Jeffrey C. Murray, MD

Portrait
Professor, Dows Institute of Dental Research
Adjunct Professor of Pediatric Dentistry
Professor of Pediatrics - Neonatology
Professor of Anatomy and Cell Biology
Professor of Biology
Professor of Epidemiology

Contact Information

Lab: 2182 ML
500 Newton Road
Iowa City, IA 52242
319-335-6897

Education

BS, Biology, Massachusetts Institute of Technology, Cambridge, Massachussetts
MD, Tufts Medical School, Boston, Massachussetts

Resident, Pediatrics, New England Medical Center Hospital
Fellow, Medical Genetics, University of Washington

Licensure and Certifications

American College of Medical Genetics, Clinical Genetics
American Board of Medical Genetics, Clinical Genetics
American Board of Pediatrics

Education/Training Program Affiliations

Interdisciplinary Graduate Program in Genetics, Interdisciplinary Graduate Program in Molecular Medicine, Interdisciplinary Graduate Program in Neuroscience, Interdisciplinary Graduate Program in Translational Biomedicine, Medical Scientist Training Program

Center, Program and Institute Affiliations

Craniofacial Research Center, Iowa Institute of Human Genetics.

Research Summary

Current projects include strategies to identify and characterize genes and environmental components in complex human disorders. We focus on conditions that affect infants and children including a common birth defect- cleft lip and palate, prematurity and two traits of young children- myopia and language development. Many of our studies are carried out using large population and epidemiologic studies of children particularly from the Philippines, Japan, Denmark, Norway, Argentina and Brazil, and we work in close collaboration with investigators in these countries. Studies of cleft lip involve using epidemiolgic databases coupled to large scale genetic evaluation (genotyping and DNA sequencing) to find how variation in normal genes affects exposure (such as smoking or poor nutrition) to induce fetal developmental abnormalities. For prematurity, a problem that affects 10% of all infants and leads to death and significant medical problems (mental retardation, blindness, deafness), we study cases and families to find genes and examine environmental triggers such as infection, stress and smoking. Our work involves collaborations with many other disciplines such as embryologists, biostatisticians and clinicians. Our lab has particular expertise in analyzing DNA from very large datasets and tying this into basic science and clinical care. In some cases we also carry out clinical trials targetted at prevention or improved treatment of these conditions. Graduate students play an active role in implementation of the studies and are often involved at many different levels of the collaboration from bench techniques to overseas coordination of sample collection.

Publications

Kaluarachchi, D. C., Smith, C. J., Klein, J. M., Murray, J. C., Dagle, J. M. & Ryckman, K. K. (2017). Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn. Pediatric Research. PMID: 28609431.

Leslie, E. J., Carlson, J. C., Shaffer, J. R., Butali, A., Buxó, C. J., Castilla, E. E., Christensen, K., Deleyiannis, F. W., Leigh Field, L., Hecht, J. T., Moreno, L., Orioli, I. M., Padilla, C., Vieira, A. R., Wehby, G. L., Feingold, E., Weinberg, S. M., Murray, J. C., Beaty, T. H. & Marazita, M. L. (2017). Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Human Genetics, 136(3), 275–286. PMID: 28054174.

Xiao, Y., Taub, M. A., Ruczinski, I., Begum, F., Hetmanski, J. B., Schwender, H., Leslie, E. J., Koboldt, D. C., Murray, J. C., Marazita, M. L. & Beaty, T. H. (2017). Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios. Genetic Epidemiology, 41(3), 244–250. PMID: 28019042.

Ersig, A. L., Schutte, D. L., Standley, J., Leslie, E., Zimmerman, B., Kleiber, C., Hanrahan, K., Murray, J. C. & McCarthy, A. M. (2017). Relationship of Genetic Variants With Procedural Pain, Anxiety, and Distress in Children. Biological Research for Nursing, 19(3), 339–349. PMID: 28413930.

Gowans, L. J., Busch, T. D., Mossey, P. A., Eshete, M. A., Adeyemo, W. L., Aregbesola, B., Donkor, P., Arthur, F. K., Agbenorku, P., Olutayo, J., Twumasi, P., Braimah, R., Oti, A. A., Plange-Rhule, G., Obiri-Yeboah, S., Abate, F., Hoyte-Williams, P. E., Hailu, T., Murray, J. C. & Butali, A. (2017). The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan Africa. Molecular Genetics & Genomic Medicine, 5(2), 164–171. PMID: 28361103.

Kutbi, H., Wehby, G. L., Moreno Uribe, L. M., Romitti, P. A., Carmichael, S., Shaw, G. M., Olshan, A. F., DeRoo, L., Rasmussen, S. A., Murray, J. C., Wilcox, A., Lie, R. T. & Munger, R. G. (2017). Maternal underweight and obesity and risk of orofacial clefts in a large international consortium of population-based studies. International Journal of Epidemiology, 46(1), 190–199. PMID: 27215617.

Carlson, J. C., Taub, M. A., Feingold, E., Beaty, T. H., Murray, J. C., Marazita, M. L. & Leslie, E. J. (2017). Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. Birth Defects Research, 109(13), 1030–1038. PMID: 28762674.

Haaland, Ø. A., Jugessur, A., Gjerdevik, M., Romanowska, J., Shi, M., Beaty, T. H., Marazita, M. L., Murray, J. C., Wilcox, A. J., Lie, R. T. & Gjessing, H. K. (2017). Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios. PloS One, 12(9), e0184358. PMID: 28898263.

Liu, H., Busch, T., Eliason, S., Anand, D., Bullard, S., Gowans, L. J., Nidey, N., Petrin, A., Augustine-Akpan, E., Saadi, I., Dunnwald, M., Lachke, S. A., Zhu, Y., Adeyemo, A., Amendt, B., Roscioli, T., Cornell, R., Murray, J. & Butali, A. (2017). Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate. Birth Defects Research, 109(1), 27–37. PMID: 28029220.

Fu, J., Beaty, T. H., Scott, A. F., Hetmanski, J., Parker, M. M., Wilson, J. E., Marazita, M. L., Mangold, E., Albacha-Hejazi, H., Murray, J. C., Bureau, A., Carey, J., Cristiano, S., Ruczinski, I. & Scharpf, R. B. (2017). Whole exome association of rare deletions in multiplex oral cleft families. Genetic Epidemiology, 41(1), 61–69. PMID: 27910131.

Gimenez, L. G., Momany, A. M., Poletta, F. A., Krupitzki, H. B., Gili, J. A., Busch, T. D., Saleme, C., Cosentino, V. R., Pawluk, M. S., Campaña, H., Gadow, E. C., Murray, J. C. & Lopez-Camelo, J. S. (2017). Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population. Pediatric Research, 82(3), 554–559. PMID: 28426651.

Lansdon, L. A., Bernabe, H. V., Nidey, N., Standley, J., Schnieders, M. J. & Murray, J. C. (2017). The Use of Variant Maps to Explore Domain-Specific Mutations of FGFR1. Journal of Dental Research, 96(11), 1339–1345. PMID: 28825856.

Moreno Uribe, L. M., Fomina, T., Munger, R. G., Romitti, P. A., Jenkins, M. M., Gjessing, H. K., Gjerdevik, M., Christensen, K., Wilcox, A. J., Murray, J. C., Lie, R. T. & Wehby, G. L. (2017). A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts. Journal of Dental Research, 96(11), 1322–1329. PMID: 28662356.

Leslie, E. J., Carlson, J. C., Shaffer, J. R., Buxó, C. J., Castilla, E. E., Christensen, K., Deleyiannis, F. W., Field, L. L., Hecht, J. T., Moreno, L., Orioli, I. M., Padilla, C., Vieira, A. R., Wehby, G. L., Feingold, E., Weinberg, S. M., Murray, J. C. & Marazita, M. L. (2017). Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. American Journal of Medical Genetics. Part A, 173(6), 1531–1538. PMID: 28425186.

Parada-Sanchez, M. T., Chu, E. Y., Cox, L. L., Undurty, S. S., Standley, J. M., Murray, J. C. & Cox, T. C. (2017). Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/Palate. Journal of Dental Research, 96(11), 1330–1338. PMID: 28767310.

Howe, B. J., Cooper, M. E., Wehby, G. L., Resick, J. M., Nidey, N. L., Valencia-Ramirez, L. C., Lopez-Palacio, A. M., Rivera, D., Vieira, A. R., Weinberg, S. M., Marazita, M. L. & Moreno Uribe, L. M. (2017). Dental Decay Phenotype in Nonsyndromic Orofacial Clefting. Journal of Dental Research, 96(10), 1106–1114. PMID: 28535364.

Smith, C. J., Ryckman, K. K., Bahr, T. M. & Dagle, J. M. (2017). Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus. Pediatric Research. PMID: 28609430.

Eshete, M. A., Liu, H., Li, M., Adeyemo, W. L., Gowans, L. J., Mossey, P. A., Busch, T., Deressa, W., Donkor, P., Olaitan, P. B., Aregbesola, B. S., Braimah, R. O., Oseni, G. O., Oginni, F., Audu, R., Onwuamah, C., James, O., Augustine-Akpan, E., Rahman, L. A., Ogunlewe, M. O., Arthur, F. K., Bello, S. A., Agbenorku, P., Twumasi, P., Abate, F., Hailu, T., Demissie, Y., Hailu, A., Plange-Rhule, G., Obiri-Yeboah, S., Dunnwald, M. M., Gravem, P. E., Marazita, M. L., Adeyemo, A. A., Murray, J. C., Cornell, R. A. & Butali, A. (2017). Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate. Journal of Dental Research, 22034517729819. PMID: 28886269.

Srinivasan, L., Page, G., Kirpalani, H., Murray, J. C., Das, A., Higgins, R. D., Carlo, W. A., Bell, E. F., Goldberg, R. N., Schibler, K., Sood, B. G., Stevenson, D. K., Stoll, B. J., Van Meurs, K. P., Johnson, K. J., Levy, J., McDonald, S. A., Zaterka-Baxter, K. M., Kennedy, K. A., Sánchez, P. J., Duara, S., Walsh, M. C., Shankaran, S., Wynn, J. L., Cotten, C. M., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2017). Genome-wide association study of sepsis in extremely premature infants. Archives of Disease in Childhood. Fetal and Neonatal Edition, 102(5), F439–F445. PMID: 28283553.

Tyrrell, J., Richmond, R. C., Palmer, T. M., Feenstra, B., Rangarajan, J., Metrustry, S., Cavadino, A., Paternoster, L., Armstrong, L. L., De Silva, N. Maneka G.,, Wood, A. R., Horikoshi, M., Geller, F., Myhre, R., Bradfield, J. P., Kreiner-Møller, E., Huikari, V., Painter, J. N., Hottenga, J., Allard, C., Berry, D. J., Bouchard, L., Das, S., Evans, D. M., Hakonarson, H., Hayes, M. G., Heikkinen, J., Hofman, A., Knight, B., Lind, P. A., McCarthy, M. I., McMahon, G., Medland, S. E., Melbye, M., Morris, A. P., Nodzenski, M., Reichetzeder, C., Ring, S. M., Sebert, S., Sengpiel, V., Sørensen, T. I., Willemsen, G., de Geus, Eco J. C.,, Martin, N. G., Spector, T. D., Power, C., Järvelin, M., Bisgaard, H., Grant, S. F., Nohr, E. A., Jaddoe, V. W., Jacobsson, B., Murray, J. C., Hocher, B., Hattersley, A. T., Scholtens, D. M., Davey Smith, G., Hivert, M., Felix, J. F., Hyppönen, E., Lowe, W. L., Frayling, T. M., Lawlor, D. A., Freathy, R. M. & Early Growth Genetics (EGG) Consortium, (2016). Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. JAMA, 315(11), 1129–1140. PMID: 26978208.

Leslie, E. J., Carlson, J. C., Shaffer, J. R., Feingold, E., Wehby, G., Laurie, C. A., Jain, D., Laurie, C. C., Doheny, K. F., McHenry, T., Resick, J., Sanchez, C., Jacobs, J., Emanuele, B., Vieira, A. R., Neiswanger, K., Lidral, A. C., Valencia-Ramirez, L. C., Lopez-Palacio, A. M., Valencia, D. R., Arcos-Burgos, M., Czeizel, A. E., Field, L. L., Padilla, C. D., Cutiongco-de la Paz, Eva Maria C., Deleyiannis, F., Christensen, K., Munger, R. G., Lie, R. T., Wilcox, A., Romitti, P. A., Castilla, E. E., Mereb, J. C., Poletta, F. A., Orioli, I. M., Carvalho, F. M., Hecht, J. T., Blanton, S. H., Buxó, C. J., Butali, A., Mossey, P. A., Adeyemo, W. L., James, O., Braimah, R. O., Aregbesola, B. S., Eshete, M. A., Abate, F., Koruyucu, M., Seymen, F., Ma, L., de Salamanca, J. E., Weinberg, S. M., Moreno, L., Murray, J. C. & Marazita, M. L. (2016). A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13. Human Molecular Genetics. PMID: 27033726.

Tyrrell, J., Richmond, R. C., Palmer, T. M., Feenstra, B., Rangarajan, J., Metrustry, S., Cavadino, A., Paternoster, L., Armstrong, L. L., De Silva, N. M., Wood, A. R., Horikoshi, M., Geller, F., Myhre, R., Bradfield, J. P., Kreiner-Møller, E., Huikari, V., Painter, J. N., Hottenga, J. J., Allard, C., Berry, D. J., Bouchard, L., Das, S., Evans, D. M., Hakonarson, H., Hayes, M. G., Heikkinen, J., Hofman, A., Knight, B., Lind, P. A., McCarthy, M. I., McMahon, G., Medland, S. E., Melbye, M., Morris, A. P., Nodzenski, M., Reichetzeder, C., Ring, S. M., Sebert, S., Sengpiel, V., Sørensen, T. I., Willemsen, G., de Geus, E. J., Martin, N. G., Spector, T. D., Power, C., Järvelin, M. R., Bisgaard, H., Grant, S. F., Nohr, E. A., Jaddoe, V. W., Jacobsson, B., Murray, J. C., Hocher, B., Hattersley, A. T., Scholtens, D. M., Davey Smith, G., Hivert, M. F., Felix, J. F., Hyppönen, E., Lowe, Jr, W. L., Frayling, T. M., Lawlor, D. A. & Freathy, R. M. (2016). Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. JAMA, 315(11), 1129-40. PMID: 26978208.

Knake, L. A., Ahuja, M., McDonald, E. L., Ryckman, K. K., Weathers, N., Burstain, T., Dagle, J. M., Murray, J. C. & Nadkarni, P. (2016). Quality of EHR data extractions for studies of preterm birth in a tertiary care center: guidelines for obtaining reliable data. BMC pediatrics, 16, 59. PMID: 27130217.

VanderMeer, J. E., Carter, T. C., Pangilinan, F., Mitchell, A., Kurnat-Thoma, E., Kirke, P. N., Troendle, J. F., Molloy, A. M., Munger, R. G., Feldkamp, M. L., Mansilla, M. A., Mills, J. L., Murray, J. C. & Brody, L. C. (2016). Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. American Journal of Medical Genetics. Part A, 170A(4), 1007–1016. PMID: 26789141.

Sampath, V., Helbling, D., Menden, H., Dimmock, D., Mulrooney, N. P., Murray, J. C., Dagle, J. M. & Garland, J. S. (2016). Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants. Journal of Pediatric Gastroenterology and Nutrition, 62(3), 420–423. PMID: 26426434.

Pedersen, D. A., Wehby, G. L., Murray, J. C. & Christensen, K. (2016). Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study. PloS One, 11(5), e0156261. PMID: 27223812.

Liu, H., Leslie, E. J., Jia, Z., Smith, T., Eshete, M., Butali, A., Dunnwald, M., Murray, J. & Cornell, R. A. (2016). Irf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate. Human Molecular Genetics, 25(4), 766–776. PMID: 26692521.

Kesterke, M. J., Raffensperger, Z. D., Heike, C. L., Cunningham, M. L., Hecht, J. T., Kau, C. H., Nidey, N. L., Moreno, L. M., Wehby, G. L., Marazita, M. L. & Weinberg, S. M. (2016). Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adults. Biology of Sex Differences, 7, 23. PMID: 27110347.

Leslie, E. J., Liu, H., Carlson, J. C., Shaffer, J. R., Feingold, E., Wehby, G., Laurie, C. A., Jain, D., Laurie, C. C., Doheny, K. F., McHenry, T., Resick, J., Sanchez, C., Jacobs, J., Emanuele, B., Vieira, A. R., Neiswanger, K., Standley, J., Czeizel, A. E., Deleyiannis, F., Christensen, K., Munger, R. G., Lie, R. T., Wilcox, A., Romitti, P. A., Field, L. L., Padilla, C. D., Cutiongco-de la Paz, Eva Maria C.,, Lidral, A. C., Valencia-Ramirez, L. C., Lopez-Palacio, A. M., Valencia, D. R., Arcos-Burgos, M., Castilla, E. E., Mereb, J. C., Poletta, F. A., Orioli, I. M., Carvalho, F. M., Hecht, J. T., Blanton, S. H., Buxó, C. J., Butali, A., Mossey, P. A., Adeyemo, W. L., James, O., Braimah, R. O., Aregbesola, B. S., Eshete, M. A., Deribew, M., Koruyucu, M., Seymen, F., Ma, L., de Salamanca, J. E., Weinberg, S. M., Moreno, L., Cornell, R. A., Murray, J. C. & Marazita, M. L. (2016). A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. American Journal of Human Genetics, 98(4), 744–754. PMID: 27018472.

Knake, L. A., Ahuja, M., McDonald, E. L., Ryckman, K. K., Weathers, N., Burstain, T., Dagle, J. M., Murray, J. C. & Nadkarni, P. (2016). Quality of EHR data extractions for studies of preterm birth in a tertiary care center: guidelines for obtaining reliable data. BMC pediatrics, 16(1), 59. PMID: 27130217.

Leslie, E. J., Koboldt, D. C., Kang, C. J., Ma, L., Hecht, J. T., Wehby, G. L., Christensen, K., Czeizel, A. E., Deleyiannis, F. W., Fulton, R. S., Wilson, R. K., Beaty, T. H., Schutte, B. C., Murray, J. C. & Marazita, M. L. (2016). IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. Clinical Genetics, 90(1), 28-34. DOI: 10.1111/cge.12675.

Ryckman, K. K., Bedell, B., Bodker, F., Li, J., Liu, H., Zhang, J., Breheny, P., Christensen, K., Dagle, J. M. & Murray, J. C. (2016). Whole exome sequencing identifies rare variants implicated in preterm birth. American Journal of Obstetrics and Gynecology, 214(1), S55–S55.

Mueller, K. L., Murray, J. C., Michaelson, J. J., Christiansen, M. H., Reilly, S. & Tomblin, J. B. (2016). Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development. PloS One, 11(4), e0152576. PMID: 27064276.

Frost, L., Hinton, R., Pratt, B. A., Murray, J., Arscott-Mills, S., Jack, S., de Francisco, A. & Kuruvilla, S. (2016). Using multistakeholder dialogues to assess policies, programmes and progress for women’s, children’s and adolescents’ health. Bulletin of the World Health Organization, 94(5), 393–395. PMID: 27147770.

Leslie, E. J., Carlson, J. C., Shaffer, J. R., Feingold, E., Wehby, G., Laurie, C. A., Jain, D., Laurie, C. C., Doheny, K. F., McHenry, T., Resick, J., Sanchez, C., Jacobs, J., Emanuele, B., Vieira, A. R., Neiswanger, K., Lidral, A. C., Valencia-Ramirez, L. C., Lopez-Palacio, A. M., Valencia, D. R., Arcos-Burgos, M., Czeizel, A. E., Field, L. L., Padilla, C. D., Cutiongco-de la Paz, Eva Maria C.,, Deleyiannis, F., Christensen, K., Munger, R. G., Lie, R. T., Wilcox, A., Romitti, P. A., Castilla, E. E., Mereb, J. C., Poletta, F. A., Orioli, I. M., Carvalho, F. M., Hecht, J. T., Blanton, S. H., Buxó, C. J., Butali, A., Mossey, P. A., Adeyemo, W. L., James, O., Braimah, R. O., Aregbesola, B. S., Eshete, M. A., Abate, F., Koruyucu, M., Seymen, F., Ma, L., de Salamanca, J. E., Weinberg, S. M., Moreno, L., Murray, J. C. & Marazita, M. L. (2016). A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13. Human Molecular Genetics, 25(13), 2862–2872. PMID: 27033726.

Shaffer, J. R., Orlova, E., Lee, M. K., Leslie, E. J., Raffensperger, Z. D., Heike, C. L., Cunningham, M. L., Hecht, J. T., Kau, C. H., Nidey, N. L., Moreno, L. M., Wehby, G. L., Murray, J. C., Laurie, C. A., Laurie, C. C., Cole, J., Ferrara, T., Santorico, S., Klein, O., Mio, W., Feingold, E., Hallgrimsson, B., Spritz, R. A., Marazita, M. L. & Weinberg, S. M. (2016). Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. PLoS genetics, 12(8), e1006149. PMID: 27560520.

Patel, P. M., Momany, A. M., Schaa, K. L., Romitti, P. A., Druschel, C., Cooper, M. E., Marazita, M. L., Murray, J. C. & Dagle, J. M. (2016). Genetic Modifiers of Patent Ductus Arteriosus in Term Infants. The Journal of Pediatrics, 176, 57–61.e1. PMID: 27344223.

Gimenez, L. G., Krupitzki, H. B., Momany, A. M., Gili, J. A., Poletta, F. A., Campaña, H., Cosentino, V. R., Saleme, C., Pawluk, M., Murray, J. C., Castilla, E. E., Gadow, E. C. & Lopez-Camelo, J. S. (2016). Maternal and neonatal epidemiological features in clinical subtypes of preterm birth. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetr, 29(19), 3153–3161. PMID: 26701680.

Weinberg, S. M., Raffensperger, Z. D., Kesterke, M. J., Heike, C. L., Cunningham, M. L., Hecht, J. T., Kau, C. H., Murray, J. C., Wehby, G. L., Moreno, L. M. & Marazita, M. L. (2016). The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 53(6), e185–e197. PMID: 26492185.

Gowans, L. J., Adeyemo, W. L., Eshete, M., Mossey, P. A., Busch, T., Aregbesola, B., Donkor, P., Arthur, F. K., Bello, S. A., Martinez, A., Li, M., Augustine-Akpan, E. A., Deressa, W., Twumasi, P., Olutayo, J., Deribew, M., Agbenorku, P., Oti, A. A., Braimah, R., Plange-Rhule, G., Gesses, M., Obiri-Yeboah, S., Oseni, G. O., Olaitan, P. B., Abdur-Rahman, L., Abate, F., Hailu, T., Gravem, P., Ogunlewe, M. O., Buxó, C. J., Marazita, M. L., Adeyemo, A. A., Murray, J. C. & Butali, A. (2016). Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations. Journal of Dental Research, 95(11), 1245–1256. PMID: 27369588.

Wallenstein, M. B., Jelliffe-Pawlowski, L. L., Yang, W., Carmichael, S. L., Stevenson, D. K., Ryckman, K. K. & Shaw, G. M. (2016). Inflammatory biomarkers and spontaneous preterm birth among obese women. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetr, 29(20), 3317–3322. PMID: 26700828.

Kaluarachchi, D. C., Momany, A. M., Busch, T. D., Gimenez, L. G., Saleme, C., Cosentino, V., Christensen, K., Dagle, J. M., Ryckman, K. K. & Murray, J. C. (2016). Polymorphisms in NR5A2, gene encoding liver receptor homolog-1 are associated with preterm birth. Pediatric Research, 79(5), 776–780. PMID: 26761123.

Leslie, E. J., Koboldt, D. C., Kang, C. J., Ma, L., Hecht, J. T., Wehby, G. L., Christensen, K., Czeizel, A. E., Deleyiannis, F. W., Fulton, R. S., Wilson, R. K., Beaty, T. H., Schutte, B. C., Murray, J. C. & Marazita, M. L. (2016). IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. Clinical Genetics, 90(1), 28–34. PMID: 26346622.

Kutbi, H., Wehby, G. L., Moreno Uribe, L. M., Romitti, P. A., Carmichael, S., Shaw, G. M., Olshan, A. F., DeRoo, L., Rasmussen, S. A., Murray, J. C., Wilcox, A., Lie, R. T. & Munger, R. G. (2016). Maternal underweight and obesity and risk of orofacial clefts in a large international consortium of population-based studies. International Journal of Epidemiology. PMID: 27215617.

Patel, P. M., Momany, A. M., Schaa, K. L., Romitti, P. A., Druschel, C., Cooper, M. E., Marazita, M. L., Murray, J. C. & Dagle, J. M. (2016). Genetic Modifiers of Patent Ductus Arteriosus in Term Infants. The Journal of Pediatrics. PMID: 27344223.

Ahmed, S. M., Rawal, L. B., Chowdhury, S. A., Murray, J., Arscott-Mills, S., Jack, S., Hinton, R., Alam, P. M. & Kuruvilla, S. (2016). Cross-country analysis of strategies for achieving progress towards global goals for women’s and children’s health. Bulletin of the World Health Organization, 94(5), 351–361. PMID: 27147765.

Jumbe, N. L., Murray, J. C. & Kern, S. (2016). Data Sharing and Inductive Learning–Toward Healthy Birth, Growth, and Development. The New England Journal of Medicine, 374(25), 2415–2417. PMID: 27168111.

Ambalavanan, N., Cotten, C. M., Page, G. P., Carlo, W. A., Murray, J. C., Bhattacharya, S., Mariani, T. J., Cuna, A. C., Faye-Petersen, O. M., Kelly, D. & Higgins, R. D. (2015). Integrated genomic analyses in bronchopulmonary dysplasia. The Journal of pediatrics, 166(3), 531-7.e13. PMID: 25449221.

Wolf, Z. T., Brand, H. A., Shaffer, J. R., Leslie, E. J., Arzi, B., Willet, C. E., Cox, T. C., McHenry, T., Narayan, N., Feingold, E., Wang, X., Sliskovic, S., Karmi, N., Safra, N., Sanchez, C., Deleyiannis, F. W., Murray, J. C., Wade, C. M., Marazita, M. L. & Bannasch, D. L. (2015). Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. PLoS genetics, 11(3), e1005059. PMID: 25798845.

Locke, A. E., Kahali, B., Berndt, S. I., Justice, A. E., Pers, T. H., Day, F. R., Powell, C., Vedantam, S., Buchkovich, M. L., Yang, J., Croteau-Chonka, D. C., Esko, T., Fall, T., Ferreira, T., Gustafsson, S., Kutalik, Z., Luan, J., Mägi, R., Randall, J. C., Winkler, T. W., Wood, A. R., Workalemahu, T., Faul, J. D., Smith, J. A., Hua Zhao, J., Zhao, W., Chen, J., Fehrmann, R., Hedman, Å. K., Karjalainen, J., Schmidt, E. M., Absher, D., Amin, N., Anderson, D., Beekman, M., Bolton, J. L., Bragg-Gresham, J. L., Buyske, S., Demirkan, A., Deng, G., Ehret, G. B., Feenstra, B., Feitosa, M. F., Fischer, K., Goel, A., Gong, J., Jackson, A. U., Kanoni, S., Kleber, M. E., Kristiansson, K., Lim, U., Lotay, V., Mangino, M., Mateo Leach, I., Medina-Gomez, C., Medland, S. E., Nalls, M. A., Palmer, C. D., Pasko, D., Pechlivanis, S., Peters, M. J., Prokopenko, I., Shungin, D., Stancáková, A., Strawbridge, R. J., Ju Sung, Y., Tanaka, T., Teumer, A., Trompet, S., van der Laan, S. 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J., Hveem, K., Kaplan, R. C., Kivimaki, M., Kuh, D., Laakso, M., Liu, Y., Martin, N. G., März, W., Melbye, M., Metspalu, A., Moebus, S., Munroe, P. B., Njølstad, I., Oostra, B. A., Palmer, C. N., Pedersen, N. L., Perola, M., Pérusse, L., Peters, U., Power, C., Quertermous, T., Rauramaa, R., Rivadeneira, F., Saaristo, T. E., Saleheen, D., Sattar, N., Schadt, E. E., Schlessinger, D., Slagboom, P. E., Snieder, H., Spector, T. D., Thorsteinsdottir, U., Stumvoll, M., Tuomilehto, J., Uitterlinden, A. G., Uusitupa, M., van der Harst, P., Walker, M., Wallaschofski, H., Wareham, N. J., Watkins, H., Weir, D. R., Wichmann, H. E., Wilson, J. F., Zanen, P., Borecki, I. B., Deloukas, P., Fox, C. S., Heid, I. M., O'Connell, J. R., Strachan, D. P., Stefansson, K., van Duijn, C. M., Abecasis, G. R., Franke, L., Frayling, T. M., McCarthy, M. I., Visscher, P. M., Scherag, A., Willer, C. J., Boehnke, M., Mohlke, K. L., Lindgren, C. M., Beckmann, J. S., Barroso, I., North, K. E., Ingelsson, E., Hirschhorn, J. N., Loos, R. J. & Speliotes, E. K. (2015). Genetic studies of body mass index yield new insights for obesity biology. Nature, 518(7538), 197-206. PMID: 25673413.

Ambalavanan, N., Cotten, C. M., Page, G. P., Carlo, W. A., Murray, J. C., Bhattacharya, S., Mariani, T. J., Cuna, A. C., Faye-Petersen, O. M., Kelly, D., Higgins, R. D., Genomics,, Cytokine Subcommittees of the Eunice Kennedy Shriver National Institute of,, Health, C. & Human Development Neonatal Research Network, (2015). Integrated genomic analyses in bronchopulmonary dysplasia. The Journal of Pediatrics, 166(3), 531–537.e13. PMID: 25449221.

Fuller, T. D., Spracklen, C. N., Ryckman, K. K., Knake, L. A., Busch, T. D., Momany, A. M., Murray, J. C. & Dagle, J. M. (2015). Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy. Pediatric research, 77(3), 472-6. PMID: 25521918.

Van 't Erve, T. J., Wagner, B. A., Martin, S. M., Knudson, C. M., Blendowski, R., Keaton, M., Holt, T., Hess, J. R., Buettner, G. R., Ryckman, K. K., Darbro, B. W., Murray, J. C. & Raife, T. J. (2015). The heritability of hemolysis in stored human red blood cells. Transfusion. PMID: 25644965.

Leslie, E. J., Taub, M. A., Liu, H., Steinberg, K. M., Koboldt, D. C., Zhang, Q., Carlson, J. C., Hetmanski, J. B., Wang, H., Larson, D. E., Fulton, R. S., Kousa, Y. A., Fakhouri, W. D., Naji, A., Ruczinski, I., Begum, F., Parker, M. M., Busch, T., Standley, J., Rigdon, J., Hecht, J. T., Scott, A. F., Wehby, G. L., Christensen, K., Czeizel, A. E., Deleyiannis, F. W., Schutte, B. C., Wilson, R. K., Cornell, R. A., Lidral, A. C., Weinstock, G. M., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2015). Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American Journal of Human Genetics, 96(3), 397–411. PMID: 25704602.

Sampath, V., Garland, J. S., Helbling, D., Dimmock, D., Mulrooney, N. P., Simpson, P. M., Murray, J. C. & Dagle, J. M. (2015). Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants. Pediatric research, 77(3), 477-83. PMID: 25518008.

Wolf, Z. T., Brand, H. A., Shaffer, J. R., Leslie, E. J., Arzi, B., Willet, C. E., Cox, T. C., McHenry, T., Narayan, N., Feingold, E., Wang, X., Sliskovic, S., Karmi, N., Safra, N., Sanchez, C., Deleyiannis, F. W., Murray, J. C., Wade, C. M., Marazita, M. L. & Bannasch, D. L. (2015). Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. PLoS genetics, 11(3), e1005059. PMID: 25798845.

Pers, T. H., Karjalainen, J. M., Chan, Y., Westra, H., Wood, A. R., Yang, J., Lui, J. C., Vedantam, S., Gustafsson, S., Esko, T., Frayling, T., Speliotes, E. K., Genetic Investigation of ANthropometric Traits (GIANT) Consortium,, Boehnke, M., Raychaudhuri, S., Fehrmann, R. S., Hirschhorn, J. N. & Franke, L. (2015). Biological interpretation of genome-wide association studies using predicted gene functions. Nature Communications, 6, 5890. PMID: 25597830.

Olsen, D. S., Goar, W. A., Nichols, B. A., Bailey, K. T., Christensen, S. L., Merriam, K. R., Reynolds, P. R., Wilson, E., Weber, K. S. & Bridgewater, L. C. (2015). Targeted Mutation of Nuclear Bone Morphogenetic Protein 2 Impairs Secondary Immune Response in a Mouse Model. BioMed Research International, 2015, 975789. PMID: 26491697.

Myers, H. I., Spracklen, C. N., Ryckman, K. K. & Murray, J. C. (2015). A retrospective study of administration of vaccination for hepatitis B among newborn infants prior to hospital discharge at a midwestern tertiary care center. Vaccine, 33(20), 2316-21. PMID: 25835577.

Fuller, T. D., Spracklen, C. N., Ryckman, K. K., Knake, L. A., Busch, T. D., Momany, A. M., Murray, J. C. & Dagle, J. M. (2015). Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy. Pediatric Research, 77(3), 472–476. PMID: 25521918.

Ment, L. R., Ådén, U., Bauer, C. R., Bada, H. S., Carlo, W. A., Kaiser, J. R., Lin, A., Cotten, C. M., Murray, J., Page, G., Hallman, M., Lifton, R. P., Zhang, H., Bryant, C., Cassady, C., Garcia, C., Johnson, Y. R., Karpen, H. E., Munden, M. M., Shores, G., Cassese, J., Hensman, A. M., Vieira, E., Vohr, B., Wallach, M., Cummings, J. J., MacGilvray, S. S., Moseley, S., Trapanotto, V., Poindexter, B., Wilson, L. D., Wright-Coltart, S., Bartocci, M., Printz, G., Hopper, A., Smith, L., Wood, B. P., Young, L., Allan, W. C., Alfsson, J., Sävman, K., Royal, S. A., Young, D. W., Cosby, S., Helms, C., Angtuaco, T., Carol Sikes, N., Mason, M. J., Whit Hall, R., Bada, H., Challa, H. R., Grider, D., Kriss, V., Whitehead, V., Abdenour, G., Bauer, C., Danton, G., Montesinos, D., Gaurav, S., Philias, W., Teomete, U., Barks, J., Christensen, M., Sanchez, R., Sieg, M., Wiggins, S., Fuller, J., Hartenberger, C., Montman, R., Williams, J. B., Williamson, S., Bose, C., Clark, C. L., Laughon, M., Abbasi, S., Cook, N. M., Mancini, T., Chaudhary, A., DeMauro, C., Schmidt, B., Dean, E., Eyal, F., Maertens, P., Boulden, T. F., Cohen, H. L., Dempsey, S., LeNoue, P., Pourcyrous, M., Bird, K., Faix, R. G., Hedlund, G., Moore, K., Osborne, K., Weaver-Lewis, K., Yoder, B. A., Mayock, D. E., Dighe, M., Brown, P. L., Michael O’Shea, T., Peters, N. & others (2015). Genes and environment in neonatal intraventricular hemorrhage. Seminars in Perinatology, 39(8), 592-603. DOI: 10.1053/j.semperi.2015.09.006.

Zhang, H., Baldwin, D. A., Bukowski, R. K., Parry, S., Xu, Y., Song, C., Andrews, W. W., Saade, G. R., Esplin, M. S., Sadovsky, Y., Reddy, U. M., Ilekis, J., Varner, M., Biggio, J. R., Archer, S. W., Copper, R. L., Files, P. B., Harris, S. L., Blair, I., Leite, R., Zimmerle, M. L., Brandon, J. L., Jordan, S., Jones, A., Vorwaller, K., Quinn, S., Morby, V. S., Jolley, K. N., Postma, J. A., Cheung, K. H., Del, B. D., Guo, X., Hu, B., Huang, H., Jin, L., Lin, A. L., Lu, C. C., Ment, L., Perley, L., Simone, L. J., Xiao, F., Rouse, D. J., Allard, D., Wapner, R., Divito, M., Bousleiman, S., Carmona, V., Alcon, R., Saravia, K., Kalemi, L., Talucci, M., Plante, L., Reid, Z., Tocci, C., Sherwood, M., Hoffman, M., Lynch, S., Bayless, A., Benson, J., Mann, J., Grossman, T., Lort, S., Vanneman, A., Lockhart, E., Kitto, C., Guzman, E., Lake, M., Davis, S., Falk, M., Perez, C., Peaceman, A. M., Stein, L., Arego, K., Ramos-Brinson, M., Mallett, G., Thorp, J. M., Dorman, K., Brody, S., Johnson, L. B., Blackwell, S. C., Hutchinson, M., Gregg, A., Cato, R. P., Clemons, T., Ghidini, A., Hirsch, E., Murray, J., Petricoin, E., Signore, C., Sing, C. F. & Wang, X. (2015). A Genome-Wide Association Study of Early Spontaneous Preterm Delivery. Genetic Epidemiology, 39(3), 217-226. DOI: 10.1002/gepi.21887.

Pitlick, M. M., Orr, K., Momany, A. M., McDonald, E. L. & Ryckman, K. K. (2015). Determining the prevalence of cytomegalovirus infection in a cohort of preterm infants. Journal of Neonatal-Perinatal Medicine, 8(4), 427. PMID: 26836826.

Li, Q., Kappil, M. A., Li, A., Dassanayake, P. S., Darrah, T. H., Friedman, A. E., Friedman, M., Lambertini, L., Landrigan, P., Stodgell, C. J., Xia, Y., Nanes, J. A., Aagaard, K. M., Schadt, E. E., Murray, J. C., Clark, E. B., Dole, N., Culhane, J., Swanson, J., Varner, M., Moye, J., Kasten, C., Miller, R. K. & Chen, J. (2015). Exploring the associations between microRNA expression profiles and environmental pollutants in human placenta from the National Children’s Study (NCS). Epigenetics, 10(9), 793–802. PMID: 26252056.

Rysavy, M. A., Li, L., Bell, E. F., Das, A., Hintz, S. R., Stoll, B. J., Vohr, B. R., Carlo, W. A., Shankaran, S., Walsh, M. C., Tyson, J. E., Cotten, C. M., Smith, P. B., Murray, J. C., Colaizy, T. T., Brumbaugh, J. E. & Higgins, R. D. (2015). Between-hospital variation in treatment and outcomes in extremely preterm infants. The New England journal of medicine, 372(19), 1801-11. PMID: 25946279.

Van ’t Erve, Thomas J.,, Wagner, B. A., Martin, S. M., Knudson, C. M., Blendowski, R., Keaton, M., Holt, T., Hess, J. R., Buettner, G. R., Ryckman, K. K., Darbro, B. W., Murray, J. C. & Raife, T. J. (2015). The heritability of hemolysis in stored human red blood cells. Transfusion, 55(6), 1178–1185. PMID: 25644965.

Li, Q., Kappil, M. A., Li, A., Dassanayake, P. S., Darrah, T. H., Friedman, A. E., Friedman, M., Lambertini, L., Landrigan, P., Stodgell, C. J., Xia, Y., Nanes, J. A., Aagaard, K. M., Schadt, E. E., Murray, J. C., Clark, E. B., Dole, N., Culhane, J., Swanson, J., Varner, M., Moye, J., Kasten, C., Miller, R. K. & Chen, J. (2015). Exploring the associations between microRNA expression profiles and environmental pollutants in human placenta from the National Children’s Study (NCS). Epigenetics, 10(9), 793–802. DOI: 10.1080/15592294.2015.1066960.

Butali, A., Mossey, P. A., Adeyemo, W. L., Mekonen, E., Gaines, L. A., Busch, T., Braimoh, R. O., Aregbesola, S. B., Rigdon, J., Emeka, C., James, O. O., Ogunlewe, M. O., Ladeinde, A. L., Abate, F., Hailu, T., Mohammed, I., Gravem, P. E., Adeyemo, A. A., Marazita, M. & Murray, J. C. (2015). Genome-wide Association Identified Candidate Genes Analysis for Non-syndromic Clefts in Two African Populations. American Journal of Medical Genetics Part A, 167(7), 1463–1464.

Rysavy, M. A., Li, L., Bell, E. F., Das, A., Hintz, S. R., Stoll, B. J., Vohr, B. R., Carlo, W. A., Shankaran, S., Walsh, M. C., Tyson, J. E., Cotten, C. M., Smith, P. B., Murray, J. C., Colaizy, T. T., Brumbaugh, J. E. & Higgins, R. D. (2015). Between-Hospital Variation in Treatment and Outcomes in Extremely Preterm Infants. Obstetrical & Gynecological Survey, 70(9), 549–551. DOI: 10.1097/01.ogx.0000471596.46762.bf.

Winkler, T. W., Justice, A. E., Graff, M., Barata, L., Feitosa, M. F., Chu, S., Czajkowski, J., Esko, T., Fall, T., Kilpeläinen, T. O., Lu, Y., Mägi, R., Mihailov, E., Pers, T. H., Rüeger, S., Teumer, A., Ehret, G. B., Ferreira, T., Heard-Costa, N. L., Karjalainen, J., Lagou, V., Mahajan, A., Neinast, M. D., Prokopenko, I., Simino, J., Teslovich, T. M., Jansen, R., Westra, H., White, C. C., Absher, D., Ahluwalia, T. S., Ahmad, S., Albrecht, E., Alves, A. C., Bragg-Gresham, J. L., de Craen, Anton J. M.,, Bis, J. C., Bonnefond, A., Boucher, G., Cadby, G., Cheng, Y., Chiang, C. W., Delgado, G., Demirkan, A., Dueker, N., Eklund, N., Eiriksdottir, G., Eriksson, J., Feenstra, B., Fischer, K., Frau, F., Galesloot, T. E., Geller, F., Goel, A., Gorski, M., Grammer, T. B., Gustafsson, S., Haitjema, S., Hottenga, J., Huffman, J. E., Jackson, A. U., Jacobs, K. B., Johansson, Å., Kaakinen, M., Kleber, M. E., Lahti, J., Mateo Leach, I., Lehne, B., Liu, Y., Lo, K. S., Lorentzon, M., Luan, J., Madden, P. A., Mangino, M., McKnight, B., Medina-Gomez, C., Monda, K. L., Montasser, M. E., Müller, G., Müller-Nurasyid, M., Nolte, I. M., Panoutsopoulou, K., Pascoe, L., Paternoster, L., Rayner, N. W., Renström, F., Rizzi, F., Rose, L. M., Ryan, K. A., Salo, P., Sanna, S., Scharnagl, H., Shi, J., Smith, A. V., Southam, L., Stancáková, A., Steinthorsdottir, V., Strawbridge, R. J., Sung, Y. J., Tachmazidou, I., Tanaka, T., Thorleifsson, G., Trompet, S., Pervjakova, N., Tyrer, J. P., Vandenput, L., van der Laan, Sander W.,, van der Velde, N., van Setten, J., van Vliet-Ostaptchouk, J. V., Verweij, N., Vlachopoulou, E., Waite, L. L., Wang, S. R., Wang, Z., Wild, S. H., Willenborg, C., Wilson, J. F., Wong, A., Yang, J., Yengo, L., Yerges-Armstrong, L. M., Yu, L., Zhang, W., Zhao, J. H., Andersson, E. A., Bakker, S. J., Baldassarre, D., Banasik, K., Barcella, M., Barlassina, C., Bellis, C., Benaglio, P., Blangero, J., Blüher, M., Bonnet, F., Bonnycastle, L. L., Boyd, H. A., Bruinenberg, M., Buchman, A. S., Campbell, H., Chen, Y. I., Chines, P. S., Claudi-Boehm, S., Cole, J., Collins, F. S., de Geus, Eco J. C.,, de Groot, Lisette C. P. G. M.,, Dimitriou, M., Duan, J., Enroth, S., Eury, E., Farmaki, A., Forouhi, N. G., Friedrich, N., Gejman, P. V., Gigante, B., Glorioso, N., Go, A. S., Gottesman, O., Gräßler, J., Grallert, H., Grarup, N., Gu, Y., Broer, L., Ham, A. C., Hansen, T., Harris, T. B., Hartman, C. A., Hassinen, M., Hastie, N., Hattersley, A. T., Heath, A. C., Henders, A. K., Hernandez, D., Hillege, H., Holmen, O., Hovingh, K. G., Hui, J., Husemoen, L. L., Hutri-Kähönen, N., Hysi, P. G., Illig, T., De Jager, P. L., Jalilzadeh, S., Jørgensen, T., Jukema, J. W., Juonala, M., Kanoni, S., Karaleftheri, M., Khaw, K. T., Kinnunen, L., Kittner, S. J., Koenig, W., Kolcic, I., Kovacs, P., Krarup, N. T., Kratzer, W., Krüger, J., Kuh, D., Kumari, M., Kyriakou, T., Langenberg, C., Lannfelt, L., Lanzani, C., Lotay, V., Launer, L. J., Leander, K., Lindström, J., Linneberg, A., Liu, Y., Lobbens, S., Luben, R., Lyssenko, V., Männistö, S., Magnusson, P. K., McArdle, W. L., Menni, C., Merger, S., Milani, L., Montgomery, G. W., Morris, A. P., Narisu, N., Nelis, M., Ong, K. K., Palotie, A., Pérusse, L., Pichler, I., Pilia, M. G., Pouta, A., Rheinberger, M., Ribel-Madsen, R., Richards, M., Rice, K. M., Rice, T. K., Rivolta, C., Salomaa, V., Sanders, A. R., Sarzynski, M. A., Scholtens, S., Scott, R. A., Scott, W. R., Sebert, S., Sengupta, S., Sennblad, B., Seufferlein, T., Silveira, A., Slagboom, P. E., Smit, J. H., Sparsø, T. H., Stirrups, K., Stolk, R. P., Stringham, H. M., Swertz, M. A., Swift, A. J., Syvänen, A., Tan, S., Thorand, B., Tönjes, A., Tremblay, A., Tsafantakis, E., van der Most, Peter J.,, Völker, U., Vohl, M., Vonk, J. M., Waldenberger, M., Walker, R. W., Wennauer, R., Widén, E., Willemsen, G., Wilsgaard, T., Wright, A. F., Zillikens, M. C., van Dijk, S. C., van Schoor, N. M., Asselbergs, F. W., de Bakker, Paul I. W.,, Beckmann, J. S., Beilby, J., Bennett, D. A., Bergman, R. N., Bergmann, S., Böger, C. A., Boehm, B. O., Boerwinkle, E., Boomsma, D. I., Bornstein, S. R., Bottinger, E. P., Bouchard, C., Chambers, J. C., Chanock, S. J., Chasman, D. I., Cucca, F., Cusi, D., Dedoussis, G., Erdmann, J., Eriksson, J. G., Evans, D. A., de Faire, U., Farrall, M., Ferrucci, L., Ford, I., Franke, L., Franks, P. W., Froguel, P., Gansevoort, R. T., Gieger, C., Grönberg, H., Gudnason, V., Gyllensten, U., Hall, P., Hamsten, A., van der Harst, P., Hayward, C., Heliövaara, M., Hengstenberg, C., Hicks, A. A., Hingorani, A., Hofman, A., Hu, F., Huikuri, H. V., Hveem, K., James, A. L., Jordan, J. M., Jula, A., Kähönen, M., Kajantie, E., Kathiresan, S., Kiemeney, Lambertus A. L. M.,, Kivimaki, M., Knekt, P. B., Koistinen, H. A., Kooner, J. S., Koskinen, S., Kuusisto, J., Maerz, W., Martin, N. G., Laakso, M., Lakka, T. A., Lehtimäki, T., Lettre, G., Levinson, D. F., Lind, L., Lokki, M., Mäntyselkä, P., Melbye, M., Metspalu, A., Mitchell, B. D., Moll, F. L., Murray, J. C., Musk, A. W., Nieminen, M. S., Njølstad, I., Ohlsson, C., Oldehinkel, A. J., Oostra, B. A., Palmer, L. J., Pankow, J. S., Pasterkamp, G., Pedersen, N. L., Pedersen, O., Penninx, B. W., Perola, M., Peters, A., Polašek, O., Pramstaller, P. P., Psaty, B. M., Qi, L., Quertermous, T., Raitakari, O. T., Rankinen, T., Rauramaa, R., Ridker, P. M., Rioux, J. D., Rivadeneira, F., Rotter, J. I., Rudan, I., den Ruijter, H. M., Saltevo, J., Sattar, N., Schunkert, H., Schwarz, P. E., Shuldiner, A. R., Sinisalo, J., Snieder, H., Sørensen, T. I., Spector, T. D., Staessen, J. A., Stefania, B., Thorsteinsdottir, U., Stumvoll, M., Tardif, J., Tremoli, E., Tuomilehto, J., Uitterlinden, A. G., Uusitupa, M., Verbeek, A. L., Vermeulen, S. H., Viikari, J. S., Vitart, V., Völzke, H., Vollenweider, P., Waeber, G., Walker, M., Wallaschofski, H., Wareham, N. J., Watkins, H., Zeggini, E., Consortium, C., Consortium, D., Consortium, G., Consortium, G., Consortium, I., Consortium, M., Chakravarti, A., Clegg, D. J., Cupples, L. A., Gordon-Larsen, P., Jaquish, C. E., Rao, D. C., Abecasis, G. R., Assimes, T. L., Barroso, I., Berndt, S. I., Boehnke, M., Deloukas, P., Fox, C. S., Groop, L. C., Hunter, D. J., Ingelsson, E., Kaplan, R. C., McCarthy, M. I., Mohlke, K. L., O’Connell, J. R., Schlessinger, D., Strachan, D. P., Stefansson, K., van Duijn, C. M., Hirschhorn, J. N., Lindgren, C. M., Heid, I. M., North, K. E., Borecki, I. B., Kutalik, Z. & Loos, R. J. (2015). The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS genetics, 11(10), e1005378. PMID: 26426971.

Leslie, E. J., O’Sullivan, J., Cunningham, M. L., Singh, A., Goudy, S. L., Ababneh, F., Alsubaie, L., Ch’ng, G., van der Laar, Ingrid M. B. H.,, Hoogeboom, A. J., Dunnwald, M., Kapoor, S., Jiramongkolchai, P., Standley, J., Manak, J. R., Murray, J. C. & Dixon, M. J. (2015). Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders. American Journal of Medical Genetics. Part A, 167A(3), 545–552. PMID: 25691407.

Gimenez, L. G., Krupitzki, H. B., Momany, A. M., Gili, J. A., Poletta, F. A., Campaña, H., Cosentino, V. R., Saleme, C., Pawluk, M., Murray, J. C., Castilla, E. E., Gadow, E. C. & Lopez-Camelo, J. S. (2015). Maternal and neonatal epidemiological features in clinical subtypes of preterm birth. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetr, 1–9. PMID: 26701680.

Borowski, K. S., Clark, E. a., Lai, Y., Wapner, R. J., Sorokin, Y., Peaceman, A. M., Iams, J. D., Leveno, K. J., Harper, M., Caritis, S. N., Miodovnik, M., Mercer, B. M., Thorp, J. M., O’Sullivan, M. J., Ramin, S. M., Carpenter, M. W., Rouse, D. J., Sibai, B., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Maternal-Fetal Medicine Units Network, (2015). Neonatal Genetic Variation in Steroid Metabolism and Key Respiratory Function Genes and Perinatal Outcomes in Single and Multiple Courses of Corticosteroids. American Journal of Perinatology, 32(12), 1126–1132. PMID: 26445141.

Ment, L. R., Ådén, U., Bauer, C. R., Bada, H. S., Carlo, W. A., Kaiser, J. R., Lin, A., Cotten, C. M., Murray, J., Page, G., Hallman, M., Lifton, R. P., Zhang, H., Gene Targets for IVH Study Group, & Network, t. N. (2015). Genes and environment in neonatal intraventricular hemorrhage. Seminars in Perinatology, 39(8), 592–603. PMID: 26516117.

Jia, Z., Leslie, E. J., Cooper, M. E., Butali, A., Standley, J., Rigdon, J., Suzuki, S., Gongorjav, A., Shonkhuuz, T. E., Natsume, N., Shi, B., Marazita, M. L. & Murray, J. C. (2015). Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans. American Journal of Medical Genetics. Part A, 167A(5), 1054–1060. PMID: 25786657.

Sampath, V., Garland, J. S., Helbling, D., Dimmock, D., Mulrooney, N. P., Simpson, P. M., Murray, J. C. & Dagle, J. M. (2015). Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants. Pediatric Research, 77(3), 477–483. PMID: 25518008.

Machiela, M. J., Zhou, W., Sampson, J. N., Dean, M. C., Jacobs, K. B., Black, A., Brinton, L. A., Chang, I., Chen, C., Chen, C., Chen, K., Cook, L. S., Crous Bou, M., De Vivo, I., Doherty, J., Friedenreich, C. M., Gaudet, M. M., Haiman, C. A., Hankinson, S. E., Hartge, P., Henderson, B. E., Hong, Y., Hosgood, H. D., Hsiung, C. A., Hu, W., Hunter, D. J., Jessop, L., Kim, H. N., Kim, Y. H., Kim, Y. T., Klein, R., Kraft, P., Lan, Q., Lin, D., Liu, J., Le Marchand, L., Liang, X., Lissowska, J., Lu, L., Magliocco, A. M., Matsuo, K., Olson, S. H., Orlow, I., Park, J. Y., Pooler, L., Prescott, J., Rastogi, R., Risch, H. A., Schumacher, F., Seow, A., Setiawan, V. W., Shen, H., Sheng, X., Shin, M., Shu, X., VanDen Berg, D., Wang, J., Wentzensen, N., Wong, M. P., Wu, C., Wu, T., Wu, Y., Xia, L., Yang, H. P., Yang, P., Zheng, W., Zhou, B., Abnet, C. C., Albanes, D., Aldrich, M. C., Amos, C., Amundadottir, L. T., Berndt, S. I., Blot, W. J., Bock, C. H., Bracci, P. M., Burdett, L., Buring, J. E., Butler, M. A., Carreón, T., Chatterjee, N., Chung, C. C., Cook, M. B., Cullen, M., Davis, F. G., Ding, T., Duell, E. J., Epstein, C. G., Fan, J., Figueroa, J. D., Fraumeni, J. F., Freedman, N. D., Fuchs, C. S., Gao, Y., Gapstur, S. M., Patiño-Garcia, A., Garcia-Closas, M., Gaziano, J. M., Giles, G. G., Gillanders, E. M., Giovannucci, E. L., Goldin, L., Goldstein, A. M., Greene, M. H., Hallmans, G., Harris, C. C., Henriksson, R., Holly, E. A., Hoover, R. N., Hu, N., Hutchinson, A., Jenab, M., Johansen, C., Khaw, K., Koh, W., Kolonel, L. N., Kooperberg, C., Krogh, V., Kurtz, R. C., LaCroix, A., Landgren, A., Landi, M. T., Li, D., Liao, L. M., Malats, N., McGlynn, K. A., McNeill, L. H., McWilliams, R. R., Melin, B. S., Mirabello, L., Peplonska, B., Peters, U., Petersen, G. M., Prokunina-Olsson, L., Purdue, M., Qiao, Y., Rabe, K. G., Rajaraman, P., Real, F. X., Riboli, E., Rodríguez-Santiago, B., Rothman, N., Ruder, A. M., Savage, S. A., Schwartz, A. G., Schwartz, K. L., Sesso, H. D., Severi, G., Silverman, D. T., Spitz, M. R., Stevens, V. L., Stolzenberg-Solomon, R., Stram, D., Tang, Z., Taylor, P. R., Teras, L. R., Tobias, G. S., Viswanathan, K., Wacholder, S., Wang, Z., Weinstein, S. J., Wheeler, W., White, E., Wiencke, J. K., Wolpin, B. M., Wu, X., Wunder, J. S., Yu, K., Zanetti, K. A., Zeleniuch-Jacquotte, A., Ziegler, R. G., de Andrade, M., Barnes, K. C., Beaty, T. H., Bierut, L. J., Desch, K. C., Doheny, K. F., Feenstra, B., Ginsburg, D., Heit, J. A., Kang, J. H., Laurie, C. A., Li, J. Z., Lowe, W. L., Marazita, M. L., Melbye, M., Mirel, D. B., Murray, J. C., Nelson, S. C., Pasquale, L. R., Rice, K., Wiggs, J. L., Wise, A., Tucker, M., Pérez-Jurado, L. A., Laurie, C. C., Caporaso, N. E., Yeager, M. & Chanock, S. J. (2015). Characterization of large structural genetic mosaicism in human autosomes. American Journal of Human Genetics, 96(3), 487–497. PMID: 25748358.

Kousa, Y. A., Roushangar, R. R., Zhu, H., Lei, Y., Finnell, R. H., Fakhouri, W. D., Busch, T. D., Murray, J. C., Bassuk, A., Shaw, G. M., Ashley-Koch, A., Gregory, S., Patel, N., Schutte, B. C., Leslie, E. J., Williams, T. J. & Chai, Y. (2015). A GENE REGULATORY NETWORK SHARED BETWEEN NEURULATION AND OROFACIAL DEVELOPMENT. Journal of Investigative Medicine, 63(4), 676–676.

Wehby, G. L., Prater, K. N., Ryckman, K. K., Kummet, C. & Murray, J. C. (2015). Candidate gene study for smoking, alcohol use, and body weight in a sample of pregnant women. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetr, 28(7), 804–811. PMID: 25014319.

Myers, H. I., Spracklen, C. N., Ryckman, K. K. & Murray, J. C. (2015). A retrospective study of administration of vaccination for hepatitis B among newborn infants prior to hospital discharge at a midwestern tertiary care center. Vaccine, 33(20), 2316–2321. PMID: 25835577.

Rysavy, M. A., Li, L., Bell, E. F., Das, A., Hintz, S. R., Stoll, B. J., Vohr, B. R., Carlo, W. A., Shankaran, S., Walsh, M. C., Tyson, J. E., Cotten, C. M., Smith, P. B., Murray, J. C., Colaizy, T. T., Brumbaugh, J. E., Higgins, R. D., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2015). Between-hospital variation in treatment and outcomes in extremely preterm infants. The New England Journal of Medicine, 372(19), 1801–1811. PMID: 25946279.

Butali, A., Mossey, P. A., Adeyemo, W. L., Eshete, M. A., Gaines, L. A., Even, D., Braimah, R. O., Aregbesola, B. S., Rigdon, J. V., Emeka, C. I., James, O., Ogunlewe, M. O., Ladeinde, A. L., Abate, F., Hailu, T., Mohammed, I., Gravem, P. E., Deribew, M., Gesses, M., Adeyemo, A. A. & Murray, J. C. (2014). Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa. Molecular Genetics & Genomic Medicine, 2(3), 254–260. PMID: 24936515.

Wolf, Z. T., Leslie, E. J., Arzi, B., Jayashankar, K., Karmi, N., Jia, Z., Rowland, D. J., Young, A., Safra, N., Sliskovic, S., Murray, J. C., Wade, C. M. & Bannasch, D. L. (2014). A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. PLoS genetics, 10(4), e1004257. PMID: 24699068.

Butali, A., Suzuki, S., Mansilla, M. A., Petrin, A. L., Leslie, E., L’Heureux, J., Cooper, M. E., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2014). Replication of GWAS Candidate Genes in Four Independent Populations Confirm the Role of Common Variants and Identifies Rare Variants in PAX7 and VAX1 Contributing to the Etiology of Non-Syndromic CL(P). American Journal of Medical Genetics Part A, 164(4), 882–883.

Fakhouri, W. D., Rahimov, F., Zhou, H., Du, T., Kouwenhoven, E. N., van Bokhoven, H., Murray, J. C. & Schutte, B. C. (2014). A Rare DNA Variant in a cis-Overlapping Motif (COM) in an IRF6 Enhancer Element is Associated With Van der Woude Syndrome. American Journal of Medical Genetics Part A, 164(4), 878–878.

Leslie, E. J., Mansilla, M. A., Biggs, L. C., Schuette, K., Bullard, S., Zhang, T., Cooper, M., Dunnwald, M., Lidral, A. C., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2014). GWAS Follow-Up Mutation Screen and Expression Analysis Implicate ARHGAP29 as a Novel Candidate Gene for Nonsyndromic Cleft Lip/Palate. American Journal of Medical Genetics Part A, 164(4), 876–876.

VanderMeer, J. E., Carter, T. C., Pangilinan, F., Mitchell, A., Kurnat-Thoma, E., Kirke, P. N., Troendle, J. F., Molloy, A. M., Munger, R. G., Feldkamp, M. L., Mansilla, M. A., Mills, J. L., Murray, J. C. & Brody, L. C. (2014). Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. American Journal of Medical Genetics Part A, 170(4), 1007–1016. DOI: 10.1002/ajmg.a.37539.

Butali, A., Mossey, P. A., Adeyemo, W. L., Eshete, M. A., Gaines, L. A., Even, D., Braimah, R. O., Aregbesola, B. S., Rigdon, J. V., Emeka, C. I., James, O., Ogunlewe, M. O., Ladeinde, A. L., Abate, F., Hailu, T., Mohammed, I., Gravem, P. E., Deribew, M., Gesses, M., Adeyemo, A. A. & Murray, J. C. (2014). Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa. Molecular genetics & genomic medicine, 2(3), 254-60. PMID: 24936515.

Wehby, G. L. (2014). Child health insurance coverage and household activity toward child development in four South American countries. Maternal and Child Health Journal, 18(4), 939–949. PMID: 23807717.

Ali, S. R., Fong, J. J., Carlin, A. F., Busch, T. D., Linden, R., Angata, T., Areschoug, T., Parast, M., Varki, N., Murray, J., Nizet, V. & Varki, A. (2014). Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus. The Journal of experimental medicine, 211(6), 1231-42. PMID: 24799499.

Wolf, Z. T., Leslie, E. J., Arzi, B., Jayashankar, K., Karmi, N., Jia, Z., Rowland, D. J., Young, A., Safra, N., Sliskovic, S., Murray, J. C., Wade, C. M. & Bannasch, D. L. (2014). A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. PLoS genetics, 10(4), e1004257. PMID: 24699068.

Ali, S. R., Fong, J. J., Carlin, A. F., Busch, T. D., Linden, R., Angata, T., Areschoug, T., Parast, M., Varki, N., Murray, J., Nizet, V. & Varki, A. (2014). Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus. The Journal of Experimental Medicine, 211(6), 1231–1242. PMID: 24799499.

Fakhouri, W. D., Rahimov, F., Attanasio, C., Kouwenhoven, E. N., De Ferreira Lima, R. L., Felix, T. M., Nitschke, L., Huver, D., Barrons, J., Kousa, Y. A., Leslie, E., Pennacchio, L. A., Van Bokhoven, H., Visel, A., Zhou, H., Murray, J. C. & Schutte, B. C. (2014). An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects. Human molecular genetics, 23(10), 2711-20. PMID: 24442519.

Fakhouri, W. D., Rahimov, F., Attanasio, C., Kouwenhoven, E. N., Ferreira De Lima, Renata L.,, Felix, T. M., Nitschke, L., Huver, D., Barrons, J., Kousa, Y. A., Leslie, E., Pennacchio, L. A., Van Bokhoven, H., Visel, A., Zhou, H., Murray, J. C. & Schutte, B. C. (2014). An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects. Human Molecular Genetics, 23(10), 2711–2720. PMID: 24442519.

Bureau, A., Parker, M. M., Ruczinski, I., Taub, M. A., Marazita, M. L., Murray, J. C., Mangold, E., Noethen, M. M., Ludwig, K. U., Hetmanski, J. B., Bailey-Wilson, J. E., Cropp, C. D., Li, Q., Szymczak, S., Albacha-Hejazi, H., Alqosayer, K., Field, L. L., Wu-Chou, Y., Doheny, K. F., Ling, H., Scott, A. F. & Beaty, T. H. (2014). Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics, 197(3), 1039–1044. PMID: 24793288.

Wu, T., Schwender, H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Parker, M. M., Wang, P., Murray, T., Taub, M., Li, S., Redett, R. J., Fallin, M. D., Liang, K. Y., Wu-Chou, Y. H., Chong, S. S., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E. W., Shi, B., Wilcox, A. J., Jee, S. H., Scott, A. F. & Beaty, T. H. (2014). Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate. PloS one, 9(2), e88088. PMID: 24516586.

Murray, J. C. (2014). 2013 Presidential Address: Just another president's speech (but it's all about you). American journal of human genetics, 94(3), 319-23. PMID: 24607380.

Wu, T., Schwender, H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Parker, M. M., Wang, P., Murray, T., Taub, M., Li, S., Redett, R. J., Fallin, M. D., Liang, K. Y., Wu-Chou, Y. H., Chong, S. S., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E. W., Shi, B., Wilcox, A. J., Jee, S. H., Scott, A. F. & Beaty, T. H. (2014). Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate. PloS One, 9(2), e88088. PMID: 24516586.

Chakraborty, H., Nyarko, K. A., Goco, N., Moore, J., Moretti-Ferreira, D., Murray, J. C. & Wehby, G. L. (2014). Folic Acid Fortification and Women’s Folate Levels in Selected Communities in Brazil - A First Look. International Journal for Vitamin and Nutrition Research, 84(5-6), 286–294. DOI: 10.1024/0300-9831/a000215.

Chakraborty, H., Nyarko, K. A., Goco, N., Moore, J., Moretti-Ferreira, D., Murray, J. C. & Wehby, G. L. (2014). Folic Acid Fortification and Women’s Folate Levels in Selected Communities in Brazil - A First Look. International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition, 84(5-6), 286–294. PMID: 26255550.

Kuruvilla, S., Schweitzer, J., Bishai, D., Chowdhury, S., Caramani, D., Frost, L., Cortez, R., Daelmans, B., de Francisco, A., Adam, T., Cohen, R., Alfonso, Y. N., Franz-Vasdeki, J., Saadat, S., Pratt, B. A., Eugster, B., Bandali, S., Venkatachalam, P., Hinton, R., Murray, J., Arscott-Mills, S., Axelson, H., Maliqi, B., Sarker, I., Lakshminarayanan, R., Jacobs, T., Jack, S., Jacks, S., Mason, E., Ghaffar, A., Mays, N., Presern, C., Bustreo, F., Women’s, S. F. & groups, C. H. (2014). Success factors for reducing maternal and child mortality. Bulletin of the World Health Organization, 92(7), 533–544B. PMID: 25110379.

Wehby, G. L., Nyarko, K. A. & Murray, J. C. (2014). Oral cleft recurrence risk and subsequent maternal fertility preferences and behavior in Brazil. Birth Defects Research. Part A, Clinical and Molecular Teratology, 100(1), 48–56. PMID: 24382743.

Murray, J. C., Marazita, M. L. (2014). Clefting, Dental, and Craniofacial Syndromes. DOI: 10.1016/B978-0-12-801238-3.05615-4.

Wehby, G. L., Nyarko, K. A. & Murray, J. C. (2014). Oral cleft recurrence risk and subsequent maternal fertility preferences and behavior in Brazil. Birth defects research. Part A, Clinical and molecular teratology, 100(1), 48-56. PMID: 24382743.

Murray, J. C. (2014). 2013 Presidential Address: Just another president’s speech (but it’s all about you). American Journal of Human Genetics, 94(3), 319–323. PMID: 24607380.

Yang, T., Jia, Z., Bryant-Pike, W., Chandrasekhar, A., Murray, J. C., Fritzsch, B. & Bassuk, A. G. (2014). Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. Molecular genetics & genomic medicine, 2(2), 138-51. PMID: 24689077.

Yang, T., Jia, Z., Bryant-Pike, W., Chandrasekhar, A., Murray, J. C., Fritzsch, B. & Bassuk, A. G. (2014). Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. Molecular Genetics & Genomic Medicine, 2(2), 138–151. PMID: 24689077.

Boghossian, N. S., Hansen, N. I., Bell, E. F., Stoll, B. J., Murray, J. C., Carey, J. C., Adams-Chapman, I., Shankaran, S., Walsh, M. C., Laptook, A. R., Faix, R. G., Newman, N. S., Hale, E. C., Das, A., Wilson, L. D., Hensman, A. M., Grisby, C., Collins, M. V., Vasil, D. M., Finkle, J., Maffett, D., Ball, M. B., Lacy, C. B., Bara, R., Higgins, R. D., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2014). Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18. Pediatrics, 133(2), 226–235. PMID: 24446439.

Peyrard-Janvid, M., Leslie, E. J., Kousa, Y. A., Smith, T. L., Dunnwald, M., Magnusson, M., Lentz, B. A., Unneberg, P., Fransson, I., Koillinen, H. K., Rautio, J., Pegelow, M., Karsten, A., Basel-Vanagaite, L., Gordon, W., Andersen, B., Svensson, T., Murray, J. C., Cornell, R. A., Kere, J. & Schutte, B. C. (2014). Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. American journal of human genetics, 94(1), 23-32. PMID: 24360809.

Boghossian, N. S., Hansen, N. I., Bell, E. F., Stoll, B. J., Murray, J. C., Carey, J. C., Adams-Chapman, I., Shankaran, S., Walsh, M. C., Laptook, A. R., Faix, R. G., Newman, N. S., Hale, E. C., Das, A., Wilson, L. D., Hensman, A. M., Grisby, C., Collins, M. V., Vasil, D. M., Finkle, J., Maffett, D., Ball, M. B., Lacy, C. B., Bara, R. & Higgins, R. D. (2014). Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18. Pediatrics, 133(2), 226-35. PMID: 24446439.

Peyrard-Janvid, M., Leslie, E. J., Kousa, Y. A., Smith, T. L., Dunnwald, M., Magnusson, M., Lentz, B. A., Unneberg, P., Fransson, I., Koillinen, H. K., Rautio, J., Pegelow, M., Karsten, A., Basel-Vanagaite, L., Gordon, W., Andersen, B., Svensson, T., Murray, J. C., Cornell, R. A., Kere, J. & Schutte, B. C. (2014). Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. American Journal of Human Genetics, 94(1), 23–32. PMID: 24360809.

Hartnett, M. E., Morrison, M. A., Smith, S., Yanovitch, T. L., Young, T. L., Colaizy, T., Momany, A., Dagle, J., Carlo, W. A., Clark, E. A., Page, G., Murray, J., DeAngelis, M. M. & Cotten, C. M. (2014). Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants. Investigative ophthalmology & visual science, 55(10), 6194-203. PMID: 25118269.

Guinan, E. C., Palmer, C. D., Mancuso, C. J., Brennan, L., Stoler-Barak, L., Kalish, L. A., Suter, E. E., Gallington, L. C., Huhtelin, D. P., Mansilla, M., Schumann, R. R., Murray, J. C., Weiss, J. & Levy, O. (2014). Identification of single nucleotide polymorphisms in hematopoietic cell transplant patients affecting early recognition of, and response to, endotoxin. Innate immunity, 20(7), 697-711. PMID: 24107515.

Butali, A., Mossey, P., Adeyemo, W., Eshete, M., Gaines, L., Braimah, R., Aregbesola, B., Rigdon, J., Emeka, C., Olutayo, J., Ogunlewe, O., Ladeinde, A., Abate, F., Hailu, T., Mohammed, I., Gravem, P., Deribew, M., Gesses, M., Adeyemo, A., Marazita, M. & Murray, J. (2014). Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population. American journal of medical genetics. Part A, 164A(10), 2567-71. PMID: 25081408.

Naderi, H. M., Murray, J. C. & Dagle, J. M. (2014). Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks). (Vols. 164A). (10), pp. 2676-8. American journal of medical genetics. Part A. PMID: 25073622.

Ryckman, K. K., Spracklen, C. N., Dagle, J. M. & Murray, J. C. (2014). Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone. Journal of pediatric endocrinology & metabolism : JPEM, 27(9-10), 929-38. PMID: 24854527.

Ryckman, K. K., Spracklen, C. N., Dagle, J. M. & Murray, J. C. (2014). Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone. Journal of pediatric endocrinology & metabolism: JPEM, 27(9-10), 929–938. PMID: 24854527.

Naderi, H. M., Murray, J. C. & Dagle, J. M. (2014). Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks). American Journal of Medical Genetics. Part A, 164A(10), 2676–2678. PMID: 25073622.

Butali, A., Mossey, P., Adeyemo, W., Eshete, M., Gaines, L., Braimah, R., Aregbesola, B., Rigdon, J., Emeka, C., Olutayo, J., Ogunlewe, O., Ladeinde, A., Abate, F., Hailu, T., Mohammed, I., Gravem, P., Deribew, M., Gesses, M., Adeyemo, A., Marazita, M. & Murray, J. (2014). Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population. American Journal of Medical Genetics. Part A, 164A(10), 2567–2571. PMID: 25081408.

Wood, A. R., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., Chu, A. Y., Estrada, K., Luan, J., Kutalik, Z., Amin, N., Buchkovich, M. L., Croteau-Chonka, D. C., Day, F. R., Duan, Y., Fall, T., Fehrmann, R., Ferreira, T., Jackson, A. U., Karjalainen, J., Lo, K. S., Locke, A. E., Mägi, R., Mihailov, E., Porcu, E., Randall, J. C., Scherag, A., Vinkhuyzen, A. A., Westra, H. J., Winkler, T. W., Workalemahu, T., Zhao, J. H., Absher, D., Albrecht, E., Anderson, D., Baron, J., Beekman, M., Demirkan, A., Ehret, G. B., Feenstra, B., Feitosa, M. F., Fischer, K., Fraser, R. M., Goel, A., Gong, J., Justice, A. E., Kanoni, S., Kleber, M. E., Kristiansson, K., Lim, U., Lotay, V., Lui, J. C., Mangino, M., Mateo Leach, I., Medina-Gomez, C., Nalls, M. A., Nyholt, D. R., Palmer, C. D., Pasko, D., Pechlivanis, S., Prokopenko, I., Ried, J. S., Ripke, S., Shungin, D., Stancáková, A., Strawbridge, R. J., Sung, Y. J., Tanaka, T., Teumer, A., Trompet, S., van der Laan, S. W., van Setten, J., Van Vliet-Ostaptchouk, J. V., Wang, Z., Yengo, L., Zhang, W., Afzal, U., Arnlöv, J., Arscott, G. M., Bandinelli, S., Barrett, A., Bellis, C., Bennett, A. J., Berne, C., Blüher, M., Bolton, J. L., Böttcher, Y., Boyd, H. A., Bruinenberg, M., Buckley, B. M., Buyske, S., Caspersen, I. H., Chines, P. S., Clarke, R., Claudi-Boehm, S., Cooper, M., Daw, E. W., De Jong, P. A., Deelen, J., Delgado, G., Denny, J. C., Dhonukshe-Rutten, R., Dimitriou, M., Doney, A. S., Dörr, M., Eklund, N., Eury, E., Folkersen, L., Garcia, M. E., Geller, F., Giedraitis, V., Go, A. S., Grallert, H., Grammer, T. B., Gräßler, J., Grönberg, H., de Groot, L. C., Groves, C. J., Haessler, J., Hall, P., Haller, T., Hallmans, G., Hannemann, A., Hartman, C. A., Hassinen, M., Hayward, C., Heard-Costa, N. L., Helmer, Q., Hemani, G., Henders, A. K., Hillege, H. L., Hlatky, M. A., Hoffmann, W., Hoffmann, P., Holmen, O., Houwing-Duistermaat, J. J., Illig, T., Isaacs, A., James, A. L., Jeff, J., Johansen, B., Johansson, Å., Jolley, J., Juliusdottir, T., Junttila, J., Kho, A. N., Kinnunen, L., Klopp, N., Kocher, T., Kratzer, W., Lichtner, P., Lind, L., Lindström, J., Lobbens, S., Lorentzon, M., Lu, Y., Lyssenko, V., Magnusson, P. K., Mahajan, A., Maillard, M., McArdle, W. L., McKenzie, C. A., McLachlan, S., McLaren, P. J., Menni, C., Merger, S., Milani, L., Moayyeri, A., Monda, K. L., Morken, M. A., Müller, G., Müller-Nurasyid, M., Musk, A. W., Narisu, N., Nauck, M., Nolte, I. M., Nöthen, M. M., Oozageer, L., Pilz, S., Rayner, N. W., Renstrom, F., Robertson, N. R., Rose, L. M., Roussel, R., Sanna, S., Scharnagl, H., Scholtens, S., Schumacher, F. R., Schunkert, H., Scott, R. A., Sehmi, J., Seufferlein, T., Shi, J., Silventoinen, K., Smit, J. H., Smith, A. V., Smolonska, J., Stanton, A. V., Stirrups, K., Stott, D. J., Stringham, H. M., Sundström, J., Swertz, M. A., Syvänen, A. C., Tayo, B. O., Thorleifsson, G., Tyrer, J. P., van Dijk, S., van Schoor, N. M., van der Velde, N., van Heemst, D., van Oort, F. V., Vermeulen, S. H., Verweij, N., Vonk, J. M., Waite, L. L., Waldenberger, M., Wennauer, R., Wilkens, L. R., Willenborg, C., Wilsgaard, T., Wojczynski, M. K., Wong, A., Wright, A. F., Zhang, Q., Arveiler, D., Bakker, S. J., Beilby, J., Bergman, R. N., Bergmann, S., Biffar, R., Blangero, J., Boomsma, D. I., Bornstein, S. R., Bovet, P., Brambilla, P., Brown, M. J., Campbell, H., Caulfield, M. J., Chakravarti, A., Collins, R., Collins, F. S., Crawford, D. C., Cupples, L. A., Danesh, J., de Faire, U., den Ruijter, H. M., Erbel, R., Erdmann, J., Eriksson, J. G., Farrall, M., Ferrannini, E., Ferrières, J., Ford, I., Forouhi, N. G., Forrester, T., Gansevoort, R. T., Gejman, P. V., Gieger, C., Golay, A., Gottesman, O., Gudnason, V., Gyllensten, U., Haas, D. W., Hall, A. S., Harris, T. B., Hattersley, A. T., Heath, A. C., Hengstenberg, C., Hicks, A. A., Hindorff, L. A., Hingorani, A. D., Hofman, A., Hovingh, G. K., Humphries, S. E., Hunt, S. C., Hypponen, E., Jacobs, K. B., Jarvelin, M. R., Jousilahti, P., Jula, A. M., Kaprio, J., Kastelein, J. J., Kayser, M., Kee, F., Keinanen-Kiukaanniemi, S. M., Kiemeney, L. A., Kooner, J. S., Kooperberg, C., Koskinen, S., Kovacs, P., Kraja, A. T., Kumari, M., Kuusisto, J., Lakka, T. A., Langenberg, C., Le Marchand, L., Lehtimäki, T., Lupoli, S., Madden, P. A., Männistö, S., Manunta, P., Marette, A., Matise, T. C., McKnight, B., Meitinger, T., Moll, F. L., Montgomery, G. W., Morris, A. D., Morris, A. P., Murray, J. C., Nelis, M., Ohlsson, C., Oldehinkel, A. J., Ong, K. K., Ouwehand, W. H., Pasterkamp, G., Peters, A., Pramstaller, P. P., Price, J. F., Qi, L., Raitakari, O. T., Rankinen, T., Rao, D. C., Rice, T. K., Ritchie, M., Rudan, I., Salomaa, V., Samani, N. J., Saramies, J., Sarzynski, M. A., Schwarz, P. E., Sebert, S., Sever, P., Shuldiner, A. R., Sinisalo, J., Steinthorsdottir, V., Stolk, R. P., Tardif, J. C., Tönjes, A., Tremblay, A., Tremoli, E., Virtamo, J., Vohl, M. C., Amouyel, P., Asselbergs, F. W., Assimes, T. L., Bochud, M., Boehm, B. O., Boerwinkle, E., Bottinger, E. P., Bouchard, C., Cauchi, S., Chambers, J. C., Chanock, S. J., Cooper, R. S., de Bakker, P. I., Dedoussis, G., Ferrucci, L., Franks, P. W., Froguel, P., Groop, L. C., Haiman, C. A., Hamsten, A., Hayes, M. G., Hui, J., Hunter, D. J., Hveem, K., Jukema, J. W., Kaplan, R. C., Kivimaki, M., Kuh, D., Laakso, M., Liu, Y., Martin, N. G., März, W., Melbye, M., Moebus, S., Munroe, P. B., Njølstad, I., Oostra, B. A., Palmer, C. N., Pedersen, N. L., Perola, M., Pérusse, L., Peters, U., Powell, J. E., Power, C., Quertermous, T., Rauramaa, R., Reinmaa, E., Ridker, P. M., Rivadeneira, F., Rotter, J. I., Saaristo, T. E., Saleheen, D., Schlessinger, D., Slagboom, P. E., Snieder, H., Spector, T. D., Strauch, K., Stumvoll, M., Tuomilehto, J., Uusitupa, M., van der Harst, P., Völzke, H., Walker, M., Wareham, N. J., Watkins, H., Wichmann, H. E., Wilson, J. F., Zanen, P., Deloukas, P., Heid, I. M., Lindgren, C. M., Mohlke, K. L., Speliotes, E. K., Thorsteinsdottir, U., Barroso, I., Fox, C. S., North, K. E., Strachan, D. P., Beckmann, J. S., Berndt, S. I., Boehnke, M., Borecki, I. B., McCarthy, M. I., Metspalu, A., Stefansson, K., Uitterlinden, A. G., van Duijn, C. M., Franke, L., Willer, C. J., Price, A. L., Lettre, G., Loos, R. J., Weedon, M. N., Ingelsson, E., O'Connell, J. R., Abecasis, G. R., Chasman, D. I., Goddard, M. E., Visscher, P. M., Hirschhorn, J. N. & Frayling, T. M. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nature genetics, 46(11), 1173-86. PMID: 25282103.

Bureau, A., Parker, M. M., Ruczinski, I., Taub, M. A., Marazita, M. L., Murray, J. C., Mangold, E., Noethen, M. M., Ludwig, K. U., Hetmanski, J. B., Bailey-Wilson, J. E., Cropp, C. D., Li, Q., Szymczak, S., Albacha-Hejazi, H., Alqosayer, K., Field, L. L., Wu-Chou, Y. H., Doheny, K. F., Ling, H., Scott, A. F. & Beaty, T. H. (2014). Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics, 197(3), 1039-44. PMID: 24793288.

Murray, J. C., Tremblay, M. A., Corriveau, H., Hamel, M. & Cabana, F. (2014). Effects of Right Lower Limb Orthopedic Immobilization on Braking Function: An On-The-Road Experimental Study With Healthy Volunteers. The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons. PMID: 25435008.

Wood, A. R., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., Chu, A. Y., Estrada, K., Luan, J., Kutalik, Z., Amin, N., Buchkovich, M. L., Croteau-Chonka, D. C., Day, F. R., Duan, Y., Fall, T., Fehrmann, R., Ferreira, T., Jackson, A. U., Karjalainen, J., Lo, K. S., Locke, A. E., Mägi, R., Mihailov, E., Porcu, E., Randall, J. C., Scherag, A., Vinkhuyzen, A. A., Westra, H., Winkler, T. W., Workalemahu, T., Zhao, J. H., Absher, D., Albrecht, E., Anderson, D., Baron, J., Beekman, M., Demirkan, A., Ehret, G. B., Feenstra, B., Feitosa, M. F., Fischer, K., Fraser, R. M., Goel, A., Gong, J., Justice, A. E., Kanoni, S., Kleber, M. E., Kristiansson, K., Lim, U., Lotay, V., Lui, J. C., Mangino, M., Mateo Leach, I., Medina-Gomez, C., Nalls, M. A., Nyholt, D. R., Palmer, C. D., Pasko, D., Pechlivanis, S., Prokopenko, I., Ried, J. S., Ripke, S., Shungin, D., Stancáková, A., Strawbridge, R. J., Sung, Y. J., Tanaka, T., Teumer, A., Trompet, S., van der Laan, Sander W.,, van Setten, J., Van Vliet-Ostaptchouk, J. V., Wang, Z., Yengo, L., Zhang, W., Afzal, U., Arnlöv, J., Arscott, G. M., Bandinelli, S., Barrett, A., Bellis, C., Bennett, A. J., Berne, C., Blüher, M., Bolton, J. L., Böttcher, Y., Boyd, H. A., Bruinenberg, M., Buckley, B. M., Buyske, S., Caspersen, I. H., Chines, P. S., Clarke, R., Claudi-Boehm, S., Cooper, M., Daw, E. W., De Jong, P. A., Deelen, J., Delgado, G., Denny, J. C., Dhonukshe-Rutten, R., Dimitriou, M., Doney, A. S., Dörr, M., Eklund, N., Eury, E., Folkersen, L., Garcia, M. E., Geller, F., Giedraitis, V., Go, A. S., Grallert, H., Grammer, T. B., Gräßler, J., Grönberg, H., de Groot, Lisette C. P. G. M.,, Groves, C. J., Haessler, J., Hall, P., Haller, T., Hallmans, G., Hannemann, A., Hartman, C. A., Hassinen, M., Hayward, C., Heard-Costa, N. L., Helmer, Q., Hemani, G., Henders, A. K., Hillege, H. L., Hlatky, M. A., Hoffmann, W., Hoffmann, P., Holmen, O., Houwing-Duistermaat, J. J., Illig, T., Isaacs, A., James, A. L., Jeff, J., Johansen, B., Johansson, Å., Jolley, J., Juliusdottir, T., Junttila, J., Kho, A. N., Kinnunen, L., Klopp, N., Kocher, T., Kratzer, W., Lichtner, P., Lind, L., Lindström, J., Lobbens, S., Lorentzon, M., Lu, Y., Lyssenko, V., Magnusson, P. K., Mahajan, A., Maillard, M., McArdle, W. L., McKenzie, C. A., McLachlan, S., McLaren, P. J., Menni, C., Merger, S., Milani, L., Moayyeri, A., Monda, K. L., Morken, M. A., Müller, G., Müller-Nurasyid, M., Musk, A. W., Narisu, N., Nauck, M., Nolte, I. M., Nöthen, M. M., Oozageer, L., Pilz, S., Rayner, N. W., Renstrom, F., Robertson, N. R., Rose, L. M., Roussel, R., Sanna, S., Scharnagl, H., Scholtens, S., Schumacher, F. R., Schunkert, H., Scott, R. A., Sehmi, J., Seufferlein, T., Shi, J., Silventoinen, K., Smit, J. H., Smith, A. V., Smolonska, J., Stanton, A. V., Stirrups, K., Stott, D. J., Stringham, H. M., Sundström, J., Swertz, M. A., Syvänen, A., Tayo, B. O., Thorleifsson, G., Tyrer, J. P., van Dijk, S., van Schoor, N. M., van der Velde, N., van Heemst, D., van Oort, Floor V. A.,, Vermeulen, S. H., Verweij, N., Vonk, J. M., Waite, L. L., Waldenberger, M., Wennauer, R., Wilkens, L. R., Willenborg, C., Wilsgaard, T., Wojczynski, M. K., Wong, A., Wright, A. F., Zhang, Q., Arveiler, D., Bakker, S. J., Beilby, J., Bergman, R. N., Bergmann, S., Biffar, R., Blangero, J., Boomsma, D. I., Bornstein, S. R., Bovet, P., Brambilla, P., Brown, M. J., Campbell, H., Caulfield, M. J., Chakravarti, A., Collins, R., Collins, F. S., Crawford, D. C., Cupples, L. A., Danesh, J., de Faire, U., den Ruijter, H. M., Erbel, R., Erdmann, J., Eriksson, J. G., Farrall, M., Ferrannini, E., Ferrières, J., Ford, I., Forouhi, N. G., Forrester, T., Gansevoort, R. T., Gejman, P. V., Gieger, C., Golay, A., Gottesman, O., Gudnason, V., Gyllensten, U., Haas, D. W., Hall, A. S., Harris, T. B., Hattersley, A. T., Heath, A. C., Hengstenberg, C., Hicks, A. A., Hindorff, L. A., Hingorani, A. D., Hofman, A., Hovingh, G. K., Humphries, S. E., Hunt, S. C., Hypponen, E., Jacobs, K. B., Jarvelin, M., Jousilahti, P., Jula, A. M., Kaprio, J., Kastelein, J. J., Kayser, M., Kee, F., Keinanen-Kiukaanniemi, S. M., Kiemeney, L. A., Kooner, J. S., Kooperberg, C., Koskinen, S., Kovacs, P., Kraja, A. T., Kumari, M., Kuusisto, J., Lakka, T. A., Langenberg, C., Le Marchand, L., Lehtimäki, T., Lupoli, S., Madden, P. A., Männistö, S., Manunta, P., Marette, A., Matise, T. C., McKnight, B., Meitinger, T., Moll, F. L., Montgomery, G. W., Morris, A. D., Morris, A. P., Murray, J. C., Nelis, M., Ohlsson, C., Oldehinkel, A. J., Ong, K. K., Ouwehand, W. H., Pasterkamp, G., Peters, A., Pramstaller, P. P., Price, J. F., Qi, L., Raitakari, O. T., Rankinen, T., Rao, D. C., Rice, T. K., Ritchie, M., Rudan, I., Salomaa, V., Samani, N. J., Saramies, J., Sarzynski, M. A., Schwarz, P. E., Sebert, S., Sever, P., Shuldiner, A. R., Sinisalo, J., Steinthorsdottir, V., Stolk, R. P., Tardif, J., Tönjes, A., Tremblay, A., Tremoli, E., Virtamo, J., Vohl, M., Records, E. M., Genomics (eMEMERGEGE) Consortium,, Consortium, M., Consortium, P., Study, L. C., Amouyel, P., Asselbergs, F. W., Assimes, T. L., Bochud, M., Boehm, B. O., Boerwinkle, E., Bottinger, E. P., Bouchard, C., Cauchi, S., Chambers, J. C., Chanock, S. J., Cooper, R. S., de Bakker, Paul I. W.,, Dedoussis, G., Ferrucci, L., Franks, P. W., Froguel, P., Groop, L. C., Haiman, C. A., Hamsten, A., Hayes, M. G., Hui, J., Hunter, D. J., Hveem, K., Jukema, J. W., Kaplan, R. C., Kivimaki, M., Kuh, D., Laakso, M., Liu, Y., Martin, N. G., März, W., Melbye, M., Moebus, S., Munroe, P. B., Njølstad, I., Oostra, B. A., Palmer, C. N., Pedersen, N. L., Perola, M., Pérusse, L., Peters, U., Powell, J. E., Power, C., Quertermous, T., Rauramaa, R., Reinmaa, E., Ridker, P. M., Rivadeneira, F., Rotter, J. I., Saaristo, T. E., Saleheen, D., Schlessinger, D., Slagboom, P. E., Snieder, H., Spector, T. D., Strauch, K., Stumvoll, M., Tuomilehto, J., Uusitupa, M., van der Harst, P., Völzke, H., Walker, M., Wareham, N. J., Watkins, H., Wichmann, H., Wilson, J. F., Zanen, P., Deloukas, P., Heid, I. M., Lindgren, C. M., Mohlke, K. L., Speliotes, E. K., Thorsteinsdottir, U., Barroso, I., Fox, C. S., North, K. E., Strachan, D. P., Beckmann, J. S., Berndt, S. I., Boehnke, M., Borecki, I. B., McCarthy, M. I., Metspalu, A., Stefansson, K., Uitterlinden, A. G., van Duijn, C. M., Franke, L., Willer, C. J., Price, A. L., Lettre, G., Loos, R. J., Weedon, M. N., Ingelsson, E., O’Connell, J. R., Abecasis, G. R., Chasman, D. I., Goddard, M. E., Visscher, P. M., Hirschhorn, J. N. & Frayling, T. M. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46(11), 1173–1186. PMID: 25282103.

Guinan, E. C., Palmer, C. D., Mancuso, C. J., Brennan, L., Stoler-Barak, L., Kalish, L. A., Suter, E. E., Gallington, L. C., Huhtelin, D. P., Mansilla, M., Schumann, R. R., Murray, J. C., Weiss, J. & Levy, O. (2014). Identification of single nucleotide polymorphisms in hematopoietic cell transplant patients affecting early recognition of, and response to, endotoxin. Innate Immunity, 20(7), 697–711. PMID: 24107515.

van ’t Erve, Thomas J.,, Doskey, C. M., Wagner, B. A., Hess, J. R., Darbro, B. W., Ryckman, K. K., Murray, J. C., Raife, T. J. & Buettner, G. R. (2014). Heritability of glutathione and related metabolites in stored red blood cells. Free Radical Biology & Medicine, 76, 107–113. PMID: 25108189.

van ’t Erve, Thomas J., Doskey, C. M., Wagner, B. A., Hess, J. R., Darbro, B. W., Ryckman, K. K., Murray, J. C., Raife, T. J. & Buettner, G. R. (2014). Heritability of glutathione and related metabolites in stored red blood cells. Free Radical Biology & Medicine, 76, 107–113. PMID: 25108189.

Ryckman, K. K., Smith, C. J., Jelliffe-Pawlowski, L. L., Momany, A. M., Berberich, S. L. & Murray, J. C. (2014). Metabolic heritability at birth: implications for chronic disease research. Human Genetics, 133(8), 1049–1057. PMID: 24850141.

Marazita, M. L., Hochheiser, H. & Murray, J. C. (2014). The FaceBase Hub: a resource for translational craniofacial genetics. American Journal of Medical Genetics Part A, 164(8), 1881–1881.

Weh, E., Reis, L. M., Tyler, R. C., Bick, D., Rhead, W. J., Wallace, S., McGregor, T. L., Dills, S. K., Chao, M., Murray, J. C. & Semina, E. V. (2014). Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical Genetics, 86(2), 142–148. PMID: 23889335.

van ’t Erve, Thomas J., Wagner, B. A., Martin, S. M., Knudson, C. M., Blendowski, R., Keaton, M., Holt, T., Hess, J. R., Buettner, G. R., Ryckman, K. K., Darbro, B. W., Murray, J. C. & Raife, T. J. (2014). The heritability of metabolite concentrations in stored human red blood cells. Transfusion, 54(8), 2055–2063. PMID: 24601981.

Wehby, G. L., Prater, K. N., Ryckman, K. K., Kummet, C. & Murray, J. C. (2014). Candidate gene study for smoking, alcohol use, and body weight in a sample of pregnant women. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstet, 1-8. PMID: 25014319.

Durda, K. M., Schutte, B. C. & Murray, J. C. (2014). IRF6-Related Disorders. In GeneReviews. (Updated) Seattle: University of Washington, Seattle.

Jelliffe-Pawlowski, L. L., Ryckman, K. K., Bedell, B., O'Brodovich, H. M., Gould, J. B., Lyell, D. J., Borowski, K. S., Shaw, G. M., Murray, J. C. & Stevenson, D. K. (2014). Combined elevated midpregnancy tumor necrosis factor alpha and hyperlipidemia in pregnancies resulting in early preterm birth. American journal of obstetrics and gynecology, 211(2), 141.e1-9. PMID: 24831886.

van ’t Erve, Thomas J.,, Wagner, B. A., Martin, S. M., Knudson, C. M., Blendowski, R., Keaton, M., Holt, T., Hess, J. R., Buettner, G. R., Ryckman, K. K., Darbro, B. W., Murray, J. C. & Raife, T. J. (2014). The heritability of metabolite concentrations in stored human red blood cells. Transfusion, 54(8), 2055–2063. PMID: 24601981.

Jelliffe-Pawlowski, L. L., Ryckman, K. K., Bedell, B., O’Brodovich, H. M., Gould, J. B., Lyell, D. J., Borowski, K. S., Shaw, G. M., Murray, J. C. & Stevenson, D. K. (2014). Combined elevated midpregnancy tumor necrosis factor alpha and hyperlipidemia in pregnancies resulting in early preterm birth. American Journal of Obstetrics and Gynecology, 211(2), 141.e1–9. PMID: 24831886.

Bureau, A., Younkin, S. G., Parker, M. M., Bailey-Wilson, J. E., Marazita, M. L., Murray, J. C., Mangold, E., Albacha-Hejazi, H., Beaty, T. H. & Ruczinski, I. (2014). Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics (Oxford, England), 30(15), 2189-96. PMID: 24740360.

Kousa, Y. A., Zhu, H., Busch, T. D., Kinoshita, A., Fakhouri, W. D., Roushangar, R. R., Smith, A. L., Dunnwald, M., Williams, T. J., Chai, Y., Amendt, B. A., Murray, J. C., Shaw, G. M., Bassuk, A. G., Finnell, R. H. & Schutte, B. C. (2014). Irf6 regulates Tfap2a and is required for neurulation. American Journal of Medical Genetics Part A, 164(8), 1883–1884.

Ryckman, K. K., Smith, C. J., Jelliffe-Pawlowski, L. L., Momany, A. M., Berberich, S. L. & Murray, J. C. (2014). Metabolic heritability at birth: implications for chronic disease research. Human genetics, 133(8), 1049-57. PMID: 24850141.

Weh, E., Reis, L. M., Tyler, R. C., Bick, D., Rhead, W. J., Wallace, S., McGregor, T. L., Dills, S. K., Chao, M. C., Murray, J. C. & Semina, E. V. (2014). Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical genetics, 86(2), 142-8. PMID: 23889335.

Hartnett, M. E., Morrison, M. A., Smith, S., Yanovitch, T. L., Young, T. L., Colaizy, T., Momany, A., Dagle, J., Carlo, W. A., Clark, E. A., Page, G., Murray, J., DeAngelis, M. M., Cotten, C. M. & Subcommittee, G. (2014). Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants. Investigative Ophthalmology & Visual Science, 55(10), 6194–6203. PMID: 25118269.

Bureau, A., Younkin, S. G., Parker, M. M., Bailey-Wilson, J. E., Marazita, M. L., Murray, J. C., Mangold, E., Albacha-Hejazi, H., Beaty, T. H. & Ruczinski, I. (2014). Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics (Oxford, England), 30(15), 2189–2196. PMID: 24740360.

Myking, S., Boyd, H. A., Myhre, R., Feenstra, B., Jugessur, A., Devold Pay, A. S., Ostensen, I. H., Morken, N. H., Busch, T., Ryckman, K. K., Geller, F., Magnus, P., Gjessing, H. K., Melbye, M., Jacobsson, B. & Murray, J. C. (2013). X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study. PloS one, 8(4), e61781. PMID: 23613933.

Alul, F. Y., Shchelochkov, O. A., Berberich, S. L., Murray, J. C. & Ryckman, K. K. (2013). Genetic associations with neonatal thyroid-stimulating hormone levels. Pediatric research, 73(4 Pt 1), 484-91. PMID: 23344678.

Alul, F. Y., Shchelochkov, O. A., Berberich, S. L., Murray, J. C. & Ryckman, K. K. (2013). Genetic associations with neonatal thyroid-stimulating hormone levels. Pediatric Research, 73(4 Pt 1), 484–491. PMID: 23344678.

Wehby, G. L. (2013). Living on higher ground reduces child neurodevelopment-evidence from South America. The Journal of Pediatrics, 162(3), 606–611.e1. PMID: 23092532.

Patel, P. J., Beaty, T. H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Wu, T., Murray, T., Rose, M., Redett, R. J., Jin, S. C., Lie, R. T., Wu-Chou, Y., Wang, H., Ye, X., Yeow, V., Chong, S., Jee, S. H., Shi, B. & Scott, A. F. (2013). X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts. European Journal of Oral Sciences, 121(2), 63–68. PMID: 23489894.

Alul, F. Y., Cook, D. E., Shchelochkov, O. A., Fleener, L. G., Berberich, S. L., Murray, J. C. & Ryckman, K. K. (2013). The heritability of metabolic profiles in newborn twins. Heredity, 110(3), 253-8. PMID: 23149456.

Miller, R. K., Stodgell, C. J., Katzman, P. J., Friedman, A. E., Jamerson, D., Friedman, M. R., Salamone, L., Ruffolo, L., Weidenborner, P., Aagaard-Tillery, K., Culhane, J., Wadlinger, S., Pacholski, M., Kent, M. A., Green, L., Wapner, R., Torres, C., Perou, J., Landrigan, P., Chen, J., Lambertini, L., Littman, L., Sheffield, P., Golden, A., Gilbert, J., Lendor, C., Allen, S., Schadt, E., Dudley, J., Leuthner, S., Szabo, S., Salafia, C. M., Dalton, J. L., Misra, D., Thiex, N., Gutzman, K., Martin, A., Specker, B., Hobbs, C., Maccleod, S., Walker, C. K., Swanson, J., Holliday, C., Butler, J., Li, A., Dassanayake, R. M. A. P. S., Nanes, J., Xia, Y., Murray, J. C., Busch, T. D., Rigdon, J., Darrah, T. H., Campbell, E., Dole, N., Thorp, J., Eucker, B., Bell, C., Clark, E. B., Varner, M. W., Taggart, E., Billy, J., Stradling, S., Leavitt, J., Bell, W., Waterfall, S., O’Brien, B., Layton, M., Todd, D., Wilson, K., Durkin, M. S., Sandoval, M., Kasten, C. & Moye, J. (2013). Use of the Human Placenta As a Biomarker for Environmental Exposures and Clinical, Genetics/Epigenetic, Morphological, and Systems Biology Assessments in the National Children’s Study (NCS). Birth Defects Research Part a-Clinical and Molecular Teratology, 97(5), 330–331.

Alul, F. Y., Cook, D. E., Shchelochkov, O. A., Fleener, L. G., Berberich, S. L., Murray, J. C. & Ryckman, K. K. (2013). The heritability of metabolic profiles in newborn twins. Heredity, 110(3), 253–258. PMID: 23149456.

Mann, P. C., Cooper, M. E., Ryckman, K. K., Comas, B., Gili, J., Crumley, S., Bream, E. N., Byers, H. M., Piester, T., Schaefer, A., Christine, P. J., Lawrence, A., Schaa, K. L., Kelsey, K. J., Berends, S. K., Momany, A. M., Gadow, E., Cosentino, V., Castilla, E. E., López Camelo, J., Saleme, C., Day, L. J., England, S. K., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2013). Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population. Journal of perinatology : official journal of the California Perinatal Association, 33(5), 336-40. PMID: 23018797.

Butali, A., Suzuki, S., Cooper, M. E., Mansilla, A. M., Cuenco, K., Leslie, E. J., Suzuki, Y., Niimi, T., Yamamoto, M., Ayanga, G., Erkhembaatar, T., Furukawa, H., Fujiwawa, K., Imura, H., Petrin, A. L., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2013). Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P). American Journal of Medical Genetics. Part A, 161A(5), 965–972. PMID: 23463464.

Leslie, E. J., Standley, J., Compton, J., Bale, S., Schutte, B. C. & Murray, J. C. (2013). Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases. Genetics in medicine : official journal of the American College of Medical Genetics, 15(5), 338-44. PMID: 23154523.

Mohamed, S., Murray, J. C., Dagle, J. M. & Colaizy, T. (2013). Hyperglycemia as a risk factor for the development of retinopathy of prematurity. BMC pediatrics, 13, 78. PMID: 23679669.

Wehby, G. L., Félix, T. M., Goco, N., Richieri-Costa, A., Chakraborty, H., Souza, J., Pereira, R., Padovani, C., Moretti-Ferreira, D. & Murray, J. C. (2013). High dosage folic acid supplementation, oral cleft recurrence and fetal growth. International journal of environmental research and public health, 10(2), 590-605. PMID: 23380913.

Butali, A., Suzuki, S., Cooper, M. E., Mansilla, A. M., Cuenco, K., Leslie, E. J., Suzuki, Y., Niimi, T., Yamamoto, M., Ayanga, G., Erkhembaatar, T., Furukawa, H., Fujiwawa, K., Imura, H., Petrin, A. L., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2013). Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P). American journal of medical genetics. Part A, 161A(5), 965-72. PMID: 23463464.

Wehby, G. L. (2013). Child health insurance and early preventive care in three South American countries. Health Policy and Planning, 28(3), 328–338. PMID: 22791558.

Mann, P. C., Cooper, M. E., Ryckman, K. K., Comas, B., Gili, J., Crumley, S., Bream, E. N., Byers, H. M., Piester, T., Schaefer, A., Christine, P. J., Lawrence, A., Schaa, K. L., Kelsey, K. J., Berends, S. K., Momany, A. M., Gadow, E., Cosentino, V., Castilla, E. E., López Camelo, J., Saleme, C., Day, L. J., England, S. K., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2013). Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population. Journal of Perinatology: Official Journal of the California Perinatal Association, 33(5), 336–340. PMID: 23018797.

Mohamed, S., Murray, J. C., Dagle, J. M. & Colaizy, T. (2013). Hyperglycemia as a risk factor for the development of retinopathy of prematurity. BMC pediatrics, 13, 78. PMID: 23679669.

Leslie, E. J., Standley, J., Compton, J., Bale, S., Schutte, B. C. & Murray, J. C. (2013). Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 15(5), 338–344. PMID: 23154523.

Zheng, X., Feingold, E., Ryckman, K. K., Shaffer, J. R., Boyd, H. A., Feenstra, B., Melbye, M., Marazita, M. L., Murray, J. C. & Cuenco, K. T. (2013). Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. Frontiers in Genetics, 4, 196. PMID: 24194744.

Bream, E. N., Leppellere, C. R., Cooper, M. E., Dagle, J. M., Merrill, D. C., Christensen, K., Simhan, H. N., Fong, C. T., Hallman, M., Muglia, L. J., Marazita, M. L. & Murray, J. C. (2013). Candidate gene linkage approach to identify DNA variants that predispose to preterm birth. Pediatric research, 73(2), 135-41. PMID: 23168575.

L'Heureux, J., Murray, J. C., Newbury, E., Shinkunas, L. & Simon, C. M. (2013). Public perspectives on biospecimen procurement: what biorepositories should consider. Biopreservation and biobanking, 11(3), 137-43. PMID: 24850089.

Ross, A. P., Mansilla, M. A., Choe, Y., Helminski, S., Sturm, R., Maute, R. L., May, S. R., Hozyasz, K. K., Wójcicki, P., Mostowska, A., Davidson, B., Adamopoulos, I. E., Pleasure, S. J., Murray, J. C. & Zarbalis, K. S. (2013). A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting. PloS One, 8(7), e69333. PMID: 23935987.

Lewinska, M., Zelenko, U., Merzel, F., Golic Grdadolnik, S., Murray, J. C. & Rozman, D. (2013). Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure. PloS one, 8(12), e82554. PMID: 24358204.

Murray, J. C., Marazita, M. L. (2013). Clefting, Dental, and Craniofacial Syndromes. DOI: 10.1016/B978-0-12-383834-6.00152-X.

Kim, J., Pitlick, M. M., Christine, P. J., Schaefer, A. R., Saleme, C., Comas, B., Cosentino, V., Gadow, E. & Murray, J. C. (2013). Genome-wide analysis of DNA methylation in human amnion. TheScientificWorldJournal, 2013, 678156. PMID: 23533356.

Myking, S., Boyd, H. A., Myhre, R., Feenstra, B., Jugessur, A., Devold Pay, A. S., Ostensen, I. H., Morken, N., Busch, T., Ryckman, K. K., Geller, F., Magnus, P., Gjessing, H. K., Melbye, M., Jacobsson, B. & Murray, J. C. (2013). X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study. PloS One, 8(4), e61781. PMID: 23613933.

Pennell, C. E., Vadillo-Ortega, F., Olson, D. M., Ha, E. H., Williams, S., Frayling, T. M., Dolan, S., Katz, M., Merialdi, M., Davey-Smith, G., Ha, E., Menon, R., Murray, J. C., Thorsen, P., Hobel, C., Petrauskas, B., Williams, S. M., Lindheimer, M., Fortunato, S., Jacobsson, B., Witkin, S. S., Dolan, S. M., Ober, C., Ward, K., Frayling, T., Campbell, M. K., Kramer, M., Moore, J. H., Morken, N. H., Relton, C., Genc, M. R., Norwitz, E. R., Vanderpoel, S. & Lye, S. (2013). Preterm Birth Genome Project (PGP) - Validation of resources for preterm birth genome-wide studies. Journal of Perinatal Medicine, 41(1), 45-49. DOI: 10.1515/jpm-2012-0145.

Lewinska, M., Zelenko, U., Merzel, F., Golic Grdadolnik, S., Murray, J. C. & Rozman, D. (2013). Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure. PloS One, 8(12), e82554. PMID: 24358204.

Falah, N., McElroy, J., Snegovskikh, V., Lockwood, C. J., Norwitz, E., Murray, J. C., Kuczynski, E., Menon, R., Teramo, K., Muglia, L. J. & Morgan, T. (2013). Investigation of genetic risk factors for chronic adult diseases for association with preterm birth. Human genetics, 132(1), 57-67. PMID: 22972380.

Kim, J., Pitlick, M. M., Christine, P. J., Schaefer, A. R., Saleme, C., Comas, B., Cosentino, V., Gadow, E. & Murray, J. C. (2013). Genome-wide analysis of DNA methylation in human amnion. TheScientificWorldJournal, 2013, 678156. PMID: 23533356.

Cousminer, D. L., Berry, D. J., Timpson, N. J., Ang, W., Thiering, E., Byrne, E., Taal, H. R., Huikari, V., Bradfield, J. P., Kerkhof, M., Groen-Blokhuis, M. M., Kreiner-Møller, E., Marinelli, M., Holst, C., Leinonen, J. T., Perry, J. R., Surakka, I., Pietiläinen, O., Kettunen, J., Anttila, V., Kaakinen, M., Sovio, U., Pouta, A., Das, S., Lagou, V., Power, C., Prokopenko, I., Evans, D. M., Kemp, J. P., Pourcain, B. S., Ring, S., Palotie, A., Kajantie, E., Osmond, C., Lehtimäki, T., Viikari, J. S., Kähönen, M., Warrington, N. M., Lye, S. J., Palmer, L. J., Tiesler, C. M., Flexeder, C., Montgomery, G. W., Medland, S. E., Hofman, A., Hakonarson, H., Guxens, M., Bartels, M., Salomaa, V., Consortium, T. R., Murabito, J., Kaprio, J., Sørensen, T. I., Ballester, F., Bisgaard, H., Boomsma, D. I., Koppelman, G. H., Grant, S. F., Jaddoe, V. W., Martin, N. G., Heinrich, J., Pennell, C. E., Raitakari, O., Eriksson, J. G., Smith, G. D., Hyppönen, E., Järvelin, M., McCarthy, M. I., Ripatti, S., Widén, E. & Consortium, for the Early Growth Genetics (EGG) (2013). Genome-wide Association and Longitudinal Analyses Reveal Genetic Loci Linking Pubertal Height Growth, Pubertal Timing, and Childhood Adiposity. Human Molecular Genetics, ddt104. PMID: 23449627.

Wehby, G. L., McCarthy, A. M. (2013). Economic gradients in early child neurodevelopment: a multi-country study. Social Science & Medicine (1982), 78, 86–95. PMID: 23273409.

Bream, E. N., Leppellere, C. R., Cooper, M. E., Dagle, J. M., Merrill, D. C., Christensen, K., Simhan, H. N., Fong, C., Hallman, M., Muglia, L. J., Marazita, M. L. & Murray, J. C. (2013). Candidate gene linkage approach to identify DNA variants that predispose to preterm birth. Pediatric Research, 73(2), 135–141. PMID: 23168575.

Wehby, G. L., Félix, T. M., Goco, N., Richieri-Costa, A., Chakraborty, H., Souza, J., Pereira, R., Padovani, C., Moretti-Ferreira, D. & Murray, J. C. (2013). High dosage folic acid supplementation, oral cleft recurrence and fetal growth. International Journal of Environmental Research and Public Health, 10(2), 590–605. PMID: 23380913.

Ryckman, K. K., Berberich, S. L., Shchelochkov, O. A., Cook, D. E. & Murray, J. C. (2013). Clinical and environmental influences on metabolic biomarkers collected for newborn screening. Clinical Biochemistry, 46(1-2), 133–138. PMID: 23010448.

Ryckman, K. K., Berberich, S. L., Shchelochkov, O. A., Cook, D. E. & Murray, J. C. (2013). Clinical and environmental influences on metabolic biomarkers collected for newborn screening. Clinical biochemistry, 46(1-2), 133-8. PMID: 23010448.

Zheng, X., Feingold, E., Ryckman, K. K., Shaffer, J. R., Boyd, H. A., Feenstra, B., Melbye, M., Marazita, M. L., Murray, J. C. & Cuenco, K. T. (2013). Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. Frontiers in genetics, 4, 196. PMID: 24194744.

Falah, N., McElroy, J., Snegovskikh, V., Lockwood, C. J., Norwitz, E., Murray, J. C., Kuczynski, E., Menon, R., Teramo, K., Muglia, L. J. & Morgan, T. (2013). Investigation of genetic risk factors for chronic adult diseases for association with preterm birth. Human Genetics, 132(1), 57–67. PMID: 22972380.

de la Garza, G., Schleiffarth, J. R., Dunnwald, M., Mankad, A., Weirather, J. L., Bonde, G., Butcher, S., Mansour, T. A., Kousa, Y. A., Fukazawa, C. F., Houston, D. W., Manak, J. R., Schutte, B. C., Wagner, D. S. & Cornell, R. A. (2013). Interferon regulatory factor 6 promotes differentiation of the periderm by activating expression of Grainyhead-like 3. The Journal of Investigative Dermatology, 133(1), 68–77. PMID: 22931925.

Patel, P. J., Beaty, T. H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Wu, T., Murray, T., Rose, M., Redett, R. J., Jin, S. C., Lie, R. T., Wu-Chou, Y. H., Wang, H., Ye, X., Yeow, V., Chong, S., Jee, S. H., Shi, B. & Scott, A. F. (2013). X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts. European journal of oral sciences, 121(2), 63-8. PMID: 23489894.

Ross, A. P., Mansilla, M. A., Choe, Y., Helminski, S., Sturm, R., Maute, R. L., May, S. R., Hozyasz, K. K., Wójcicki, P., Mostowska, A., Davidson, B., Adamopoulos, I. E., Pleasure, S. J., Murray, J. C. & Zarbalis, K. S. (2013). A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting. PloS one, 8(7), e69333. PMID: 23935987.

Ryckman, K. K., Shchelochkov, O. A., Cook, D. E., Berberich, S. L., Copeland, S., Dagle, J. M. & Murray, J. C. (2013). The influence of maternal disease on metabolites measured as part of newborn screening. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstet, 26(14), 1380-3. PMID: 23550828.

Ryckman, K. K., Shchelochkov, O. A., Cook, D. E., Berberich, S. L., Copeland, S., Dagle, J. M. & Murray, J. C. (2013). The influence of maternal disease on metabolites measured as part of newborn screening. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetr, 26(14), 1380–1383. PMID: 23550828.

Leslie, E. J., Mancuso, J. L., Schutte, B. C., Cooper, M. E., Durda, K. M., L'heureux, J., Zucchero, T. M., Marazita, M. L. & Murray, J. C. (2013). Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American journal of medical genetics. Part A, 161A(10), 2535-44. PMID: 23949966.

Feenstra, B., Geller, F., Carstensen, L., Romitti, P. A., Körberg, I. B., Bedell, B., Krogh, C., Fan, R., Svenningsson, A., Caggana, M., Nordenskjöld, A., Mills, J. L., Murray, J. C. & Melbye, M. (2013). Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. JAMA, 310(7), 714-21. PMID: 23989729.

McElroy, J. J., Gutman, C. E., Shaffer, C. M., Busch, T. D., Puttonen, H., Teramo, K., Murray, J. C., Hallman, M. & Muglia, L. J. (2013). Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. Human genetics, 132(8), 935-42. PMID: 23591632.

Kim, J., Stirling, K. J., Cooper, M. E., Ascoli, M., Momany, A. M., McDonald, E. L., Ryckman, K. K., Rhea, L., Schaa, K. L., Cosentino, V., Gadow, E., Saleme, C., Shi, M., Hallman, M., Plunkett, J., Teramo, K. A., Muglia, L. J., Feenstra, B., Geller, F., Boyd, H. A., Melbye, M., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2013). Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study. BMC medical genetics, 14, 77. PMID: 23889750.

Feenstra, B., Geller, F., Carstensen, L., Romitti, P. A., Körberg, I. B., Bedell, B., Krogh, C., Fan, R., Svenningsson, A., Caggana, M., Nordenskjöld, A., Mills, J. L., Murray, J. C. & Melbye, M. (2013). Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. JAMA, 310(7), 714–721. PMID: 23989729.

McElroy, J. J., Gutman, C. E., Shaffer, C. M., Busch, T. D., Puttonen, H., Teramo, K., Murray, J. C., Hallman, M. & Muglia, L. J. (2013). Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. Human Genetics, 132(8), 935–942. PMID: 23591632.

Leslie, E. J., Mancuso, J. L., Schutte, B. C., Cooper, M. E., Durda, K. M., L’Heureux, J., Zucchero, T. M., Marazita, M. L. & Murray, J. C. (2013). Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American Journal of Medical Genetics. Part A, 161A(10), 2535–2544. PMID: 23949966.

Leslie, E. J., Murray, J. C. (2013). Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate. Clinical genetics, 84(5), 496-500. PMID: 22978696.

Lackritz, E. M., Wilson, C. B., Guttmacher, A. E., Howse, J. L., Engmann, C. M., Rubens, C. E., Mason, E. M., Muglia, L. J., Gravett, M. G., Goldenberg, R. L., Murray, J. C., Spong, C. Y. & Simpson, J. L. (2013). A solution pathway for preterm birth: accelerating a priority research agenda. The Lancet. Global health, 1(6), e328-30. PMID: 25104592.

Lackritz, E. M., Wilson, C. B., Guttmacher, A. E., Howse, J. L., Engmann, C. M., Rubens, C. E., Mason, E. M., Muglia, L. J., Gravett, M. G., Goldenberg, R. L., Murray, J. C., Spong, C. Y., Simpson, J. L. & Preterm Birth Research Priority Setting Group, (2013). A solution pathway for preterm birth: accelerating a priority research agenda. The Lancet. Global Health, 1(6), e328–330. PMID: 25104592.

Boghossian, N. S., Page, G. P., Bell, E. F., Stoll, B. J., Murray, J. C., Cotten, C. M., Shankaran, S., Walsh, M. C., Laptook, A. R., Newman, N. S., Hale, E. C., McDonald, S. A., Das, A. & Higgins, R. D. (2013). Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births. The Journal of pediatrics, 162(6), 1120-4, 1124.e1. PMID: 23324523.

Adén, U., Lin, A., Carlo, W., Leviton, A., Murray, J. C., Hallman, M., Lifton, R. P., Zhang, H., Ment, L. R. & Gene Targets for Intraventricular Hemorrhage Study Group, (2013). Candidate gene analysis: severe intraventricular hemorrhage in inborn preterm neonates. The Journal of Pediatrics, 163(5), 1503–1506.e1. PMID: 23896193.

Leslie, E. J., Murray, J. C. (2013). Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate. Clinical Genetics, 84(5), 496–500. PMID: 22978696.

Adén, U., Lin, A., Carlo, W., Leviton, A., Murray, J. C., Hallman, M., Lifton, R. P., Zhang, H. & Ment, L. R. (2013). Candidate gene analysis: severe intraventricular hemorrhage in inborn preterm neonates. The Journal of pediatrics, 163(5), 1503-6.e1. PMID: 23896193.

Brinkley, J. F., Borromeo, C., Clarkson, M., Cox, T. C., Cunningham, M. J., Detwiler, L. T., Heike, C. L., Hochheiser, H., Mejino, J. L., Travillian, R. S. & Shapiro, L. G. (2013). The ontology of craniofacial development and malformation for translational craniofacial research. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 163C(4), 232–245. PMID: 24124010.

Leslie, E. J., Marazita, M. L. (2013). Genetics of cleft lip and cleft palate. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 163C(4), 246–258. PMID: 24124047.

Gaines, L., Butali, A. & Murray, J. C. (2013). IRF6 mutations causing Van der Woude Syndrome and Popliteal Pterygium Syndrome in the African Population. ABRCMS meeting in Nashville, TN, November 13-16.

Adams-Chapman, I., Hansen, N. I., Shankaran, S., Bell, E. F., Boghossian, N. S., Murray, J. C., Laptook, A. R., Walsh, M. C., Carlo, W. A., Sánchez, P. J., Van Meurs, K. P., Das, A., Hale, E. C., Newman, N. S., Ball, M. B., Higgins, R. D., Stoll, B. J., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2013). Ten-year review of major birth defects in VLBW infants. Pediatrics, 132(1), 49–61. PMID: 23733791.

Krupitzki, H. B., Gadow, E. C., Gili, J. A., Comas, B., Cosentino, V. R., Saleme, C., Murray, J. C. & Lopez Camelo, J. S. (2013). Environmental risk factors and perinatal outcomes in preterm newborns, according to family recurrence of prematurity. American Journal of Perinatology, 30(6), 451–461. PMID: 23132119.

Ryckman, K. K., Dagle, J. M., Shchelochkov, O. A., Ehinger, N., Poole, S. D., Berberich, S. L., Reese, J. & Murray, J. C. (2013). Association of amino acids with common complications of prematurity. Pediatric Research, 73(6), 700–705. PMID: 23481552.

Alleman, B. W., Smith, A. R., Byers, H. M., Bedell, B., Ryckman, K. K., Murray, J. C. & Borowski, K. S. (2013). A proposed method to predict preterm birth using clinical data, standard maternal serum screening, and cholesterol. American Journal of Obstetrics and Gynecology, 208(6), 472.e1–11. PMID: 23500456.

Boghossian, N. S., Page, G. P., Bell, E. F., Stoll, B. J., Murray, J. C., Cotten, C. M., Shankaran, S., Walsh, M. C., Laptook, A. R., Newman, N. S., Hale, E. C., McDonald, S. A., Das, A., Higgins, R. D., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2013). Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births. The Journal of Pediatrics, 162(6), 1120–1124, 1124.e1. PMID: 23324523.

Alleman, B. W., Smith, A. R., Byers, H. M., Bedell, B., Ryckman, K. K., Murray, J. C. & Borowski, K. S. (2013). A proposed method to predict preterm birth using clinical data, standard maternal serum screening, and cholesterol. American journal of obstetrics and gynecology, 208(6), 472.e1-11. PMID: 23500456.

Krupitzki, H. B., Gadow, E. C., Gili, J. A., Comas, B., Cosentino, V. R., Saleme, C., Murray, J. C. & Lopez Camelo, J. S. (2013). Environmental risk factors and perinatal outcomes in preterm newborns, according to family recurrence of prematurity. American journal of perinatology, 30(6), 451-61. PMID: 23132119.

Gutierrez, J. A., Hannoush, Z. C., Vargas, L. G., Momany, A., Garcia, C. C., Murray, J. C. & Dunnwald, M. (2013). A Novel non-sense Mutation in Keratin 10 Causes a Familial Case of Recessive Epidermolytic Ichthyosis. Molecular genetics & genomic medicine, 1(2), 108-112. PMID: 23957016.

Ryckman, K. K., Dagle, J. M., Shchelochkov, O. A., Ehinger, N., Poole, S. D., Berberich, S. L., Reese, J. & Murray, J. C. (2013). Association of amino acids with common complications of prematurity. Pediatric research, 73(6), 700-5. PMID: 23481552.

L’Heureux, J., Murray, J. C., Newbury, E., Shinkunas, L. & Simon, C. M. (2013). Public perspectives on biospecimen procurement: what biorepositories should consider. Biopreservation and Biobanking, 11(3), 137–143. PMID: 24850089.

Gutierrez, J. A., Hannoush, Z. C., Vargas, L. G., Momany, A., Garcia, C. C., Murray, J. C. & Dunnwald, M. (2013). A Novel non-sense Mutation in Keratin 10 Causes a Familial Case of Recessive Epidermolytic Ichthyosis. Molecular Genetics & Genomic Medicine, 1(2), 108–112. PMID: 23957016.

Vila-Nova, C., Wehby, G. L., Queirós, F. C., Chakraborty, H., Félix, T. M., Goco, N., Moore, J., Gewehr, E. V., Lins, L., Affonso, C. M. & Murray, J. C. (2013). Periconceptional use of folic acid and risk of miscarriage - findings of the Oral Cleft Prevention Program in Brazil. Journal of perinatal medicine, 41(4), 461-6. PMID: 23669628.

Kim, J., Stirling, K. J., Cooper, M. E., Ascoli, M., Momany, A. M., McDonald, E. L., Ryckman, K. K., Rhea, L., Schaa, K. L., Cosentino, V., Gadow, E., Saleme, C., Shi, M., Hallman, M., Plunkett, J., Teramo, K. A., Muglia, L. J., Feenstra, B., Geller, F., Boyd, H. A., Melbye, M., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2013). Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study. BMC medical genetics, 14, 77. PMID: 23889750.

Beaty, T. H., Taub, M. A., Scott, A. F., Murray, J. C., Marazita, M. L., Schwender, H., Parker, M. M., Hetmanski, J. B., Balakrishnan, P., Mansilla, M. A., Mangold, E., Ludwig, K. U., Noethen, M. M., Rubini, M., Elcioglu, N. & Ruczinski, I. (2013). Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Human genetics, 132(7), 771-81. PMID: 23512105.

Alleman, B. W., Bell, E. F., Li, L., Dagle, J. M., Smith, P. B., Ambalavanan, N., Laughon, M. M., Stoll, B. J., Goldberg, R. N., Carlo, W. A., Murray, J. C., Cotten, C. M., Shankaran, S., Walsh, M. C., Laptook, A. R., Ellsbury, D. L., Hale, E. C., Newman, N. S., Wallace, D. D., Das, A. & Higgins, R. D. (2013). Individual and center-level factors affecting mortality among extremely low birth weight infants. Pediatrics, 132(1), e175-84. PMID: 23753096.

Adams-Chapman, I., Hansen, N. I., Shankaran, S., Bell, E. F., Boghossian, N. S., Murray, J. C., Laptook, A. R., Walsh, M. C., Carlo, W. A., Sánchez, P. J., Van Meurs, K. P., Das, A., Hale, E. C., Newman, N. S., Ball, M. B., Higgins, R. D. & Stoll, B. J. (2013). Ten-year review of major birth defects in VLBW infants. Pediatrics, 132(1), 49-61. PMID: 23733791.

Beaty, T. H., Taub, M. A., Scott, A. F., Murray, J. C., Marazita, M. L., Schwender, H., Parker, M. M., Hetmanski, J. B., Balakrishnan, P., Mansilla, M. A., Mangold, E., Ludwig, K. U., Noethen, M. M., Rubini, M., Elcioglu, N. & Ruczinski, I. (2013). Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Human Genetics, 132(7), 771–781. PMID: 23512105.

Cousminer, D. L., Berry, D. J., Timpson, N. J., Ang, W., Thiering, E., Byrne, E. M., Taal, H. R., Huikari, V., Bradfield, J. P., Kerkhof, M., Groen-Blokhuis, M. M., Kreiner-Møller, E., Marinelli, M., Holst, C., Leinonen, J. T., Perry, J. R., Surakka, I., Pietiläinen, O., Kettunen, J., Anttila, V., Kaakinen, M., Sovio, U., Pouta, A., Das, S., Lagou, V., Power, C., Prokopenko, I., Evans, D. M., Kemp, J. P., St Pourcain, B., Ring, S., Palotie, A., Kajantie, E., Osmond, C., Lehtimäki, T., Viikari, J. S., Kähönen, M., Warrington, N. M., Lye, S. J., Palmer, L. J., Tiesler, C. M., Flexeder, C., Montgomery, G. W., Medland, S. E., Hofman, A., Hakonarson, H., Guxens, M., Bartels, M., Salomaa, V., Consortium, R., Murabito, J. M., Kaprio, J., Sørensen, T. I., Ballester, F., Bisgaard, H., Boomsma, D. I., Koppelman, G. H., Grant, S. F., Jaddoe, V. W., Martin, N. G., Heinrich, J., Pennell, C. E., Raitakari, O. T., Eriksson, J. G., Smith, G. D., Hyppönen, E., Järvelin, M., McCarthy, M. I., Ripatti, S., Widén, E. & Early Growth Genetics (EGG) Consortium, (2013). Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Human Molecular Genetics, 22(13), 2735–2747. PMID: 23449627.

Alleman, B. W., Bell, E. F., Li, L., Dagle, J. M., Smith, P. B., Ambalavanan, N., Laughon, M. M., Stoll, B. J., Goldberg, R. N., Carlo, W. A., Murray, J. C., Cotten, C. M., Shankaran, S., Walsh, M. C., Laptook, A. R., Ellsbury, D. L., Hale, E. C., Newman, N. S., Wallace, D. D., Das, A., Higgins, R. D., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2013). Individual and center-level factors affecting mortality among extremely low birth weight infants. Pediatrics, 132(1), e175–184. PMID: 23753096.

Vila-Nova, C., Wehby, G. L., Queirós, F. C., Chakraborty, H., Félix, T. M., Goco, N., Moore, J., Gewehr, E. V., Lins, L., Affonso, C. M. & Murray, J. C. (2013). Periconceptional use of folic acid and risk of miscarriage - findings of the Oral Cleft Prevention Program in Brazil. Journal of Perinatal Medicine, 41(4), 461–466. PMID: 23669628.

Zheng, X., Shaffer, J. R., McHugh, C. P., Laurie, C. C., Feenstra, B., Melbye, M., Murray, J. C., Marazita, M. L. & Feingold, E. (2012). Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies. Genetic Epidemiology, 36(3), 253–262. PMID: 22714937.

Biggs, L. C., Le, M., Rhea, L., Kinoshita, A., Murray, J. C., Schutte, B. C. & Dunnwald, M. (2012). Interferon Regulatory Factor 6, a novel transcriptional regulator of embryonic development and wound healing. Faseb Journal, 26.

Radhakrishna, U., Nath, S. K., McElreavey, K., Ratnamala, U., Sun, C., Maiti, A. K., Gagnebin, M., Béna, F., Newkirk, H. L., Sharp, A. J., Everman, D. B., Murray, J. C., Schwartz, C. E., Antonarakis, S. E. & Butler, M. G. (2012). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. Journal of Medical Genetics, 49(4), 270–276. PMID: 22499347.

Kim, J., Zhao, K., Jiang, P., Lu, Z. X., Wang, J., Murray, J. C. & Xing, Y. (2012). Transcriptome landscape of the human placenta. BMC genomics, 13, 115. PMID: 22448651.

Shi, M., Murray, J. C., Marazita, M. L., Munger, R. G., Ruczinski, I., Hetmanski, J. B., Wu, T., Murray, T., Redett, R. J., Wilcox, A. J., Lie, R. T., Jabs, E. W., Wu-Chou, Y. H., Chen, P. K., Wang, H., Ye, X., Yeow, V., Chong, S. S., Shi, B., Christensen, K., Scott, A. F., Patel, P., Cheah, F. & Beaty, T. H. (2012). Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. American Journal of Medical Genetics. Part A, 158A(4), 784–794. PMID: 22419666.

Butali, A., Suzuki, S., Mansilla, M. A., Dragan, E., Suzuki, Y., Niimi, T., Yamamoto, M., Ayanga, G., Wekhembaatar, T., Furukawa, H., Fujiwawa, K., Imura, H., Petrin, A. L., Leslie, E., L'Heureux, J., Lidral, A. C., Cooper, M. E., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2012). Replication of GWAS Candidate Genes in Four Independent Populations Confirm the Role of Common Variants and Identifies Rare Variants in PAX7 and VAX1 contributing to the Etiology of Non-Syndromic CL(P). American Association for Dental Research Annual Meeting, Tampa, Florida, March 20-24.

Allen, C., Mansilla, A. & Murray, J. C. (2012). GWAS Follow-up Studies: NTN1 and NOG, New Candidates for NSCL/P. University of Iowa College of Dentistry, Iowa City, Iowa, February 14, 2012. National AADR, Tampa, Florida.

Ryckman, K. K., Shchelochkov, O. A., Ehinger, N., Poole, S. D., Berberich, S. L., Copeland, S., Reese, J., Dagle, J. M. & Murray, J. C. (2012). Essential Amino Acids are associated with Patent Ductus Arteriosus in Preterm Newborns. University of Iowa Medical Research Week (April 2-6, 2012) and Pediatric Research Day (April 13, 2012), Iowa City, Iowa.

Kim, J., Zhao, K., Jiang, P., Lu, Z., Wang, J., Murray, J. C. & Xing, Y. (2012). Transcriptome landscape of the human placenta. BMC genomics, 13, 115. PMID: 22448651.

Wehby, G. L., Pedersen, D. A., Murray, J. C. & Christensen, K. (2012). The effects of oral clefts on hospital use throughout the lifespan. BMC health services research, 12, 58. PMID: 22405490.

Wehby, G. L., Murray, J. C., Wilcox, A. & Lie, R. T. (2012). Smoking and body weight: evidence using genetic instruments. Economics and Human Biology, 10(2), 113–126. PMID: 22024417.

Wehby, G. L., Pedersen, D. A., Murray, J. C. & Christensen, K. (2012). The effects of oral clefts on hospital use throughout the lifespan. BMC health services research, 12, 58. PMID: 22405490.

Wehby, G. L., Murray, J. C., Wilcox, A. & Lie, R. T. (2012). Smoking and body weight: evidence using genetic instruments. Economics and human biology, 10(2), 113-26. PMID: 22024417.

Cook, D. E., Ryckman, K. K., Murray, J. C., Berberich, S. L. & Weber, P. J. (2012). Mapping Newborn Screen Data: A Geographic Exploration. University of Iowa, Medical Research Day.

L'Heureux, J. L., Murray, J. C., Winkour, P., Weiner, G., Newbury, E., Shinkunas, L., Zimmerman, B. & Simon, C. M. (2012). Development of a comprehensive DNA and tissue Biobank at the University of Iowa: The UI Bank. University of Iowa Medical Research Week (April 2-6 2012), Iowa City, Iowa.

Cook, D. E., Ryckman, K. K., Murray, J. C., Berberich, S. L. & Weyer, P. J. (2012). Mapping Newborn Screen Data: A Geographic Exploration. University of Iowa Pediatric Research Day Iowa City, Iowa.

Biggs, L., Leslie, E., DeMali, K., Soll, D., Murray, J. C. & Dunnwald, M. (2012). Interferon Regulatory Factor 6 regulates Arhgap29 to modulate keratinocyte migration. University of Iowa, Pediatric Research Day, Iowa City, Iowa.

Alul, F., Ryckman, K. K., Shchelochkov, O. A., Berberich, S. L. & Murray, J. C. (2012). Genotype Associations with Thyroid Stimulating Hormone Concentration in Newborns. Iowa City: University of Iowa, Pediatric Research Day.

Feenstra, B., Geller, F., Krogh, C., Hollegaard, M. V., Gørtz, S., Boyd, H. A., Murray, J. C., Hougaard, D. M. & Melbye, M. (2012). Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis. Nature genetics, 44(3), 334-7. PMID: 22306654.

Momany, A., Rhea, L., Middleton, K., Busch, T., Berends, S., Murray, J. & Dagle, J. (2012). Genetics Contributions to Preterm Patent Ductus Arteriosus. University of Iowa, Pediatric Research Day, Iowa City, Iowa.

McCarthy, A. M., Wehby, G. L., Barron, S., Aylward, G. P., Castilla, E. E., Javois, L. C., Goco, N. & Murray, J. C. (2012). Application of neurodevelopmental screening to a sample of South American infants: the Bayley Infant Neurodevelopmental Screener (BINS). Infant behavior & development, 35(2), 280-94. PMID: 22244313.

Shi, M., Murray, J. C., Marazita, M. L., Munger, R. G., Ruczinski, I., Hetmanski, J. B., Wu, T., Murray, T., Redett, R. J., Wilcox, A. J., Lie, R. T., Jabs, E. W., Wu-Chou, Y. H., Chen, P. K., Wang, H., Ye, X., Yeow, V., Chong, S. S., Shi, B., Christensen, K., Scott, A. F., Patel, P., Cheah, F. & Beaty, T. H. (2012). Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. American journal of medical genetics. Part A, 158A(4), 784-94. PMID: 22419666.

Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H. A., Sigurdsson, S., Ropele, S., Taal, H. R., Mook-Kanamori, D. O., Coker, L. H., Longstreth, W. T., Niessen, W. J., DeStefano, A. L., Beiser, A., Zijdenbos, A. P., Struchalin, M., Jack, C. R., Rivadeneira, F., Uitterlinden, A. G., Knopman, D. S., Hartikainen, A., Pennell, C. E., Thiering, E., Steegers, E. A., Hakonarson, H., Heinrich, J., Palmer, L. J., Jarvelin, M., McCarthy, M. I., Grant, S. F., St Pourcain, B., Timpson, N. J., Smith, G. D., Sovio, U., Consortium, E. G., Nalls, M. A., Au, R., Hofman, A., Gudnason, H., van der Lugt, A., Harris, T. B., Meeks, W. M., Vernooij, M. W., van Buchem, M. A., Catellier, D., Jaddoe, V. W., Gudnason, V., Windham, B. G., Wolf, P. A., van Duijn, C. M., Mosley, T. H., Schmidt, H., Launer, L. J., Breteler, M. M., DeCarli, C., Heart, C. f. & Aging Research in Genomic Epidemiology Consortium, (2012). Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, 44(5), 539–544. PMID: 22504418.

Taal, H. R., Pourcain, B. S., Thiering, E., Das, S., Mook-Kanamori, D. O., Warrington, N. M., Kaakinen, M., Kreiner-Møller, E., Bradfield, J. P., Freathy, R. M., Geller, F., Guxens, M., Cousminer, D. L., Kerkhof, M., Timpson, N. J., Ikram, M. A., Beilin, L. J., Bønnelykke, K., Buxton, J. L., Charoen, P., Chawes, B. L., Eriksson, J., Evans, D. M., Hofman, A., Kemp, J. P., Kim, C. E., Klopp, N., Lahti, J., Lye, S. J., McMahon, G., Mentch, F. D., Müller, M., O’Reilly, P. F., Prokopenko, I., Rivadeneira, F., Steegers, E. A., Sunyer, J., Tiesler, C., Yaghootkar, H., Heart, C. f., Aging Research in Genetic Epidemiology (CHARGE) Consortium,, Breteler, M. M., Debette, S., Fornage, M., Gudnason, V., Launer, L. J., van der Lugt, A., Mosley, T. H., Seshadri, S., Smith, A. V., Vernooij, M. W., Early Genetics & Lifecourse Epidemiology (EAGLE) consortium,, Blakemore, A. I., Chiavacci, R. M., Feenstra, B., Fernandez-Benet, J., Grant, S. F., Hartikainen, A., van der Heijden, Albert J.,, Iñiguez, C., Lathrop, M., McArdle, W. L., Mølgaard, A., Newnham, J. P., Palmer, L. J., Palotie, A., Pouta, A., Ring, S. M., Sovio, U., Standl, M., Uitterlinden, A. G., Wichmann, H., Vissing, N. H., DeCarli, C., van Duijn, C. M., McCarthy, M. I., Koppelman, G. H., Estivill, X., Hattersley, A. T., Melbye, M., Bisgaard, H., Pennell, C. E., Widen, E., Hakonarson, H., Smith, G. D., Heinrich, J., Jarvelin, M., Early Growth Genetics (EGG) Consortium, & Jaddoe, V. W. (2012). Common variants at 12q15 and 12q24 are associated with infant head circumference. Nature Genetics, 44(5), 532–538. PMID: 22504419.

McCarthy, A. M., Wehby, G. L., Barron, S., Aylward, G. P., Castilla, E. E., Javois, L. C., Goco, N. & Murray, J. C. (2012). Application of neurodevelopmental screening to a sample of South American infants: the Bayley Infant Neurodevelopmental Screener (BINS). Infant Behavior & Development, 35(2), 280–294. PMID: 22244313.

Radhakrishna, U., Nath, S. K., McElreavey, K., Ratnamala, U., Sun, C., Maiti, A. K., Gagnebin, M., Béna, F., Newkirk, H. L., Sharp, A. J., Everman, D. B., Murray, J. C., Schwartz, C. E., Antonarakis, S. E. & Butler, M. G. (2012). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. Journal of medical genetics, 49(4), 270-6. PMID: 22499347.

Zheng, X., Shaffer, J. R., McHugh, C. P., Laurie, C. C., Feenstra, B., Melbye, M., Murray, J. C., Marazita, M. L. & Feingold, E. (2012). Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies. Genetic epidemiology, 36(3), 253-62. PMID: 22714937.

Marazita, M. L. (2012). The evolution of human genetic studies of cleft lip and cleft palate. Annual Review of Genomics and Human Genetics, 13, 263–283. PMID: 22703175.

Boghossian, N. S., Horbar, J. D., Murray, J. C. & Carpenter, J. H. (2012). Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: the VON charts. American journal of medical genetics. Part A, 158A(2), 322-32. PMID: 22246859.

Jugessur, A., Skare, Ø., Lie, R. T., Wilcox, A. J., Christensen, K., Christiansen, L., Nguyen, T. T., Murray, J. C. & Gjessing, H. K. (2012). X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia. PloS One, 7(6), e39240. PMID: 22723972.

Ryckman, K. K., Cook, D. E., Berberich, S. L., Shchelochkov, O. A., Berends, S. K., Busch, T., Dagle, J. M. & Murray, J. C. (2012). Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns. Journal of pediatric endocrinology & metabolism: JPEM, 25(3-4), 301–305. PMID: 22768660.

Letra, A., Fakhouri, W., Fonseca, R. F., Menezes, R., Kempa, I., Prasad, J. L., McHenry, T. G., Lidral, A. C., Moreno, L., Murray, J. C., Daack-Hirsch, S., Marazita, M. L., Castilla, E. E., Lace, B., Orioli, I. M., Granjeiro, J. M., Schutte, B. C. & Vieira, A. R. (2012). Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate. PloS One, 7(9), e45441. PMID: 23029012.

Jugessur, A., Skare, Ø., Lie, R. T., Wilcox, A. J., Christensen, K., Christiansen, L., Nguyen, T. T., Murray, J. C. & Gjessing, H. K. (2012). X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia. PloS one, 7(6), e39240. PMID: 22723972.

Jugessur, A., Wilcox, A. J., Murray, J. C., Gjessing, H. K., Nguyen, T. T., Nilsen, R. M. & Lie, R. T. (2012). Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data. Norsk Epidemiologi = Norwegian Journal of Epidemiology, 21(2), 241–250. PMID: 26451072.

Pinnaro, C., Borowski, K., Ryckman, K., Bedell, B., Feenstra, B., Melbye, M. & Murray, J. (2012). Evaluation of Maternal Cholesterol and Inflammation for Contributions to Spontaneous Preterm Labor (sPTL). University of Iowa, Pediatric Research Day, Iowa City, Iowa.

Mitchell, K., O’Sullivan, J., Missero, C., Blair, E., Richardson, R., Anderson, B., Antonini, D., Murray, J. C., Shanske, A. L., Schutte, B. C., Romano, R., Sinha, S., Bhaskar, S. S., Black, G. C., Dixon, J. & Dixon, M. J. (2012). Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus. American Journal of Human Genetics, 90(1), 69–75. PMID: 22197488.

Dietz, A., Pedersen, D. A., Jacobsen, R., Wehby, G. L., Murray, J. C. & Christensen, K. (2012). Risk of breast cancer in families with cleft lip and palate. Annals of Epidemiology, 22(1), 37–42. PMID: 22037380.

Ryckman, K. K., Feenstra, B., Shaffer, J. R., Bream, E. N., Geller, F., Feingold, E., Weeks, D. E., Gadow, E., Cosentino, V., Saleme, C., Simhan, H. N., Merrill, D., Fong, C., Busch, T., Berends, S. K., Comas, B., Camelo, J. L., Boyd, H., Laurie, C. C., Crosslin, D., Zhang, Q., Doheny, K. F., Pugh, E., Melbye, M., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2012). Replication of a genome-wide association study of birth weight in preterm neonates. The Journal of Pediatrics, 160(1), 19–24.e4. PMID: 21885063.

Wehby, G. L., Tyler, M. C., Lindgren, S., Romitti, P., Robbins, J. & Damiano, P. (2012). Oral clefts and behavioral health of young children. Oral Diseases, 18(1), 74–84. PMID: 21883709.

Rahimov, F., Jugessur, A. & Murray, J. C. (2012). Genetics of nonsyndromic orofacial clefts. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 49(1), 73–91. PMID: 21545302.

Biggs, L. C., Rhea, L., Schutte, B. C. & Dunnwald, M. (2012). Interferon regulatory factor 6 is necessary, but not sufficient, for keratinocyte differentiation. The Journal of Investigative Dermatology, 132(1), 50–58. PMID: 21918538.

Dietz, A., Pedersen, D. A., Jacobsen, R., Wehby, G. L., Murray, J. C. & Christensen, K. (2012). Risk of breast cancer in families with cleft lip and palate. Annals of epidemiology, 22(1), 37-42. PMID: 22037380.

Ryckman, K. K., Cook, D. E., Berberich, S. L., Shchelochkov, O. A., Berends, S. K., Busch, T., Dagle, J. M. & Murray, J. C. (2012). Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns. Journal of pediatric endocrinology & metabolism : JPEM, 25(3-4), 301-5. PMID: 22768660.

Wu, T., Fallin, M. D., Shi, M., Ruczinski, I., Liang, K. Y., Hetmanski, J. B., Wang, H., Ingersoll, R. G., Huang, S., Ye, X., Wu-Chou, Y., Chen, P. K., Jabs, E. W., Shi, B., Redett, R., Scott, A. F., Murray, J. C., Marazita, M. L., Munger, R. G. & Beaty, T. H. (2012). Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. Birth Defects Research. Part A, Clinical and Molecular Teratology, 94(2), 76–83. PMID: 22241686.

Feenstra, B., Geller, F., Krogh, C., Hollegaard, M. V., Gørtz, S., Boyd, H. A., Murray, J. C., Hougaard, D. M. & Melbye, M. (2012). Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis. Nature Genetics, 44(3), 334–337. PMID: 22306654.

Boghossian, N. S., Horbar, J. D., Murray, J. C., Carpenter, J. H. & Network, V. O. (2012). Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: the VON charts. American Journal of Medical Genetics. Part A, 158A(2), 322–332. PMID: 22246859.

Wu, T., Fallin, M. D., Shi, M., Ruczinski, I., Liang, K. Y., Hetmanski, J. B., Wang, H., Ingersoll, R. G., Huang, S., Ye, X., Wu-Chou, Y. H., Chen, P. K., Jabs, E. W., Shi, B., Redett, R., Scott, A. F., Murray, J. C., Marazita, M. L., Munger, R. G. & Beaty, T. H. (2012). Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. Birth defects research. Part A, Clinical and molecular teratology, 94(2), 76-83. PMID: 22241686.

Byers, H. M., Dagle, J. M., Klein, J. M., Ryckman, K. K., McDonald, E. L., Murray, J. C. & Borowski, K. S. (2012). Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn. Pediatric research, 71(2), 162-7. PMID: 22258127.

Weirather, J. L., Wilson, M. E. & Donelson, J. E. (2012). Mapping of VSG similarities in Trypanosoma brucei. Molecular and Biochemical Parasitology, 181(2), 141–152. PMID: 22079099.

Byers, H. M., Dagle, J. M., Klein, J. M., Ryckman, K. K., McDonald, E. L., Murray, J. C. & Borowski, K. S. (2012). Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn. Pediatric Research, 71(2), 162–167. PMID: 22258127.

Ryckman, K. K., Feenstra, B., Shaffer, J. R., Bream, E. N., Geller, F., Feingold, E., Weeks, D. E., Gadow, E., Cosentino, V., Saleme, C., Simhan, H. N., Merrill, D., Fong, C. T., Busch, T., Berends, S. K., Comas, B., Camelo, J. L., Boyd, H., Laurie, C. C., Crosslin, D., Zhang, Q., Doheny, K. F., Pugh, E., Melbye, M., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2012). Replication of a genome-wide association study of birth weight in preterm neonates. The Journal of pediatrics, 160(1), 19-24.e4. PMID: 21885063.

Letra, A., Fakhouri, W., Fonseca, R. F., Menezes, R., Kempa, I., Prasad, J. L., McHenry, T. G., Lidral, A. C., Moreno, L., Murray, J. C., Daack-Hirsch, S., Marazita, M. L., Castilla, E. E., Lace, B., Orioli, I. M., Granjeiro, J. M., Schutte, B. C. & Vieira, A. R. (2012). Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate. PloS one, 7(9), e45441. PMID: 23029012.

Rahimov, F., Jugessur, A. & Murray, J. C. (2012). Genetics of nonsyndromic orofacial clefts. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 49(1), 73-91. PMID: 21545302.

Mitchell, K., O'Sullivan, J., Missero, C., Blair, E., Richardson, R., Anderson, B., Antonini, D., Murray, J. C., Shanske, A. L., Schutte, B. C., Romano, R. A., Sinha, S., Bhaskar, S. S., Black, G. C., Dixon, J. & Dixon, M. J. (2012). Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus. American journal of human genetics, 90(1), 69-75. PMID: 22197488.

Bertolacini, C. D., Ribeiro-Bicudo, L. A., Petrin, A., Richieri-Costa, A. & Murray, J. C. (2012). Clinical findings in patients with GLI2 mutations--phenotypic variability. Clinical genetics, 81(1), 70-5. PMID: 21204792.

Bertolacini, C. D., Ribeiro-Bicudo, L. A., Petrin, A., Richieri-Costa, A. & Murray, J. C. (2012). Clinical findings in patients with GLI2 mutations–phenotypic variability. Clinical Genetics, 81(1), 70–75. PMID: 21204792.

Wehby, G. L., McCarthy, A. M., Castilla, E. E. & Murray, J. C. (2012). The Impact of Household Investments on Early Child Neurodevelopment and on Racial and Socioeconomic Developmental Gaps - Evidence from South America. Forum for health economics & policy, 14(2). PMID: 22639558.

Geller, F., Feenstra, B., Melbye, M., Myhre, R., Myking, S., Sorensen, T. A., Magnus, P., Marazita, M. L., Murray, J. C. & Jacobsson, B. (2012). Genome-wide association study of preterm delivery in mothers. (#3028T), pp. 775. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Wehby, G. L., Moreno, L. M., Romitti, P., Christensen, K., DeRoo, L., Wilcox, A., Munger, R., Lie, R. & Murray, J. C. (2012). Genetic instrumental variable studies of the effects of maternal risk factors in oral clefts. (#1564F), pp. 331. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Alul, F., Shchelochkov, O., Berberich, S., Murray, J. & Ryckman, K. (2012). Genetic associations with neonatal thyroid stimulating hormone levels. (#1882T), pp. 425. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Leslie, E. J., Mansilla, M. A., Biggs, L. C., Schuette, K., Bullard, S., Cooper, M., Dunnwald, M., Lidral, A. C., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2012). Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth Defects Research. Part A, Clinical and Molecular Teratology, 94(11), 934–942. PMID: 23008150.

Ryckman, K. K., Dagle, J. M., Shchelochkov, O. A., Berberich, S. L. & Murray, J. C. (2012). Genetic associations with essential aminon acids in infants with patent ductus arteriosus. (Vols. #1344T). pp. 272. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10, 2012.

Miller, S., Nidney, N., Weinberg, S., Marazita, M. L., Murray, J. C., Wehby, G. L. & Moreno, L. M. (2012). Genotype-phenotype correlations of facial shape and asymmetry in unaffected relatives of children with non-syndromic cleft lip/palate and controls. (#1937F), pp. 442. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Falah, N., McElroy, J., Snegovskikh, V., Lockwood, C., Kuczynski, E., Norwitz, E., Murray, J., Menon, R., Teramo, K., Uglia, K. M. & Morgan, T. (2012). Investigation of genetic risk factors for chronic adult diseases in preterm birth. (#3030T), pp. 775. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Bailey-Wilson, J. E., Parker, M. M., Szymczak, S., Li, Q., Cropp, C. D., Nothen, M. M., Hetmanski, J. B., Ling, H., Pugh, E. W., Duggal, P., Taub, M. A., Ruczinski, I., Scott, A. F., Marazita, M. L., Murray, J. C., Mangold, E. & Beaty, T. H. (2012). Using Whole Exome Sequencing to Identify Rare Causal Variants for Oral Clefts in Multiplex Families with a Focus on Syrian Families. Genetic Epidemiology, 36(7), 738–739.

Beaty, T. H., Ruczinski, I., Parker, M. M., Hetmanski, J. B., Duggal, P., Taub, M. A., Szymczak, S., Li, Q., Crop, C., Ling, H., Pugh, E. W., Wu-Chou, Y. H., Bailey-Wilson, J. `., Marazita, M. L., Murray, J. C., Mangold, E., Noethen, M. M., Ludwig, K. & Scott, A. F. (2012). Using whole exome sequencing to identify rare causal variants for oral clects in multiplex families. (#1512T), pp. 318. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Leslie, E. J., Goudy, S., Cunningham, M. & Murray, J. C. (2012). RIPK4 mutations explain a portion of IRF6-negative popliteal p terygium cases. (#2762T), pp. 697. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Alleman, B. W., Myking, S., Ryckman, K. K., Myhre, R., Feingold, E., Feenstra, B., Geller, F., Boyd, H. A., Shaffer, J. R., Zhang, Q., Begum, F., Crosslin, D., Doheny, K., Pugh, E., Pay, A. S., Ostensen, I. H., Morken, N., Magnus, P., Marazita, M. L., Jacobsson, B., Melbye, M., Murray, J. C., Gene, Environment Association Studies (GENEVA) Consortium,, Mother, N. & Child Cohort Study (MoBA) Genome-Wide Association Study Group, (2012). No observed association for mitochondrial SNPs with preterm delivery and related outcomes. Pediatric Research, 72(5), 539–544. PMID: 22902432.

Wehby, G. L., Goco, N., Moretti-Ferreira, D., Felix, T., Richieri-Costa, A., Padovani, C., Queiros, F., Guimaraes, C. V., Pereira, R., Litavecz, S., Hartwell, T., Chakraborty, H., Javois, L. & Murray, J. C. (2012). Oral cleft prevention program (OCPP). BMC pediatrics, 12, 184. PMID: 23181832.

Wu, T., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Murray, T., Redett, R. J., Fallin, M. D., Liang, K. Y., Patel, P. J., Jin, S. C., Zhang, T. X., Schwender, H., Wu-Chou, Y. H., Chen, P. K., Chong, S. S., Cheah, F., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E. W., Shi, B., Wilcox, A. J., Lie, R. T., Jee, S. H., Christensen, K., Scott, A. F. & Beaty, T. H. (2012). Evidence of gene-environment interaction for the chromosome 4 and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. (#1472W), pp. 307. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10, 2012.

Harris, C., Leslie, E., Fulton, R., Miner, T., Appelbaum, E., Fronick, C., Mead, M., Larson, D., Mansilla, M. A., Lidral, A., Moreno, L., Hecht, J., Marazita, M., Scott, A., Beaty, T., Murray, J., Wilson, R. & Weinstock, G. (2012). Deep sequencing of genomic regions associated with cleft lilp susceptibility. (#2325W), pp. 567. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Reis, L. M., Tyler, R. C., Volkmann Kloss, B. A., Schilter, K. F., Levin, A. V., Lowry, R. B., Zwijnenburg, P. J., Stroh, E., Broeckel, U., Murray, J. C. & Semina, E. V. (2012). PITX2 and FOXC1 spectrum of mutations in ocular syndromes. European journal of human genetics : EJHG, 20(12), 1224-33. PMID: 22569110.

Pappas, A., Shankaran, S., Hansen, N. I., Bell, E. F., Stoll, B. J., Laptook, A. R., Walsh, M. C., Das, A., Bara, R., Hale, E. C., Newman, N. S., Boghossian, N. S., Murray, J. C., Cotten, C. M., Adams-Chapman, I., Hamrick, S. & Higgins, R. D. (2012). Outcome of extremely preterm infants (<1,000 g) with congenital heart defects from the National Institute of Child Health and Human Development Neonatal Research Network. Pediatric cardiology, 33(8), 1415-26. PMID: 22644414.

Dagle, J. M., Murray, J. C. (2012). Applying deep DNA sequencing to common, complex pediatric traits. Pediatrics, 130(6), e1677-8. PMID: 23166345.

Butali, A., Suzuki, S., Mansilla, M. A., Cooper, M. E., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2012). Additional Evidence for the Role of GWAS Candidate Genes (PAX7 and VAX1) in the Etiology of Non-syndromic CL(P). American Cleft Palate-Craniofacial Association Annual Meeting, San Jose, California, April 17-21.

Tyrrell, J., Huikari, V., Christie, J. T., Cavadino, A., Bakker, R., Brion, M. J., Geller, F., Paternoster, L., Myhre, R., Potter, C., Johnson, P. C., Ebrahim, S., Feenstra, B., Hartikainen, A. L., Hattersley, A. T., Hofman, A., Kaakinen, M., Lowe, L. P., Magnus, P., McConnachie, A., Melbye, M., Ng, J. W., Nohr, E. A., Power, C., Ring, S. M., Sebert, S. P., Sengpiel, V., Taal, H. R., Watt, G. C., Sattar, N., Relton, C. L., Jacobsson, B., Frayling, T. M., Sørensen, T. I., Murray, J. C., Lawlor, D. A., Pennell, C. E., Jaddoe, V. W., Hypponen, E., Lowe, Jr, W. L., Jarvelin, M. R., Davey Smith, G. & Freathy, R. M. (2012). Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight. Human molecular genetics, 21(24), 5344-58. PMID: 22956269.

Tyrrell, J., Huikari, V., Christie, J. T., Cavadino, A., Bakker, R., Brion, M. A., Geller, F., Paternoster, L., Myhre, R., Potter, C., Johnson, P. C., Ebrahim, S., Feenstra, B., Hartikainen, A., Hattersley, A. T., Hofman, A., Kaakinen, M., Lowe, L. P., Magnus, P., McConnachie, A., Melbye, M., Ng, J. W., Nohr, E. A., Power, C., Ring, S. M., Sebert, S. P., Sengpiel, V., Taal, H. R., Watt, G. C., Sattar, N., Relton, C. L., Jacobsson, B., Frayling, T. M., Sørensen, T. I., Murray, J. C., Lawlor, D. A., Pennell, C. E., Jaddoe, V. W., Hypponen, E., Lowe, W. L., Jarvelin, M., Davey Smith, G., Freathy, R. M. & Early Growth Genetics (EGG) Consortium, (2012). Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight. Human Molecular Genetics, 21(24), 5344–5358. PMID: 22956269.

Pappas, A., Shankaran, S., Hansen, N. I., Bell, E. F., Stoll, B. J., Laptook, A. R., Walsh, M. C., Das, A., Bara, R., Hale, E. C., Newman, N. S., Boghossian, N. S., Murray, J. C., Cotten, C. M., Adams-Chapman, I., Hamrick, S. & Higgins, R. D. (2012). Outcome of extremely preterm infants (<1,000 g) with congenital heart defects from the National Institute of Child Health and Human Development Neonatal Research Network. Pediatric Cardiology, 33(8), 1415–1426. PMID: 22644414.

Cook, D., Dagle, J., Ryckman, K. & Murray, J. (2012). dbGENO: A web based complex disease curation pipeline. (#3537F), pp. 916. American Society of Human Genetics 62nd Annual Meeting, San Francisco, California, November 6-10.

Alleman, B. W., Myking, S., Ryckman, K. K., Myhre, R., Feingold, E., Feenstra, B., Geller, F., Boyd, H. A., Shaffer, J. R., Zhang, Q., Begum, F., Crosslin, D., Doheny, K., Pugh, E., Pay, A. S., Ostensen, I. H., Morken, N. H., Magnus, P., Marazita, M. L., Jacobsson, B., Melbye, M. & Murray, J. C. (2012). No observed association for mitochondrial SNPs with preterm delivery and related outcomes. Pediatric research, 72(5), 539-44. PMID: 22902432.

Leslie, E. J., Mansilla, M. A., Biggs, L. C., Schuette, K., Bullard, S., Cooper, M., Dunnwald, M., Lidral, A. C., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2012). Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth defects research. Part A, Clinical and molecular teratology, 94(11), 934-42. PMID: 23008150.

Reis, L. M., Tyler, R. C., Volkmann Kloss, B. A., Schilter, K. F., Levin, A. V., Lowry, R. B., Zwijnenburg, P. J., Stroh, E., Broeckel, U., Murray, J. C. & Semina, E. V. (2012). PITX2 and FOXC1 spectrum of mutations in ocular syndromes. European journal of human genetics: EJHG, 20(12), 1224–1233. PMID: 22569110.

Wehby, G. L., Goco, N., Moretti-Ferreira, D., Felix, T., Richieri-Costa, A., Padovani, C., Queiros, F., Guimaraes, C. V., Pereira, R., Litavecz, S., Hartwell, T., Chakraborty, H., Javois, L. & Murray, J. C. (2012). Oral cleft prevention program (OCPP). BMC pediatrics, 12, 184. PMID: 23181832.

Dagle, J. M., Murray, J. C. (2012). Applying deep DNA sequencing to common, complex pediatric traits. Pediatrics, 130(6), e1677–1678. PMID: 23166345.

Boghossian, N. S., Horbar, J. D., Carpenter, J. H., Murray, J. C. & Bell, E. F. (2012). Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network. The Journal of pediatrics, 160(5), 774-780.e11. PMID: 22177989.

Ryckman, K. K., Shchelochkov, O. A., Ehinger, N., Poole, S. D., Berberich, S. L., Copeland, S., Reese, J., Dagle, J. M. & Murray, J. C. (2012). Essential Amino Acids are associated with Patent Ductus Arteriosus in Preterm Newborns. Annual Meeting of the Pediatric Academic Society (April 28-May 1, 2012), Boston, Massachusetts.

Laurie, C. C., Laurie, C. A., Rice, K., Doheny, K. F., Zelnick, L. R., McHugh, C. P., Ling, H., Hetrick, K. N., Pugh, E. W., Amos, C., Wei, Q., Wang, L., Lee, J. E., Barnes, K. C., Hansel, N. N., Mathias, R., Daley, D., Beaty, T. H., Scott, A. F., Ruczinski, I., Scharpf, R. B., Bierut, L. J., Hartz, S. M., Landi, M. T., Freedman, N. D., Goldin, L. R., Ginsburg, D., Li, J., Desch, K. C., Strom, S. S., Blot, W. J., Signorello, L. B., Ingles, S. A., Chanock, S. J., Berndt, S. I., Le Marchand, L., Henderson, B. E., Monroe, K. R., Heit, J. A., de Andrade, M., Armasu, S. M., Regnier, C., Lowe, W. L., Hayes, M. G., Marazita, M. L., Feingold, E., Murray, J. C., Melbye, M., Feenstra, B., Kang, J. H., Wiggs, J. L., Jarvik, G. P., McDavid, A. N., Seshan, V. E., Mirel, D. B., Crenshaw, A., Sharopova, N., Wise, A., Shen, J., Crosslin, D. R., Levine, D. M., Zheng, X., Udren, J. I., Bennett, S., Nelson, S. C., Gogarten, S. M., Conomos, M. P., Heagerty, P., Manolio, T., Pasquale, L. R., Haiman, C. A., Caporaso, N. & Weir, B. S. (2012). Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics, 44(6), 642–650. PMID: 22561516.

Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H. A., Sigurdsson, S., Ropele, S., Taal, H. R., Mook-Kanamori, D. O., Coker, L. H., Longstreth, W. T., Niessen, W. J., DeStefano, A. L., Beiser, A., Zijdenbos, A. P., Struchalin, M., Jack, C. R., Rivadeneira, F., Uitterlinden, A. G., Knopman, D. S., Hartikainen, A., Pennell, C. E., Thiering, E., Steegers, E. A., Hakonarson, H., Heinrich, J., Palmer, L. J., Jarvelin, M., McCarthy, M. I., Grant, S. F., St Pourcain, B., Timpson, N. J., Smith, G. D., Sovio, U., Nalls, M. A., Au, R., Hofman, A., Gudnason, H., van der Lugt, A., Harris, T. B., Meeks, W. M., Vernooij, M. W., van Buchem, M. A., Catellier, D., Jaddoe, V. W., Gudnason, V., Windham, B. G., Wolf, P. A., van Duijn, C. M., Mosley, T. H., Schmidt, H., Launer, L. J., Breteler, M. M., DeCarli, C., Adair, L. S., Ang, W., Atalay, M., vanBeijsterveldt, T., Bergen, N., Benke, K., Berry, D., Coin, L., Davis, O. S., Elliott, P., Flexeder, C., Frayling, T., Gaillard, R., Groen-Blokhuis, M., Goh, L., Haworth, C. M., Hadley, D., Hedebrand, J., Hinney, A., Hirschhorn, J. N., Holloway, J. W., Holst, C., Hottenga, J. J., Horikoshi, M., Huikari, V., Hypponen, E., Kilpelainen, T. O., Kirin, M., Kowgier, M., Lakka, H., Lange, L. A., Lawlor, D. A., Lehtimaki, T., Lewin, A., Lindgren, C., Lindi, V., Maggi, R., Marsh, J., Middeldorp, C., Millwood, I., Murray, J. C., Nivard, M., Nohr, E. A., Ntalla, I., Oken, E., Panoutsopoulou, K., Pararajasingham, J., Rodriguez, A., Salem, R. M., Sebert, S., Siitonen, N., Strachan, D. P., Teo, Y., Valcarcel, B., Willemsen, G., Zeggini, E., Boomsma, D. I., Cooper, C., Gillman, M., Hocher, B., Lakka, T. A., Mohlke, K. L., Dedoussis, G. V., Ong, K. K., Pearson, E. R., Price, T. S., Power, C., Raitakari, O. T., Saw, S., Scherag, A., Simell, O., Sorensen, T. I. & Wilson, J. F. (2012). Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, 44(5), 539–+. DOI: 10.1038/ng.2245.

Skare, O., Jugessur, A., Lie, R. T., Wilcox, A. J., Murray, J. C., Lunde, A., Nguyen, T. T. & Gjessing, H. K. (2012). Application of a novel hybrid study design to explore gene-environment interactions in orofacial clefts. Annals of Human Genetics, 76(3), 221–236. PMID: 22497478.

Taal, H. R., St Pourcain, B., Thiering, E., Das, S., Mook-Kanamori, D. O., Warrington, N. M., Kaakinen, M., Kreiner-Moller, E., Bradfield, J. P., Freathy, R. M., Geller, F., Guxens, M., Cousminer, D. L., Kerkhof, M., Timpson, N. J., Ikram, M. A., Beilin, L. J., Bonnelykke, K., Buxton, J. L., Charoen, P., Chawes, B. L., Eriksson, J., Evans, D. M., Hofman, A., Kemp, J. P., Kim, C. E., Klopp, N., Lahti, J., Lye, S. J., McMahon, G., Mentch, F. D., Mueller-Nurasyid, M., O’Reilly, P. F., Prokopenko, I., Rivadeneira, F., Steegers, E. A., Sunyer, J., Tiesler, C., Yaghootkar, H., Breteler, M. M., Debette, S., Fornage, M., Gudnason, V., Launer, L. J., van der Lugt, A., Mosley, T. H., Seshadri, S., Smith, A. V., Vernooij, M. W., Blakemore, A. I., Chiavacci, R. M., Feenstra, B., Fernandez-Banet, J., Grant, S. F., Hartikainen, A., van der Heijden, Albert J., Iniguez, C., Lathrop, M., McArdle, W. L., Molgaard, A., Newnham, J. P., Palmer, L. J., Palotie, A., Pouta, A., Ring, S. M., Sovio, U., Standl, M., Uitterlinden, A. G., Wichmann, H., Vissing, N. H., DeCarli, C., van Duijn, C. M., McCarthy, M. I., Koppelman, G. H., Estivill, X., Hattersley, A. T., Melbye, M., Bisgaard, H., Pennell, C. E., Widen, E., Hakonarson, H., Smith, G. D., Heinrich, J., Jarvelin, M., Jaddoe, V. W., Adair, L. S., Ang, W., Atalay, M., van Beijsterveldt, T., Bergen, N., Benke, K., Berry, D., Bradfield, J. P., Charoen, P., Coin, L., Cousminer, D. L., Das, S., Davis, O. S., Elliott, P., Evans, D. M., Feenstra, B., Flexeder, C., Frayling, T., Freathy, R. M., Gaillard, R., Geller, F., Groen-Blokhuis, M., Goh, L., Guxens, M., Haworth, C. M., Hadley, D., Hedebrand, J., Hinney, A., Hirschhorn, J. N., Holloway, J. W., Holst, C., Hottenga, J. J., Horikoshi, M., Huikari, V., Hypponen, E., Iniguez, C., Kaakinen, M., Kilpelainen, T. O., Kirin, M., Kowgier, M., Lakka, H., Lange, L. A., Lawlor, D. A., Lehtimaki, T., Lewin, A., Lindgren, C., Lindi, V., Maggi, R., Marsh, J., Middeldorp, C., Millwood, I., Mook-Kanamori, D. O., Murray, J. C., Nivard, M., Nohr, E. A., Ntalla, I., Oken, E., O’Reilly, P. F., Palmer, L. J., Panoutsopoulou, K., Pararajasingham, J., Prokopenko, I., Rodriguez, A., Salem, R. M., Sebert, S., Siitonen, N., Sovio, U., St Pourcain, B., Strachan, D. P., Sunyer, J., Taal, H. R., Teo, Y., Thiering, E., Tiesler, C., Uitterlinden, A. G., Valcarcel, B., Warrington, N. M., White, S., Willemsen, G., Yaghootkar, H., Zeggini, E., Boomsma, D. I., Cooper, C., Estivill, X., Gillman, M., Grant, S. F., Hakonarson, H., Hattersley, A. T., Heinrich, J., Hocher, B., Jaddoe, V. W., Jarvelin, M., Lakka, T. A., McCarthy, M. I., Melbye, M., Mohlke, K. L., Dedoussis, G. V., Ong, K. K., Pearson, E. R., Pennell, C. E., Price, T. S., Power, C., Raitakari, O. T., Saw, S., Scherag, A., Simell, O., Sorensen, T. I., Timpson, N. J., Widen, E., Wilson, J. F., Ang, W., van Beijsterveldt, T., Bergen, N., Benke, K., Berry, D., Bradfield, J. P., Charoen, P., Coin, L., Cousminer, D. L., Das, S., Elliott, P., Evans, D. M., Frayling, T., Freathy, R. M., Gaillard, R., Groen-Blokhuis, M., Guxens, M., Hadley, D., Hottenga, J. J., Huikari, V., Hypponen, E., Kaakinen, M., Kowgier, M., Lawlor, D. A., Lewin, A., Lindgren, C., Marsh, J., Middeldorp, C., Millwood, I., Mook-Kanamori, D. O., Nivard, M., O’Reilly, P. F., Palmer, L. J., Prokopenko, I., Rodriguez, A., Sebert, S., Sovio, U., St Pourcain, B., Standl, M., Strachan, D. P., Sunyer, J., Taal, H. R., Thiering, E., Tiesler, C., Uitterlinden, A. G., Valcarcel, B., Warrington, N. M., White, S., Willemsen, G., Yaghootkar, H., Boomsma, D. I., Estivill, X., Grant, S. F., Hakonarson, H., Hattersley, A. T., Heinrich, J., Jaddoe, V. W., Jarvelin, M., McCarthy, M. I., Pennell, C. E., Power, C., Timpson, N. J., Widen, E., Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H. A., Sigurdsson, S., Ropele, S., Coker, L. H., Longstreth, W. T., Niessen, W. J., DeStefano, A. L., Beiser, A., Zijdenbos, A. P., Struchalin, M., Jack, C. R., Nalls, M. A., Au, R., Hofman, A., Gudnason, H., van der Lugt, A., Harris, T. B., Meeks, W. M., Vernooij, M. W., van Buchem, M. A., Catellier, D., Gudnason, V., Windham, B. G., Wolf, P. A., van Duijn, C. M., Mosley, T. H., Schmidt, H., Launer, L. J., Breteler, M. M. & DeCarli, C. (2012). Common variants at 12q15 and 12q24 are associated with infant head circumference. Nature Genetics, 44(5), 532–+. DOI: 10.1038/ng.2238.

Murray, T., Taub, M. A., Ruczinski, I., Scott, A. F., Hetmanski, J. B., Schwender, H., Patel, P., Zhang, T. X., Munger, R. G., Wilcox, A. J., Ye, X., Wang, H., Wu, T., Wu-Chou, Y. H., Shi, B., Jee, S. H., Chong, S., Yeow, V., Murray, J. C., Marazita, M. L. & Beaty, T. H. (2012). Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genetic Epidemiology, 36(4), 392–399. PMID: 22508319.

Miller, R. K., Stodgell, C. J., Katzman, P. J., Friedman, A., Rinderknecht, A. L., Hoffman, L., Salamone, L., Ruffolo, L., Penmetsa, A., Weidenborner, P., Aagaard-Tillery, K., Culhane, J., Wadlinger, S., Pacholski, M., Kent, M. A., Green, L., Wapner, R., Torres, C., Perou, J., Leuthner, S., Szabo, S., Landrigan, P., Chen, J., Lambertini, L., Littman, L., Sheffield, P., Golden, A., Gilbert, J., Lendor, C., Allen, S., Mantilla, K., Ma, Y., Salafia, C. M., Dalton, J. L., Misra, D., Thiex, N., Gutzman, K., Martin, A., Specker, B., Walker, C. K., Swanson, J., Holliday, C., Butler, J., Li, A., Dassanayake, R. M. A. P. S., Nanes, J., Xia, Y., Murray, J. C., Busch, T. D., Rigdon, J., Darrah, T. H., Campbell, E., Dole, N., Thorp, J., Eucker, B., Bell, C., Clark, E. B., Varner, M. W., Taggart, E., Billy, J., Stradling, S., Leavitt, J., Bell, W., Waterfall, S., O’Brien, B., Layton, M., Todd, D., Wilson, K., Durkin, M. S. & Sandoval, M. (2012). Field Experience: Use of the Human Placenta As a Biomarker for Environmental Exposures, Epigenetic, and Morphological Assessments in the National Children’s Study. Birth Defects Research Part a-Clinical and Molecular Teratology, 94(5), 383–383.

Tabor, H. K., Murray, J. C., Gammill, H. S., Kitzman, J. O., Snyder, M. W., Ventura, M., Lewis, A. P., Qiu, R., Simmons, L. E., Rubens, C. E., Santillan, M. K., Eichler, E. E., Cheng, E. Y., Bamshad, M. J. & Shendure, J. (2012). Non-invasive fetal genome sequencing: opportunities and challenges. (Vols. 158A). (10), pp. 2382-4. American journal of medical genetics. Part A. PMID: 22887792.

Pinnaro, C., McDonald, L., Bream, E., Evans, K., Smebak, L., Busch, T., Berends, S., Dagle, J. & Murray, J. (2012). Maternal Genetics and Spontaneous Preterm Birth (sPTB). Pediatric Academic Society Annual Meeting, Boston, Massachusetts, April 27-May 1.

Cook, D. E., Ryckman, K. K., Murray, J. C., Berberich, S. L. & Weyer, P. J. (2012). Mapping Newborn Screen Data: A Geographic Exploration. Annual Meeting of the Pediatric Academic Society (April 28-May 1, 2012), Boston, Massachusetts.

Stodgell, C. J., Miller, R. K., Penmetsa, A., Ruffolo, L., Busch, T., Rigdon, J., Walker, C., Szabo, S., Leuthner, S. & Murray, J. C. (2012). Gene Expression in the Human Placenta As a Function of Time: A National Children’s Study Formative Research Project. Birth Defects Research Part a-Clinical and Molecular Teratology, 94(5), 381–381.

Boghossian, N. S., Horbar, J. D., Carpenter, J. H., Murray, J. C., Bell, E. F. & Network, V. O. (2012). Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network. The Journal of Pediatrics, 160(5), 774–780.e11. PMID: 22177989.

Ryckman, K. K., Dagle, J. M., Kelsey, K., Momany, A. M. & Murray, J. C. (2012). Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates. Journal of Perinatology: Official Journal of the California Perinatal Association, 32(5), 349–355. PMID: 21960125.

Hartz, S. M., Short, S. E., Saccone, N. L., Culverhouse, R., Chen, L., Schwantes-An, T., Coon, H., Han, Y., Stephens, S. H., Sun, J., Chen, X., Ducci, F., Dueker, N., Franceschini, N., Frank, J., Geller, F., Gubjartsson, D., Hansel, N. N., Jiang, C., Keskitalo-Vuokko, K., Liu, Z., Lyytikäinen, L., Michel, M., Rawal, R., Rosenberger, A., Scheet, P., Shaffer, J. R., Teumer, A., Thompson, J. R., Vink, J. M., Vogelzangs, N., Wenzlaff, A. S., Wheeler, W., Xiao, X., Yang, B., Aggen, S. H., Balmforth, A. J., Baumeister, S. E., Beaty, T., Bennett, S., Bergen, A. W., Boyd, H. A., Broms, U., Campbell, H., Chatterjee, N., Chen, J., Cheng, Y., Cichon, S., Couper, D., Cucca, F., Dick, D. M., Foroud, T., Furberg, H., Giegling, I., Gu, F., Hall, A. S., Hällfors, J., Han, S., Hartmann, A. M., Hayward, C., Heikkilä, K., Hewitt, J. K., Hottenga, J. J., Jensen, M. K., Jousilahti, P., Kaakinen, M., Kittner, S. J., Konte, B., Korhonen, T., Landi, M., Laatikainen, T., Leppert, M., Levy, S. M., Mathias, R. A., McNeil, D. W., Medland, S. E., Montgomery, G. W., Muley, T., Murray, T., Nauck, M., North, K., Pergadia, M., Polasek, O., Ramos, E. M., Ripatti, S., Risch, A., Ruczinski, I., Rudan, I., Salomaa, V., Schlessinger, D., Styrkársdóttir, U., Terracciano, A., Uda, M., Willemsen, G., Wu, X., Abecasis, G., Barnes, K., Bickeböller, H., Boerwinkle, E., Boomsma, D. I., Caporaso, N., Duan, J., Edenberg, H. J., Francks, C., Gejman, P. V., Gelernter, J., Grabe, H. J., Hops, H., Jarvelin, M., Viikari, J., Kähönen, M., Kendler, K. S., Lehtimäki, T., Levinson, D. F., Marazita, M. L., Marchini, J., Melbye, M., Mitchell, B. D., Murray, J. C., Nöthen, M. M., Penninx, B. W., Raitakari, O., Rietschel, M., Rujescu, D., Samani, N. J., Sanders, A. R., Schwartz, A. G., Shete, S., Shi, J., Spitz, M., Stefansson, K., Swan, G. E., Thorgeirsson, T., Völzke, H., Wei, Q., Wichmann, H., Amos, C. I., Breslau, N., Cannon, D. S., Ehringer, M., Grucza, R., Hatsukami, D., Heath, A., Johnson, E. O., Kaprio, J., Madden, P., Martin, N. G., Stevens, V. L., Stitzel, J. A., Weiss, R. B., Kraft, P. & Bierut, L. J. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry, 69(8), 854–860. PMID: 22868939.

Kokitsu-Nakata, N. M., Petrin, A. L., Heard, J. P., Vendramini-Pittoli, S., Henkle, L. E., dos Santos, Daniela Vera Cruz,, Murray, J. C. & Richieri-Costa, A. (2012). Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American Journal of Medical Genetics. Part A, 158A(8), 2003–2008. PMID: 22740433.

Ludwig, K. U., Mangold, E., Herms, S., Nowak, S., Reutter, H., Paul, A., Becker, J., Herberz, R., AlChawa, T., Nasser, E., Böhmer, A. C., Mattheisen, M., Alblas, M. A., Barth, S., Kluck, N., Lauster, C., Braumann, B., Reich, R. H., Hemprich, A., Pötzsch, S., Blaumeiser, B., Daratsianos, N., Kreusch, T., Murray, J. C., Marazita, M. L., Ruczinski, I., Scott, A. F., Beaty, T. H., Kramer, F. J., Wienker, T. F., Steegers-Theunissen, R. P., Rubini, M., Mossey, P. A., Hoffmann, P., Lange, C., Cichon, S., Propping, P., Knapp, M. & Nöthen, M. M. (2012). Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nature genetics, 44(9), 968-71. PMID: 22863734.

Ludwig, K. U., Mangold, E., Herms, S., Nowak, S., Reutter, H., Paul, A., Becker, J., Herberz, R., AlChawa, T., Nasser, E., Böhmer, A. C., Mattheisen, M., Alblas, M. A., Barth, S., Kluck, N., Lauster, C., Braumann, B., Reich, R. H., Hemprich, A., Pötzsch, S., Blaumeiser, B., Daratsianos, N., Kreusch, T., Murray, J. C., Marazita, M. L., Ruczinski, I., Scott, A. F., Beaty, T. H., Kramer, F., Wienker, T. F., Steegers-Theunissen, R. P., Rubini, M., Mossey, P. A., Hoffmann, P., Lange, C., Cichon, S., Propping, P., Knapp, M. & Nöthen, M. M. (2012). Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nature Genetics, 44(9), 968–971. PMID: 22863734.

Tabor, H. K., Murray, J. C., Gammill, H. S., Kitzman, J. O., Snyder, M. W., Ventura, M., Lewis, A. P., Qiu, R., Simmons, L. E., Rubens, C. E., Santillan, M. K., Eichler, E. E., Cheng, E. Y., Bamshad, M. J. & Shendure, J. (2012). Non-invasive fetal genome sequencing: opportunities and challenges. American Journal of Medical Genetics. Part A, 158A(10), 2382–2384. PMID: 22887792.

Ryckman, K. K., Dagle, J. M., Kelsey, K., Momany, A. M. & Murray, J. C. (2012). Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates. Journal of perinatology : official journal of the California Perinatal Association, 32(5), 349-55. PMID: 21960125.

Wehby, G. L., McCarthy, A. M., Castilla, E. E. & Murray, J. C. (2012). The Impact of Household Investments on Early Child Neurodevelopment and on Racial and Socioeconomic Developmental Gaps - Evidence from South America. Forum for Health Economics & Policy, 14(2). PMID: 22639558.

Kokitsu-Nakata, N. M., Petrin, A. L., Heard, J. P., Vendramini-Pittoli, S., Henkle, L. E., dos Santos, D. V., Murray, J. C. & Richieri-Costa, A. (2012). Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American journal of medical genetics. Part A, 158A(8), 2003-8. PMID: 22740433.

Kitzman, J. O., Snyder, M. W., Ventura, M., Lewis, A. P., Qiu, R., Simmons, L. E., Gammill, H. S., Rubens, C. E., Santillan, D. A., Murray, J. C., Tabor, H. K., Bamshad, M. J., Eichler, E. E. & Shendure, J. (2012). Noninvasive whole-genome sequencing of a human fetus. Science Translational Medicine, 4(137), 137ra76. PMID: 22674554.

Skare, O., Jugessur, A., Lie, R. T., Wilcox, A. J., Murray, J. C., Lunde, A., Nguyen, T. T. & Gjessing, H. K. (2012). Application of a novel hybrid study design to explore gene-environment interactions in orofacial clefts. Annals of human genetics, 76(3), 221-36. PMID: 22497478.

Laurie, C. C., Laurie, C. A., Rice, K., Doheny, K. F., Zelnick, L. R., McHugh, C. P., Ling, H., Hetrick, K. N., Pugh, E. W., Amos, C., Wei, Q., Wang, L. E., Lee, J. E., Barnes, K. C., Hansel, N. N., Mathias, R., Daley, D., Beaty, T. H., Scott, A. F., Ruczinski, I., Scharpf, R. B., Bierut, L. J., Hartz, S. M., Landi, M. T., Freedman, N. D., Goldin, L. R., Ginsburg, D., Li, J., Desch, K. C., Strom, S. S., Blot, W. J., Signorello, L. B., Ingles, S. A., Chanock, S. J., Berndt, S. I., Le Marchand, L., Henderson, B. E., Monroe, K. R., Heit, J. A., de Andrade, M., Armasu, S. M., Regnier, C., Lowe, W. L., Hayes, M. G., Marazita, M. L., Feingold, E., Murray, J. C., Melbye, M., Feenstra, B., Kang, J. H., Wiggs, J. L., Jarvik, G. P., McDavid, A. N., Seshan, V. E., Mirel, D. B., Crenshaw, A., Sharopova, N., Wise, A., Shen, J., Crosslin, D. R., Levine, D. M., Zheng, X., Udren, J. I., Bennett, S., Nelson, S. C., Gogarten, S. M., Conomos, M. P., Heagerty, P., Manolio, T., Pasquale, L. R., Haiman, C. A., Caporaso, N. & Weir, B. S. (2012). Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature genetics, 44(6), 642-50. PMID: 22561516.

Kitzman, J. O., Snyder, M. W., Ventura, M., Lewis, A. P., Qiu, R., Simmons, L. E., Gammill, H. S., Rubens, C. E., Santillan, D. A., Murray, J. C., Tabor, H. K., Bamshad, M. J., Eichler, E. E. & Shendure, J. (2012). Noninvasive whole-genome sequencing of a human fetus. Science translational medicine, 4(137), 137ra76. PMID: 22674554.

Hartz, S. M., Short, S. E., Saccone, N. L., Culverhouse, R., Chen, L., Schwantes-An, T. H., Coon, H., Han, Y., Stephens, S. H., Sun, J., Chen, X., Ducci, F., Dueker, N., Franceschini, N., Frank, J., Geller, F., Gubjartsson, D., Hansel, N. N., Jiang, C., Keskitalo-Vuokko, K., Liu, Z., Lyytikäinen, L. P., Michel, M., Rawal, R., Rosenberger, A., Scheet, P., Shaffer, J. R., Teumer, A., Thompson, J. R., Vink, J. M., Vogelzangs, N., Wenzlaff, A. S., Wheeler, W., Xiao, X., Yang, B. Z., Aggen, S. H., Balmforth, A. J., Baumeister, S. E., Beaty, T., Bennett, S., Bergen, A. W., Boyd, H. A., Broms, U., Campbell, H., Chatterjee, N., Chen, J., Cheng, Y. C., Cichon, S., Couper, D., Cucca, F., Dick, D. M., Foroud, T., Furberg, H., Giegling, I., Gu, F., Hall, A. S., Hällfors, J., Han, S., Hartmann, A. M., Hayward, C., Heikkilä, K., Hewitt, J. K., Hottenga, J. J., Jensen, M. K., Jousilahti, P., Kaakinen, M., Kittner, S. J., Konte, B., Korhonen, T., Landi, M. T., Laatikainen, T., Leppert, M., Levy, S. M., Mathias, R. A., McNeil, D. W., Medland, S. E., Montgomery, G. W., Muley, T., Murray, T., Nauck, M., North, K., Pergadia, M., Polasek, O., Ramos, E. M., Ripatti, S., Risch, A., Ruczinski, I., Rudan, I., Salomaa, V., Schlessinger, D., Styrkársdóttir, U., Terracciano, A., Uda, M., Willemsen, G., Wu, X., Abecasis, G., Barnes, K., Bickeböller, H., Boerwinkle, E., Boomsma, D. I., Caporaso, N., Duan, J., Edenberg, H. J., Francks, C., Gejman, P. V., Gelernter, J., Grabe, H. J., Hops, H., Jarvelin, M. R., Viikari, J., Kähönen, M., Kendler, K. S., Lehtimäki, T., Levinson, D. F., Marazita, M. L., Marchini, J., Melbye, M., Mitchell, B. D., Murray, J. C., Nöthen, M. M., Penninx, B. W., Raitakari, O., Rietschel, M., Rujescu, D., Samani, N. J., Sanders, A. R., Schwartz, A. G., Shete, S., Shi, J., Spitz, M., Stefansson, K., Swan, G. E., Thorgeirsson, T., Völzke, H., Wei, Q., Wichmann, H. E., Amos, C. I., Breslau, N., Cannon, D. S., Ehringer, M., Grucza, R., Hatsukami, D., Heath, A., Johnson, E. O., Kaprio, J., Madden, P., Martin, N. G., Stevens, V. L., Stitzel, J. A., Weiss, R. B., Kraft, P. & Bierut, L. J. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of general psychiatry, 69(8), 854-60. PMID: 22868939.

Murray, T., Taub, M. A., Ruczinski, I., Scott, A. F., Hetmanski, J. B., Schwender, H., Patel, P., Zhang, T. X., Munger, R. G., Wilcox, A. J., Ye, X., Wang, H., Wu, T., Wu-Chou, Y. H., Shi, B., Jee, S. H., Chong, S., Yeow, V., Murray, J. C., Marazita, M. L. & Beaty, T. H. (2012). Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genetic epidemiology, 36(4), 392-9. PMID: 22508319.

Mossey, P. A., Shaw, W. C., Munger, R. G., Murray, J. C., Murthy, J. & Little, J. (2011). Global oral health inequalities: challenges in the prevention and management of orofacial clefts and potential solutions. Advances in Dental Research, 23(2), 247–258. PMID: 21490237.

Momany, A. M., Dallas, L. M., Berends, S. K., Murray, J. C. & Dagle, J. M. (2011). Genetic Variants in TFAP2B in Preterm Infants with Patent Ductus Arteriosus. poster presentation at the Pediatric Academic Societies and Asian Society for Pediatric Research Conference (PAS/SPR); Denver, CO.

Ryckman, K. K., Cook, D. E., Berberich, S. L., Shchelochkov, O. A., Copeland, S., Berends, S. K., Busch, T., Dagle, J. M. & Murray, J. C. (2011). Clinical and Genetic Associations with 17-hydroxyprogesterone in Preterm Neonates. poster presentation at the Pediatric Academic Societies and Asian Society for Pediatric Research Conference (PAS/SPR); Denver, CO.

O’Sullivan, J., Bitu, C. C., Daly, S. B., Urquhart, J. E., Barron, M. J., Bhaskar, S. S., Martelli-Júnior, H., dos Santos Neto, Pedro Eleuterio,, Mansilla, M. A., Murray, J. C., Coletta, R. D., Black, G. C. & Dixon, M. J. (2011). Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. American Journal of Human Genetics, 88(5), 616–620. PMID: 21549343.

Grosen, D., Bille, C., Petersen, I., Skytthe, A., Hjelmborg, Jacob von Bornemann,, Pedersen, J. K., Murray, J. C. & Christensen, K. (2011). Risk of oral clefts in twins. Epidemiology (Cambridge, Mass.), 22(3), 313–319. PMID: 21423016.

Petrin, A. L., Daack-Hirsch, S., L’Heureux, J. & Murray, J. C. (2011). A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 48(2), 222–230. PMID: 20500065.

Butali, A., Moussey, P. A., Adeyemo, W. L., Jezewski, P. A., Onwuamah, C. K., Ugboko, V. I., Adigun, A. I., Mansilla, M. A., Osaguona, A. O., Olasoji, H. O., Olaitan, P. B. & Murray, J. C. (2011). The NigeriaCRAN collaboration. Genetic studies in the Nigerian population implicate a MSX1 mutation in complex oral facial clefting disorders. American Cleft Palate-Craniofacial Association, 68th Annual Meeting,San Juan, Puerto Rico, April 5-9.

Bennett, S. N., Caporaso, N., Fitzpatrick, A. L., Agrawal, A., Barnes, K., Boyd, H. A., Cornelis, M. C., Hansel, N. N., Heiss, G., Heit, J. A., Kang, J. H., Kittner, S. J., Kraft, P., Lowe, W., Marazita, M. L., Monroe, K. R., Pasquale, L. R., Ramos, E. M., van Dam, R. M., Udren, J., Williams, K. & Consortium, G. (2011). Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience. Genetic Epidemiology, 35(3), 159–173. PMID: 21284036.

Hansen, T. G., Pedersen, J. K., Henneberg, S. W., Pedersen, D. A., Murray, J. C., Morton, N. S. & Christensen, K. (2011). Academic performance in adolescence after inguinal hernia repair in infancy: a nationwide cohort study. Anesthesiology, 114(5), 1076–1085. PMID: 21368654.

Cornelis, M. C., Monda, K. L., Yu, K., Paynter, N., Azzato, E. M., Bennett, S. N., Berndt, S. I., Boerwinkle, E., Chanock, S., Chatterjee, N., Couper, D., Curhan, G., Heiss, G., Hu, F. B., Hunter, D. J., Jacobs, K., Jensen, M. K., Kraft, P., Landi, M. T., Nettleton, J. A., Purdue, M. P., Rajaraman, P., Rimm, E. B., Rose, L. M., Rothman, N., Silverman, D., Stolzenberg-Solomon, R., Subar, A., Yeager, M., Chasman, D. I., van Dam, R. M. & Caporaso, N. E. (2011). Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. PLoS genetics, 7(4), e1002033. PMID: 21490707.

Mossey, P. A., Shaw, W. C., Munger, R. G., Murray, J. C., Murthy, J. & Little, J. (2011). Global oral health inequalities: challenges in the prevention and management of orofacial clefts and potential solutions. Advances in dental research, 23(2), 247-58. PMID: 21490237.

Grosen, D., Bille, C., Petersen, I., Skytthe, A., Hjelmborg Jv, Pedersen, J. K., Murray, J. C. & Christensen, K. (2011). Risk of oral clefts in twins. Epidemiology (Cambridge, Mass.), 22(3), 313-9. PMID: 21423016.

Hochheiser, H., Aronow, B. J., Artinger, K., Beaty, T. H., Brinkley, J. F., Chai, Y., Clouthier, D., Cunningham, M. L., Dixon, M., Donahue, L. R., Fraser, S. E., Hallgrimsson, B., Iwata, J., Klein, O., Marazita, M. L., Murray, J. C., Murray, S., de Villena, F. P., Postlethwait, J., Potter, S., Shapiro, L., Spritz, R., Visel, A., Weinberg, S. M. & Trainor, P. A. (2011). The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. Developmental Biology, 355(2), 175–182. PMID: 21458441.

Dixon, M. J., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2011). Cleft lip and palate: understanding genetic and environmental influences. Nature Reviews. Genetics, 12(3), 167–178. PMID: 21331089.

Ryckman, K. K., Dagle, J. M., Kelsey, K., Momany, A. M. & Murray, J. C. (2011). Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates. Pediatric Research, 70(1), 90–95. PMID: 21659962.

Rorick, N. K., Kinoshita, A., Weirather, J. L., Peyrard-Janvid, M., de Lima, Renata L. L. Ferreira,, Dunnwald, M., Shanske, A. L., Moretti-Ferreira, D., Koillinen, H., Kere, J., Mansilla, M. A., Murray, J. C., Goudy, S. L. & Schutte, B. C. (2011). Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome. American Journal of Medical Genetics. Part A, 155A(6), 1314–1321. PMID: 21574244.

Mutti, D. O., Cooper, M. E., Dragan, E., Jones-Jordan, L. A., Bailey, M. D., Marazita, M. L., Murray, J. C., Zadnik, K. & Group, C. S. (2011). Vitamin D receptor (VDR) and group-specific component (GC, vitamin D-binding protein) polymorphisms in myopia. Investigative Ophthalmology & Visual Science, 52(6), 3818–3824. PMID: 21357399.

Hansen, T. G., Pedersen, J. K., Henneberg, S. W., Pedersen, D. A., Murray, J. C., Morton, N. S. & Christensen, K. (2011). Academic performance in adolescence after inguinal hernia repair in infancy: a nationwide cohort study. Anesthesiology, 114(5), 1076-85. PMID: 21368654.

O'Sullivan, J., Bitu, C. C., Daly, S. B., Urquhart, J. E., Barron, M. J., Bhaskar, S. S., Martelli-Júnior, H., dos Santos Neto, P. E., Mansilla, M. A., Murray, J. C., Coletta, R. D., Black, G. C. & Dixon, M. J. (2011). Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. American journal of human genetics, 88(5), 616-20. PMID: 21549343.

Mutti, D. O., Cooper, M. E., Dragan, E., Jones-Jordan, L. A., Bailey, M. D., Marazita, M. L., Murray, J. C. & Zadnik, K. (2011). Vitamin D receptor (VDR) and group-specific component (GC, vitamin D-binding protein) polymorphisms in myopia. Investigative ophthalmology & visual science, 52(6), 3818-24. PMID: 21357399.

Rorick, N. K., Kinoshita, A., Weirather, J. L., Peyrard-Janvid, M., de Lima, R. L., Dunnwald, M., Shanske, A. L., Moretti-Ferreira, D., Koillinen, H., Kere, J., Mansilla, M. A., Murray, J. C., Goudy, S. L. & Schutte, B. C. (2011). Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome. American journal of medical genetics. Part A, 155A(6), 1314-21. PMID: 21574244.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Nguyen, T. T., Christiansen, L., Lidral, A. C. & Murray, J. C. (2011). Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia. Birth Defects Research. Part A, Clinical and Molecular Teratology, 91(2), 85–92. PMID: 21319277.

Kao, J. S., Dawson, J. D., Murray, J. C., Dagle, J. M., Berends, S. K., Gillen, S. B. & Bell, E. F. (2011). Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity. Acta Paediatrica (Oslo, Norway: 1992), 100(3), 347–351. PMID: 20969622.

Wehby, G. L., Fletcher, J. M., Lehrer, S. F., Moreno, L. M., Murray, J. C., Wilcox, A. & Lie, R. T. (2011). A genetic instrumental variables analysis of the effects of prenatal smoking on birth weight: evidence from two samples. Biodemography and social biology, 57(1), 3-32. PMID: 21845925.

Byers, H., Bedell, B., Murray, J. C., Ryckman, K. K. & Borowski, K. S. (2011). Rate of change of lipid levels in pregnancy associated with first trimester lipid levels and maternal factors. American Journal of Obstetrics and Gynecology, 204, S226–S226. DOI: 10.1016/j.ajog.2010.10.585.

Byers, H., Bedell, B., Murray, J. C., Ryckman, K. K. & Borowski, K. S. (2011). Genes of cholesterol metabolism and transport are associated with increases in lipid levels that occurs in pregnancy. American Journal of Obstetrics and Gynecology, 204, S282–S283. DOI: 10.1016/j.ajog.2010.10.739.

Wehby, G. L., Fletcher, J. M., Lehrer, S. F., Moreno, L. M., Murray, J. C., Wilcox, A. & Lie, R. T. (2011). A genetic instrumental variables analysis of the effects of prenatal smoking on birth weight: evidence from two samples. Biodemography and Social Biology, 57(1), 3–32. PMID: 21845925.

Murray, J. C. (2011). Chapter 17, Impact of the Human Genome Project on Neonatal Care. In Avery's Diseases of the Newborn: Expert Consult Online and Print. (9) Saunders and Elsevier Inc.

Wehby, G., Jugessur, A., Murray, J. C., Moreno, L., Wilcox, A. & Lie, R. T. (2011). GENES AS INSTRUMENTS FOR STUDYING RISK BEHAVIOR EFFECTS: AN APPLICATION TO MATERNAL SMOKING AND OROFACIAL CLEFTS. Health Services & Outcomes Research Methodology, 11(1-2), 54–78. PMID: 22102793.

Wehby, G. L., Prater, K., McCarthy, A. M., Castilla, E. E. & Murray, J. C. (2011). The Impact of Maternal Smoking during Pregnancy on Early Child Neurodevelopment. Journal of Human Capital, 5(2), 207–254. PMID: 22272363.

Murray, J. C. (2011). Journeys From Bedside to Bench and Back. In Medicine Science and Dreams. The Making of Physician-Scientists. (1) Springer.

Vieira, A. R., Deeley, K. B., Callahan, N. F., Noel, J. B., Anjomshoaa, I., Carricato, W. M., Schulhof, L. P., Desensi, R. S., Gandhi, P., Resick, J. M., Brandon, C. A., Rozhon, C., Patir, A., Yildirim, M., Poletta, F. A., Mereb, J. C., Letra, A., Menezes, R., Wendell, S., Lopez-Camelo, J. S., Castilla, E. E., Orioli, I. M., Seymen, F., Weyant, R. J., Crout, R., McNeil, D. W., Modesto, A. & Marazita, M. L. (2011). Detection of Streptococcus mutans Genomic DNA in Human DNA Samples Extracted from Saliva and Blood. ISRN dentistry, 2011, 543561. PMID: 21731912.

Haataja, R., Karjalainen, M. K., Luukkonen, A., Teramo, K., Puttonen, H., Ojaniemi, M., Varilo, T., Chaudhari, B. P., Plunkett, J., Murray, J. C., McCarroll, S. A., Peltonen, L., Muglia, L. J., Palotie, A. & Hallman, M. (2011). Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. PLoS genetics, 7(2), e1001293. PMID: 21304894.

Ghassibe-Sabbagh, M., Desmyter, L., Langenberg, T., Claes, F., Boute, O., Bayet, B., Pellerin, P., Hermans, K., Backx, L., Mansilla, M. A., Imoehl, S., Nowak, S., Ludwig, K. U., Baluardo, C., Ferrian, M., Mossey, P. A., Noethen, M., Dewerchin, M., François, G., Revencu, N., Vanwijck, R., Hecht, J., Mangold, E., Murray, J., Rubini, M., Vermeesch, J. R., Poirel, H. A., Carmeliet, P. & Vikkula, M. (2011). FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish. The American Journal of Human Genetics, 88(2), 150–161. DOI: 10.1016/j.ajhg.2011.01.003.

Kao, J. S., Dawson, J. D., Murray, J. C., Dagle, J. M., Berends, S. K., Gillen, S. B. & Bell, E. F. (2011). Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity. Acta paediatrica (Oslo, Norway : 1992), 100(3), 347-51. PMID: 20969622.

Dixon, M. J., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2011). Cleft lip and palate: understanding genetic and environmental influences. Nature reviews. Genetics, 12(3), 167-78. PMID: 21331089.

Petrin, A. L., Daack-Hirsch, S., L'Heureux, J. & Murray, J. C. (2011). A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 48(2), 222-30. PMID: 20500065.

Day, L. J., Schaa, K. L., Ryckman, K. K., Cooper, M., Dagle, J. M., Fong, C., Simhan, H. N., Merrill, D. C., Marazita, M. L., Murray, J. C. & England, S. K. (2011). Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birth. Reproductive Sciences (Thousand Oaks, Calif.), 18(3), 286–295. PMID: 21266667.

Day, L. J., Schaa, K. L., Ryckman, K. K., Cooper, M., Dagle, J. M., Fong, C. T., Simhan, H. N., Merrill, D. C., Marazita, M. L., Murray, J. C. & England, S. K. (2011). Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birth. Reproductive sciences (Thousand Oaks, Calif.), 18(3), 286-95. PMID: 21266667.

Byers, H. M., Bedell, B., Ryckman, K. K., Murray, J. C. & Borowski, K. S. (2011). First Trimester Lipid Level and Maternal Factors Associated with Rate of Change of Lipid Levels in Pregnancy. poster presentation at The Society for Maternal-Fetal Medicine (SMFM) 31st Annual Meeting; San Francisco, CA.

Ghassibe-Sabbagh, M., Desmyter, L., Langenberg, T., Claes, F., Boute, O., Bayet, B., Pellerin, P., Hermans, K., Backx, L., Mansilla, M. A., Imoehl, S., Nowak, S., Ludwig, K. U., Baluardo, C., Ferrian, M., Mossey, P. A., Noethen, M., Dewerchin, M., François, G., Revencu, N., Vanwijck, R., Hecht, J., Mangold, E., Murray, J., Rubini, M., Vermeesch, J. R., Poirel, H. A., Carmeliet, P. & Vikkula, M. (2011). FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish. American Journal of Human Genetics, 88(2), 150–161. PMID: 21295280.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Nguyen, T. T., Christiansen, L., Lidral, A. C. & Murray, J. C. (2011). Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia. Birth defects research. Part A, Clinical and molecular teratology, 91(2), 85-92. PMID: 21319277.

Haataja, R., Karjalainen, M. K., Luukkonen, A., Teramo, K., Puttonen, H., Ojaniemi, M., Varilo, T., Chaudhari, B. P., Plunkett, J., Murray, J. C., McCarroll, S. A., Peltonen, L., Muglia, L. J., Palotie, A. & Hallman, M. (2011). Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. PLoS genetics, 7(2), e1001293. PMID: 21304894.

Byers, H. M., Bedell, B., Ryckman, K. K., Murray, J. C. & Borowski, K. K. (2011). Genes of Cholesterol Metabolism and Transport Significantly Related to the Increase in Lipid Levels that Occur in Pregnancy. a poster presentation at The Society for Maternal-Fetal Medicine (SMFM) 31st Annual Meeting; San Francisco, CA.

Wehby, G., Jugessur, A., Murray, J. C., Moreno, L., Wilcox, A. & Lie, R. T. (2011). GENES AS INSTRUMENTS FOR STUDYING RISK BEHAVIOR EFFECTS: AN APPLICATION TO MATERNAL SMOKING AND OROFACIAL CLEFTS. Health services & outcomes research methodology, 11(1-2), 54-78. PMID: 22102793.

Myers, H., Busch, T. & Murray, J. C. (2011). Impact of Follicle Stimulating Hormone Receptor on Preterm Birth. poster presentation at University of Iowa Pediatrics Research Day, Iowa City, Iowa.

Leslie, E. J., Mansilla, M. A., Biggs, L. C., Schuette, K., Bullard, S., Zhang, T., Cooper, M., Dunnwald, M., Lidral, A. C., FitzPatrick, D., Marazita, M. L., Beaty, T. H. & Murray, J. C. (2011). GWAS follow-up mutation screen and expression analysis implicate ARHGAP29 as a novel candidate gene for nonsyndromic cleft lip/palate. poster presentation at the American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

Mansilla, A. M., Cooper, M. E., Christensen, K., Munger, R. G., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2011). Evidence of genetics interaction between SNPs in candidate genes that may confer increased risk of oral clefts. poster presentation at the American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

Butali, A., Mossey, P. A., Adeyemo, W. L., Jezewski, P. A., Onwuamah, C. K., Ogunlewe, M. O., Ugboko, V. I., Adejuyigbe, O., Adigun, A. I., Abdur-Rahman, L. O., Onah, I. I., Audu, R. A., Idigbe, E. O., Mansilla, M. A., Dragan, E. A., Petrin, A. L., Bullard, S. A., Uduezue, A. O., Akpata, O., Osaguona, A. O., Olasoji, H. O., Ligali, T. O., Kejeh, B. M., Iseh, K. R., Olaitan, P. B., Adebola, A. R., Efunkoya, E., Adesina, O. A., Oluwatosin, O. M., Murray, J. C. & Collaboration, N. (2011). Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 48(6), 646–653. PMID: 21740177.

Petrin, A. L., Dierforfff, J., Lentz, B. A., Hong, X., de la Garza, G., Cornell, R. A., Murray, J. C. & Manak, J. R. (2011). Identification of a novel clefting locus through genome-wide CNV analysis. poster presentation at the American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

L'Heureux, J., Murray, J. C. & Simon, C. M. (2011). Public views of sample collection methods for biobanks. poster presentation at the American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

Smith, A. (2011). Genetics of Preterm Birth: The Influence of Maternal Cholesterol. poster presentation at the University of Iowa Pediatrics Research Day, Iowa City, Iowa.

Knake, L. (2011). Enhancing International Collaborative Research Efforts on the Genetics of Preterm Birth in Argentina. poster presentation at the University of Iowa Pediatrics Research Day, Iowa City, Iowa.

Ryckman, K. K., Berberich, S. L., Shchelochkov, O. A., Copeland, S. & Murray, J. C. (2011). The Heritability of Metabolic Profiles in Preterm Twins. poster presentation at the American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

Butali, A., Suzuki, S., Mansilla, M. A., Dragan, E., Suzuki, Y., Nimi, T., Yamamoto, M., Ayanga, G., Erkhembaatar, T., Furukawa, H., Fujiwawa, K., Imura, H., Petrin, A. L., Leslie, E., L'Heureux, J., Lidral, A. C., Cooper, M. E., Natsume, N., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2011). Replication of GWAS Candidate Genes in Four Independent Populations Confirm the Role of Common Variants and Identifies Rare Variants in PAX7 and VAX1 contributing to the Etiology of Non-syndromic CL(P). poster presentation at American Society of Human Genetics Annual Meeting, Montreal, Canada, October 11-15.

Butali, A., Mossey, P. A., Adeyemo, W. L., Jezewski, P. A., Onwuamah, C. K., Ogunlewe, M. O., Ugboko, V. I., Adejuyigbe, O., Adigun, A. I., Abdur-Rahman, L. O., Onah, I. I., Audu, R. A., Idigbe, E. O., Mansilla, M. A., Dragan, E. A., Petrin, A. L., Bullard, S. A., Uduezue, A. O., Akpata, O., Osaguona, A. O., Olasoji, H. O., Ligali, T. O., Kejeh, B. M., Iseh, K. R., Olaitan, P. B., Adebola, A. R., Efunkoya, E., Adesina, O. A., Oluwatosin, O. M. & Murray, J. C. (2011). Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 48(6), 646-53. PMID: 21740177.

Myers, H. L., Busch, T. & Murray, J. C. (2011). Evaluating the Impact of Follicle Stimulating Hormone Receptor on Preterm Birth. 2011 AMA-MSS Interim Meeting, Joint Research Symposium, New Orleans, Louisiana.

Paternoster, L., Standl, M., Chen, C. M., Ramasamy, A., Bønnelykke, K., Duijts, L., Ferreira, M. A., Alves, A. C., Thyssen, J. P., Albrecht, E., Baurecht, H., Feenstra, B., Sleiman, P. M., Hysi, P., Warrington, N. M., Curjuric, I., Myhre, R., Curtin, J. A., Groen-Blokhuis, M. M., Kerkhof, M., Sääf, A., Franke, A., Ellinghaus, D., Fölster-Holst, R., Dermitzakis, E., Montgomery, S. B., Prokisch, H., Heim, K., Hartikainen, A. L., Pouta, A., Pekkanen, J., Blakemore, A. I., Buxton, J. L., Kaakinen, M., Duffy, D. L., Madden, P. A., Heath, A. C., Montgomery, G. W., Thompson, P. J., Matheson, M. C., Le Souëf, P., St Pourcain, B., Smith, G. D., Henderson, J., Kemp, J. P., Timpson, N. J., Deloukas, P., Ring, S. M., Wichmann, H. E., Müller-Nurasyid, M., Novak, N., Klopp, N., Rodríguez, E., McArdle, W., Linneberg, A., Menné, T., Nohr, E. A., Hofman, A., Uitterlinden, A. G., van Duijn, C. M., Rivadeneira, F., de Jongste, J. C., van der Valk, R. J., Wjst, M., Jogi, R., Geller, F., Boyd, H. A., Murray, J. C., Kim, C., Mentch, F., March, M., Mangino, M., Spector, T. D., Bataille, V., Pennell, C. E., Holt, P. G., Sly, P., Tiesler, C. M., Thiering, E., Illig, T., Imboden, M., Nystad, W., Simpson, A., Hottenga, J. J., Postma, D., Koppelman, G. H., Smit, H. A., Söderhäll, C., Chawes, B., Kreiner-Møller, E., Bisgaard, H., Melén, E., Boomsma, D. I., Custovic, A., Jacobsson, B., Probst-Hensch, N. M., Palmer, L. J., Glass, D., Hakonarson, H., Melbye, M., Jarvis, D. L., Jaddoe, V. W., Gieger, C., Strachan, D. P., Martin, N. G., Jarvelin, M. R., Heinrich, J., Evans, D. M. & Weidinger, S. (2011). Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nature genetics, 44(2), 187-92. PMID: 22197932.

Wehby, G. L., Castilla, E. E., Goco, N., Rittler, M., Cosentino, V., Javois, L., Kindem, M., Chakraborty, H., Dutra, G., López-Camelo, J. S., Orioli, I. M. & Murray, J. C. (2011). The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts. BMC pediatrics, 11, 121. PMID: 22204448.

Saadi, I., Alkuraya, F. S., Gisselbrecht, S. S., Goessling, W., Cavallesco, R., Turbe-Doan, A., Petrin, A. L., Harris, J., Siddiqui, U., Grix, A. W., Hove, H. D., Leboulch, P., Glover, T. W., Morton, C. C., Richieri-Costa, A., Murray, J. C., Erickson, R. P. & Maas, R. L. (2011). Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics, 89(1), 44–55. PMID: 21703590.

Shaffer, J. R., Wang, X., Feingold, E., Lee, M., Begum, F., Weeks, D. E., Cuenco, K. T., Barmada, M. M., Wendell, S. K., Crosslin, D. R., Laurie, C. C., Doheny, K. F., Pugh, E. W., Zhang, Q., Feenstra, B., Geller, F., Boyd, H. A., Zhang, H., Melbye, M., Murray, J. C., Weyant, R. J., Crout, R., McNeil, D. W., Levy, S. M., Slayton, R. L., Willing, M. C., Broffitt, B., Vieira, A. R. & Marazita, M. L. (2011). Genome-wide association scan for childhood caries implicates novel genes. Journal of dental research, 90(12), 1457-62. PMID: 21940522.

Wehby, G. L., Murray, J. C., McCarthy, A. M. & Castilla, E. E. (2011). Racial gaps in child health insurance coverage in four South American countries: the role of wealth, human capital, and other household characteristics. Health services research, 46(6pt2), 2119-38. PMID: 21210797.

Wehby, G. L., Castilla, E. E., Goco, N., Rittler, M., Cosentino, V., Javois, L., Kindem, M., Chakraborty, H., Dutra, G., López-Camelo, J. S., Orioli, I. M. & Murray, J. C. (2011). The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts. BMC pediatrics, 11, 121. PMID: 22204448.

Wehby, G. L., Murray, J. C., McCarthy, A. M. & Castilla, E. E. (2011). Racial gaps in child health insurance coverage in four South American countries: the role of wealth, human capital, and other household characteristics. Health Services Research, 46(6pt2), 2119–2138. PMID: 21210797.

Paternoster, L., Standl, M., Chen, C., Ramasamy, A., Bønnelykke, K., Duijts, L., Ferreira, M. A., Alves, A. C., Thyssen, J. P., Albrecht, E., Baurecht, H., Feenstra, B., Sleiman, P. M., Hysi, P., Warrington, N. M., Curjuric, I., Myhre, R., Curtin, J. A., Groen-Blokhuis, M. M., Kerkhof, M., Sääf, A., Franke, A., Ellinghaus, D., Fölster-Holst, R., Dermitzakis, E., Montgomery, S. B., Prokisch, H., Heim, K., Hartikainen, A., Pouta, A., Pekkanen, J., Blakemore, A. I., Buxton, J. L., Kaakinen, M., Duffy, D. L., Madden, P. A., Heath, A. C., Montgomery, G. W., Thompson, P. J., Matheson, M. C., Le Souëf, P., Australian Asthma Genetics Consortium (AAGC),, St Pourcain, B., Smith, G. D., Henderson, J., Kemp, J. P., Timpson, N. J., Deloukas, P., Ring, S. M., Wichmann, H., Müller-Nurasyid, M., Novak, N., Klopp, N., Rodríguez, E., McArdle, W., Linneberg, A., Menné, T., Nohr, E. A., Hofman, A., Uitterlinden, A. G., van Duijn, C. M., Rivadeneira, F., de Jongste, J. C., van der Valk, Ralf J. P.,, Wjst, M., Jogi, R., Geller, F., Boyd, H. A., Murray, J. C., Kim, C., Mentch, F., March, M., Mangino, M., Spector, T. D., Bataille, V., Pennell, C. E., Holt, P. G., Sly, P., Tiesler, C. M., Thiering, E., Illig, T., Imboden, M., Nystad, W., Simpson, A., Hottenga, J., Postma, D., Koppelman, G. H., Smit, H. A., Söderhäll, C., Chawes, B., Kreiner-Møller, E., Bisgaard, H., Melén, E., Boomsma, D. I., Custovic, A., Jacobsson, B., Probst-Hensch, N. M., Palmer, L. J., Glass, D., Hakonarson, H., Melbye, M., Jarvis, D. L., Jaddoe, V. W., Gieger, C., Genetics of Overweight Young Adults (GOYA) Consortium,, Strachan, D. P., Martin, N. G., Jarvelin, M., Heinrich, J., Evans, D. M., Weidinger, S. & EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium, (2011). Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nature Genetics, 44(2), 187–192. PMID: 22197932.

Shaffer, J. R., Wang, X., Feingold, E., Lee, M., Begum, F., Weeks, D. E., Cuenco, K. T., Barmada, M. M., Wendell, S. K., Crosslin, D. R., Laurie, C. C., Doheny, K. F., Pugh, E. W., Zhang, Q., Feenstra, B., Geller, F., Boyd, H. A., Zhang, H., Melbye, M., Murray, J. C., Weyant, R. J., Crout, R., McNeil, D. W., Levy, S. M., Slayton, R. L., Willing, M. C., Broffitt, B., Vieira, A. R. & Marazita, M. L. (2011). Genome-wide association scan for childhood caries implicates novel genes. Journal of Dental Research, 90(12), 1457–1462. PMID: 21940522.

Ryckman, K. K., Berberich, S. L., Shchelochkov, O. A., Copeland, S. & Murray, J. C. (2011). 2011 Newborn Screening and Genetic Testing Symposium, Sheraton San Diego Hotel and Mariana, San Diego, CA, November 7-10.

Gaines, L. A., Mansilla, M. A. & Murray, J. C. (2011). Reassessing the role of Jarid 2 in Cleft Lip/Palate. poster presentation at SURC (Summer Undergraduate Research Conference) University of Iowa, Iowa City, Iowa.

Letra, A., Menezes, R., Cooper, M. E., Fonseca, R. F., Tropp, S., Govil, M., Granjeiro, J. M., Imoehl, S. R., Mansilla, M. A., Murray, J. C., Castilla, E. E., Orioli, I. M., Czeizel, A. E., Ma, L., Chiquet, B. T., Hecht, J. T., Vieira, A. R. & Marazita, M. L. (2011). CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 48(4), 363-70. PMID: 20815724.

Rittler, M., Cosentino, V., López-Camelo, J. S., Murray, J. C., Wehby, G. & Castilla, E. E. (2011). Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up. American journal of medical genetics. Part A, 155A(7), 1588-96. PMID: 21671378.

Hochheiser, H., Aronow, B. J., Artinger, K., Beaty, T. H., Brinkley, J. F., Chai, Y., Clouthier, D., Cunningham, M. L., Dixon, M., Donahue, L. R., Fraser, S. E., Hallgrimsson, B., Iwata, J., Klein, O., Marazita, M. L., Murray, J. C., Murray, S., de Villena, F. P., Postlethwait, J., Potter, S., Shapiro, L., Spritz, R., Visel, A., Weinberg, S. M. & Trainor, P. A. (2011). The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. Developmental biology, 355(2), 175-82. PMID: 21458441.

Saadi, I., Alkuraya, F. S., Gisselbrecht, S. S., Goessling, W., Cavallesco, R., Turbe-Doan, A., Petrin, A. L., Harris, J., Siddiqui, U., Grix, Jr, A. W., Hove, H. D., Leboulch, P., Glover, T. W., Morton, C. C., Richieri-Costa, A., Murray, J. C., Erickson, R. P. & Maas, R. L. (2011). Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American journal of human genetics, 89(1), 44-55. PMID: 21703590.

Dagle, J. M., Fisher, T. J., Haynes, S. E., Berends, S. K., Brophy, P. D., Morriss, Jr, F. H. & Murray, J. C. (2011). Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit. The Journal of pediatrics, 159(1), 104-9. PMID: 21353244.

Ryckman, K. K., Dagle, J. M., Kelsey, K., Momany, A. M. & Murray, J. C. (2011). Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates. Pediatric research, 70(1), 90-5. PMID: 21659962.

Simon, C. M., L'heureux, J., Murray, J. C., Winokur, P., Weiner, G., Newbury, E., Shinkunas, L. & Zimmerman, B. (2011). Active choice but not too active: public perspectives on biobank consent models. Genetics in medicine : official journal of the American College of Medical Genetics, 13(9), 821-31. PMID: 21555942.

Letra, A., Menezes, R., Cooper, M. E., Fonseca, R. F., Tropp, S., Govil, M., Granjeiro, J. M., Imoehl, S. R., Mansilla, M. A., Murray, J. C., Castilla, E. E., Orioli, I. M., Czeizel, A. E., Ma, L., Chiquet, B. T., Hecht, J. T., Vieira, A. R. & Marazita, M. L. (2011). CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 48(4), 363–370. PMID: 20815724.

Rittler, M., Cosentino, V., López-Camelo, J. S., Murray, J. C., Wehby, G. & Castilla, E. E. (2011). Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up. American Journal of Medical Genetics. Part A, 155A(7), 1588–1596. PMID: 21671378.

Wehby, G. L., Prater, K., McCarthy, A. M., Castilla, E. E. & Murray, J. C. (2011). The Impact of Maternal Smoking during Pregnancy on Early Child Neurodevelopment. Journal of human capital, 5(2), 207-254. PMID: 22272363.

Dagle, J. M., Fisher, T. J., Haynes, S. E., Berends, S. K., Brophy, P. D., Morriss, F. H. & Murray, J. C. (2011). Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit. The Journal of Pediatrics, 159(1), 104–109. PMID: 21353244.

Moussey, P. A., Butali, A. (2011). Genetics and Environmental Factors in the Aetiology of Orofacial Clefts in Nigeria. Lodz, Poland: 5th International Conference for Birth Defects and Disabilities in Developing Countries / WHO Birth Defects Meeting.

Beaty, T. H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Murray, T., Redett, R. J., Fallin, M. D., Liang, K. Y., Wu, T., Patel, P. J., Jin, S., Zhang, T. X., Schwender, H., Wu-Chou, Y. H., Chen, P. K., Chong, S. S., Cheah, F., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E. W., Shi, B., Wilcox, A. J., Lie, R. T., Jee, S. H., Christensen, K., Doheny, K. F., Pugh, E. W., Ling, H. & Scott, A. F. (2011). Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genetic Epidemiology, 35(6), 469–478. PMID: 21618603.

Simon, C. M., L’heureux, J., Murray, J. C., Winokur, P., Weiner, G., Newbury, E., Shinkunas, L. & Zimmerman, B. (2011). Active choice but not too active: public perspectives on biobank consent models. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 13(9), 821–831. PMID: 21555942.

Geller, F., Feenstra, B., Zhang, H., Shaffer, J. R., Hansen, T., Esserlind, A. L., Boyd, H. A., Nohr, E. A., Timpson, N. J., Fatemifar, G., Paternoster, L., Evans, D. M., Weyant, R. J., Levy, S. M., Lathrop, M., Smith, G. D., Murray, J. C., Olesen, J., Werge, T., Marazita, M. L., Sørensen, T. I. & Melbye, M. (2011). Genome-wide association study identifies four loci associated with eruption of permanent teeth. PLoS genetics, 7(9), e1002275. PMID: 21931568.

Beaty, T. H., Ruczinski, I., Murray, J. C., Marazita, M. L., Munger, R. G., Hetmanski, J. B., Murray, T., Redett, R. J., Fallin, M. D., Liang, K. Y., Wu, T., Patel, P. J., Jin, S. C., Zhang, T. X., Schwender, H., Wu-Chou, Y. H., Chen, P. K., Chong, S. S., Cheah, F., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E. W., Shi, B., Wilcox, A. J., Lie, R. T., Jee, S. H., Christensen, K., Doheny, K. F., Pugh, E. W., Ling, H. & Scott, A. F. (2011). Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genetic epidemiology, 35(6), 469-78. PMID: 21618603.

Jobling, R., Ferrier, R. A., McLeod, R., Petrin, A. L., Murray, J. C. & Thomas, M. A. (2011). Monozygotic twins with variable expression of Van der Woude syndrome. American Journal of Medical Genetics. Part A, 155A(8), 2008–2010. PMID: 21739575.

Geller, F., Feenstra, B., Zhang, H., Shaffer, J. R., Hansen, T., Esserlind, A., Boyd, H. A., Nohr, E. A., Timpson, N. J., Fatemifar, G., Paternoster, L., Evans, D. M., Weyant, R. J., Levy, S. M., Lathrop, M., Smith, G. D., Murray, J. C., Olesen, J., Werge, T., Marazita, M. L., Sørensen, T. I. & Melbye, M. (2011). Genome-wide association study identifies four loci associated with eruption of permanent teeth. PLoS genetics, 7(9), e1002275. PMID: 21931568.

Jobling, R., Ferrier, R. A., McLeod, R., Petrin, A. L., Murray, J. C. & Thomas, M. A. (2011). Monozygotic twins with variable expression of Van der Woude syndrome. American journal of medical genetics. Part A, 155A(8), 2008-10. PMID: 21739575.

O’Sullivan, J., Bitu, C. C., Daly, S. B., Urquhart, J. E., Barron, M. J., Bhaskar, S. S., Martelli-Ju’nior, H., dos Santos Neto, P. Eleuterio, Mansilla, M. A., Murray, J. C., Coletta, R. D., Black, G. C. & Dixon, M. J. (2011). Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome. Journal of Medical Genetics, 48, S17–S17.

Murray, J. C., Manak, J. R., Petrin, A. L., Mansilla, M. A., Marazita, M. L., Beaty, T. H., Leslie, E. J., Cooper, M. E., Dunnwald, M., Christensen, K., Butali, A. & Jensen, C. (2011). Multiple Genomic Approaches to the Identification of Genetic Etiologies for Cleft Lip and Palate. Lodz, Poland: 5th International Conference for Birth Defects and Disabilities in Developing Countries / WHO Birth Defects Meeting.

King, J. L., Yang, B., Sparks, A. E., Mains, L. M., Murray, J. C. & Van Voorhis, B. J. (2010). Skewed X inactivation and IVF-conceived infants. Reproductive biomedicine online, 20(5), 660-3. PMID: 20207584.

Boghossian, N. S., Hansen, N. I., Bell, E. F., Stoll, B. J., Murray, J. C., Laptook, A. R., Shankaran, S., Walsh, M. C., Das, A., Higgins, R. D. (2010). Survival and morbidity outcomes of very low birth weight infants with Down syndrome. poster presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Ryckman, K., Berberich, S., Copeland, S. & Murray, J. C. (2010). The influence of gender, gestational age, birthweight and seasonality of analytes utilized in newborn screening. poster presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Munger, R. G., Mansilla, M. A., Tamura, T., Feldkamp, M., Johnson, K., Botto, L. D. & Murray, J. C. (2010). Maternal Plasma Folate, Dihydrofolate Reductase Genotype and Risk of Isolated Cleft Lip with or without Cleft Palate: Findings from a Population-Based Study. Birth Defects Research Part a-Clinical and Molecular Teratology, 88(5), 368–368.

King, J. L., Yang, B., Sparks, A. E., Mains, L. M., Murray, J. C. & Van Voorhis, B. J. (2010). Skewed X inactivation and IVF-conceived infants. Reproductive Biomedicine Online, 20(5), 660–663. PMID: 20207584.

Köttgen, A., Pattaro, C., Böger, C. A., Fuchsberger, C., Olden, M., Glazer, N. L., Parsa, A., Gao, X., Yang, Q., Smith, A. V., O’Connell, J. R., Li, M., Schmidt, H., Tanaka, T., Isaacs, A., Ketkar, S., Hwang, S., Johnson, A. D., Dehghan, A., Teumer, A., Paré, G., Atkinson, E. J., Zeller, T., Lohman, K., Cornelis, M. C., Probst-Hensch, N. M., Kronenberg, F., Tönjes, A., Hayward, C., Aspelund, T., Eiriksdottir, G., Launer, L. J., Harris, T. B., Rampersaud, E., Mitchell, B. D., Arking, D. E., Boerwinkle, E., Struchalin, M., Cavalieri, M., Singleton, A., Giallauria, F., Metter, J., de Boer, I. H., Haritunians, T., Lumley, T., Siscovick, D., Psaty, B. M., Zillikens, M. C., Oostra, B. A., Feitosa, M., Province, M., de Andrade, M., Turner, S. T., Schillert, A., Ziegler, A., Wild, P. S., Schnabel, R. B., Wilde, S., Munzel, T. F., Leak, T. S., Illig, T., Klopp, N., Meisinger, C., Wichmann, H., Koenig, W., Zgaga, L., Zemunik, T., Kolcic, I., Minelli, C., Hu, F. B., Johansson, A., Igl, W., Zaboli, G., Wild, S. H., Wright, A. F., Campbell, H., Ellinghaus, D., Schreiber, S., Aulchenko, Y. S., Felix, J. F., Rivadeneira, F., Uitterlinden, A. G., Hofman, A., Imboden, M., Nitsch, D., Brandstätter, A., Kollerits, B., Kedenko, L., Mägi, R., Stumvoll, M., Kovacs, P., Boban, M., Campbell, S., Endlich, K., Völzke, H., Kroemer, H. K., Nauck, M., Völker, U., Polasek, O., Vitart, V., Badola, S., Parker, A. N., Ridker, P. M., Kardia, S. L., Blankenberg, S., Liu, Y., Curhan, G. C., Franke, A., Rochat, T., Paulweber, B., Prokopenko, I., Wang, W., Gudnason, V., Shuldiner, A. R., Coresh, J., Schmidt, R., Ferrucci, L., Shlipak, M. G., van Duijn, C. M., Borecki, I., Krämer, B. K., Rudan, I., Gyllensten, U., Wilson, J. F., Witteman, J. C., Pramstaller, P. P., Rettig, R., Hastie, N., Chasman, D. I., Kao, W. H., Heid, I. M. & Fox, C. S. (2010). New loci associated with kidney function and chronic kidney disease. Nature Genetics, 42(5), 376–384. PMID: 20383146.

Bream, E., Busch, T. D., Berends, S. K., Cooper, M. E., Marazita, M. L., Grosen, D., Anshoj, B., Christensen, K. & Murray, J. C. (2010). Linkage analysis of preterm delivery. oral presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Ryckman, K., Begum, F., Fenstra, B., Feingold, E., Geller, F., Boyd, H., Shaffer, J., Laurie, C., Zhang, Q., Doheny, K., Pugh, E., Manolio, T., Marazita, M., Murray, J. C., Mebye, M. (2010). A genome-wide association study of birthweight in preterm and term neonates. poster presentation at the 2010 University of Iowa, Carver College of Medicine Research Week, Iowa City, Iowa.

Cornelis, M. C., Agrawal, A., Cole, J. W., Hansel, N. N., Barnes, K. C., Beaty, T. H., Bennett, S. N., Bierut, L. J., Boerwinkle, E., Doheny, K. F., Feenstra, B., Feingold, E., Fornage, M., Haiman, C. A., Harris, E. L., Hayes, M. G., Heit, J. A., Hu, F. B., Kang, J. H., Laurie, C. C., Ling, H., Manolio, T. A., Marazita, M. L., Mathias, R. A., Mirel, D. B., Paschall, J., Pasquale, L. R., Pugh, E. W., Rice, J. P., Udren, J., van Dam, R. M., Wang, X., Wiggs, J. L., Williams, K., Yu, K. & Consortium, G. (2010). The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genetic Epidemiology, 34(4), 364–372. PMID: 20091798.

Ryckman, K. K., Murray, J. C., Copeland, S. & Berberich, S. L. (2010). Gestational Age, Birthweight and Month of Birt Impact Analytes Collected for Newborn Screening. oral presentation at the 2010 Newborn Screening and Genetic Testing Symposium, Orlando, Florida.

Alleman, B., Ryckman, K., Feingold, E., Fenestra, B., Geller, F., Boyd, H., Shaffer, J., Laurie, C., Zhang, Q., Doheny, K., Pugh, E., Manolio, T., Marazita, M., Melbye, M., Murray, J. C. (2010). Lack of mitochrondria association with preterm birth in mothers and neonates. poster presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Berends, S., Knosp, L. K., Dagle, J. M. & Murray, J. C. (2010). Developing an infrastructure to study genetic and environmental contributions to preterm birth. poster presentation at the Advanced Practice Nursing Forum, Washington DC.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Nguyen, T. T., Christiansen, L., Lidral, A. C. & Murray, J. C. (2010). Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. PloS One, 5(7), e11493. PMID: 20634891.

Schmidt, R. J., Romitti, P. A., Burns, T. L., Murray, J. C., Browne, M. L., Druschel, C. M., Olney, R. S. & National Birth Defects Prevention Study, (2010). Caffeine, selected metabolic gene variants, and risk for neural tube defects. Birth Defects Research. Part A, Clinical and Molecular Teratology, 88(7), 560–569. PMID: 20641098.

Beaty, T. H., Murray, J. C., Marazita, M. L., Munger, R. G., Ruczinski, I., Hetmanski, J. B., Liang, K. Y., Wu, T., Murray, T., Fallin, M. D., Redett, R. A., Raymond, G., Schwender, H., Jin, S. C., Cooper, M. E., Dunnwald, M., Mansilla, M. A., Leslie, E., Bullard, S., Lidral, A. C., Moreno, L. M., Menezes, R., Vieira, A. R., Petrin, A., Wilcox, A. J., Lie, R. T., Jabs, E. W., Wu-Chou, Y. H., Chen, P. K., Wang, H., Ye, X., Huang, S., Yeow, V., Chong, S. S., Jee, S. H., Shi, B., Christensen, K., Melbye, M., Doheny, K. F., Pugh, E. W., Ling, H., Castilla, E. E., Czeizel, A. E., Ma, L., Field, L. L., Brody, L., Pangilinan, F., Mills, J. L., Molloy, A. M., Kirke, P. N., Scott, J. M., Arcos-Burgos, M. & Scott, A. F. (2010). A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nature genetics, 42(6), 525-9. PMID: 20436469.

Beaty, T. H., Murray, J. C., Marazita, M. L., Munger, R. G., Ruczinski, I., Hetmanski, J. B., Liang, K. Y., Wu, T., Murray, T., Fallin, M. D., Redett, R. A., Raymond, G., Schwender, H., Jin, S., Cooper, M. E., Dunnwald, M., Mansilla, M. A., Leslie, E., Bullard, S., Lidral, A. C., Moreno, L. M., Menezes, R., Vieira, A. R., Petrin, A., Wilcox, A. J., Lie, R. T., Jabs, E. W., Wu-Chou, Y. H., Chen, P. K., Wang, H., Ye, X., Huang, S., Yeow, V., Chong, S. S., Jee, S. H., Shi, B., Christensen, K., Melbye, M., Doheny, K. F., Pugh, E. W., Ling, H., Castilla, E. E., Czeizel, A. E., Ma, L., Field, L. L., Brody, L., Pangilinan, F., Mills, J. L., Molloy, A. M., Kirke, P. N., Scott, J. M., Scott, J. M., Arcos-Burgos, M. & Scott, A. F. (2010). A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nature Genetics, 42(6), 525–529. PMID: 20436469.

Butali, A., Adeyemo, W. L., Ogunlewe, O. M., Mossey, P. A. & Murray, J. C. (2010). Investigating the genetic causes of Orofacial cleffts in Nigerian family. poster presentation at the Pediatric Academic Society meeting, Vancouver, BC, Canada.

Boghossian, N. S., Page, G. P., Bell, E. F., Stoll, B. J., Murray, J. C., Shankaran, S., Walsh, M. C., Laptook, A. R., Das, A., Higgins, R. D. (2010). Familial and genetic susceptibility to sepsis in very low birth weight twins. poster presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Ryckman, K., Begum, F., Feenstra, B., Feingold, E., Geller, F., Boyd, H., Shaffer, J., Laurie, C., Zhang, Q., Doheny, K., Pugh, E., Manolio, T., Marazita, M., Murray, J. C., Mebye, M. (2010). A genome-wide association study of birthweight in preterm and term neonates. oral presentation at the Pediatric Academic Society meeting, Vancouver, BC Canada.

Leslie, E., Mansilla, M. A. & Murray, J. C. (2010). Evaluation of ABCA4 as a candidate gene for nonsyndromic cleft lip and palate. poster session at the Graduate Student session at the 2010 Health Sciences Research Week, University of Iowa, Iowa City, Iowa.

Wehby, G. L., Murray, J. C. (2010). Folic acid and orofacial clefts: a review of the evidence. Oral diseases, 16(1), 11-9. PMID: 20331806.

Butali, A., Mossey, P., Adeyemo, W., Murray, J. (2010). Genetic studies in the Nigerian population implicate a MSX1 mutation in oral facial clefting. poster session at the Post Doctoral/Staff session at the 2010 Health Sciences Research Week, University of Iowa, Iowa City, Iowa.

Bille, C., Pedersen, D. A., Andersen, A. N., Mansilla, M. A., Murray, J. C., Christensen, K., Ballard, J. L., Gorman, E. B., Cabrera, R. M. & Finnell, R. H. (2010). Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. Pediatric Research, 67(3), 274–279. PMID: 19952865.

Grosen, D., Chevrier, C., Skytthe, A., Bille, C., Mølsted, K., Sivertsen, A., Murray, J. C. & Christensen, K. (2010). A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance. Journal of Medical Genetics, 47(3), 162–168. PMID: 19752161.

Bille, C., Pedersen, D. A., Andersen, A. M., Mansilla, M. A., Murray, J. C., Christensen, K., Ballard, J. L., Gorman, E. B., Cabrera, R. M. & Finnell, R. H. (2010). Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. Pediatric research, 67(3), 274-9. PMID: 19952865.

Haija, A. E., McCarthy, A., Kleiber, C., Marazita, M. L., Cooper, M. E., Zimmerman, B., Hanrahan, K., Ersig, A. L. & Murray, J. C. (2010). Cortisol response varies by genotype under stressful conditions. poster presentation at the 2010 Annual Clinical Genetics Meeting, Albuquerque, New Mexico, March 24-28.

Da Silva, A. L., Hong, X., Mangold, E., Marazita, M. L., Manak, J. R. & Murray, J. C. (2010). Microdeletion screening in the new candidate locus 8q24 for cleft lip and palate. poster presentation at the 67th Annual Meeting American Cleft Palate-Craniofacial Association, Fort Worth, Texas, March 15-March 20.

Brustolin, S., Giugliani, R. & Félix, T. M. (2010). Genetics of homocysteine metabolism and associated disorders. Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas, 43(1), 1–7. PMID: 19967264.

Wehby, G. L., Murray, J. C. (2010). Folic acid and orofacial clefts: a review of the evidence. Oral Diseases, 16(1), 11–19. PMID: 20331806.

Day, L. J., Schaa, K., Murray, J. C. & England, S. K. (2010). Single Nucleotide Polymorphisms (SNPs) in KCNN3 (SK3 Channel) Associate with Preterm Birth. Reproductive Sciences, 17(3), 255A–256A.

Mansilla, M. A., Christensen, K., Lie, R. T., Beaty, T. H., Hetmanski, J. B., Marazita, M. L. & Murray, J. C. (2010). Molecular genetic findings and their future clinical impact in CL/P. poster presentation at the 67th Annual Meeting American Cleft Palate-Craniofacial Association, Fort Worth, Texas, March 15-March 20.

Grosen, D., Chevrier, C., Skytthe, A., Bille, C., Mølsted, K., Sivertsen, A., Murray, J. C. & Christensen, K. (2010). A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance. Journal of medical genetics, 47(3), 162-8. PMID: 19752161.

Imoehl, S. R., Mansilla, M. A. & Murray, J. C. (2010). The role between variations in alcohol metabolism and orofacial clefts. poster presentation at the American Association for Dental Research (AADR) Meeting, Washington DC.

Mansilla, M. A., Leslie, E., Bullard, S., Dunnwald, M., Christensen, K., Lie, R. T., Beaty, J. B., Hetmanski, J. B., Marazita, M. L. & Murray, J. C. (2010). Role of MAFB and ABCA4 in the etiology of CLP. poster presentation at the Gordon Research Conference, Cranofacial Morphogenesis and Tissue Regeneration, Lucca (Barqa) Italy, April 10-April 16.

Petrin, A. L., Manak, J. R. & Murray, J. C. (2010). Detection of etiological microdeletion/microduplication in cases with cleft lip and palate using high-resolution array CGH. poster presentation at the Gordon Research Conference, Cranofacial Morphogenesis and Tissue Regeneration, Lucca (Barqa) Italy, April 10-April 16.

Bream, E., Zimmerman, C. R., Ahra, D., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2010). Linkage analysis of preterm delivery. poster session at the Graduate Student session at the 2010 Health Sciences Research Week, University of Iowa, Iowa City, Iowa.

Olson, L. C., Schutte, B. C., Murray, J. C. & Dunnwald, M. (2010). The potential role for Interferon regulatory factor 6 in keratinocyte adhesion and/or migration. Faseb Journal, 24.

Cook, D. E., Ryckman, K. K., Berbereich, S., Schchelochkov, O. A., Copeland, S. & Murray, J. C. (2010). Influence of clinical characteristics on 17-Hydroxyprogesterone in newborns. poster presentatin at the Spring Undergraduate Research Festival, University of Iowa, Iowa City, Iowa.

Ryckman, K., Berberich, S., Copeland, S. & Murray, J. C. (2010). The influence of gender, gestational age, birthweight and seasonality of analytes utilized in newborn screening. poster presentation at Pediatric Research Week, University of Iowa, Iowa City, Iowa.

Alul, F., Ryckman, K., Dagle, J. & Murray, J. C. (2010). Replication of a genome-wide association study for prematurity. poster presentation at Pediatric Research Week, University of Iowa, Iowa City, Iowa.

Bream, E., Zimmerman, C. R., Ahra, D., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2010). Linkage analysis of preterm delivery. poster presentation at Pediatric Research Week, University of Iowa, Iowa City, Iowa.

Leslie, E., Mansilla, M. A. & Murray, J. C. (2010). Evaluation of ABCA4 as a candidate gene for nonsyndromic cleft lip and palate. poster presentation at Pediatric Research Week, University of Iowa, Iowa City, Iowa.

Schmidt, R. J., Romitti, P. A., Burns, T. L., Murray, J. C., Browne, M. L., Druschel, C. M. & Olney, R. S. (2010). Caffeine, selected metabolic gene variants, and risk for neural tube defects. Birth defects research. Part A, Clinical and molecular teratology, 88(7), 560-9. PMID: 20641098.

Patel, P. J., Beaty, T. H., Murray, J. C., Marazita, M. L., Munger, R. G., Ruczinski, I., Hetmanski, J. B., Liang, K. Y., Wu, T., Rose, M., Redett, R. A., Jin, S. C., Wilcox, A., Lie, R. T., Wu-Chou, T. Y., Wang, H., Ye, X., Huang, S., Yeow, V., Chong, S. S., Jee, S. H., Shi, B., Christensen, K., Doheny, K., Pugh, E. W., Ling, H. & Scott, A. F. (2010). X-linked genetic factors in DMD associated with oral clefts. oral presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Butali, A., Mansila, M. A., Suzuki, S., Beaty, T. H., Marazita, M. L. & Murray, J. C. (2010). Common and rare variants in the PAX7 and VAX1 genes contribute to Orofacial cleft etiology. poster presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Mahajan, V. B., Olney, A. H., Garrett, P., Chary, A., Dragan, E., Lerner, G., Murray, J. & Bassuk, A. G. (2010). Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia. American Journal of Medical Genetics. Part A, 152A(11), 2875–2879. PMID: 20799329.

Mahajan, V. B., Olney, A. H., Garrett, P., Chary, A., Dragan, E., Lerner, G., Murray, J. & Bassuk, A. G. (2010). Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia. American Journal of Medical Genetics Part A, 152A(11), 2875–2879. DOI: 10.1002/ajmg.a.33621.

Kim, j., Lin, L., Shen, S., Murray, J. C. & Xing, Y. (2010). Genome-wide transcriptome analysis of human placenta. oral presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Shaffer, J. R., Feingold, E., Ryckman, K., Begun, F., Feenstra, B., Geller, F., Boyd, H. A., Weeks, D. E., Barmada, M. M., Laurie, C., Zhang, Q., Doheny, K., Pugh, E., Marazita, M. L., Melbye, M. & Murray, J. C. (2010). Intergenerational allelic Interaction: Excess maternal-fetal allele sharing in the HLA genomic region is associated with preterm birth. poster presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Zheng, X., Shaffer, J. R., McHugh, C., Laurie, C., Melbye, M., Murray, J. C., Marazita, M. L. & Feingold, E. (2010). Using family data as a verification standard to evaluate CNV calling strategies. oral presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Ryckman, K. K., Bream, E., Shaffer, J., Feingold, E., Berends, S. K., Gadow, E., Saleme, C., Simhan, H. N., Merrill, D., Fong, C. T., Busch, T., Feenstra, B., Geller, F., Melbye, M., Marazita, M., Dagle, J. M. & Murray, J. C. (2010). Replication of a genome-wide association study of birthweight in preterm neonates. poster presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Jugessur, A., Skare, O., Gjessing, H. K., Wilcox, A. J., Trung Nguyen, T., Lie, R. T. & Murray, J. C. (2010). Lack of evidence for gene-environment interactions in a population-based sample of isolated CL/P from Norway: A combined case-control and offspring-parent triad study-design. oral presentation at the 60th Annual American Society of Human Genetics (ASHG) conference, Washington DC, November 2-6.

Elks, C. E., Perry, J. R., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K., Smith, E. N., Ulivi, S., Warrington, N. M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G. S., Bergmann, S., Blackburn, H., Boerwinkle, E., Buring, J. E., Busonero, F., Campbell, H., Chanock, S. J., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., d’Adamo, P., de Faire, U., de Geus, Eco J. C.,, Deloukas, P., Döring, A., Smith, G. D., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Geller, F., Gieger, C., Consortium, G., Gudnason, V., Hall, P., Hankinson, S. E., Ferreli, L., Heath, A. C., Hernandez, D. G., Hofman, A., Hu, F. B., Illig, T., Järvelin, M., Johnson, A. D., Karasik, D., Khaw, K., Kiel, D. P., Kilpeläinen, T. O., Kolcic, I., Kraft, P., Launer, L. J., Laven, J. S., Li, S., Liu, J., Levy, D., Martin, N. G., McArdle, W. L., Melbye, M., Mooser, V., Murray, J. C., Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., Oostra, B. A., Peacock, M., Palmer, L. J., Palotie, A., Paré, G., Parker, A. N., Pedersen, N. L., Peltonen, L., Pennell, C. E., Pharoah, P., Polasek, O., Plump, A. S., Pouta, A., Porcu, E., Rafnar, T., Rice, J. P., Ring, S. M., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Schork, N. J., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Soranzo, N., Sovio, U., Srinivasan, S. R., Strachan, D. P., Tammesoo, M., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., van Dam, R. M., van Meurs, Joyce B. J.,, Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Willemsen, G., Wilson, J. F., Wright, A. F., Young, L., Zhai, G., Zhuang, W. V., Bierut, L. J., Boomsma, D. I., Boyd, H. A., Crisponi, L., Demerath, E. W., van Duijn, C. M., Econs, M. J., Harris, T. B., Hunter, D. J., Loos, R. J., Metspalu, A., Montgomery, G. W., Ridker, P. M., Spector, T. D., Streeten, E. A., Stefansson, K., Thorsteinsdottir, U., Uitterlinden, A. G., Widen, E., Murabito, J. M., Ong, K. K. & Murray, A. (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, 42(12), 1077–1085. PMID: 21102462.

Boghossian, N. S., Hansen, N. I., Bell, E. F., Stoll, B. J., Murray, J. C., Laptook, A. R., Shankaran, S., Walsh, M. C., Das, A., Higgins, R. D., Eunice Kennedy Shriver National Institute of Child Health, & Human Development Neonatal Research Network, (2010). Survival and morbidity outcomes for very low birth weight infants with Down syndrome. Pediatrics, 126(6), 1132–1140. PMID: 21098157.

Boghossian, N. S., Horbar, J. D., Carpenter, J. H., Murray, J. C., Bell, E. F. (2010). Major Chromosomal Anomalies Among Very Low Birth Weight Infants in the Vermont Oxford Network. ral presentation at the Vermont Oxford meeting in Washington, DC.

Mumtaz, G., Nassar, A. H., Mahfoud, Z., El-Khamra, A., Al-Choueiri, N., Adra, A., Murray, J. C., Zalloua, P. & Yunis, K. A. (2010). Consanguinity: a risk factor for preterm birth at less than 33 weeks' gestation. American journal of epidemiology, 172(12), 1424-30. PMID: 20978088.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Nguyen, T. T., Christiansen, L., Lidral, A. C. & Murray, J. C. (2010). Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. PloS one, 5(7), e11493. PMID: 20634891.

Petrin, A. L., Giacheti, C. M., Maximino, L. P., Abramides, D. V., Zanchetta, S., Rossi, N. F., Richieri-Costa, A. & Murray, J. C. (2010). Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American journal of medical genetics. Part A, 152A(12), 3164-72. PMID: 21108403.

Boghossian, N. S., Hansen, N. I., Bell, E. F., Stoll, B. J., Murray, J. C., Laptook, A. R., Shankaran, S., Walsh, M. C., Das, A. & Higgins, R. D. (2010). Survival and morbidity outcomes for very low birth weight infants with Down syndrome. Pediatrics, 126(6), 1132-40. PMID: 21098157.

Geller, F., Feenstra, B., Zhang, H., Boyd, H. A., Ryckman, K. K., Shaffer, J. R., Dagle, J., Weeks, D. E., Marazita, M., Feingold, E., Murray, J. C. & Melbye, M. (2010). Set Level Association Testing in a GWA Study on Preterm Birth. Genetic Epidemiology, 34(8), 974–974.

Petrin, A. L., Giacheti, C. M., Maximino, L. P., Abramides, D. V., Zanchetta, S., Rossi, N. F., Richieri-Costa, A. & Murray, J. C. (2010). Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American Journal of Medical Genetics. Part A, 152A(12), 3164–3172. PMID: 21108403.

Mumtaz, G., Nassar, A. H., Mahfoud, Z., El-Khamra, A., Al-Choueiri, N., Adra, A., Murray, J. C., Zalloua, P. & Yunis, K. A. (2010). Consanguinity: a risk factor for preterm birth at less than 33 weeks’ gestation. American Journal of Epidemiology, 172(12), 1424–1430. PMID: 20978088.

Elks, C. E., Perry, J. R., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K., Smith, E. N., Ulivi, S., Warrington, N. M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G. S., Bergmann, S., Blackburn, H., Boerwinkle, E., Buring, J. E., Busonero, F., Campbell, H., Chanock, S. J., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., d'Adamo, P., de Faire, U., de Geus, E. J., Deloukas, P., Döring, A., Smith, G. D., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Geller, F., Gieger, C., Gudnason, V., Hall, P., Hankinson, S. E., Ferreli, L., Heath, A. C., Hernandez, D. G., Hofman, A., Hu, F. B., Illig, T., Järvelin, M. R., Johnson, A. D., Karasik, D., Khaw, K. T., Kiel, D. P., Kilpeläinen, T. O., Kolcic, I., Kraft, P., Launer, L. J., Laven, J. S., Li, S., Liu, J., Levy, D., Martin, N. G., McArdle, W. L., Melbye, M., Mooser, V., Murray, J. C., Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., Oostra, B. A., Peacock, M., Palmer, L. J., Palotie, A., Paré, G., Parker, A. N., Pedersen, N. L., Peltonen, L., Pennell, C. E., Pharoah, P., Polasek, O., Plump, A. S., Pouta, A., Porcu, E., Rafnar, T., Rice, J. P., Ring, S. M., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Schork, N. J., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Soranzo, N., Sovio, U., Srinivasan, S. R., Strachan, D. P., Tammesoo, M. L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., van Dam, R. M., van Meurs, J. B., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Willemsen, G., Wilson, J. F., Wright, A. F., Young, L., Zhai, G., Zhuang, W. V., Bierut, L. J., Boomsma, D. I., Boyd, H. A., Crisponi, L., Demerath, E. W., van Duijn, C. M., Econs, M. J., Harris, T. B., Hunter, D. J., Loos, R. J., Metspalu, A., Montgomery, G. W., Ridker, P. M., Spector, T. D., Streeten, E. A., Stefansson, K., Thorsteinsdottir, U., Uitterlinden, A. G., Widen, E., Murabito, J. M., Ong, K. K. & Murray, A. (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature genetics, 42(12), 1077-85. PMID: 21102462.

Sheehan-Rooney, K., Pálinkášová, B., Eberhart, J. K. & Dixon, M. J. (2010). A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages. Developmental Dynamics: An Official Publication of the American Association of Anatomists, 239(12), 3481–3491. PMID: 21089028.

Momany, A. M., Dallas, L. M., Berends, S. K., Murray, J. C. & Dagle, J. M. (2010). Genetic variants in TFAP2B in preterm infants with patent ductus arteriosus. poster presentation at the 2010 Midwest Society for Pediatric Research, Iowa City, Iowa, October 21-22.

Ryckman, K. K., Cook, D. E., Berberich, S. L., Shchelochkov, O. A., Copeland, S., Berends, S. K., Busch, T., Dagle, J. M. & Murray, J. C. (2010). Genotype and phenotype correlations with 17-hydroxyprogesterone concentration in premature newborns. oral presentation at the 2010 Midwest Society for Pediatric Research, Iowa City, Iowa, October 21-22.

Ryckman, K. K., Cook, D. E., Berberich, S. L., Shchelochkov, O. A., Copeland, S., Berends, S. K., Busch, T., Dagle, J. K. & Murray, J. C. (2010). GENOTYPE AND PHENOTYPE CORRELATIONS WITH 17-HYDROXYPRO-GESTERONE CONCENTRATION IN PREMATURE NEWBORNS. Pediatric Research, 68(4), 357–357.

Momany, A. M., Dallas, L. M., Berends, S. K., Murray, J. C. & Dagle, J. M. (2010). Genetic variants’ in TFAP2B in preterm infants with patent ductus arteriosus. poster presentation at the 2010 Midwest Society for Pediatric Research, Iowa City, Iowa, October 21-22.

Boyles, A. L., DeRoo, L. A., Lie, R. T., Taylor, J. A., Jugessur, A., Murray, J. C. & Wilcox, A. J. (2010). Maternal alcohol consumption, alcohol metabolism genes, and the risk of oral clefts: a population-based case-control study in Norway, 1996-2001. American Journal of Epidemiology, 172(8), 924–931. PMID: 20810466.

Waleh, N., Hodnick, R., Jhaveri, N., McConaghy, S., Dagle, J., Seidner, S., McCurnin, D., Murray, J. C., Ohls, R. & Clyman, R. I. (2010). Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency. Pediatric Research, 68(4), 292–297. PMID: 20581741.

Brémond-Gignac, D., Bitoun, P., Reis, L. M., Copin, H., Murray, J. C. & Semina, E. V. (2010). Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia. Molecular Vision, 16, 1705–1711. PMID: 20806047.

Boyles, A. L., DeRoo, L. A., Lie, R. T., Taylor, J. A., Jugessur, A., Murray, J. C. & Wilcox, A. J. (2010). Maternal alcohol consumption, alcohol metabolism genes, and the risk of oral clefts: a population-based case-control study in Norway, 1996-2001. American journal of epidemiology, 172(8), 924-31. PMID: 20810466.

Brémond-Gignac, D., Bitoun, P., Reis, L. M., Copin, H., Murray, J. C. & Semina, E. V. (2010). Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia. Molecular vision, 16, 1705-11. PMID: 20806047.

Jones, J. L., Canady, J. W., Brookes, J. T., Wehby, G. L., L'Heureux, J., Schutte, B. C., Murray, J. C. & Dunnwald, M. (2010). Wound complications after cleft repair in children with Van der Woude syndrome. The Journal of craniofacial surgery, 21(5), 1350-3. PMID: 20856020.

Jones, J. L., Canady, J. W., Brookes, J. T., Wehby, G. L., L’Heureux, J., Schutte, B. C., Murray, J. C. & Dunnwald, M. (2010). Wound complications after cleft repair in children with Van der Woude syndrome. The Journal of Craniofacial Surgery, 21(5), 1350–1353. PMID: 20856020.

Petrin, A. L., Hong, X., Mangold, E., Marazita, M. L., Visel, A., Manak, J. R. & Murray, J. C. (2010). Screening of the Locus 8q24 in patients with cleft lip and palate. poster presentation at the 2010 Midwest Society for Pediatric Research, Iowa City, Iowa, October 21-22.

L'Heureux, J. L., Murray, J. C. & Simon, C. (2010). How should biobanks obtain consent? Public perceptions and preferences expressed in focus groups. poster presentation at the National Society of Genetic Counselors Annual Education Conference, Dallas, Texas.

Grosen, D., Bille, C., Pedersen, J. K., Skytthe, A., Murray, J. C. & Christensen, K. (2010). Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort. American Journal of Medical Genetics. Part A, 152A(10), 2468–2474. PMID: 20799319.

Félix, T. M., Petrin, A. L., Sanseverino, M. T. & Murray, J. C. (2010). Further characterization of microdeletion syndrome involving 2p15-p16.1. American Journal of Medical Genetics. Part A, 152A(10), 2604–2608. PMID: 20799320.

Félix, T. M., Petrin, A. L., Sanseverino, M. T. & Murray, J. C. (2010). Further characterization of microdeletion syndrome involving 2p15-p16.1. American journal of medical genetics. Part A, 152A(10), 2604-8. PMID: 20799320.

Abu-Maziad, A., Schaa, K., Bell, E. F., Dagle, J. M., Cooper, M., Marazita, M. L. & Murray, J. C. (2010). Role of polymorphic variants as genetic modulators of infection in neonatal sepsis. Pediatric Research, 68(4), 323–329. PMID: 20463618.

Waleh, N., Hodnick, R., Jhaveri, N., McConaghy, S., Dagle, J., Seidner, S., McCurnin, D., Murray, J. C., Ohls, R. & Clyman, R. I. (2010). Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency. Pediatric research, 68(4), 292-7. PMID: 20581741.

Abu-Maziad, A., Schaa, K., Bell, E. F., Dagle, J. M., Cooper, M., Marazita, M. L. & Murray, J. C. (2010). Role of polymorphic variants as genetic modulators of infection in neonatal sepsis. Pediatric research, 68(4), 323-9. PMID: 20463618.

Grosen, D., Bille, C., Pedersen, J. K., Skytthe, A., Murray, J. C. & Christensen, K. (2010). Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort. American journal of medical genetics. Part A, 152A(10), 2468-74. PMID: 20799319.

Mansilla, M. A., Cooper, M. E., Christensen, K., Beaty, T. H., Marazita, M. L. & Murray, J. (2010). Evidence of genetic interaction between SNPs in candidate genes that may confer increased risk for CL/P. poster presentation at the 2010 Midwest Society for Pediatric Research, Iowa City, Iowa, October 21-22.

Boyles, A. L., Wilcox, A. J., Taylor, J. A., Shi, M., Weinberg, C. R., Meyer, K., Fredriksen, A., Ueland, P. M., Johansen, A. M., Drevon, C. A., Jugessur, A., Trung, T. N., Gjessing, H. K., Vollset, S. E., Murray, J. C., Christensen, K. & Lie, R. T. (2009). Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study. Genetic epidemiology, 33(3), 247-55. PMID: 19048631.

Dagle, J. M., Lepp, N. T., Cooper, M. E., Schaa, K. L., Kelsey, K. J., Orr, K. L., Caprau, D., Zimmerman, C. R., Steffen, K. M., Johnson, K. J., Marazita, M. L. & Murray, J. C. (2009). Determination of genetic predisposition to patent ductus arteriosus in preterm infants. Pediatrics, 123(4), 1116–1123. PMID: 19336370.

Boyles, A. L., Wilcox, A. J., Taylor, J. A., Shi, M., Weinberg, C. R., Meyer, K., Fredriksen, A., Ueland, P. M., Johansen, A. M., Drevon, C. A., Jugessur, A., Trung, T. N., Gjessing, H. K., Vollset, S. E., Murray, J. C., Christensen, K. & Lie, R. T. (2009). Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study. Genetic Epidemiology, 33(3), 247–255. PMID: 19048631.

de Lima, R. L., Hoper, S. A., Ghassibe, M., Cooper, M. E., Rorick, N. K., Kondo, S., Katz, L., Marazita, M. L., Compton, J., Bale, S., Hehr, U., Dixon, M. J., Daack-Hirsch, S., Boute, O., Bayet, B., Revencu, N., Verellen-Dumoulin, C., Vikkula, M., Richieri-Costa, A., Moretti-Ferreira, D., Murray, J. C. & Schutte, B. C. (2009). Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genetics in medicine : official journal of the American College of Medical Genetics, 11(4), 241-7. PMID: 19282774.

Suzuki, S., Marazita, M. L., Cooper, M. E., Miwa, N., Hing, A., Jugessur, A., Natsume, N., Shimozato, K., Ohbayashi, N., Suzuki, Y., Niimi, T., Minami, K., Yamamoto, M., Altannamar, T. J., Erkhembaatar, T., Furukawa, H., Daack-Hirsch, S., L’heureux, J., Brandon, C. A., Weinberg, S. M., Neiswanger, K., Deleyiannis, F. W., de Salamanca, J. E., Vieira, A. R., Lidral, A. C., Martin, J. F. & Murray, J. C. (2009). Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. American Journal of Human Genetics, 84(3), 406–411. PMID: 19249007.

D'Alessandro, D. M., D'Alessandro, M. P. & Murray, J. C. (2009). Using web 2.0 tools to enhance communication and collaboration at a Pediatric Research Institute. special CTSA platform session at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Dagle, J. M., Lepp, N. T., Cooper, M. E., Schaa, K. L., Kelsey, K. J., Orr, K. L., Caprau, D., Zimmerman, C. R., Steffen, K. M., Johnson, K. J., Marazita, M. L. & Murray, J. C. (2009). Determination of genetic predisposition to patent ductus arteriosus in preterm infants. Pediatrics, 123(4), 1116-23. PMID: 19336370.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Prenatal care demand and its effects on birth outcomes by birth defect status in Argentina. Economics and Human Biology, 7(1), 84–95. PMID: 19059012.

Mohamed, S., Colaizy, T., Murray, J. C. & Dagle, J. M. (2009). Hyperglycemia as a risk factor for the development of retinopathy of prematurity. poster presentation at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Kelsey, K., Cooper, M. E., Schaa, K. L., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2009). Identification of fetal genetic variation involved in preterm delivery. poster presentation at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Prenatal care effectiveness and utilization in Brazil. Health Policy and Planning, 24(3), 175–188. PMID: 19282483.

Imoehl, S. R., Mansilla, M. A., Marazita, M. L. & Murray, J. C. (2009). Association between FAF1 and Non-syndromic cleft palate. poster presentation at the International Assocation for Dental Research (IADR) Meeting, Miami, Florida.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Prenatal care effectiveness and utilization in Brazil. Health policy and planning, 24(3), 175-88. PMID: 19282483.

Wehby, G. L., Castilla, E. E., Lopez-Camelo, J. S. & Murray, J. C. (2009). Predictors of multivitamin use during pregnancy in Brazil. International journal of public health, 54(2), 78-87. PMID: 19296054.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Prenatal care demand and its effects on birth outcomes by birth defect status in Argentina. Economics and human biology, 7(1), 84-95. PMID: 19059012.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Trung, T. N., Bille, C., Lidral, A. C. & Murray, J. C. (2009). Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. PloS One, 4(4), e5385. PMID: 19401770.

Marazita, M. L., Lidral, A. C., Murray, J. C., Field, L. L., Maher, B. S., Goldstein McHenry, T., Cooper, M. E., Govil, M., Daack-Hirsch, S., Riley, B., Jugessur, A., Felix, T., Morene, L., Mansilla, M. A., Vieira, A. R., Doheny, K., Pugh, E., Valencia-Ramirez, C. & Arcos-Burgos, M. (2009). Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Human Heredity, 68(3), 151–170. PMID: 19521098.

Wehby, G. L., Castilla, E. E., Lopez-Camelo, J. S. & Murray, J. C. (2009). Predictors of multivitamin use during pregnancy in Brazil. International Journal of Public Health, 54(2), 78–87. PMID: 19296054.

Gurol, E. S., Keegan, K., Consention, V., Gadow, E. C., Saleme, C., Cooper, M. E., Marazita, M. L., Simhan, H. & Murray, J. C. (2009). Genetic variation in the Vitamin D receptor is a risk factor for preterm birth. Platform Presentation at the 2009 Pediatric Academic Societies’ Annual Meeting, Baltimore, Maryland, May 2-5.

Wambach, J. A., Wegner, D. J., An, P., Cole, F. S., Hamvas, A., Dagle, J. M. & Murray, J. C. (2009). Surfactant Protein-C (SFTPC) Promotor Variant Associated with Neonatal Respiratory Distress Syndrome. American Journal of Respiratory and Critical Care Medicine, 179.

Shi, M., Mostowska, A., Jugessur, A., Johnson, M. K., Mansilla, M. A., Christensen, K., Lie, R. T., Wilcox, A. J. & Murray, J. C. (2009). Identification of microdeletions in candidate genes for cleft lip and/or palate. Birth defects research. Part A, Clinical and molecular teratology, 85(1), 42-51. PMID: 19137569.

Marazita, M. L., Lidral, A. C., Murray, J. C., Field, L. L., Maher, B. S., Goldstein McHenry, T., Cooper, M. E., Govil, M., Daack-Hirsch, S., Riley, B., Jugessur, A., Felix, T., Morene, L., Mansilla, M. A., Vieira, A. R., Doheny, K., Pugh, E., Valencia-Ramirez, C. & Arcos-Burgos, M. (2009). Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Human heredity, 68(3), 151-70. PMID: 19521098.

Smith, B. J., Mansilla, M. A., Cooper, M. E., Imoehl, S. R., Marazita, M. L. & Murray, J. C. (2009). TP63 associated with nonsyndromic cleft lip with or without palate. poster presentation at the Iowa AADR, The University of Iowa College of Dentistry, Iowa City, Iowa.

Suzuki, S., Marazita, M. L., Cooper, M. E., Miwa, N., Hing, A., Jugessur, A., Natsume, N., Shimozato, K., Ohbayashi, N., Suzuki, Y., Niimi, T., Minami, K., Yamamoto, M., Altannamar, T. J., Erkhembaatar, T., Furukawa, H., Daack-Hirsch, S., L'heureux, J., Brandon, C. A., Weinberg, S. M., Neiswanger, K., Deleyiannis, F. W., de Salamanca, J. E., Vieira, A. R., Lidral, A. C., Martin, J. F. & Murray, J. C. (2009). Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. American journal of human genetics, 84(3), 406-11. PMID: 19249007.

Petrin, A. L., Daack-Hirsh, S., L'Heureux, J. L. & Murray, J. C. (2009). Detection of a 3q29 microdeletion syndrome case diagnosed by CGH-array. University of Iowa Biosciences Program, February Interview Weekend, Iowa City, Iowa.

Mohamed, S., Schaa, K., Cooper, M. E., Ahrens, E., Alvarado, A., Colaizy, T., Marazita, M. L., Murray, J. C. & Dagle, J. M. (2009). Genetic contributions to the development of retinopathy of prematurity. Pediatric research, 65(2), 193-7. PMID: 18787502.

Shi, M., Mostowska, A., Jugessur, A., Johnson, M. K., Mansilla, M. A., Christensen, K., Lie, R. T., Wilcox, A. J. & Murray, J. C. (2009). Identification of microdeletions in candidate genes for cleft lip and/or palate. Birth Defects Research. Part A, Clinical and Molecular Teratology, 85(1), 42–51. PMID: 19137569.

Mohamed, S., Schaa, K., Cooper, M. E., Ahrens, E., Alvarado, A., Colaizy, T., Marazita, M. L., Murray, J. C. & Dagle, J. M. (2009). Genetic contributions to the development of retinopathy of prematurity. Pediatric Research, 65(2), 193–197. PMID: 18787502.

Jugessur, A., Shi, M., Gjessing, H. K., Lie, R. T., Wilcox, A. J., Weinberg, C. R., Christensen, K., Boyles, A. L., Daack-Hirsch, S., Trung, T. N., Bille, C., Lidral, A. C. & Murray, J. C. (2009). Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. PloS one, 4(4), e5385. PMID: 19401770.

Goto, T., Mansilla, M. A., Petrin, A. L., Bullard, S. A., Dierdorf, J., Lidral, A. L., Christensen, K., Durda, K., Marazita, M., Cooper, M., Sunakawa, H., Moreno-Uribe, L. M. & Murray, J. C. (2009). Replication of genome-wide association signal on 8q associated with cleft lip and palate. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Bertolacini, C., Petrin, A. L., Ribiro-Bicudo, L. A., Costa, A. R. & Murray, J. C. (2009). Investigation of the genes PTCH1 and GL12 in the etiology Anophthalmia and Holoprosencephaly in Brazilian cases. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Tomblin, J. B., O’Brien, M., Shriberg, L. D., Williams, C., Murray, J., Patil, S., Bjork, J., Anderson, S. & Ballard, K. (2009). Language Features in a Mother and Daughter of a Chromosome 7;13 Translocation Involving FOXP2. Journal of Speech Language and Hearing Research, 52(5), 1157. DOI: 10.1044/1092-4388(2009/07-0162).

Tomblin, J. B., O’Brien, M., Shriberg, L. D., Williams, C., Murray, J., Patil, S., Bjork, J., Anderson, S. & Ballard, K. (2009). Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2. Journal of speech, language, and hearing research: JSLHR, 52(5), 1157–1174. PMID: 19797137.

Mansilla, M. A., Pate, S., Ryckman, K., Feldkamp, M. L., Munger, R. G. & Murray, J. C. (2009). Positive association for FOXE1 and loci in 8q24 in CL/P cases. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-24.

Leslie, E. J., Petrin, A. L., Marazita, M., Cooper, M., Rahiomov, F. & Murray, J. C. (2009). New common IRF6 variant associated with specific risk for cleft lip and palate. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Petrin, A., Felix, T., Daack-Hirsch, S. & Murray, J. C. (2009). Identification of genomic imbalances in cases with cleft lip and palate using array CGH. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Petrin, R. J., Petrin, A. L. & Murray, J. C. (2009). Copy number variation detection in cleft lip and palate using high resolution array-CGH. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Moreno, L. M., Mansilla, M. A., Bullard, S. A., Cooper, M. E., Busch, T. D., Machida, J., Johnson, M. K., Brauer, D., Krahn, K., Daack-Hirsch, S., L'heureux, J., Valencia-Ramirez, C., Rivera, D., López, A. M., Moreno, M. A., Hing, A., Lammer, E. J., Jones, M., Christensen, K., Lie, R. T., Jugessur, A., Wilcox, A. J., Chines, P., Pugh, E., Doheny, K., Arcos-Burgos, M., Marazita, M. L., Murray, J. C. & Lidral, A. C. (2009). FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Human molecular genetics, 18(24), 4879-96. PMID: 19779022.

Mohamed, S., Colaizy, T., Murray, J. C. & Dagle, J. M. (2009). Genetic polymorphisms of complement factor H and the develoment of retinopathy of prematurity. poster presentation at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Boyd, H. A., Poulsen, G., Wohlfahrt, J., Murray, J. C., Feenstra, B. & Melbye, M. (2009). Maternal contributions to preterm delivery. American journal of epidemiology, 170(11), 1358-64. PMID: 19854807.

Moreno, L. M., Mansilla, M. A., Bullard, S. A., Cooper, M. E., Busch, T. D., Machida, J., Johnson, M. K., Brauer, D., Krahn, K., Daack-Hirsch, S., L’heureux, J., Valencia-Ramirez, C., Rivera, D., López, A. M., Moreno, M. A., Hing, A., Lammer, E. J., Jones, M., Christensen, K., Lie, R. T., Jugessur, A., Wilcox, A. J., Chines, P., Pugh, E., Doheny, K., Arcos-Burgos, M., Marazita, M. L., Murray, J. C. & Lidral, A. C. (2009). FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Human Molecular Genetics, 18(24), 4879–4896. PMID: 19779022.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Quantile effects of prenatal care utilization on birth weight in Argentina. Health economics, 18(11), 1307-21. PMID: 19142894.

Boyd, H. A., Poulsen, G., Wohlfahrt, J., Murray, J. C., Feenstra, B. & Melbye, M. (2009). Maternal contributions to preterm delivery. American Journal of Epidemiology, 170(11), 1358–1364. PMID: 19854807.

Wehby, G. L., Murray, J. C., Castilla, E. E., Lopez-Camelo, J. S. & Ohsfeldt, R. L. (2009). Quantile effects of prenatal care utilization on birth weight in Argentina. Health Economics, 18(11), 1307–1321. PMID: 19142894.

Genisca, A. E., Frías, J. L., Broussard, C. S., Honein, M. A., Lammer, E. J., Moore, C. A., Shaw, G. M., Murray, J. C., Yang, W., Rasmussen, S. A. & National Birth Defects Prevention Study, (2009). Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. American Journal of Medical Genetics. Part A, 149A(6), 1149–1158. PMID: 19441124.

Genisca, A. E., Frías, J. L., Broussard, C. S., Honein, M. A., Lammer, E. J., Moore, C. A., Shaw, G. M., Murray, J. C., Yang, W. & Rasmussen, S. A. (2009). Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. American journal of medical genetics. Part A, 149A(6), 1149-58. PMID: 19441124.

Choi, S. J., Marazita, M. L., Hart, P. S., Sulima, P. P., Field, L. L., McHenry, T. G., Govil, M., Cooper, M. E., Letra, A., Menezes, R., Narayanan, S., Mansilla, M. A., Granjeiro, J. M., Vieira, A. R., Lidral, A. C., Murray, J. C. & Hart, T. C. (2009). The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P. European journal of human genetics: EJHG, 17(6), 774–784. PMID: 19092777.

Dagle, J. M., Fisher, T. J., Kelsey, K., Schaa, K. L., Morriss, F. H., Berends, S. K., Brophy, P. D. & Murray, J. C. (2009). Gene polymorphisms associated with post-discharge elevated blood pressures in infants born < 32 weeks gestation. platform session at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Mann, P. C., Ahrens, E., Byers, H., Cromley, S., Piester, T., Gadow, E., Cosentino, V., Castilla, E. E., Saleme, C., Dagle, J. & Murray, J. C. (2009). Candidate genes affecting premature birth in Argentina. poster session at the Pediatric Academic Societies Meeting, Baltimore, Maryland, May 2-5.

Kimani, J. W., Yoshiura, K., Shi, M., Jugessur, A., Moretti-Ferreira, D., Christensen, K. & Murray, J. C. (2009). Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate. Twin Research and Human Genetics: The Official Journal of the International Society for Twin Studies, 12(5), 462–468. PMID: 19803774.

Stirling, K., Gadow, E., Cosentino, V., Saleme, C., Dagle, J. M., Galet, C., Ascoli, M. & Murray, J. C. (2009). Functional characterization of mutations in the Oxytocin Recpetor in families with prematurity. platform presentation at the 2009 Pediatric Academic Societies’ Annual Meeting, Baltimore, Maryland, May 2-5.

Choi, S. J., Marazita, M. L., Hart, P. S., Sulima, P. P., Field, L. L., McHenry, T. G., Govil, M., Cooper, M. E., Letra, A., Menezes, R., Narayanan, S., Mansilla, M. A., Granjeiro, J. M., Vieira, A. R., Lidral, A. C., Murray, J. C. & Hart, T. C. (2009). The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P. European journal of human genetics : EJHG, 17(6), 774-84. PMID: 19092777.

Erickson, B. N., Kim, J., Christensen, K., Marazita, M. L. & Murray, J. C. (2009). Variation of FGFR2 expression correlates with genotypes at SNPs associated with nonsyndromic cleft lip/palate and breast cancer. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Machida, J., Félix, T. M., Murray, J. C., Yoshiura, K., Tanemura, M., Kamamoto, M., Shimozato, K., Sonta, S. & Ono, T. (2009). Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 46(5), 532-40. PMID: 19929093.

Kim, J., Dunnwald, M. & Murray, J. C. (2009). SNP and expression analyses of candidate genes for orofacial clefts. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Masiero, E., Mansilla, M. A., Carinci, F. & Murray, J. C. (2009). Study of the possible role of MKX in non- syndromic cleft lip and palate. poster presentation at the 59th Annual Meeting of the American Society of Human Genetics, Honolulu, Hawaii, October 20-October 24.

Kimani, J. W., Yoshiura, K., Shi, M., Jugessur, A., Moretti-Ferreira, D., Christensen, K. & Murray, J. C. (2009). Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate. Twin research and human genetics : the official journal of the International Society for Twin Studies, 12(5), 462-8. PMID: 19803774.

Machida, J., Félix, T. M., Murray, J. C., Yoshiura, K., Tanemura, M., Kamamoto, M., Shimozato, K., Sonta, S. & Ono, T. (2009). Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 46(5), 532–540. PMID: 19929093.

Petrin, A. L., Felix, T. M., Daack-Hirsch, S. E. & Murray, J. C. (2009). Identification of genomic imbalances in cases with craniofacial abnormalities using array CGH. oral presentation at the Cleft 2009 Meeting in Fortaleza, Brazil.

Mann, P., Crumley, S., Gadow, E., Cosentino, V., Castilla, E., Saleme, C. & Murray, J. (2008). Genetic factors influencing preterm delivery in Argentina. Pediatric Academic Society Annual Meeting in Honolulu, HI, May 2-6.

Vieira, A. R., McHenry, T. G., Daack-Hirsch, S., Murray, J. C. & Marazita, M. L. (2008). A genome wide linkage scan for cleft lip and palate and dental anomalies. American journal of medical genetics. Part A, 146A(11), 1406-13. PMID: 18442096.

Wehby, G. L., Gastilla, E. E., Goco, N., Rittler, M., Consentino, V., Javois, L., Harris, H., Chakraborty, H., Dutra, G., Lopez-Camelo, J. S., Orioli, I. M. & Murray, J. C. (2008). The Impact of Systematic Pediatric Care on Neonatal Mortality of Infants Born with Cleft Lip and Palate. 65th Annual Meeting of the American Cleft Palate-Craniofaical Association, Philadelphia, PA, June 14-18.

Vieira, A. R., McHenry, T. G., Daack-Hirsch, S., Murray, J. C. & Marazita, M. L. (2008). A genome wide linkage scan for cleft lip and palate and dental anomalies. American Journal of Medical Genetics. Part A, 146A(11), 1406–1413. PMID: 18442096.

Berends, S., Dagle, J. & Murray, J. (2008). Genetics of Prematurity. 11th Annual Neonatal Advanced Nursing Forum, Washington DC, June 4-6.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2008). ’Mendelian randomization’ equals instrumental variable analysis with genetic instruments. Statistics in Medicine, 27(15), 2745–2749. PMID: 18344186.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2008). A genetic instrumental variables analysis of the effects of maternal smoking on birth outcomes. American Society of Health Economists (ASHE), Durham, North Carolina, June 22-25.

Romitti, P. A., Rose, K. L., Sun, L., Malville-Shipan, K. & Murray, J. C. (2008). Alcohol dehydrogenase genes, alcohol consumption and risk of orofacial clefts. Alcoholism-Clinical and Experimental Research, 32(6), 209A–209A.

Osoegawa, K., Vessere, G. M., Utami, K. H., Mansilla, M. A., Johnson, M. K., Riley, B. M., L’Heureux, J., Pfundt, R., Staaf, J., van der Vliet, W. A.,, Lidral, A. C., Schoenmakers, E. F. P. M.,, Borg, A., Schutte, B. C., Lammer, E. J., Murray, J. C. & de Jong, P. J. (2008). Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. Journal of Medical Genetics, 45(2), 81–86. PMID: 17873121.

Davis, L. K., Meyer, K. J., Rudd, D. S., Librant, A. L., Epping, E. A., Sheffield, V. C. & Wassink, T. H. (2008). Pax6 3’ deletion results in aniridia, autism and mental retardation. Human Genetics, 123(4), 371–378. PMID: 18322702.

Osoegawa, K., Vessere, G. M., Utami, K. H., Mansilla, M. A., Johnson, M. K., Riley, B. M., L'Heureux, J., Pfundt, R., Staaf, J., van der Vliet, W. A., Lidral, A. C., Schoenmakers, E. F., Borg, A., Schutte, B. C., Lammer, E. J., Murray, J. C. & de Jong, P. J. (2008). Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. Journal of medical genetics, 45(2), 81-6. PMID: 17873121.

Schutte, B. C., Dixon, M. J. & Murray, J. C. (2008). Interferon Regulatory Factor 6 (IRF6) is Casual in Van der Woude and Popliteal Pterygium Syndromes and Contributes to the Risk for Nonsyndromic Cleft Lip and Palate. In Inborn Errors of Development. (2), pp. 1069-1072. New York, NY: Oxford University Press.

Jugessur, A., Rahimov, F., Lie, R. T., Wilcox, A. J., Gjessing, H. K., Nilsen, R. M., Nguyen, T. T. & Murray, J. C. (2008). Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway. Genetic Epidemiology, 32(5), 413–424. PMID: 18278815.

Wehby, G. L., Murray, J. C. (2008). The effects of prenatal use of folic acid and other dietary supplements on early child development. Maternal and child health journal, 12(2), 180-7. PMID: 17554612.

Shi, M., Wehby, G. L. & Murray, J. C. (2008). Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects. Birth defects research. Part C, Embryo today : reviews, 84(1), 16-29. PMID: 18383123.

Abu-Maziad, A., Schaa, K. L., Dagle, J. M. & Murray, J. C. (2008). The role of polymorphic variants in inflammatory cytokines, cytokine receptors, surface receptors, and Toll-like receptor genes in neonatal sepsis. Pediatric Academic Society Meeting, Honolulu, Hawaii, May 2-6.

Shi, M., Wehby, G. L. & Murray, J. C. (2008). Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects. Birth Defects Research. Part C, Embryo Today: Reviews, 84(1), 16–29. PMID: 18383123.

Wehby, G. L., Murray, J. C. (2008). The effects of prenatal use of folic acid and other dietary supplements on early child development. Maternal and Child Health Journal, 12(2), 180–187. PMID: 17554612.

Stirling, K. J., Johnson, M. K., Rahimov, F., Shi, M. & Murray, J. C. (2008). Investigations into the role of the oxytocin receptor in preterm labor. Pediatric Academic Societies Annual Meeting in Honolulu, HI, May 2-6.

Petrin, A. L., L'Heureux, J., Daack-Hirsch, S. & Murray, J. C. (2008). Detection of a 3q29 microdeletion syndrome case diagnosed by CGH-array. 58th Annual Meeting of the American Socieity of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Mansilla, M. A., Moreno, L. M., Machida, J., Bullard, S. A., Busch, T., Cooper, M. E., Jugessur, A., Lie, R. T., Wilcox, A., Christensen, K., Chines, P., Lidral, A. C., Marazita, M. L. & Murray, J. C. (2008). Association between FOXE1 and cleft palate. 58th Annual Meeting of the American Society of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Erickson, B. N., Christensen, K., Marazita, M. L. & Murray, J. C. (2008). Association of cleft lip/palate with mutations in FGFR2 found in breast cancer patients. 58th Annual Meeting of the American Society of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Marazita, M. L., Cooper, M. E., Vieira, A. R., Letra, A., Menezes, R., Mansilla, M., Murray, J. C., Castilla, E. E., Orioli, I. M., Czeizel, A. E., Martin, A., Chiquet, B. C. & Hecht, J. T. (2008). CRISPLD2 assessed with multiple orofacial cleft (OFC) phenotypes in multiple ethnicities. 58th Annual Meeting of the American Society of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Vieira, A. R., Howe, A. & Murray, J. C. (2008). Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts. American journal of medical genetics. Part A, 146A(21), 2828-30. PMID: 18837046.

Petrin, A. L., L'Heureux, J., Daack-Hirsch, S. & Murray, J. C. (2008). Detection of a 3q29 microdeletion syndrome case diagnosed by CGH-array. Society of Craniofacial Genetics Meeting, Philadelphia, PA.

Jugessur, A., Rahimov, F., Lie, R. T., Wilcox, A. J., Gjessing, H. K., Nilsen, R. M., Nguyen, T. T. & Murray, J. C. (2008). Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway. Genetic epidemiology, 32(5), 413-24. PMID: 18278815.

Mansilla, M. A., Moreno, L. M., Machida, J., Bullard, S. A., Busch, T., Johnson, M., Cooper, M. E., Jugessur, A., Lie, R. T., Wilcox, A., Christensen, K., McHenry, T. H., Maher, B. S., Chines, P., Lidral, A. C., Marazita, M. L. & Murray, J. C. (2008). A major role for FOXE1 in NSCL/P. Society of Craniofacial Genetics Meeting, Philadelphia, PA.

Erickson, B. N., Christensen, K., Marazita, M. L. & Murray, J. C. (2008). Association of cleft lip/palate with mutations in FGFR2 found in breast cancer patients. Society of Craniofacial Genetics Meeting, Philadelphia, PA.

Rahimov, F., Marazita, M. L., Visel, A., Cooper, M. E., Hitchler, M. J., Rubini, M., Domann, F. E., Govil, M., Christensen, K., Bille, C., Melbye, M., Jugessur, A., Lie, R. T., Wilcox, A. J., Fitzpatrick, D. R., Green, E. D., Mossey, P. A., Little, J., Steegers-Theunissen, R. P., Pennacchio, L. A., Schutte, B. C. & Murray, J. C. (2008). Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Nature genetics, 40(11), 1341-7. PMID: 18836445.

Vieira, A. R., McHenry, T. G., Daack-Hirsch, S., Murray, J. C. & Marazita, M. L. (2008). Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 10(9), 668–674. PMID: 18978678.

Vieira, A. R., McHenry, T. G., Daack-Hirsch, S., Murray, J. C. & Marazita, M. L. (2008). Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts. Genetics in medicine : official journal of the American College of Medical Genetics, 10(9), 668-74. PMID: 18978678.

Rahimov, F., Marazita, M. L., Visel, A., Cooper, M. E., Hitchler, M. J., Rubini, M., Domann, F. E., Govil, M., Christensen, K., Bille, C., Melbye, M., Jugessur, A., Lie, R. T., Wilcox, A. J., Fitzpatrick, D. R., Green, E. D., Mossey, P. A., Little, J., Steegers-Theunissen, R. P., Pennacchio, L. A., Schutte, B. C. & Murray, J. C. (2008). Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Nature Genetics, 40(11), 1341–1347. PMID: 18836445.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2008). 'Mendelian randomization' equals instrumental variable analysis with genetic instruments. Statistics in medicine, 27(15), 2745-9. PMID: 18344186.

Murray, J. C., Shi, M., Mostowska, A., Mansilla, M. A., Christensen, K., Marazita, M., Cooper, M., Lidral, A., Rahimov, F. & Suzuki, S. (2008). Cleft Palate. Journal of Medical Genetics, 45, S15–S15.

Vieira, A. R., Howe, A. & Murray, J. C. (2008). Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts. American Journal of Medical Genetics. Part A, 146A(21), 2828–2830. PMID: 18837046.

Brustolin, S., Cooper, M. E., Silva, A., Marazita, M. L., Santos, M. M., Giugliani, R., Murray, J. C. & Felix, T. M. (2008). Folate pathway genes and biochemical studies in orofacial clefts. 58th Annual Meeting of the American Society of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Cooper, M. E., Abu-Maziad, A. S., Schaa, K. L., Marazita, M. L., Dagle, J. M. & Murray, J. C. (2008). Sepsis in premature infants: Investigation of candidate genes. 58th Annual Meeting of the American Society of Human Genetics (ASHG), Philadelphia, Pennsylvania, November 11-15.

Davis, L. K., Hazlett, H. C., Librant, A. L., Nopoulos, P., Sheffield, V. C., Piven, J. & Wassink, T. H. (2008). Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics, 147B(7), 1145–1151. PMID: 18361446.

Damiano, P. C., Tyler, M. C., Romitti, P. A., Momany, E. T., Jones, M. P., Canady, J. W., Karnell, M. P. & Murray, J. C. (2007). Health-related quality of life among preadolescent children with oral clefts: the mother's perspective. Pediatrics, 120(2), e283-90. PMID: 17671039.

Damiano, P. C., Tyler, M. C., Romitti, P. A., Momany, E. T., Jones, M. P., Canady, J. W., Karnell, M. P. & Murray, J. C. (2007). Health-related quality of life among preadolescent children with oral clefts: the mother’s perspective. Pediatrics, 120(2), e283–290. PMID: 17671039.

Machida, J., Moreno, L. M., Mansilla, M. A., Bullard, S. B., Busch, T. D., Johnson, M. K., McHenry, T., Cooper, M. E., Valencia-Ramirez, C., Arcos-Burgos, M., Hing, A., Lammer, E. J., Jones, M., Christensen, K., Murray, J. C., Marazita, M. L. & Lidral, A. C. (2007). The role of FOXE1 in the etiology of cleft lip. 57th Annual Meeting of the American society of Human Genetics in San Diego, CA, October 23-27.

Abidi, F. E., Miano, M. G., Murray, J. C. & Schwartz, C. E. (2007). A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate. Clinical Genetics, 72(1), 19–22. PMID: 17594395.

Govil, M., Daack-Hirsch, S., Lidral, A. C., Vieland, V. J., Murray, J. C. & Marazita, M. L. (2007). Non-syndromic cleft lip with or without cleft palate (CL/P) analysis sequentially updated over phenotypic subgroups reveals a Philippines-specific linkage to a region on chromosome 6q. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Riley, B. M., Murray, J. C. (2007). Sequence evaluation of FGF and FGFR gene conserved non-coding elements in nonsyndromic cleft lip and palate cases. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Abidi, F. E., Miano, M. G., Murray, J. C. & Schwartz, C. E. (2007). A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate. Clinical Genetics, 72(1), 19–22. DOI: 10.1111/j.1399-0004.2007.00817.x.

Suzuki, S., Marazita, M. L., Miwa, N., Jugessur, A., Natsume, N., Shimozato, K., Shi, M., Ohbayashi, N., Suzuki, Y., Niimi, T., Yamamoto, M., Altannamar, T. J., Erkhembaatar, T., Furukawa, H., Daack-Hirsch, S., Vieira, A., Lidral, A. C., Martin, J. F. & Murray, J. C. (2007). Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Iyengar, S. K., Tomblin, J. B., Kelsey, K. J., Bjork, J. B., Sucheston, L. E., Samelson, B. K. & Murray, J. C. (2007). Replication of DCDC2 and KIAA0319 in a single population with language disorder. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Kimani, J. W., Yoshiura, K. & Murray, J. C. (2007). Search for genomic alterations in monozygotic twins discordant for cleft lip and palate. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Stirling, K. J., Johnson, M., Welter, S., Dagle, J. M. & Murray, J. C. (2007). Evidence that the oxytocin receptor plays a role in preterm birth. Platform Presentation, 2007 Pediatrics Academic Society Annual Meeting, Toronto, Canada.

Wehby, G., Murray, J., Castilla, E., Camelo, J. & Ohsfeldt, R. (2007). Prenatal care utilization and its effects on infant health in samples of normal versus abnormal births from South America. 6th World Congress of the International Health Economics Association in Copenhagen, Denmark, July 8-11.

Borowski, K., Dagle, J. & Murray, J. C. (2007). Genetic variation in term and late preterm infants with neonatal respiratory distress. 48th Annual Short Course on Craniofacial & Experimental Mammalian Genetics, Bar Harbor, Maine, June 15-25.

Kinoshita, A., Dunnwald, M., Trout, K. J., Richardson, R., Dixon, M., Yang, B., Murray, J. C. & Schutte, B. C. (2007). Irf6 allelic series in mouse shows differential defects in oral adhesions without cleft palate. 57th Annual Meeting of the American society of Human Genetics in San Diego, CA, October 23-27.

Riley, B. M., Schultz, R. E., Cooper, M. E., Goldstein-McHenry, T., Daack-Hirsch, S., Lee, K. T., Dragan, E., Vieira, A. R., Lidral, A. C., Marazita, M. L. & Murray, J. C. (2007). A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23. American journal of medical genetics. Part A, 143A(8), 846-52. PMID: 17366557.

Nopoulos, P., Richman, L., Andreasen, N., Murray, J. C. & Schutte, B. (2007). Cognitive dysfunction in adults with Van der Woude syndrome. Genetics in medicine : official journal of the American College of Medical Genetics, 9(4), 213-8. PMID: 17438385.

Mostowska, A., Govil, M., McHenry, T. H., Cooper, M. E., FitzPatrick, D. R., Vieland, V. J., Marazita, M. L. & Murray, J. C. (2007). Evidence for the role of BACH2 in chromosomal region 6q14-6q16.3 with nonsyndromic cleft lip and palate. 48th Annual Short Course on Craniofacial & Experimental Mammalian Genetics, Bar Harbor, Maine, June 15-25.

Rahimov, F., Hitchler, M. J., Domann, F. E., Jugessur, A., Lie, R. T., Wilcox, A. J., Christensen, K., Green, E. D., Marazita, M. L., Schutte, B. C. & Murray, J. C. (2007). Disruptive of AP-2 binding site upstream of IRF6 is commonly associated with nonsyndromic cleft lip and palate. 48th Annual Short Course on Craniofacial & Experimental Mammalian Genetics, Bar Harbor, Maine, June 15-25.

Mutti, D. O., Cooper, M. E., O'Brien, S., Jones, L. A., Marazita, M. L., Murray, J. C. & Zadnik, K. (2007). Candidate gene and locus analysis of myopia. Molecular vision, 13, 1012-9. PMID: 17653045.

Nopoulos, P., Richman, L., Andreasen, N. C., Murray, J. C. & Schutte, B. (2007). Abnormal brain structure in adults with Van der Woude syndrome. Clinical genetics, 71(6), 511-7. PMID: 17539900.

Nopoulos, P., Richman, L., Andreasen, N. C., Murray, J. C. & Schutte, B. (2007). Abnormal brain structure in adults with Van der Woude syndrome. Clinical Genetics, 71(6), 511–517. PMID: 17539900.

Cosentino, S. C., Gili, J. A., Murray, J. C. & Gadow, E. (2007). Clinical epidemiological study on risk factors for the recurrence of preterm birth. Poster presentation, 3rd International Conference on Birth Defects and disabilities in the developing World, Rio de Janeiro, Brazil, June 17-21.

Tomblin, J. B., Christiansen, M. H., Bjork, J. B., Iyengar, S. K. & Murray, J. C. (2007). Association of FOXP2 genetic markers with procedural learning and language. 57th Annual Meeting of the American Society of Human Genetics, October 23-27.

Rorick, N. K., Kinoshita, A., Peyrard, M., Goudy, S. L., Weirather, J., de Lima, R., Moretti-Ferreira, D., Koillinen, H., Kere, J., Murray, J. C. & Schutte, B. C. (2007). Genomic strategy identifies Stratifin (SFN) and WD-Repeat Domain 65 (Wdr65) as candidate genes for cleft lip and palate. 57th Annual Meeting of the American society of Human Genetics in San Diego, CA, October 23-27.

Freitas, E. L., Martinhago, C. D., Ramos, E. S., Murray, J. C. & Gil-da-Silva-Lopes, V. L. (2007). Preliminary molecular studies on blepharocheilodontic syndrome. American Journal of Medical Genetics Part A, 143A(22), 2757–2759. DOI: 10.1002/ajmg.a.32010.

Freitas, E. L., Martinhago, C. D., Ramos, E. S., Murray, J. C. & Gil-da-Silva-Lopes, V. L. (2007). Preliminary molecular studies on blepharocheilodontic syndrome. American Journal of Medical Genetics. Part A, 143A(22), 2757–2759. PMID: 17937431.

Merialdi, M., Murray, J. C. (2007). The changing face of preterm birth. Pediatrics, 120(5), 1133–1134. PMID: 17974752.

Ehn, N. L., Cooper, M. E., Orr, K., Shi, M., Johnson, M. K., Caprau, D., Dagle, J., Steffen, K., Johnson, K., Marazita, M. L., Merrill, D. & Murray, J. C. (2007). Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth. Pediatric research, 62(5), 630-5. PMID: 17805208.

Steffen, K. M., Cooper, M. E., Shi, M., Caprau, D., Simhan, H. N., Dagle, J. M., Marazita, M. L. & Murray, J. C. (2007). Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. Journal of Perinatology: Official Journal of the California Perinatal Association, 27(11), 672–680. PMID: 17855807.

Ehn, N. L., Cooper, M. E., Orr, K., Shi, M., Johnson, M. K., Caprau, D., Dagle, J., Steffen, K., Johnson, K., Marazita, M. L., Merrill, D. & Murray, J. C. (2007). Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth. Pediatric Research, 62(5), 630–635. PMID: 17805208.

Riley, B. M., Murray, J. C. (2007). Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases. American journal of medical genetics. Part A, 143A(24), 3228-34. PMID: 17963255.

Kimani, J. W., Shi, M., Daack-Hirsch, S., Christensen, K., Moretti-Ferreira, D., Marazita, M. L., Field, L. L., Canady, J. W. & Murray, J. C. (2007). X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. American journal of medical genetics. Part A, 143A(24), 3267-72. PMID: 18000982.

Riley, B. M., Murray, J. C. (2007). Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases. American Journal of Medical Genetics. Part A, 143A(24), 3228–3234. PMID: 17963255.

Kimani, J. W., Shi, M., Daack-Hirsch, S., Christensen, K., Moretti-Ferreira, D., Marazita, M. L., Field, L. L., Canady, J. W. & Murray, J. C. (2007). X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. American Journal of Medical Genetics. Part A, 143A(24), 3267–3272. PMID: 18000982.

Steffen, K. M., Cooper, M. E., Shi, M., Caprau, D., Simhan, H. N., Dagle, J. M., Marazita, M. L. & Murray, J. C. (2007). Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. Journal of perinatology : official journal of the California Perinatal Association, 27(11), 672-80. PMID: 17855807.

Merialdi, M., Murray, J. C. (2007). The changing face of preterm birth. Pediatrics, 120(5), 1133-4. PMID: 17974752.

Bjork, B. C., Vieira, A. R., Davis, S. W., Camper, S. A., Murray, J. C. & Beier, D. R. (2007). ENU-induced, targeted and sporadic mutations reveal an important role for Prdm 16 during mouse and human craniofacial development. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Stirling, K., Johnson, M., Cooper, M., Marazita, M., Shi, M., Dagle, J. & Murray, J. (2007). Evidence that the oxytocin receptor plays a role in preterm labor. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Kelsey, K. J., Tomlin, J. B., Bjork, J. B., Iyengar, S. K., Sucheston, L. E., Samelson, B. K. & Murray, J. C. (2007). Genes showing accelerated evolutionary properties associate with communication abilities in humans. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Patel, P. M., Schaa, K., Romitti, P. A., Dagle, J. M. & Murray, J. C. (2007). Genetic determinants of patent ductus arteriosus in term infants. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Rahimov, F., Hitchler, M. J., Domann, F. E., Jessur, A., Lie, R. T., Wilcox, A. J., Christensen, K., Green, E. D., Marazita, M. L., Schutte, B. C. & Murray, J. C. (2007). Disruption of an AP-2 binding site upstream IRF6 is commonly associated with nonsyndromic cleft lip and palate. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Shi, M., Jugessur, A., Gjessing, H., Wilcox, A. J., Lie, R. T., Weinberg, C. R., Trung, T. N., Christensen, K. & Murray, J. C. (2007). Detecting deletions in candidate genes for cleft lip and palate. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Wehby, G. L., Marcinow, A., Quin, X., Mansilla, A. & Murray, J. C. (2007). A genetic instrumental variables analysis of the effects of maternal smoking on oral cleft risks. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Chevrier, C., Grosen, D., Bille, C., Murray, J. C. & Christensen, K. (2007). Analysis of familial recurrence patterns of nonsyndromic oral clefts in Denmark: a registry study with 6,811 probands. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Bjork, J. B., Tomlin, J. B., Williams, C. A., Patil, S. R., O'Brien, M. R. & Murray, J. C. (2007). Characterization of a balanced translocation breakpoint to within the FOXP2 gene in a two-generation family with language impairment. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Jugessur, A., Shi, M., Gjessing, H., Wilcox, A., Lie, R., Weinberg, C., Trung, T., Lidral, A., Christensen, K. & Murray, J. (2007). Comprehensive analysis of 331 candidate genes for orofacial clefting in a population-based infant-parent case-control study for Norway. 57th Annual Meeting of the American Society of Human Genetics in San Diego, CA, October 23-27.

Riley, B. M., Schultz, R. E., Cooper, M. E., Goldstein-McHenry, T., Daack-Hirsch, S., Lee, K. T., Dragan, E., Vieira, A. R., Lidral, A. C., Marazita, M. L. & Murray, J. C. (2007). A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23. American Journal of Medical Genetics. Part A, 143A(8), 846–852. PMID: 17366557.

Wehby, G. L., Castilla, E. E., Goco, N., Rittler, M., Cosentino, V., Javois, L., McCarthy, A. M., Bobashev, G., Litavecz, S., Mariona, A., Dutra, G., López-Camelo, J. S., Orioli, I. M. & Murray, J. C. (2006). Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149]. BMC pediatrics, 6, 9. PMID: 16563165.

Rorick, N. K., Gakhar, L., Waldschmidt, T. R., Schipper, Murray, J. C. & Schutte, B. C. (2006). Structrual and DNA binding differences between VWS and PPS mutations in IRF6. (Vols. 79S). pp. 333. Am J Hum Gen.

Lepp, N., Dagle, J. M., Caprau, D., Marazita, M. L., Cooper, M. E., Johnson, K. & Murray, J. C. (2006). Single nucleotide polymorphisms (SNPs) in smooth muscle regulation genes as risk factors for spontaneous preterm delivery. Platform presentation, 2006 PAS Meeting, San Francisco, CA, Apr 29-May 2.

Riley, B. M., Mansilla, M. A., Raffensperger, L., Maher, B., Marazita, M. L., Mohammadi, M. & Murray, J. C. (2006). Mutations in FGF signaling pathway genes contribute to cleft lip and palate. Plenary Presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Lepp, N., Dagle, J. M., Caprau, D., Marazita, M. L., Cooper, M. E., Johnson, K. & Murray, J. C. (2006). The determination of a genetic predisposition to patent ductus arteriosus in preterm infants. 2006 PAS meeting, San Francisco, CA, Apr 29-May 2.

Lepp, N. T., Dagle, J. M., Caprau, D., Marazita, M. L., Cooper, M. E., Johnson, K. & Murray, J. C. (2006). The determination of a genetic predisposition to patent ductus arteriosus in preterm infants. Society for Pediatric Research meeting, San Francisco, CA, Apr 29-May 2.

Mansilla, M. A., Cooper, M. E., Goldstein, T., Castilla, E. E., Lopez Camelo, J. S., Marazita, M. L. & Murray, J. C. (2006). Contributions of PTCH gene variants to isolated cleft lip and palate. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 43(1), 21-9. PMID: 16405370.

Ingraham, C. R., Kinoshita, A., Yang, B., Kondo, S., Trout, K. J., Malik, M. I., Murray, J. C. & Schutte, B. C. (2006). Irf6, the mouse ortholog of the gen mutated in VWS, is essential for craniofacial, skin, and limb development. Gordon Research Conference, Ventura, CA, Jan 22-27.

Moreno, L. M., Mansilla, M. A., Johnson, M., Riley, B., Arcos-Burgos, M., Valencia-Ramirez, C., Busch, T., Cooper, M., McHenry, T., Marazita, M. L., Murray, J. C. & Lidral, A. C. (2006). Fine mapping the 9q22-33 region in nonsyndromic CL/P populations from Southeast Asia and South America. American Cleft Palate-Craniofacial Association annual meeting, Vancouver, BC, Jan 22-27.

Mansilla, M. A., Cooper, M. E., Goldstein, T., Castilla, E. E., Lopez Camelo, J. S., Marazita, M. L. & Murray, J. C. (2006). Contributions of PTCH gene variants to isolated cleft lip and palate. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 43(1), 21–29. PMID: 16405370.

Govil, M., Marazita, M. L., Murray, J. C., Field, L. L. & Vieland, V. J. (2006). Multipoint PPL analysis of cleft lip with/out cleft palate (CL/P) provides compelling evidence in favor of linkage. Poster presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Ehn, N., Merrill, D., Caprau, D., Dagle, J., Johnson, K., Johnson, M., Marazita, M., Cooper, M. & Murray, J. C. (2006). Genetic variation in the progesterone receptor gene is a risk factor for preterm birth. Platform presentation, 2006 PAS meeting, San Francisco, CA, Apr 29-May 2.

Wehby, G. L., Castilla, E. E., Goco, N., Rittler, M., Cosentino, V., Javois, L., McCarthy, A. M., Bobashev, G., Litavecz, S., Mariona, A., Dutra, G., López-Camelo, J. S., Orioli, I. M. & Murray, J. C. (2006). Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149]. BMC pediatrics, 6, 9. PMID: 16563165.

Saadi, I., Toro, R., Kuburas, A., Semina, E., Murray, J. C. & Russo, A. F. (2006). An unusual class of PITX2 mutations in Axenfeld-Rieger syndrome. Birth Defects Research. Part A, Clinical and Molecular Teratology, 76(3), 175–181. PMID: 16498627.

Saadi, I., Toro, R., Kuburas, A., Semina, E., Murray, J. C. & Russo, A. F. (2006). An unusual class of PITX2 mutations in Axenfeld-Rieger syndrome. Birth defects research. Part A, Clinical and molecular teratology, 76(3), 175-81. PMID: 16498627.

Yoshiura, K., Kinoshita, A., Ishida, T., Ninokata, A., Ishikawa, T., Kaname, T., Bannai, M., Tokunaga, K., Sonoda, S., Komaki, R., Ihara, M., Saenko, V. A., Alipov, G. K., Sekine, I., Komatsu, K., Takahashi, H., Nakashima, M., Sosonkina, N., Mapendano, C. K., Ghadami, M., Nomura, M., Liang, D. S., Miwa, N., Kim, D. K., Garidkhuu, A., Natsume, N., Ohta, T., Tomita, H., Kaneko, A., Kikuchi, M., Russomando, G., Hirayama, K., Ishibashi, M., Takahashi, A., Saitou, N., Murray, J. C., Saito, S., Nakamura, Y. & Niikawa, N. (2006). A SNP in the ABCC11 gene is the determinant of human earwax type. Nature genetics, 38(3), 324-30. PMID: 16444273.

Yankowitz, J., Zeng, S., Merrill, D. & Murray, J. (2006). Association between FLT-1 htSNPs and preeclampsia. SMFM 26th Annual Scientific meeting, Jan 30-Feb 6.

Marazita, M. L., Maher, B. S., Murray, J. C., Lidral, A. C., Field, L. L., Goldstein McHenry, T., Cooper, M. E., Daak-Hirsch, S., Jugessur, A., Riley, B., Moreno, L. & Chines, P. (2006). Candidate gene analyses for nonsyndromic cleft lip (CL) with or without cleft palate (CP) in families from six countries. Platform presentation, 2006 Annual Meeting, New Orleans, LA, October 9-13.

Steffen, K. M., Simhan, H. N., Caprau, D., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2006). Genetic variation in genes of cholesterol metabolism influence gestational age at delivery and birthweight. PAS Meeting, San Francisco, CA, Apr 29-May 2.

Caprau, D. M., Orr, K., Cooper, M. E., Dagle, J., Zimmerman, C., Johnson, K. J., Hostager, B., Marazita, M. L. & Murray, J. C. (2006). Fetal genetic variation in inflammation and detoxification paths are risk factors for preterm delivery. Platform presentation, 2006 PAS meeting, San Francisco, CA, Apr 29-May 2.

Vieira, A. R., Gamboa, G., Orbiso, M., McHenry, T. H., Cooper, M. E., Daack-Hirsch, S., Marazita, M. L. & Murray, J. C. (2006). Dental Anomalies as an Extended Phenotype of Orofacial Clefts: Genome Wide Reanalysis of 12 Multiplex Filipino Families. Poster presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Osoeqawa, K., Vessere, G., Pfundt, R., Schoenmakers, E., Staaf, J., Borg, A., Mansilla, M. A., Schutte, B. C., Lammer, E., Murray, J. C. & DeJong, P. J. (2006). CGH Screening to find loci associated with cleft lip and palate. Poster presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Wyszynski, D. F., Maestri, N., McIntosh, I., Smith, E. A., Lewanda, A. F., Garcia-Delgado, C., Vinageras-Guarneros, E., Wulfsberg, E. & Beaty, T. H. Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families. Human Genetics, 99(1), 22–26. DOI: 10.1007/s004390050303.

Pinnaro, C., Bedell, B., Ryckman, K., Smith, A., Feenstra, B., Melbye, M., Borowski, K. & Murray, J. C. Evaluation of Maternal Cholesterol and Inflammatory Markers for Contributions to Spontaneous Preterm Birth (sPTB). Doris Duke Clinical Research Fellows Meeting, Yale University.

Bille, C., Murray, J. C. & Olsen, S. F. (2007). Folic acid and birth malformations. (Vols. 334). (7591), pp. 433-4. BMJ (Clinical research ed.). PMID: 17332537.

Riley, B. M., Mansilla, M. A., Ma, J., Daack-Hirsch, S., Maher, B. S., Raffensperger, L. M., Russo, E. T., Vieira, A. R., Dodé, C., Mohammadi, M., Marazita, M. L. & Murray, J. C. (2007). Impaired FGF signaling contributes to cleft lip and palate. Proceedings of the National Academy of Sciences of the United States of America, 104(11), 4512–4517. PMID: 17360555.

Vieira, A. R., Modesto, A., Meira, R., Barbosa, A. R., Lidral, A. C. & Murray, J. C. (2007). Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. American Journal of Medical Genetics. Part A, 143A(6), 538–545. PMID: 17318851.

Riley, B. M., Mansilla, M. A., Ma, J., Daack-Hirsch, S., Maher, B. S., Raffensperger, L. M., Russo, E. T., Vieira, A. R., Dodé, C., Mohammadi, M., Marazita, M. L. & Murray, J. C. (2007). Impaired FGF signaling contributes to cleft lip and palate. Proceedings of the National Academy of Sciences of the United States of America, 104(11), 4512-7. PMID: 17360555.

Christensen, K., Murray, J. C. (2007). What genome-wide association studies can do for medicine. The New England journal of medicine, 356(11), 1094-7. PMID: 17360987.

Nopoulos, P., Richman, L., Andreasen, N., Murray, J. C. & Schutte, B. (2007). Cognitive dysfunction in adults with Van der Woude syndrome. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 9(4), 213–218. PMID: 17438385.

Felix, T. M., Tansey, M. J., Patil, S. R., Murray, J. C. & Dagle, J. M. (2007). Double paternal nondisjunction in an infant with transient neonatal diabetes mellitus and Klinefelter syndrome. American Journal of Medical Genetics Part A, 143A(8), 895–898. DOI: 10.1002/ajmg.a.31659.

Murray, J., Wehby, G., Mastroiacovo, P., Goco, N., Moretti-Ferreira, D., Felix, T. & Padovani, C. (2007). Randomized clinical trials of folic acid for prevention of recurrences of cleft lip and palate. Platform presentation, 64th Annual Meeting of the American Cleft Palate-Craniofacial Association Conference, Broomfield, Colorado, April 23-28.

Vieira, A. R., Modesto, A., Meira, R., Barbosa, A. R., Lidral, A. C. & Murray, J. C. (2007). Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. American journal of medical genetics. Part A, 143A(6), 538-45. PMID: 17318851.

Kleiber, C., Schutte, D. L., McCarthy, A. M., Floria-Santos, M., Murray, J. C. & Hanrahan, K. (2007). Predictors of topical anesthetic effectiveness in children. The Journal of Pain: Official Journal of the American Pain Society, 8(2), 168–174. PMID: 17010672.

Kleiber, C., Schutte, D. L., McCarthy, A. M., Floria-Santos, M., Murray, J. C. & Hanrahan, K. (2007). Predictors of topical anesthetic effectiveness in children. The journal of pain : official journal of the American Pain Society, 8(2), 168-74. PMID: 17010672.

Dietz, F. R., Murray, J. C. (2007). Genetic Basis of Disorders with Orthopaetic Manifestations. In Orthopaedic Basic Science, Foundations of Clinical Practice. (3), pp. 25-47.

Wehby, G. L., Castilla, E. E., Camelo, J. L. & Murray, J. C. (2007). An international trial of folic acid for prevention of recurrences of CLP. Platform presentation, 64th Annual Meeting of the American Cleft Palate-Craniofacial Association Conference, Broomfield, Colorado, April 23-28.

Wang, W., Yoshiura, K., Murray, J. & Lufkin, T. Assignment of the murine Hmx1 homeobox gene to the proximal region of mouse Chromosome 5. Mammalian Genome, 8(11), 869–870. DOI: 10.1007/s003359900598.

Klewer, S. E., Williamson, K. A., Lauer, R. M. & Murray, J. C. Association of candidate genes with atrioventricular septal defects in trisomy 21 and nonsyndromic cases. Society of Pediatric Research.

Johnson, K., Berends, S. & Murray, J. C. (2007). Development of a repository for genetic studies in infants. Platform presentation, Iowa Department of Public Health Conference, Ames, Iowa, April 3-4.

Gurnett, C. A., Bowcock, A. M., Dietz, F. R., Morcuende, J. A., Murray, J. C. & Dobbs, M. B. (2007). Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly. American journal of medical genetics. Part A, 143A(1), 27-32. PMID: 17152067.

Weinberg, S. M., Jenkins, E. A., Marazita, M. L. & Maher, B. S. (2007). Minor physical anomalies in schizophrenia: a meta-analysis. Schizophrenia Research, 89(1-3), 72–85. PMID: 17079117.

Shi, M., Christensen, K., Weinberg, C. R., Romitti, P., Bathum, L., Lozada, A., Morris, R. W., Lovett, M. & Murray, J. C. (2007). Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants. American Journal of Human Genetics, 80(1), 76–90. PMID: 17160896.

Bille, C., Olsen, J., Vach, W., Knudsen, V. K., Olsen, S. F., Rasmussen, K., Murray, J. C., Andersen, A. M. & Christensen, K. (2007). Oral clefts and life style factors--a case-cohort study based on prospective Danish data. European journal of epidemiology, 22(3), 173-81. PMID: 17295096.

Shi, M., Christensen, K., Weinberg, C. R., Romitti, P., Bathum, L., Lozada, A., Morris, R. W., Lovett, M. & Murray, J. C. (2007). Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants. American journal of human genetics, 80(1), 76-90. PMID: 17160896.

Warrington, A., Vieira, A. R., Christensen, K., Orioli, I. M., Castilla, E. E., Romitti, P. A. & Murray, J. C. (2006). Genetic evidence for the role of loci at 19q13 in cleft lip and palate. (Vols. 43). (6), pp. e26. Journal of medical genetics. PMID: 16740910.

Lourenco-Silva, A., Ribeiro, L. A., Cooper, M. E., Marazita, M. L., Moretti-Ferrieria, D. & Murray, J. C. (2006). Analysis of candidate genes for nonsyndromic cleft lip and/or palate in Brazilian trios with both a parent and offspring affected. Abstract presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Noorchashm, N., Deleyiannis, F., Weinberg, S., Neiswanger, K., Brandon, C., Scott, N., Bardi, K., Cooper, M. E., Vieira, A., Murray, J. C. & Marazita, M. L. (2006). A study of candidate markers for oral-facial clefts in Guatemalan families. Platform presentation, 63rd annual meeting of the American Cleft Palate-Craniofacial Association, Vancouver, BC, Apr 3-8.

Damiano, P. C., Tyler, M. C., Romitti, P. A., Momany, E. T., Canady, J. W., Karnell, M. P. & Murray, J. C. (2006). Type of oral cleft and mothers' perceptions of care, health status, and outcomes for preadolescent children. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 43(6), 715-21. PMID: 17105335.

Mostowska, A., Vieira, A. R., Govil, M., Lidral, A. C., Vieland, V. J., Mansilla, M. A., Marazita, M. L. & Murray, J. C. (2006). Association of chromosomal region 6q14-6q16.3 with nonsyndromic cleft lip and palate. Oral presentation, 29th Annual Meeting and Scientific Symposium, Society of Craniofacial Genetics, New Orleans, LA.

Brandon, C. A., Goldstein McHenry, T. H., Cooper, M. E., Maher, B. S., Bardi, K. M., Avila, J. R., Murray, J. C., Vieira, A. R. & Marazita, M. L. (2006). Analysis of ancestral origins of three populations using structure. Poster presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Félix, T. M., Hanshaw, B. C., Mueller, R., Bitoun, P. & Murray, J. C. (2006). CHD7 gene and non-syndromic cleft lip and palate. American journal of medical genetics. Part A, 140(19), 2110-4. PMID: 16763960.

Damiano, P. C., Tyler, M. C., Romitti, P. A., Momany, E. T., Canady, J. W., Karnell, M. P. & Murray, J. C. (2006). Type of oral cleft and mothers’ perceptions of care, health status, and outcomes for preadolescent children. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 43(6), 715–721. PMID: 17105335.

Ingraham, C. R., Kinoshita, A., Kondo, S., Yang, B., Sajan, S., Trout, K. J., Malik, M. I., Dunnwald, M., Goudy, S. L., Lovett, M., Murray, J. C. & Schutte, B. C. (2006). Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature Genetics, 38(11), 1335–1340. PMID: 17041601.

Rahimov, F., Ribeiro, L. A., de Miranda, E., Richieri-Costa, A. & Murray, J. C. (2006). GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?. American Journal of Medical Genetics. Part A, 140(23), 2571–2576. PMID: 17096318.

Avila, J. R., Jezewski, P. A., Vieira, A. R., Orioli, I. M., Castilla, E. E., Christensen, K., Daack-Hirsch, S., Romitti, P. A. & Murray, J. C. (2006). PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. American Journal of Medical Genetics. Part A, 140(23), 2562–2570. PMID: 17089422.

Rahimov, F., Ribeiro, L. A., de Miranda, E., Richieri-Costa, A. & Murray, J. C. (2006). GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?. American journal of medical genetics. Part A, 140(23), 2571-6. PMID: 17096318.

Avila, J. R., Jezewski, P. A., Vieira, A. R., Orioli, I. M., Castilla, E. E., Christensen, K., Daack-Hirsch, S., Romitti, P. A. & Murray, J. C. (2006). PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. American journal of medical genetics. Part A, 140(23), 2562-70. PMID: 17089422.

Ribeiro, L. A., Murray, J. C. & Richieri-Costa, A. (2006). PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American journal of medical genetics. Part A, 140(23), 2584-6. PMID: 17001668.

Ingraham, C. R., Kinoshita, A., Kondo, S., Yang, B., Sajan, S., Trout, K. J., Malik, M. I., Dunnwald, M., Goudy, S. L., Lovett, M., Murray, J. C. & Schutte, B. C. (2006). Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature genetics, 38(11), 1335-40. PMID: 17041601.

Schutte, D. L., McCarthy, A. M., Floria-Santos, M., Hanrahan, K., Murray, J. C. & Kleiber, C. (2006). Integrating molecular genetics analyses into clinical research. Biological research for nursing, 8(1), 67-77. PMID: 16766630.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2006). Health professionals’ assessment of health-related quality of life values for oral clefting by age using a visual analogue scale method. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 43(4), 383–391. PMID: 16854194.

Schutte, D. L., McCarthy, A. M., Floria-Santos, M., Hanrahan, K., Murray, J. C. & Kleiber, C. (2006). Integrating molecular genetics analyses into clinical research. Biological Research for Nursing, 8(1), 67–77. PMID: 16766630.

Jiang, R., Bush, J. O. & Lidral, A. C. (2006). Development of the upper lip: morphogenetic and molecular mechanisms. Developmental Dynamics: An Official Publication of the American Association of Anatomists, 235(5), 1152–1166. PMID: 16292776.

Félix, T. M., Hanshaw, B. C., Mueller, R., Bitoun, P. & Murray, J. C. (2006). CHD7 gene and non-syndromic cleft lip and palate. American Journal of Medical Genetics. Part A, 140(19), 2110–2114. PMID: 16763960.

Neiswanger, K., Deleyiannis, F. W., Avila, J. R., Cooper, M. E., Brandon, C. A., Vieira, A. R., Noorchashm, N., Weinberg, S. M., Bardi, K. M., Murray, J. C. & Marazita, M. L. (2006). Candidate genes for oral-facial clefts in Guatemalan families. Annals of plastic surgery, 56(5), 518-21; discussion 521. PMID: 16641627.

Rahimov, F., Murray, J. C. (2006). Expression analysis of the IRF6 gene in placental tissue. 2006 ASHG Meeting, New Orleans, LA, October 9-13.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2006). Health professionals' assessment of health-related quality of life values for oral clefting by age using a visual analogue scale method. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 43(4), 383-91. PMID: 16854194.

Kimani, J., Murray, J. C. (2006). DNA methylation analysis of the GABRB3 promoter in monozygotic twin pairs discordant for non-syndromic cleft lip and/or palate. Abstract presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Borowski, K. S., Dagle, J. M. & Murray, J. C. (2006). Neonatal RDS and polymorphisms in the corticosteroid metabolism pathway. Abstract presentation, 2006 ASHG Annual Meeting, New Orleans, LA, October 9-13.

Maciolek, N. L., Alward, W. L., Murray, J. C., Semina, E. V. & McNally, M. T. (2006). Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome. BMC medical genetics, 7, 59. PMID: 16834779.

Mansilla, M. A., Moreno, L. M., Johnson, M., Bullard, S. A., Jugessur, A., Lie, R. T., Wilcox, A., Christensen, K., McHenry, T. H., Maher, B. S., Cooper, M. E., Chines, P., Lidral, A. C., Marazita, M. L. & Murray, J. C. (2006). Variants in FOXE1 are highly associated with non-syndromic cleft lip with or without cleft palate. 2006 ASHG Meeting, New Orleans, LA, October 9-13.

Dietz, F. R., Cole, W. G., Tosi, L. L., Carroll, N. C., Werner, R. D., Comstock, D. & Murray, J. C. (2005). A search for the gene(s) predisposing to idiopathic clubfoot. (Vols. 67). (4), pp. 361-2. Clinical genetics. PMID: 15733275.

Dietz, F. R., Cole, W. G., Tosi, L. L., Carroll, N. C., Werner, R. D., Comstock, D. & Murray, J. C. (2005). A search for the gene(s) predisposing to idiopathic clubfoot. Clinical Genetics, 67(4), 361–362. PMID: 15733275.

Bille, C., Skytthe, A., Vach, W., Knudsen, L. B., Andersen, A. M., Murray, J. C. & Christensen, K. (2005). Parent's age and the risk of oral clefts. Epidemiology (Cambridge, Mass.), 16(3), 311-6. PMID: 15824545.

Vieira, A. R., Murray, J. C., Trembath, D., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L., Lennon-Graham, F. & Speer, M. (2005). Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects. (Vols. 135). (2), pp. 220-3. American journal of medical genetics. Part A. PMID: 15880745.

Scott, N. M., Weinberg, S. M., Neiswanger, K., Brandon, C. A., Daack-Hirsch, S., Murray, J. C., Liu, Y. E. & Marazita, M. L. (2005). Dermatoglyphic fingerprint heterogeneity among individuals with nonsyndromic cleft lip with or without cleft palate and their unaffected relatives in China and the Philippines. Human biology, 77(2), 257-66. PMID: 16201141.

Mansilla, M. A., Kimani, J., Mitchell, L. E., Christensen, K., Boomsma, D. I., Daack-Hirsch, S., Nepomucena, B., Wyszynski, D. F., Felix, T. M., Martin, N. G. & Murray, J. C. (2005). Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits. Twin Research and Human Genetics: The Official Journal of the International Society for Twin Studies, 8(1), 39–46. PMID: 15836809.

Espinoza, H. M., Ganga, M., Vadlamudi, U., Martin, D. M., Brooks, B. P., Semina, E. V., Murray, J. C. & Amendt, B. A. (2005). Protein kinase C phosphorylation modulates N- and C-terminal regulatory activities of the PITX2 homeodomain protein. Biochemistry, 44(10), 3942-54. PMID: 15751970.

Jugessur, A., Murray, J. C. (2005). Orofacial clefting: recent insights into a complex trait. Current opinion in genetics & development, 15(3), 270-8. PMID: 15917202.

Van Westen, L., Krahn, K. B., Mach, A., Bullard, S., Bader, P., Beck, A., Braddock, S., Clark, R., Cunningham, M. L., McCarrier, J., Miller, M., Murray, J., Nino, M., Slavotinek, A. & Lidral, A. C. (2005). Craniofrontonasal dysplasia. (Vols. A). pp. 1278. J Dent Res Spec Issue.

Mansilla, M. A., Kimani, J., Mitchell, L. E., Christensen, K., Boomsma, D. I., Daack-Hirsch, S., Nepomucena, B., Wyszynski, D. F., Felix, T. M., Martin, N. G. & Murray, J. C. (2005). Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits. Twin research and human genetics : the official journal of the International Society for Twin Studies, 8(1), 39-46. PMID: 15836809.

Marazita, M. L., Murray, J. C. & Zucchero, T. (2005). The IRF6 p.274V polymorphism is not a risk factor for isolated cleft lip - Response. Genetics in Medicine, 7(3), 209–210. DOI: 10.1097/01.GIM.0000157124.29731.AB.

Lepp, N., Dagle, J., Caprau, D., Marazita, M., Johnson, K. & Murray, J. (2005). Single nucleotide polymorphisms (SNPs) in smooth muscle regulation genes as risk. Midwest Society for Pediatric Research Meeting, St Louis, MO, Oct 21-22.

Riley, B. M., Mansilla, M. A., Maher, B. S., Trump, B. C., Russo, E. T., Vieira, A. R., Marazita, M. L. & Murray, J. C. (2005). Mutations in the FGF/FGFR pathway play a role in nonsyndromic cleft lip and palate. Poster presentation, American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Marazita, M. L., Murray, J. C., Lidral, A., Cooper, M. E., Goldstein McHenry, T., Maher, B. S., Moreno, L., Daack-Hirsch, S., Field, L. L., Arcos-Burgos, M., Valencia, C., Risk, J., Hecht, J. C., Dohemy, K., Pugh, E. & Boehm, C. (2005). Genome scans for nonsyndromic cleft lip with or without cleft palate in families from seven countries. Poster presentation, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Ingraham, C. R., Richardson, R., Yang, B., Dixon, J., Trout, K. J., Malik, M. I., Murray, J. C., Dixon, M. J. & Schutte, B. C. (2005). Interferon Regulatory Factor 6 (IRF6), the mouse ortholog of the gene mutated in Van der Woude syndrome, is essential for craniofacial, skin, and limb development. Am J Hum Gen 77S:49; Platform session, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Schutte, B., Kleiber, C., McCarthy, A. M., Floria-Santos, M., Murray, J. C. & Hanrahan, K. (2005). Association between pain response and an endothelin receptor A (EDNRA) polymorphism in children undergoing an IV insertion.

Govil, M., Murray, J. C., Marazita, M. L., Lidral, A., Field, L. L., Arcos-Burgos, M., Moreno, L., Doheny, K., Pugh, E., Boehm, C. & Vieland, V. J. (2005). Bayesian genome scan for cleft lip with or without cleft palate (CL/P). Poster presentation, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Bille, C., Winther, J. F., Bautz, A., Murray, J. C., Olsen, J. & Christensen, K. (2005). Cancer risk in persons with oral cleft--a population-based study of 8,093 cases. American journal of epidemiology, 161(11), 1047-55. PMID: 15901625.

Rahimov, F., Jugessur, A., Wilcox, A. J., Rolv, T. L., Gjessing, H. K. & Murray, J. C. (2005). Genetic variants in the IRF6 gene are strongly associated with orofacial clefts in a Norwegian population. Poster presentation, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Vieira, A. R., Avila, J. R., Daack-Hirsch, S., Dragan, E., Félix, T. M., Rahimov, F., Harrington, J., Schultz, R. R., Watanabe, Y., Johnson, M., Fang, J., O'Brien, S. E., Orioli, I. M., Castilla, E. E., Fitzpatrick, D. R., Jiang, R., Marazita, M. L. & Murray, J. C. (2005). Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS genetics, 1(6), e64. PMID: 16327884.

Di Paola, J., Jugessur, A., Goldman, T., Reiland, J., Tallman, D., Sayago, C. & Murray, J. C. (2005). Platelet glycoprotein I(b)alpha and integrin alpha2 beta1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. Journal of thrombosis and haemostasis: JTH, 3(7), 1511–1521. PMID: 15978109.

Jugessur, A., Murray, J. C. (2005). Orofacial clefting: recent insights into a complex trait. Current Opinion in Genetics & Development, 15(3), 270–278. PMID: 15917202.

Di Paola, J., Jugessur, A., Goldman, T., Reiland, J., Tallman, D., Sayago, C. & Murray, J. C. (2005). Platelet glycoprotein I(b)alpha and integrin alpha2 beta1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. Journal of thrombosis and haemostasis : JTH, 3(7), 1511-21. PMID: 15978109.

De Lima, R., Ghassibe, M., Rorick, N., Hoper, S., Schipper, D., Kondo, S., Doxon, M., Hehr, U., Compton, J., Vikkula, M., Richieri-Costa, A., Moretti-Ferreira, D., Murray, J. & Schutte, B. (2005). Prevalence and distribution of exonic mutations in Interferon Regulatory Factor 6 identified in two large cohorts with Van der Woude Syndrome. (Vols. 77S). pp. 389. Am J Hum Gen; Poster presentation, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Scott, N. M., Weinberg, S. M., Neiswanger, K., Daack-Hirsch, S., O'Brien, S., Murray, J. C. & Marazita, M. L. (2005). Dermatoglyphic pattern types in subjects with nonsyndromic cleft lip with or without cleft palate (CL/P) and their unaffected relatives in the Philippines. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 42(4), 362-6. PMID: 16001916.

Kimani, J. W., Shi, M., Field, L. L., Marazita, M. L. & Murray, J. C. (2005). X-chromosome inactivation patterns in females with non-syndromic cleft lip and/or palate. Poster presentation, Annual meeting of the American Society of Human Genetics, Salt Lake City, UT, Oct 25-29.

Vieira, A. R., Avila, J. R., Daack-Hirsch, S., Dragan, E., Félix, T. M., Rahimov, F., Harrington, J., Schultz, R. R., Watanabe, Y., Johnson, M., Fang, J., O’Brien, S. E., Orioli, I. M., Castilla, E. E., Fitzpatrick, D. R., Jiang, R., Marazita, M. L. & Murray, J. C. (2005). Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS genetics, 1(6), e64. PMID: 16327884.

Etheredge, A. J., Christensen, K., Del Junco, D., Murray, J. C. & Mitchell, L. E. (2005). Evaluation of two methods for assessing gene-environment interactions using data from the Danish case-control study of facial clefts. Birth defects research. Part A, Clinical and molecular teratology, 73(8), 541-6. PMID: 15965987.

Vieira, A., Santiago, S., Schultz, R., Kondo, S., Avila, J., Warrington, A., Watanabe, Y., Schutte, B., Bjork, B. & Murray, J. (2004). Sequencing of candidate genes for non-syndromic cleft lip and palate find rare etiologic variants. 61st Annual Meeting of the American Cleft Palate-Craniofacial Association, Page 74, Mar 15-20.

Schultz, R. E., Cooper, M. E., Daack-Hirsch, S., Shi, M., Nepomucena, B., Graf, K. A., O'Brien, E. K., O'Brien, S. E., Marazita, M. L. & Murray, J. C. (2004). Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. American journal of medical genetics. Part A, 125A(1), 17-22. PMID: 14755461.

Bitoun, P., Bremond-Gignac, D., Even, D., Frees, K., Benzacken, B., Benzacken, L., Murray, J. C. & Semina, E. (2004). Identification of PAX6 and FOXE3 mutations in a sample of congenital cataracts and aniridia patients. Investigative Ophthalmology & Visual Science, 45, U943–U943.

Wehby, G., Ohsfeldt, R. & Murray, J. (2004). Cost-effectiveness/utility analysis of prenatal genetic and ultrasound screening for Van der Woude syndrome. 61st annual meeting of the American Cleft Palate-Craniofacial Association, Page 78, Mar 15-20.

Trembath, D. G., Semina, E. V., Jones, D. H., Patil, S. R., Qian, Q., Amendt, B. A., Russo, A. F. & Murray, J. C. (2004). Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome. Birth defects research. Part A, Clinical and molecular teratology, 70(2), 82-91. PMID: 14991915.

Mintz-Hittner, H. A., Semina, E. V., Frishman, L. J., Prager, T. C. & Murray, J. C. (2004). VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. Ophthalmology, 111(4), 828-36. PMID: 15051220.

Scott, N. M., Weinberg, S. M., Neiswanger, K., Brandon, C. A., Murray, J. C., Liu, Y. & Marazita, M. L. (2004). Dermatoglyphic phenotypic heterogeneity among individuals with non syndromic cleft lip with or without cleft palate (CL/P) and their relatives in China and the Philippines. American Journal of Physical Anthropology, 177–177.

Shi, M., Caprau, D., Dagle, J., Christiansen, L., Christensen, K. & Murray, J. C. (2004). Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes. Birth defects research. Part A, Clinical and molecular teratology, 70(2), 65-74. PMID: 14991913.

Marçano, A. C., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., Richieri-Costa, A., Lidral, A. C., Murray, J. C., Moore, G. E. & Stanier, P. (2004). TBX22 mutations are a frequent cause of cleft palate. (Vols. 41). (1), pp. 68-74. Journal of medical genetics. PMID: 14729838.

Suzuki, Y., Jezewski, P. A., Machida, J., Watanabe, Y., Shi, M., Cooper, M. E., le Viet, T., Nguyen, T. D., Hai, H., Natsume, N., Shimozato, K., Marazita, M. L. & Murray, J. C. (2004). In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genetics in medicine : official journal of the American College of Medical Genetics, 6(3), 117-25. PMID: 15354328.

Marcano, A. C., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., Richieri-Costa, A., Lidral, A. C., Murray, J. C., Moore, G. E. & Stanier, P. (2004). TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, 41(1), 68–74. DOI: 10.1136/jmg.2003.010868.

Schultz, R. E., Cooper, M. E., Daack-Hirsch, S., Shi, M., Nepomucena, B., Graf, K. A., O’Brien, E. K., O’Brien, S. E., Marazita, M. L. & Murray, J. C. (2004). Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. American Journal of Medical Genetics. Part A, 125A(1), 17–22. PMID: 14755461.

Trembath, D. G., Semina, E. V., Jones, D. H., Patil, S. R., Qian, Q., Amendt, B. A., Russo, A. F. & Murray, J. C. (2004). Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger’s syndrome. Birth Defects Research. Part A, Clinical and Molecular Teratology, 70(2), 82–91. PMID: 14991915.

Shi, M., Caprau, D., Dagle, J., Christiansen, L., Christensen, K. & Murray, J. C. (2004). Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes. Birth Defects Research. Part A, Clinical and Molecular Teratology, 70(2), 65–74. PMID: 14991913.

Wehby, G., Castilla, E., Javois, L., Goco, N. & Murray, J. (2004). Birth defects treatment and prevention program: Tertiary prevention by systematic pediatric care in South America. 61st annual meeting of the American Cleft Palate-Craniofacial Association, Page 74, Mar 15-20.

Zucchero, T. M., Cooper, M. E., Maher, B. S., Daack-Hirsch, S., Nepomuceno, B., Ribeiro, L., Caprau, D., Christensen, K., Suzuki, Y., Machida, J., Natsume, N., Yoshiura, K., Vieira, A. R., Orioli, I. M., Castilla, E. E., Moreno, L., Arcos-Burgos, M., Lidral, A. C., Field, L. L., Liu, Y. E., Ray, A., Goldstein, T. H., Schultz, R. E., Shi, M., Johnson, M. K., Kondo, S., Schutte, B. C., Marazita, M. L. & Murray, J. C. (2004). Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. The New England journal of medicine, 351(8), 769-80. PMID: 15317890.

Vieira, A. R., Meira, R., Modesto, A. & Murray, J. C. (2004). MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. Journal of Dental Research, 83(9), 723–727. PMID: 15329380.

Zeng, S. M., Murray, J. C., Widness, J. A., Strauss, R. G. & Yankowitz, J. (2004). Association of single nucleotide polymorphisms in the thrombopoietin-receptor gene, but not the thrombopoietin gene, with differences in platelet count. American journal of hematology, 77(1), 12-21. PMID: 15307100.

Vieira, A. R., Meira, R., Modesto, A. & Murray, J. C. (2004). MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. Journal of dental research, 83(9), 723-7. PMID: 15329380.

Katz, L. A., Schultz, R. E., Semina, E. V., Torfs, C. P., Krahn, K. N. & Murray, J. C. (2004). Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromes. American Journal of Medical Genetics. Part A, 130A(3), 277–283. PMID: 15378534.

Katz, L. A., Schultz, R. E., Semina, E. V., Torfs, C. P., Krahn, K. N. & Murray, J. C. (2004). Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromes. American journal of medical genetics. Part A, 130A(3), 277-83. PMID: 15378534.

Murray, J. C., Schutte, B. C. (2004). Cleft palate: players, pathways, and pursuits. The Journal of Clinical Investigation, 113(12), 1676–1678. PMID: 15199400.

Lidral, A. C., Murray, J. C. (2004). Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model. Birth Defects Research. Part A, Clinical and Molecular Teratology, 70(12), 893–901. PMID: 15578714.

Lidral, A. C., Murray, J. C. (2004). Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model. Birth defects research. Part A, Clinical and molecular teratology, 70(12), 893-901. PMID: 15578714.

Zeng, S. M., Murray, J. C., Widness, J. A., Strauss, R. G. & Yankowitz, J. (2004). Association of single nucleotide polymorphisms in the thrombopoietin-receptor gene, but not the thrombopoietin gene, with differences in platelet count. American Journal of Hematology, 77(1), 12–21. PMID: 15307100.

Vieira, A. R., Castillo Taucher, S., Aravena, T., Astete, C., Sanz, P., Tastets, M. E., Monasterio, L. & Murray, J. C. (2004). Análisis mutacional del gen Homeobox de segmento muscular 1 (MSX1) en chilenos con fisuras orales [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]. Revista médica de Chile, 132(7). DOI: 10.4067/S0034-98872004000700005.

Vieira, A. R., Castillo Taucher, S., Aravena, T., Astete, C., Sanz, P., Tastets, M. E., Monasterio, L. & Murray, J. C. (2004). [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]. Revista medica de Chile, 132(7), 816-22. PMID: 15379328.

Murray, J. C., Vieira, A., Santiago, S., Mansilla, A., Riley, B. & Miwa, N. (2004). Candidate gene resequencing identifies gene variants in isolated cleft lip and palate cases. The Third Structural Birth Defects meeting, St Louis, MO.

Christensen, K., Juel, K., Herskind, A. M. & Murray, J. C. (2004). Long term follow up study of survival associated with cleft lip and palate at birth. BMJ (Clinical research ed.), 328(7453), 1405. PMID: 15145797.

Marazita, M. L., Murray, J. C., Lidral, A. C., Arcos-Burgos, M., Cooper, M. E., Goldstein, T., Maher, B. S., Daack-Hirsch, S., Schultz, R., Mansilla, M. A., Field, L. L., Liu, Y. E., Prescott, N., Malcolm, S., Winter, R., Ray, A., Moreno, L., Valencia, C., Neiswanger, K., Wyszynski, D. F., Bailey-Wilson, J. E., Albacha-Hejazi, H., Beaty, T. H., McIntosh, I., Hetmanski, J. B., Tunçbilek, G., Edwards, M., Harkin, L., Scott, R. & Roddick, L. G. (2004). Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American journal of human genetics, 75(2), 161-73. PMID: 15185170.

Murray, J. C., Schutte, B. C. (2004). Cleft palate: players, pathways, and pursuits. The Journal of clinical investigation, 113(12), 1676-8. PMID: 15199400.

Zucchero, T. M., Cooper, M. E., Maher, B. S., Daack-Hirsch, S., Nepomuceno, B., Ribeiro, L., Caprau, D., Christensen, K., Suzuki, Y., Machida, J., Natsume, N., Yoshiura, K., Vieira, A. R., Orioli, I. M., Castilla, E. E., Moreno, L., Arcos-Burgos, M., Lidral, A. C., Field, L. L., Liu, Y., Ray, A., Goldstein, T. H., Schultz, R. E., Shi, M., Johnson, M. K., Kondo, S., Schutte, B. C., Marazita, M. L. & Murray, J. C. (2004). Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. The New England Journal of Medicine, 351(8), 769–780. PMID: 15317890.

Murray, J. C., Vieira, A., Santiago, S., Mansilla, A., Riley, B. & Miwa, N. (2004). Candidate gene resequencing identifies gene variants in isolated cleft lip and palate cases. 25th Annual David W Smith Workshop on Malformations and Morphogenesis, Snowbird, UT, Aug 18-21.

Murray, J. C., Marazita, M. (2004). Single gene contributions to isolated cleft lip and/or palate. Genetics in Medicine, 6(4), 382–382.

Vieira, A. R., Castillo Taucher, S., Aravena, T., Astete, C., Sanz, P., Tastets, M. E., Monasterio, L. & Murray, J. C. (2004). [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]. Revista Medica De Chile, 132(7), 816–822. PMID: 15379328.

Collins, D. R., Murray, J. C., Tomlin, J. B. & Bullard, S. A. (2003). Detection of the 22q11.2 deletion within a population containing specific language impairment (SLI) subjects. (Vols. 73). pp. 405. Am J Hum Genet.

Zinkevich, N., Bosenko, D., Frees, K., Shi, M., Trembath, Y., Murray, J. C., Link, B. & Semina, E. V. (2003). Identification and characterization of regions involved in regulation of Pitx2 expression. (Vols. 73). pp. 356. Am J Hum Genet.

Scott, N. M., Weinberg, S. M., Daach-Hirsch, S., Neiswanger, K., O'Brien, S., Nepomuceno, B., Murray, J. C. & Marazita, M. L. (2003). Dermatoglyphics in Filipinos with nonsyndromic cleft lip with or without cleft palate (NS CL/P), and their relatives. (Vols. 73). pp. 286. Am J Hum Genet.

Meira, R., Vieira, A. R., Modesto, A. & Murray, J. (2003). Associação dos genes MSX1 e TGFA com agenesia dentária isolada em uma população brasileira. (Vols. 17). (2), pp. 210. Pesqui Odontol Bras.

Ferreira, R., Schultz, R., Marazita, M., Moretti-Ferreira, D., Richieri-Costa, A. & Murray, J. C. (2003). Candidate regions to Richieri-Costa Pereira syndrome. (Vols. 73). pp. 490. Am J Hum Genet.

Kayano, S., Kure, S., Suzuki, Y., Kanno, K., Aoki, Y., Kondo, S., Schutte, B. C., Murray, J. C., Yamada, A. & Matsubara, Y. (2003). Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. Journal of human genetics, 48(12), 622-8. PMID: 14618417.

Schultz, R., Cooper, M., Riley, B., Goldstein, T., Daack-Hirsch, S., Nepomucena, B., Marazita, M. & Murray, J. (2003). A two stage genome-wide linkage scan for nonsyndromic cleft lip with or without cleft palate in 220 Filipino families shows evidence of linkage to 2p21, 6q23, and 8p21. (Vols. 73). pp. 536. Am J Hum Genet.

Miwa, N., Johnson, M., Hoper, S., Kondo, S., Zucchero, T., Murray, J. C. & Schutte, B. (2003). Identification of cryptic mutations in IRF6 using real time deletion assays and genomic sequencing. (Vols. 73). pp. 558. Am J Hum Genet.

Jugessur, A., Lie, R. T., Wilcox, A. J., Murray, J. C., Taylor, J. A., Saugstad, O. D., Vindenes, H. A. & Abyholm, F. (2003). Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysis. Genetic epidemiology, 24(3), 230-9. PMID: 12652527.

Zucchero, T., Cooper, M., Caprau, D., Ribiero, L., Suzuki, Y., Yoshiura, K., Christensen, K., Moreno, L., Johnson, M., Gill, M., Lidral, A., Kondo, S., Schutte, B., Marazita, M. & Murray, J. C. (2003). IRF6 is a major modifier for nonsyndromic cleft lip and palate. (Vols. 73). pp. 162. Am J Hum Genet.

(2003). Rieger Syndrome. In The NORD Guide to Rare Disorders. pp. 243-244. Philadelphia, PA: Williams & Wilkins.

Knight, A. S., Rorick, N. K., Malik, M. I., Murray, J. C., Dixon, M. J. & Schutte, B. C. (2003). Structure and expression analysis of Interferion Regulatory Factor 6 (IRF6). (Vols. 73). pp. 566. Am J Hum Genet.

Vieira, A. R., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2003). Variants in SKI, IRF6, and RFC1 are associated with cleft lip/palate in a South American population. (Vols. 73). pp. 519. Am J Hum Genet.

DiPaola, J., Goldman, T., Reiland, J., Sayago, C., Tallman, D. & Murray, J. (2003). Platelet membrane glycoprotein Ib? and integrin 21 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. (Vols. 102). pp. 11. Blood.

Bjork, B. C., Herron, B. J., Vieira, A. R., Murray, J. C. & Beier, D. R. (2003). Phenotypic characterization and positional cloning of two recessive ENU-induced mouse models of cleft palate. (Vols. 73). pp. 331. Am J Hum Genet.

Shi, M., Christensen, K., Lozada, A., Romitti, P. & Murray, J. (2003). Maternal cigarette smoking and variants in GSTP1 and GSTT1 contribute to the etiology of orofacial clefting. (Vols. 73). pp. 388. Am J Hum Genet.

Mansilla, M., Castilla, E., Lopez Camelo, J. & Murray, J. (2003). Mutations in PTCH may be rare causes of nonsyndromic cleft lip and palate. (Vols. 73). (519) Am J Hum Genet.

Kayano, S., Kanno, K., Yamada, A., Kondo, S., Schutte, B. C., Murray, J. C., Suzuki, Y., Kure, S. & Matsubara, Y. (2003). Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. (Vols. 73). pp. 557. Am J Hum Genet.

Wehby, G. L., Ohsfeldt, R. L. & Murray, J. C. (2003). Cost effectiveness of prenatal genetic and ultrasound screening for Van der Woude syndrome. (Vols. 73). pp. 417. Am J Hum Genet.

Shi, M., Caprau, D., Romitti, P., Christensen, K. & Murray, J. C. (2003). Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2. Birth defects research. Part A, Clinical and molecular teratology, 67(8), 545-9. PMID: 14632302.

Murray, J. C. (2003). Genetic Drift. Prenatal diagnosis is for the DR, not just for the OR. American Journal of Medical Genetics. Part A, 120A(4), 594–595. PMID: 12884446.

Shi, M., Caprau, D., Romitti, P., Christensen, K. & Murray, J. C. (2003). Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2. Birth Defects Research. Part A, Clinical and Molecular Teratology, 67(8), 545–549. PMID: 14632302.

Murray, J. C., Mansilla, M. A., Kimani, J., Mitchell, L., Christensen, K., Trench, G. C., Daack-Hirsch, S., Nepomucena, B., Wyszynski, D. & Moreno, L. (2003). Studies of discordant MZ twins as a model for understanding complex birth defects. Proc Greenwood Genet Center 2003, David W Smith Symposium, Vancouver, BC.

Murray, J. C. (2003). Genetic Drift. Prenatal diagnosis is for the DR, not just for the OR. American journal of medical genetics. Part A, 120A(4), 594-5. PMID: 12884446.

de Ferreira Lima, R. L., Moretti-Ferreira, D., Richieri-Costa, A. & Murray, J. C. (2003). Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. American journal of medical genetics. Part A, 122A(1), 56-8. PMID: 12949973.

Knight, A. S., Rorick, N. K., Malik, M. I., Murray, J. C., Dixon, M. J. & Schutte, B. C. (2003). Structure and expression analysis of Interferon Regulatory Factor 6 (IRF6). American Journal of Human Genetics, 73(5), 566–566.

Katz, L. A., Kondo, S., Schutte, B. C., Johnson, M. K., Zucchero, T. M., Krahn, K. N. & Murray, J. C. (2003). Genetic variations in the coding sequence of the IRF6 gene occur in different ethnic populations. Pediatric Research, 54(5), 774–774.

Zucchero, M., Cooper, M., Caprau, D., Ribiero, L., Suzuki, Y., Yoshiura, K., Christensen, K., Moreno, L., Johnson, M., Field, L., Liu, Y., Ray, A., Maher, B., Goldstein, T., Lidral, A., Kondo, S., Schutte, B., Marazita, M. & Murray, J. C. (2003). IRF6 is a major modifier for nonsyndromic cleft with or without cleft palate. American Journal of Human Genetics, 73(5), 162–162.

Marazita, M. L., Murray, J. C., Cooper, M., Goldstein, T., Schultz, R., Daack-Hirsch, S., Field, L., Liu, Y., Tunçbilek, G., Ray, A., Prescott, N., Winter, R., Wyszynski, D., Bailey-Wilson, J., Albacha-Hejazi, H., Lidral, A., Moreno, L., Arcos-Burgos, M. & Beaty, T. (2003). Meta-analysis of 11 genome scans for cleft lip with or without cleft palate. Society of Craniofacial Genetics 26th annual meeting and Scientific Symposium, Los Angeles, CA, Nov 4.

Di Paola, J. A., Goldman, T., Reiland, J., Sayago, C., Tallman, D. & Murray, J. C. (2003). Platelet membrane glycoproteins Ib alpha and Ia IIa polymorphisms: Gene frequencies and linkage disequilibrium in a population diversity panel. Blood, 102(11), 784A–784A.

Vieira, A. R., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2003). MSX1 and TGFB3 contribute to clefting in South America. Journal of dental research, 82(4), 289-92. PMID: 12651933.

Jezewski, P. A., Vieira, A. R., Nishimura, C., Ludwig, B., Johnson, M., O’Brien, S. E., Daack-Hirsch, S., Schultz, R. E., Weber, A., Nepomucena, B., Romitti, P. A., Christensen, K., Orioli, I. M., Castilla, E. E., Machida, J., Natsume, N. & Murray, J. C. (2003). Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. Journal of Medical Genetics, 40(6), 399–407. PMID: 12807959.

Semina, E. V., Frees, K., Tomarev, S., Cvekl, A. & Murray, J. C. (2003). Identification of promoter and other regulatory regions of Pitx3 gene. Investigative Ophthalmology & Visual Science, 44, U82–U82.

Katz, L. A., Kondo, S., Schutte, B. C., Johnson, M. K., Zucchero, T. M., Krahn, K. N. & Murray, J. C. (2003). Genetic variation in IRF6 within different ethnic populations. Pediatric Research, 53(4), 262A–262A.

Vieira, A. R., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2003). MSX1 and TGFB3 contribute to clefting in South America. Journal of Dental Research, 82(4), 289–292. PMID: 12651933.

O’Brien, E. K., d’Alencon, C., Schoenebeck, J., Murray, J. C., Allende, M. L., Gelb, B. D., Yelon, D., Eisen, J. S. & Cornell, R. A. (2003). Transcription factor AP-2 knockdown in zebrafish embryos disrupts head skeleton, autonomic neurons, and melanocytes. Developmental Biology, 259(2), 503–503.

Slayton, R. L., Williams, L., Murray, J. C., Wheeler, J. J., Lidral, A. C. & Nishimura, C. J. (2003). Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 40(3), 274-9. PMID: 12733956.

Jugessur, A., Wilcox, A. J., Lie, R. T., Murray, J. C., Taylor, J. A., Ulvik, A., Drevon, C. A., Vindenes, H. A. & Abyholm, F. E. (2003). Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads. American journal of epidemiology, 157(12), 1083-91. PMID: 12796044.

Jugessur, A., Lie, R. T., Wilcox, A. J., Murray, J. C., Taylor, J. A., Saugstad, O. D., Vindenes, H. A. & Abyholm, F. E. (2003). Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: assessing gene-environment interactions in case-parent triads. Genetic epidemiology, 25(4), 367-74. PMID: 14639706.

Mitchell, L. E., Murray, J. C., O'Brien, S. & Christensen, K. (2003). Retinoic acid receptor alpha gene variants, multivitamin use, and liver intake as risk factors for oral clefts: a population-based case-control study in Denmark, 1991-1994. American journal of epidemiology, 158(1), 69-76. PMID: 12835288.

O'Brien, E. K., Zhang, X., Nishimura, C., Tomblin, J. B. & Murray, J. C. (2003). Association of specific language impairment (SLI) to the region of 7q31. American journal of human genetics, 72(6), 1536-43. PMID: 12721956.

Jezewski, P. A., Vieira, A. R., Nishimura, C., Ludwig, B., Johnson, M., O'Brien, S. E., Daack-Hirsch, S., Schultz, R. E., Weber, A., Nepomucena, B., Romitti, P. A., Christensen, K., Orioli, I. M., Castilla, E. E., Machida, J., Natsume, N. & Murray, J. C. (2003). Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. Journal of medical genetics, 40(6), 399-407. PMID: 12807959.

O’Brien, E. K., Zhang, X., Nishimura, C., Tomblin, J. B. & Murray, J. C. (2003). Association of specific language impairment (SLI) to the region of 7q31. American Journal of Human Genetics, 72(6), 1536–1543. PMID: 12721956.

Dagle, J. M., Even, D. A., Tansey, M. J., Patil, S. R. & Murray, J. C. (2002). Double paternal nondisjunction in an infant with neonatal diabetes mellitus and Klinefelter Syndrome. Pediatric Research, 51(4), 225A–225A.

Caprau, D. M., Murray, J. C., Romitti, P. A. & Grady, R. (2002). A TDT and candidate gene analysis demonstrates a role for genes of folate metabolism (RFC1, MTHFR) in clefting. Pediatric Research, 51(4), 66A–66A.

Semina, E. V., Even, D., Frees, K., Bitoun, P., Mintz-Hittner, H. A., Summers, K. M., Alward, W. L., Hanson, I., van Heyningen, V. & Murray, J. C. (2002). Analysis of patients with various anterior segment disorders for mutations in PITX2, PITX3, FOXE3 and VSX1 genes. Investigative Ophthalmology & Visual Science, 43, U571–U571.

Barrow, L. L., Wines, M. E., Romitti, P. A., Holdener, B. C. & Murray, J. C. (2002). Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts. Teratology, 66(2), 85-90. PMID: 12210012.

Vieira, A. R., Trembath, D., Vandyke, D. C., Murray, J. C., Marker, S., Lerner, G., Bonner, E. & Speer, M. (2002). Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defects. (Vols. 111). (2), pp. 218-9. American journal of medical genetics. PMID: 12210356.

Barrow, L. L., van Bokhoven, H., Daack-Hirsch, S., Andersen, T., van Beersum, S. E., Gorlin, R. & Murray, J. C. (2002). Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Journal of medical genetics, 39(8), 559-66. PMID: 12161593.

Kim, Y. J., Williamson, R. A., Murray, J. C. & Merrill, D. C. (2002). Factor v Leiden mutation and preeclampsia - Reply. American Journal of Obstetrics and Gynecology, 186(4), 853–854. DOI: 10.1067/mob.2002.122442.

Vieira, A. R., Karras, J. C., Orioli, M., Castilla, E. E. & Murray, J. C. (2002). Frequency of mtDNA population-specific variants in a nonsyndromic clefting South American population. (Vols. 81). pp. A408. J Dent Res.

Murray, J. C. (2002). Gene/environment causes of cleft lip and/or palate. Clinical Genetics, 61(4), 248–256. PMID: 12030886.

Vieira, A. R., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2002). MSX1 and TGFB3 are associated to nonsyndromic oral-facial clefts is South America. (Vols. 81). pp. A306. J Dent Res.

Barrow, L. L., Wines, M. E., Romitti, P. A., Holdener, B. C. & Murray, J. C. (2002). Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts. Teratology, 66(2), 85–90. PMID: 12210012.

Colmenares, C., Heilstedt, H. A., Shaffer, L. G., Schwartz, S., Berk, M., Murray, J. C. & Stavnezer, E. (2002). Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice. Nature genetics, 30(1), 106-9. PMID: 11731796.

Mitchell, L. E., Beaty, T. H., Lidral, A. C., Munger, R. G., Murray, J. C., Saal, H. M. & Wyszynski, D. F. (2002). Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 39(1), 93-100. PMID: 11772175.

Murray, J. C. (2002). Gene/environment causes of cleft lip and/or palate. Clinical genetics, 61(4), 248-56. PMID: 12030886.

Vieira, A. R., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2002). MSX1 and TGFB3 are associated to nonsyndromic oral-facial clefts in South America. Journal of Dental Research, 81, A306–A306.

Rasmussen, S. A., Lammer, E. J., Shaw, G. M., Finnell, R. H., McGehee, Jr, R. E., Gallagher, M., Romitti, P. A. & Murray, J. C. (2002). Integration of DNA sample collection into a multi-site birth defects case-control study. Teratology, 66(4), 177-84. PMID: 12353214.

Vieira, A. R., Orioli, I. M. & Murray, J. C. (2002). Maternal age and oral clefts: a reappraisal. Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics, 94(5), 530-5. PMID: 12424443.

Vieira, A. R., Orioli, I. M. & Murray, J. C. (2002). Maternal age and oral clefts: a reappraisal. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 94(5), 530–535. PMID: 12424443.

Watanabe, Y., Benson, D. W., Yano, S., Akagi, T., Yoshino, M. & Murray, J. C. (2002). Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD. Journal of Medical Genetics, 39(11), 807–811. DOI: 10.1136/jmg.39.11.807.

Mutti, D. O., Semina, E., Marazita, M., Cooper, M., Murray, J. C. & Zadnik, K. (2002). Genetic loci for pathological myopia are not associated with juvenile myopia. American journal of medical genetics, 112(4), 355-60. PMID: 12376937.

Vieira, A. R., Karras, J. C., Orioli, I. M., Castilla, E. E. & Murray, J. C. (2002). Genetic origins in a South American clefting population. Clinical genetics, 62(6), 458-63. PMID: 12485193.

Zeng, S. M., Yankowitz, J. & Murray, J. C. (2002). Conjoined twins in a monozygotic triplet pregnancy: prenatal diagnosis and X-inactivation. Teratology, 66(6), 278-81. PMID: 12486760.

Karplus, T. M., Jeronimo, S. M., Chang, H., Helms, B. K., Burns, T. L., Murray, J. C., Mitchell, A. A., Pugh, E. W., Braz, R. F., Bezerra, F. L. & Wilson, M. E. (2002). Association between the tumor necrosis factor locus and the clinical outcome of Leishmania chagasi infection. Infection and Immunity, 70(12), 6919–6925. PMID: 12438370.

Zeng, S. M., Yankowitz, J. & Murray, J. C. (2002). Conjoined twins in a monozygotic triplet pregnancy: prenatal diagnosis and X-inactivation. Teratology, 66(6), 278–281. PMID: 12486760.

Barrow, L. L., van Bokhoven, H., Daack-Hirsch, S., Andersen, T., van Beersum, S. E. C.,, Gorlin, R. & Murray, J. C. (2002). Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Journal of Medical Genetics, 39(8), 559–566. PMID: 12161593.

Karplus, T. M., Jeronimo, S. M., Chang, H., Helms, B. K., Burns, T. L., Murray, J. C., Mitchell, A. A., Pugh, E. W., Braz, R. F., Bezerra, F. L. & Wilson, M. E. (2002). Association between the tumor necrosis factor locus and the clinical outcome of Leishmania chagasi infection. Infection and immunity, 70(12), 6919-25. PMID: 12438370.

Vieira, A. R., Karras, J. C., Orioli, I. M., Castilla, E. E. & Murray, J. C. (2002). Genetic origins in a South American clefting population. Clinical Genetics, 62(6), 458–463. PMID: 12485193.

Kondo, S., Schutte, B. C., Richardson, R. J., Bjork, B. C., Knight, A. S., Watanabe, Y., Howard, E., de Lima, Renata L. L. Ferreira,, Daack-Hirsch, S., Sander, A., McDonald-McGinn, D. M., Zackai, E. H., Lammer, E. J., Aylsworth, A. S., Ardinger, H. H., Lidral, A. C., Pober, B. R., Moreno, L., Arcos-Burgos, M., Valencia, C., Houdayer, C., Bahuau, M., Moretti-Ferreira, D., Richieri-Costa, A., Dixon, M. J. & Murray, J. C. (2002). Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics, 32(2), 285–289. PMID: 12219090.

Nishimura, C. J., Harrington, J., Ludwig, B., Allaman, J., Vieira, A., Jezewski, P., Schultz, R., Kondo, S., Avila, J., Warrington, A., Watanabe, Y. & Murray, J. C. (2002). Sequencing of candidate genes for non-syndromic cleft lip and palate finds rare etiologic variants. American Journal of Human Genetics, 71(4), 514–514.

Kondo, S., Schutte, B. C., Richardson, R. J., Bjork, B. C., Knight, A. S., Watanabe, Y., Howard, E., de Lima, R. L., Daack-Hirsch, S., Sander, A., McDonald-McGinn, D. M., Zackai, E. H., Lammer, E. J., Aylsworth, A. S., Ardinger, H. H., Lidral, A. C., Pober, B. R., Moreno, L., Arcos-Burgos, M., Valencia, C., Houdayer, C., Bahuau, M., Moretti-Ferreira, D., Richieri-Costa, A., Dixon, M. J. & Murray, J. C. (2002). Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature genetics, 32(2), 285-9. PMID: 12219090.

Schultz, R. E., Cooper, M. E., O’Brien, E. K., Graf, K. A., Marazita, M. L. & Murray, J. C. (2002). A targeted linkage scan for nonsyndromic cleft lip and palate. American Journal of Human Genetics, 71(4), 444–444.

Okur, H., Vargel, I., Kondo, S., Schutte, B. C., Ozgur, F., Balci, S., Ozusta, S., Cekirge, I., Girgin, B., Erk, Y., Murray, J. C. & Akarsu, A. N. (2002). Phenotype description of Van der Woude Syndrome (VWS) unlinked to chromosome 1 containing IRF6. American Journal of Human Genetics, 71(4), 285–285.

Kondo, S., Schutte, B. C., Richardson, R. J., Bjork, B. C., Knight, A. S., Watanabe, Y., Howard, E., Dixon, M. J. & Murray, J. C. (2002). Interferon regulatory facter 6 (IRF6) is mutated in two orofacial clefting disorders, Van der Woude and Popliteal Pterygium syndromes. American Journal of Human Genetics, 71(4), 209–209.

Watanabe, Y., Park, E., O’Brien, S., Nishimura, C., Ludwig, B. & Murray, J. C. (2002). Genetic and sequence based analysis of the human TGFB3 in cleft lip and palate and cross-species homology comparisons. American Journal of Human Genetics, 71(4), 372–372.

Vieira, A. R., Karras, J. C., Orioli, I. M., Castilla, E. & Murray, J. C. (2002). Genetic origins in a south American clefting population. American Journal of Human Genetics, 71(4), 436–436.

Caprau, D. M., Murray, J. C., Romitti, P. A. & Grady, R. (2002). A TDT and candidate gene analysis demonstrates a role for genes of folate metabolism (RFC1, MTHFR) in clefting. American Journal of Human Genetics, 71(4), 281–281.

Slayton, R. L., Williams, L., Murray, J. C., Wheeler, J. J., Lidral, A. C. & Nishimura, C. (2001). Candidate gene analysis of cleft lip/palate with hypodontia outside the cleft. (Vols. 69). (4S), pp. 561. Am J Hum Genet.

Shi, M., Dagle, J., Caprau, D. & Murray, J. C. (2001). Application of kinetic PCR and molecular beacon technology to pooled sample and high-sensitivity analysis of the MTHFR gene. (Vols. 69). (4(S)), pp. 226. Am J Hum Genet.

Schutte, C. L., Maas, M., Buckwalter, K. C., Murray, J. C. & Schutte, B. C. (2001). A low density lipoprotein receptor related protein-associated protein 1 Del/Ins polymorphism and phenotypic variablility in Alzheimer disease. (Vols. 69). (4S), pp. 564. Am J Hum Genet.

Murray, J. C. (2001). Advances in Molecular Genetics. In BSCS Biology, A Molecular Approach, Blue Version. (8), pp. 390-411.

Watanabe, Y., Yano, S., Akagi, T., Yoshino, M. & Murray, J. C. (2001). A new phenotype of familial visceral inversus/atrial fibrillation/ASD caused by a novel 7bp deletion in the CSX/NKX2.5 gene. (Vols. 69). (4S), pp. 606. Am J Hum Genet.

Park, E. A., Watanabe, Y., Daack-Hirsch, S., O'Brien, S. O., Schultz, R., Vieira, A., Shi, M. & Murray, J. C. (2001). A TDT and candidate gene analysis shows TGFB3 involved in non-syndromic clefting in an Asian population. (Vols. 69). (4S), pp. 557. Am J Hum Genet.

Schutte, B. C., Watanabe, Y., Bjork, B. C., Howard, E. L., Hoper, S. A., Malik, M. I., Fang, M. M., Hemerson, P. I., Dixon, M. J. & Murray, J. C. (2001). Mutation and deletion analysis of the Van der Woude syndrome locusat chromosome 1q32-q41. (Vols. 69). (4S), pp. 627. Am J Hum Genet.

Caprau, D. M., Murray, J. C., Mertz, H. L., Kim, Y. & Merrill, D. C. (2001). Genetic susceptibility to preeclampsia: evaluation of eNos, TGFB3, and AGT mutations. (Vols. 69). (4S), pp. 552. Am J Hum Genet.

Zucchero, T. M., Schutte, B. C., Daack-Hirsch, S. & Murray, J. C. (2001). TGFA is a genetic modifier of Van der Woude syndrome. (Vols. 69). (4S), pp. 568. Am J Hum Genet.

Green, P. D., Hjalt, T. A., Kirk, D. E., Sutherland, L. B., Thomas, B. L., Sharpe, P. T., Snead, M. L., Murray, J. C., Russo, A. F. & Amendt, B. A. (2001). Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development. Gene expression, 9(6), 265-81. PMID: 11763998.

Murray, J. C., Semina, E. V. (2001). PITX2 Gene in Development. In Genotype to Phenotype. (2), pp. 229-238.

Brownell, I., Semina, E. V., Mintz-Hittner, H. A., Murray, J. C. & Jamrich, M. (2001). Mutations in the human forkhead transcription factor FOXE3 cause autosomal dominant cataracts and anterior segment ocular dysgenesis. (Vols. 42). (4), pp. S459. Invest Ophthalmol Vis Sci.

Bitoun, P., Machinis, K., Semina, E., Jesuran-Perelroizen, M., Feingold, M., Odent, S., Le Marec, B., Dastot, F., Gaudelus, J., Murray, J. C., Amselem, S. & Cacheux, V. (2001). Heterozygous PITX2?RIEG1 gene deletion associated with GH deficiency in Rieger syndrome. (Vols. 69). (4S), pp. 611. Am J Hum Genet.

Vieira, A. R., Orioli, M., Castilla, E. E., Cooper, M. E., Marazita, M. L. & Murray, J. C. (2001). MSX1 Variant is associated with cleft lip/palate in a South American population. (Vols. 69). (4S), pp. 557. Am J Hum Genet.

Jezewski, P., Vieira, A., Schultz, R., Machida, J., Suzuki, Y., Ludwig, B., Daack-Hirsch, S., O'Brien, S., Nishimura, C., Johnson, M. & Murray, J. C. (2001). Mutations in MSX1 are associated with nonsyndromic orofacial clefting. (Vols. 69). (4S), pp. 558. Am J Hum Genet.

Bjork, B. C., Schutte, B. C., Watanabe, Y., Gregory, S., Howard, E. H., Malik, M. I., Dixon, M. & Murray, J. C. (2001). Characterization of 41 genes identified through the analysis of 1 Mb of sequence surrounding the Van der Woude syndrome (VWS) critical region at 1q32-q41. Cytogenetics and Cell Genetics, 92(1-2), 42–42.

Murray, J. C. (2001). Time for T. (Vols. 29). (2), pp. 107-9. Nature genetics. PMID: 11586288.

Murray, J. C., Allaman, J., Daack-Hirsch, S. E., Jezewski, P., Ludwig, B., Nishimura, C., Shi, M. & Vieira, A. (2001). Diagnostic resequencing of candidate genes for cleft lip and palate. Society of Craniofacial Genetics-Education, Research, Communication, Oct 12.

Schutte, B. C., Watanabe, Y., Bjork, B. C., Howard, E. L., Hoper, S. A., Malik, M. I., Fang, M. M., Hemerson, P. I., Dixon, M. J. & Murray, J. C. (2001). Mutation and deletion analysis of the Van der Woude syndrome locus at chromosome 1q32-q41. American Journal of Human Genetics, 69(4), 627–627.

Jezewski, P., Vieira, A., Schultz, R., Machida, J., Suzuki, Y., Ludwig, B., Daack-Hirsch, S., O’Brien, S., Nishimura, C., Johnson, M. & Murray, J. C. (2001). Mutations in MSX1 are associated with Non-Syndromic Orofacial Clefting. American Journal of Human Genetics, 69(4), 558–558.

Semina, E. V., Brownell, I., Mintz-Hittner, H. A., Murray, J. C. & Jamrich, M. (2001). Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Human molecular genetics, 10(3), 231-6. PMID: 11159941.

Murray, J. C. (2001). The unending string. (Vols. 155). (11), pp. 1193-4. Archives of pediatrics & adolescent medicine. PMID: 11695925.

Watanabe, Y., Murray, J. C., Bjork, B. C., Bird, C. P., Chiang, P. W., Gregory, S. G., Kurnit, D. M. & Schutte, B. C. (2001). Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41. Human Mutation, 18(5), 422–434. PMID: 11668635.

Kim, Y. J., Williamson, R. A., Chen, K., Smith, J. L., Murray, J. C. & Merrill, D. C. (2001). Lipoprotein lipase gene mutations and the genetic susceptibility of preeclampsia. Hypertension, 38(5), 992-6. PMID: 11711487.

Watanabe, Y., Murray, J. C., Bjork, B. C., Bird, C. P., Chiang, P. W., Gregory, S. G., Kurnit, D. M. & Schutte, B. C. (2001). Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41. Human mutation, 18(5), 422-34. PMID: 11668635.

Schutte, D. L., Maas, M., Buckwalter, K. C., Murray, J. C. & Schutte, B. C. (2001). A Low Density Lipoprotein Receptor Related Protein-Associated Protein 1 del/ins polymorphism and phenotypic variability in Alzheimer disease. American Journal of Human Genetics, 69(4), 564–564.

Kim, Y. J., Williamson, R. A., Murray, J. C., Andrews, J., Pietscher, J. J., Peraud, P. J. & Merrill, D. C. (2001). Genetic susceptibility to preeclampsia: roles of cytosineto-thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor V Leiden mutation. American Journal of Obstetrics and Gynecology, 184(6), 1211–1217. PMID: 11349190.

Bitoun, P., Semina, E., Daack-Hirsch, S., Murray, J. C. & Gaudelus, J. (2001). Isolated anterior segment dysgenesis and prenatal ecstasy exposure in a fullterm new born male. Investigative Ophthalmology & Visual Science, 42(4), S67–S67.

Semina, E. V., Brownell, I., Mintz-Hittner, H. A., Murray, J. C. & Jamrich, M. (2001). Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Human Molecular Genetics, 10(3), 231–236. PMID: 11159941.

Hjalt, T. A., Amendt, B. A. & Murray, J. C. (2001). PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: Implications for the pathology of Rieger syndrome. Journal of Cell Biology, 152(3), 545–552. DOI: 10.1083/jcb.152.3.545.

Saadi, I., Semina, E. V., Amendt, B. A., Harris, D. J., Murphy, K. P., Murray, J. C. & Russo, A. F. (2001). Identification of a dominant negative homeodomain mutation in Rieger syndrome. The Journal of biological chemistry, 276(25), 23034-41. PMID: 11301317.

Hjalt, T. A., Amendt, B. A. & Murray, J. C. (2001). PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndrome. The Journal of Cell Biology, 152(3), 545–552. PMID: 11157981.

Mitchell, L. E., Murray, J. C. (2001). A Case-Control Study of Genetic Risk Factors for Oral Clefts in Denmark. Congress of Epidemiology, Jun 13-16.

Saadi, I., Semina, E. V., Amendt, B. A., Harris, D. J., Murphy, K. P., Murray, J. C. & Russo, A. F. (2001). Identification of a dominant negative homeodomain mutation in Rieger syndrome. The Journal of Biological Chemistry, 276(25), 23034–23041. PMID: 11301317.

Mitchell, L. E., Murray, J. C., O'Brien, S. & Christensen, K. (2001). Evaluation of two putative susceptibility loci for oral clefts in the Danish population. American journal of epidemiology, 153(10), 1007-15. PMID: 11384957.

Kim, Y. J., Williamson, R. A., Murray, J. C., Andrews, J., Pietscher, J. J., Peraud, P. J. & Merrill, D. C. (2001). Genetic susceptibility to preeclampsia: Roles of cytosine-to-thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor V Leiden mutation. American Journal of Obstetrics and Gynecology, 184(6), 1211–1217. DOI: 10.1067/mob.2001.110411.

Bjork, B. C., Schutte, B. C., Watanabe, Y., Hockenhull, E. L., Malik, M. I., Dixon, M. J., Yuan, B. & Murray, J. C. (2000). Characterization of 41 genes identified through the analysis of 1Mb of sequence surrounding the Van der Woude syndrome critical region at 1q32. (Vols. 67S). pp. 269. Am J Hum Genet.

Barrow, L. L., Daack-Hirsch, S., Faaborg, T., van Bokhoven, H. & Murray, J. C. (2000). Analysis of the p63 gene in classic EEC syndrome, related syndromes, and nonsyndromic orofacial clefts. (Vols. 67S). (119) Am J Hum Genet.

Vieira, A. R., Orioli, I. M., Castilla, E. E., O'Brien, S. E., Marazita, M. L., Cooper, M. E. & Murray, J. C. (2000). Association of MSX1 with nonsyndromic orofacial clefting in ECLAMC. (Vols. 67S). pp. 228. Am J Hum Genet.

Watanabe, Y., Murray, J. C., Bjork, B. C., Bird, C. P., Chiang, P. W., Gregory, S. G., Kumit, D. M. & Schutte, B. C. (2000). Characterization of two unusual polymorphisms identified by sequence comparison. (Vols. 67S). (316) Am J Hum Genet.

Semina, E. V., Harris, D. J., Murphy, K. P., Murray, J. C. & Russo, A. F. (2000). Identification of a dominant negative Rieger syndrome mutation in PITX2. (Vols. 67S). pp. 188. Am J Hum Genet.

Kinoshita, A., Saito, T., Ghadami, M., Tomita, H., Makita, Y., Yamada, K., Ikegawa, S., Nishimura, G., Fukushima, Y., Murray, J. C., Taniguchi, N., Nikawa, N. & Yoshiura, K. (2000). Domain-specific mutations in the human transforming growth factor beta gene (TGFB1) result in Camurati-Engelmann Disease. (Vols. 67S). pp. 370. Am J Hum Genet.

Merrill, D. C., Kim, Y. J., Williamson, R. A., Andrews, J. & Murray, J. C. (2000). Lipoprotein lipase gene mutations and risk of preeclampsia. SGI annual meeting.

Ferreira de Lima, R., Moretti-Ferreira, D., Richieri-Costa, A., Marazita, M. & Murray, J. C. (2000). Identity by descent and candidate gene mapping of Richieri-Costa-Pereira syndrome. (Vols. 67S). pp. 310. Am J Hum Genet.

Schutte, B. C., Malik, M. I., Gregory, S., Fang, M. & Murray, J. C. (2000). A 700 kb contig of sequence-ready bacterial clones from mouse chromosome 1H spanning the syntenic region for the Van der Woude syndrome locus at human chromosome 1q32-q41. (Vols. 67S). pp. 260. Am J Hum Genet.

Semina, E. V., Mintz-Hittner, H. A. & Murray, J. C. (2000). Isolation and Characterization of a Novel Human paired-like Homeodomain-Containing Transcription Factor Gene, VSX1, Expressed in Ocular Tissues. Genomics, 63(2), 289–293. DOI: 10.1006/geno.1999.6093.

Dobbs, M. B., Dietz, F. R., Gurnett, C. A., Morcuende, J. A., Steyers, C. M. & Murray, J. C. (2000). Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36. Journal of Orthopaedic Research: Official Publication of the Orthopaedic Research Society, 18(3), 340–344. PMID: 10937618.

Dobbs, M. B., Dietz, F. R., Gurnett, C. A., Morcuende, J. A., Steyers, C. M. & Murray, J. C. (2000). Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36. Journal of Orthopaedic Research, 18(3), 340–344. DOI: 10.1002/jor.1100180303.

Semina, E. V., Murray, J. C., Reiter, R., Hrstka, R. F. & Graw, J. (2000). Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Human Molecular Genetics, 9(11), 1575–1585. PMID: 10861284.

Semina, E. V., Murray, J. C., Reiter, R., Hrstka, R. F. & Graw, J. (2000). Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Human Molecular Genetics, 9(11), 1575–1585. PMID: 10861284.

Jezewski, P., Schultz, R., Vieira, A., Machida, J., Suzuki, Y., Lidral, A., Johnson, M., Ludwig, B., Daack-Hirsh, S., O'Brien, S., Slayton, R., Natsume, N., Orioli, I., Castilla, E. & Murray, J. (2000). MSX1 Mutation search in diverse populations of individuals with clefting. American Society for Human Genetics meeting, Philadelphia, PA, Oct 3-7.

Kinoshita, A., Saito, T., Tomita, H., Makita, Y., Yoshida, K., Ghadami, M., Yamada, K., Kondo, S., Ikegawa, S., Nishimura, G., Fukushima, Y., Nakagomi, T., Saito, H., Sugimoto, T., Kamegaya, M., Hisa, K., Murray, J. C., Taniguchi, N., Niikawa, N. & Yoshiura, K. (2000). Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. Nature Genetics, 26(1), 19–20. DOI: 10.1038/79128.

Vieira, A. R., Orioli, I. M., Castilla, E. E., O'Brien, S. E., Marazita, M. L., Cooper, M. E. & Murray, J. C. (2000). Association of MSX1 with nonsyndromic orofacial clefting in ECLAMC. American Society for Human Genetics meeting, Philadelphia, PA, Oct 3-7.

Schutte, B. C., Bjork, B. C., Coppage, K. B., Malik, M. I., Gregory, S. G., Scott, D. J., Brentzell, L. M., Watanabe, Y., Dixon, M. J. & Murray, J. C. (2000). A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. Genome research, 10(1), 81-94. PMID: 10645953.

Semina, E. V., Mintz-Hittner, H. A. & Murray, J. C. (2000). Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues. Genomics, 63(2), 289–293. PMID: 10673340.

Hjalt, T. A., Semina, E. V., Amendt, B. A. & Murray, J. C. (2000). The Pitx2 protein in mouse development. Developmental Dynamics, 218(1), 195–200. DOI: 10.1002/(SICI)1097-0177(200005)218:1<195::AID-DVDY.

Schutte, B. C., Bjork, B. C., Coppage, K. B., Malik, M. I., Gregory, S. G., Scott, D. J., Brentzell, L. M., Watanabe, Y., Dixon, M. J. & Murray, J. C. (2000). A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. Genome Research, 10(1), 81–94. PMID: 10645953.

St Amand, T. R., Zhang, Y., Semina, E. V., Zhao, X., Hu, Y., Nguyen, L., Murray, J. C. & Chen, Y. (2000). Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage. Developmental biology, 217(2), 323-32. PMID: 10625557.

Lin, A. E., Semina, E. V., Daack-Hirsch, S., Roeder, E. R., Curry, C. J., Rosenbaum, K., Weaver, D. D. & Murray, J. C. (2000). Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. American Journal of Medical Genetics, 91(5), 387–390. DOI: 10.1002/(SICI)1096-8628(20000424)91:5<387::AID-AJM.

Hjalt, T. A., Semina, E. V., Amendt, B. A. & Murray, J. C. (2000). The Pitx2 protein in mouse development. Developmental Dynamics: An Official Publication of the American Association of Anatomists, 218(1), 195–200. PMID: 10822271.

Zeng, S., Yankowitz, J., Murray, J. C., Widness, J. A. & Strauss, R. G. (1999). Association of sequence-based polymorphisms in the thrombopoietin and thombopoietin receptor genes with absolute and sex related differences in platelet count and hematocrit. (Vols. 6). pp. 713A. J Soc Gynecol Investig.

Schutte, B. C., Basart, A. M., Watanabe, Y., Laffin, J. J., Coppage, K., Bjork, B. C., Daack-Hirsch, S., Patil, S., Dixon, M. J. & Murray, J. C. (1999). Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. American Journal of Medical Genetics, 84(2), 145–150. PMID: 10323740.

Hjalt, T. A., Murray, J. C. (1999). Genomic structure of the human retinoic acid receptor-alpha1 gene. Mammalian genome : official journal of the International Mammalian Genome Society, 10(5), 528-9. PMID: 10337631.

Hjalt, T. A., Murray, J. C. (1999). Genomic structure of the human retinoic acid receptor-alpha1 gene. Mammalian Genome: Official Journal of the International Mammalian Genome Society, 10(5), 528–529. PMID: 10337631.

Christensen, K., Olsen, J., Nørgaard-Pedersen, B., Basso, O., Støvring, H., Milhollin-Johnson, L. & Murray, J. C. (1999). Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994. American journal of epidemiology, 149(3), 248-55. PMID: 9927220.

Trembath, D., Sherbondy, A. L., Vandyke, D. C., Shaw, G. M., Todoroff, K., Lammer, E. J., Finnell, R. H., Marker, S., Lerner, G. & Murray, J. C. (1999). Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population. Teratology, 59(5), 331–341. PMID: 10332959.

Hjalt, T., Semina, E. S., Amendt, B. A. & Murray, J. C. (1999). Expression of the Rieger syndrome Pitx2 protein in mouse development. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Romitti, P. A., Lidral, A. C., Munger, R. G., Daack-Hirsch, S., Burns, T. L. & Murray, J. C. (1999). Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts. Teratology, 59(1), 39–50. PMID: 9988882.

Trembath, D., Sherbondy, A. L., Vandyke, D. C., Shaw, G. M., Todoroff, K., Lammer, E. J., Finnell, R. H., Marker, S., Lerner, G. & Murray, J. C. (1999). Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population. Teratology, 59(5), 331-41. PMID: 10332959.

Schutte, B. C., Murray, J. C. (1999). The many faces and factors of orofacial clefts. Human Molecular Genetics, 8(10), 1853–1859. PMID: 10469837.

(1999). Motility. Glendale, CA: Audio-Digest Foundation.

Rao, S. S., Conklin, J. L., Johlin, F. C., Murray, J. A., Schulze-Delrieu, K. S. & Summers, R. W. (1999). Gastrointestinal Motility: Tests and Problem-Oriented Approach. Boston, MA: Springer US.

Romitti, P. A., Lidral, A. C., Munger, R. G., Daack-Hirsch, S., Burns, T. L. & Murray, J. C. (1999). Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts. Teratology, 59(1), 39-50. PMID: 9988882.

Schutte, B. C., Murray, J. C. (1999). The many faces and factors of orofacial clefts. Human molecular genetics, 8(10), 1853-9. PMID: 10469837.

Bjork, B. C., Schutte, B. C., Malik, M. I., Coppage, K., Gregory, S. G., Scott, D. J., Brentzell, L., Watanabe, Y., Dixon, M. J. & Murray, J. C. (1999). A primary transcript map for the Van der Woude syndrome (VWS) critical region derived from 900 kb of genomic sequence at 1q32-q41. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Trembath, D. G., Semina, E. V., Zabel, B. U., Carey, J. C., Jones, D. H. & Murray, J. C. (1999). Analysis of chromosomal breakpoints in patients with Rieger syndrome: effects on PITX2. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Mintz-Hittner, H. A., Semina, E. V. & Murray, J. C. (1999). A three generation-family with anterior segment mesenchymal dysgenesis and mutation in a novel homeobox-containing gene, VSX1. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Jugessur, A., Lie, R. T., Wilcox, A., Abyholm, F., Vindness, H. & Murray, J. C. (1999). Allelic variants of candidate genes TGFA, TGFB3 and MSX1 and orofacial clefting in Norway: a case-parent triad approach. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Watanabe, Y., Bjork, B. C., Chiang, P., Gregory, S. G., Kumit, C. M., Murray, J. C. & Schutte, B. C. (1999). An 8 kb deletion/insertion polymorphism in the Van der Woude syndrome critical region at 1q32-q41. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Yang, B., Semina, E., Hjalt, T., Cao, X., Reiter, R. S., Kirby, P. A., Hrstka, R. F., Lin, J. J., Williamson, R. A. & Murray, J. C. (1999). A mouse model for Rieger syndrome. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Schutte, B. C., Basart, A. M., Watanabe, Y., Laffin, J. J., Coppage, K., Bjork, B. C., Daack-Hirsch, S., Patil, S., Dixon, M. J. & Murray, J. C. (1999). Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. American journal of medical genetics, 84(2), 145-50. PMID: 10323740.

Hjalt, T. A., Murray, J. C. (1999). The human BARX2 gene: genomic structure, chromosomal localization, and single nucleotide polymorphisms. Genomics, 62(3), 456-9. PMID: 10644443.

Hjalt, T. A., Murray, J. C. (1999). The human BARX2 gene: genomic structure, chromosomal localization, and single nucleotide polymorphisms. Genomics, 62(3), 456–459. PMID: 10644443.

Machida, J., Yoshiura, K. i., Funkhauser, C. D., Natsume, N., Kawai, T. & Murray, J. C. (1999). Transforming growth factor-alpha (TGFA): genomic structure, boundary sequences, and mutation analysis in nonsyndromic cleft lip/palate and cleft palate only. Genomics, 61(3), 237–242. PMID: 10552925.

Machida, J., Yoshiura Ki, Funkhauser, C. D., Natsume, N., Kawai, T. & Murray, J. C. (1999). Transforming growth factor-alpha (TGFA): genomic structure, boundary sequences, and mutation analysis in nonsyndromic cleft lip/palate and cleft palate only. Genomics, 61(3), 237-42. PMID: 10552925.

Semina, E. V., Funkhauser, C., Bitoun, P., Alward, W., Daack-Hirsch, S., Amendt, B., Ludwig, B. & Murray, J. C. (1999). Spectrum and frequency of PITX2/RIEG mutations in patients with Rieger syndrome and related ocular anomalies. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Torfs, C. P., Semina, E. V., Knipp, M., Lorey, F. & Murray, J. C. (1999). Study of genetic factors contributing to both isolated and MCA cases of omphalocele. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Fuller, B. P., Kahn, M. J., Barr, P. A., Biesecker, L., Crowley, E., Garber, J., Mansoura, M. K., Murphy, P., Murray, J., Phillips, J., Rothenberg, K., Rothstein, M., Stopfer, J., Swergold, G., Weber, B., Collins, F. S. & Hudson, K. L. (1999). Privacy in Genetics Research. Science, 285(5432), 1359–1361. PMID: 10490410.

Bitoun, P., Semina, E., Gaudelus, J. & Murray, J. C. (1999). Autosomal dominant hyperopia and strabismus in patients from 3-generation family associated with mutation in LIM-domain interacting factor CLIM2 gene. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Zeng, S., Yankowitz, J. & Murray, J. C. (1999). X-inactivation patterns in cytotrophoblast vs tissues of human female fetuses. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Barrow, L. L., Wines, M. E., Romitti, P. A., Holdener, B. C. & Murray, J. C. (1999). Positive association of nonsyndromic cleft palate only (CPO) and aryl hydrocarbon receptor nuclear translocator 2 (ARNT2). American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Yankowitz, J., Zeng, S., Murray, J. C., Widness, J. A. & Strauss, R. G. (1999). Sequence-based polymorphisms in members of the apoptosis Bcl-2 gene family and their association with hematocrit level. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Kim, Y. J., Andrews, J., Peraud, P., Williamson, R. A., Murray, J. C. & Merrill, D. C. (1999). Genetic susceptibility to preeclampsia: roles of Factor V Leiden and lipoprotein lipase mutations. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Schultz, R. E., McColley, A. & Murray, J. C. (1999). Screening endothelin-1 by SSCp analysis for mutations associated with nonsyndromic cleft lip and palate in individuals of Filipino origin. American Society for Human Genetics meeting, San Francisco, CA, Oct 19-23.

Alward, W. L., Semina, E. V., Kalenak, J. W., Héon, E., Sheth, B. P., Stone, E. M. & Murray, J. C. (1998). Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. American Journal of Ophthalmology, 125(1), 98–100. PMID: 9437321.

Romitti, P. A., Munger, R. G., Murray, J. C., Daack-Hirsch, S., Hanson, J. W. & Burns, T. L. (1998). The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations. European journal of epidemiology, 14(2), 129-38. PMID: 9556171.

Alward, W. L., Semina, E. V., Kalenak, J. W., Héon, E., Sheth, B. P., Stone, E. M. & Murray, J. C. (1998). Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. American journal of ophthalmology, 125(1), 98-100. PMID: 9437321.

Romitti, P. A., Munger, R. G., Murray, J. C., Daack-Hirsch, S., Hanson, J. W. & Burns, T. L. (1998). The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations. European Journal of Epidemiology, 14(2), 129–138. PMID: 9556171.

Bitoun, P., Semina, E., Ferrell, R. E., Mintz-Hittner, H. A., Gaudelus, J. & Murray, J. C. (1998). Mutations in PITX3; a novel homeobox transcription factor gene homologous to RIEG1 cause dominant cataracts and glaucoma. European Journal of Human Genetics, 6, 36–37.

Lysaught, M. T., Milhollin, L., Peirce, R., Getchell, J., Rhead, W., Susanin, J., Anderson, J. & Murray, J. C. (1998). A Pilot Test of DNA-based Analysis Using Anonymized Newborn Screening Cards in Iowa. In Stored Tissue Samples: Ethical and Public Policy Implications. pp. 3-31.

Bjork, B. C., Schutte, B. C., Malik, M. I., Coppage, K. B., Brentzell, L., Dixon, M. J. & Murray, J. C. (1998). Transcript mapping and mutation analysis of candidate genes for Van der Woude syndrome. (Vols. 63S). pp. A352. Am J Hum Genet.

Schutte, B. C., Basart, A. M., Coppage, K. B., Bjork, B. C., Malik, M. I., Laffin, J., Patil, S., Dixon, M. J. & Murray, J. C. (1998). Microdeletions at 1q32-q41 as a cause of VWS. (Vols. 63S). pp. A384. Am J Hum Genet.

Brentzell, L. M., Schutte, B., Murray, J. C. & Dixon, M. J. (1998). Mapping of the Van der Woude syndrome critical region. Journal of Dental Research, 77, 885–885.

Semina, E. V., Reiter, R. S. & Murray, J. C. (1998). A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse. Human Molecular Genetics, 7(3), 415–422. PMID: 9466998.

Schutte, B. C., Coppage, K. B., Bjork, B. C., Basart, A. M., Malik, M. I., Edwards, S. J., Dixon, M. J. & Murray, J. C. (1998). A sequence-ready BAC contig across the Van der Woude syndrome critical region in 1q32-q41 and microdeletions as a cause of VWS. Cytogenet Cell Genet.

Broman, K. W., Murray, J. C., Sheffield, V. C., White, R. L. & Weber, J. L. (1998). Comprehensive human genetic maps: individual and sex-specific variation in recombination. American journal of human genetics, 63(3), 861-9. PMID: 9718341.

Semina, E. V., Altherr, M. R. & Murray, J. C. (1998). Cloning and chromosomal localization of two novel human genes encoding LIM-domain binding factors CLIM1 and CLIM2/LDB1/NLI. Mammalian Genome: Official Journal of the International Mammalian Genome Society, 9(11), 921–924. PMID: 9799849.

Broman, K. W., Murray, J. C., Sheffield, V. C., White, R. L. & Weber, J. L. (1998). Comprehensive human genetic maps: individual and sex-specific variation in recombination. American Journal of Human Genetics, 63(3), 861–869. PMID: 9718341.

Yoshiura, K., Machida, J., Daack-Hirsch, S., Patil, S. R., Ashworth, L. K., Hecht, J. T. & Murray, J. C. (1998). Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. Genomics, 54(2), 231-40. PMID: 9828125.

Yoshiura, K., Machida, J., Daack-Hirsch, S., Patil, S. R., Ashworth, L. K., Hecht, J. T. & Murray, J. C. (1998). Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. Genomics, 54(2), 231–240. PMID: 9828125.

Semina, E. V., Altherr, M. R. & Murray, J. C. (1998). Cloning and chromosomal localization of two novel human genes encoding LIM-domain binding factors CLIM1 and CLIM2/LDB1/NLI. Mammalian genome : official journal of the International Mammalian Genome Society, 9(11), 921-4. PMID: 9799849.

Hewett, P. W., Daft, E. L. & Murray, J. C. (1998). Cloning and partial characterization of the human tie-2 receptor tyrosine kinase gene promoter. Biochemical and biophysical research communications, 252(3), 546-51. PMID: 9837743.

Semina, E. V., Reiter, R. S. & Murray, J. C. (1998). A new human homeobox gene OG12X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse. Human Molecular Genetics, 7(3), 415–422. PMID: 9466998.

Yoshiura, K., Leysens, N. J., Reiter, R. S. & Murray, J. C. (1998). Cloning, characterization, and mapping of the mouse homeobox gene Hmx1. Genomics, 50(1), 61-8. PMID: 9628823.

Yoshiura, K., Leysens, N. J., Reiter, R. S. & Murray, J. C. (1998). Cloning, characterization, and mapping of the mouse homeobox gene Hmx1. Genomics, 50(1), 61–68. PMID: 9628823.

Yoshioka, H., Meno, C., Koshiba, K., Sugihara, M., Itoh, H., Ishimaru, Y., Inoue, T., Ohuchi, H., Semina, E. V., Murray, J. C., Hamada, H. & Noji, S. (1998). Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry. Cell, 94(3), 299-305. PMID: 9708732.

el-Shanti, H., Murray, J. C., Semina, E. V., Beutow, K. H., Scherpbier, T. & al-Alami, J. (1998). Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. European journal of human genetics : EJHG, 6(3), 251-6. PMID: 9781029.

Semina, E. V., Ferrell, R. E., Mintz-Hittner, H. A., Bitoun, P., Alward, W. L., Reiter, R. S., Funkhauser, C., Daack-Hirsch, S. & Murray, J. C. (1998). A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nature genetics, 19(2), 167-70. PMID: 9620774.

Shaw, G. M., Wasserman, C. R., Murray, J. C. & Lammer, E. J. (1998). Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 35(4), 366-70. PMID: 9684776.

Lidral, A. C., Romitti, P. A., Basart, A. M., Doetschman, T., Leysens, N. J., Daack-Hirsch, S., Semina, E. V., Johnson, L. R., Machida, J., Burds, A., Parnell, T. J., Rubenstein, J. L. & Murray, J. C. (1998). Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. American journal of human genetics, 63(2), 557-68. PMID: 9683588.

Semina, E. V., Ferrell, R. E., Mintz-Hittner, H. A., Bitoun, P., Alward, W. L., Reiter, R. S., Funkhauser, C., Daack-Hirsch, S. & Murray, J. C. (1998). A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nature Genetics, 19(2), 167–170. PMID: 9620774.

Zeng, S. M., Yankowitz, J., Murray, J. C., Widness, J. A. & Strauss, R. G. (1997). Association of sequence-based polymorphisms in the erythropoietin receptor and thombopoietin genes with hematocrit. Annual American Society of Human Genetics meeting, Baltimore, MD.

Trembath, D., Sherbondy, A., VanDyke, D., Marker, S., Lerner, G. & Murray, J. C. (1997). Analysis of three folate pathway genes in a midwestern neural tube defect population. Annual American Society of Human Genetics meeting, Baltimore, MD.

Lidral, A. C., Murray, J. C., Buetow, K. H., Basart, A. M., Schearer, H., Shiang, R., Naval, A., Layda, E., Magee, K. & Magee, W. (1997). Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 34(1), 1-6. PMID: 9003904.

Yankowitz, J., Zeng, S. M., Murray, J. C., Widness, J. A. & Strauss, R. G. (1997). A novel sequence-based polymorphism in the 3’ untranslated region of the thombopoietin gene and its association with human platelet count. Annual American Society of Human Genetics meeting, Baltimore, MD.

Gaudelus, J., Murray, J. C. & Bitoun, P. (1997). Bilateral microphthalmos, pulmonary hypoplasia and diaphragmatic hernia: a non lethal case and further delineation of the MATTHEW-WOOD syndrome. Annual American Society of Human Genetics meeting, Baltimore, MD.

Coppage, K. B., Schutte, B. C., Bjork, B., Malik, M., Edwards, S., Dixon, M. & Murray, J. C. (1997). A BAC/cosmid contig of the Van der Woude syndrome critical region on Ch1q32. Annual American Society of Human Genetics meeting, Baltimore, MD.

O’Brien, S., Even, D. A. & Murray, J. C. (1997). Complex trinucleotide repeat polymorphism in the HOX B6 gene. Human Mutation, 9(3), 280–281. PMID: 9090534.

Semina, E. V., Reiter, R., Alward, S., Bitoun, P., Ferrell, R., Daack-Hirsch, S., Wise, M., Funkhauser, C. D., Nishimura, C. J., Ludwig, B. & Murray, J. C. (1997). Characterization of the PITX/RIEG homeobox-containing gene family and its involvement in the formation of anterior eye structures. Annual American Society of Human Genetics meeting, Baltimore, MD.

Semina, E. V., Reiter, R., Alward, W., Bitoun, P. & Murray, J. C. (1997). Progress in Rieger syndrome genes search and mutation screening. ARVO Annual Meeting.

O'Brien, S., Even, D. A. & Murray, J. C. (1997). Complex trinucleotide repeat polymorphism in the HOX B6 gene. Human mutation, 9(3), 280-1. PMID: 9090534.

Schutte, B. C., Bjork, B. C., Reiter, R. & Murray, J. C. (1997). Identification, genomic structure, mapping and expression of a new human CaM kinase I-like gene. (Vols. 38S). pp. 201. Epilepsia.

Lidral, A., Romitti, P., Basart, A., Leysens, N., Machida, J., Daack-Hirsch, S., Burds, A., Leysens, M., Milhollin, L., Christensen, K. & Murray, J. (1997). Genetic analysis of TGFB3, MSX1, and DLX2 as etiologic candidates for nonsyndromic cleft lip and palate. Annual meeting of the International/American Association of Dental Research, Orlando, FL.

Bjork, B. C., Schutte, B. C., Basart, A., Malik, M. & Murray, J. C. (1997). Cloning and characterization of a novel human gene from the Van der Woude syndrome (VWS) locus with homology to a hypothetical protein in yeast. Annual American Society of Human Genetics meeting, Baltimore, MD.

Yoshiura, K., Machida, J., Daack-Hirsch, S., Ashworth, L. K., Hecht, J. T. & Murray, J. C. (1997). Cloning of the gene disrupted by a chromosomal translocation in a three generation family with cleft lip and palate. Annual American Society of Human Genetics meeting, Baltimore, MD.

Murray, J. C., Thompson, M. E., Kingsmore, S. F., Bereano, P. L. & Wakeland, E. K. (1997). The Human Genome Project. Journal of Dental Research, 76, 1900–1900.

Yankowitz, J., Zeng, S. M., Murray, J. C., Widness, J. A. & Strauss, R. G. (1997). A novel sequence-based polymorphism in the 3 ’-untranslated region of the thrombopoietin gene and its association with human platelet count. American Journal of Human Genetics, 61(4), A404–A404.

Yoshiura, K., Leysens, N. J., Chang, J., Ward, D., Murray, J. C. & Muenke, M. (1997). Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes. American journal of medical genetics, 72(3), 354-62. PMID: 9332670.

Yoshiura, K. I., Murray, J. C. (1997). Sequence and chromosomal assignment of human BAPX1, a bagpipe-related gene, to 4p16.1: a candidate gene for skeletal dysplasia. Genomics, 45(2), 425-8. PMID: 9344671.

Peiffer-Schneider, S., Schutte, B. C., Murray, J. C., Frees, K. L., Williamson, K., Leysens, N. J. & Schwartz, D. A. (1997). Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus. Mammalian genome : official journal of the International Mammalian Genome Society, 8(10), 785-6. PMID: 9321479.

Semina, E. V., Reiter, R. S. & Murray, J. C. (1997). Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Human molecular genetics, 6(12), 2109-16. PMID: 9328475.

Semina, E. V., Reiter, R. S. & Murray, J. C. (1997). Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Human Molecular Genetics, 6(12), 2109–2116. PMID: 9328475.

Murray, J. C., Daack-Hirsch, S., Buetow, K. H., Munger, R., Espina, L., Paglinawan, N., Villanueva, E., Rary, J., Magee, K. & Magee, W. (1997). Clinical and epidemiologic studies of cleft lip and palate in the Philippines. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 34(1), 7-10. PMID: 9003905.

Romitti, P. A., Burns, T. L. & Murray, J. C. (1997). Maternal interview reports of family history of birth defects: evaluation from a population-based case-control study of orofacial clefts. American Journal of Medical Genetics, 72(4), 422–429. PMID: 9375725.

Romitti, P. A., Burns, T. L. & Murray, J. C. (1997). Maternal interview report of family history of birth defects: Evaluation from a population-based case-control study of orofacial clefts. American Journal of Medical Genetics, 72(4), 422–429. DOI: 10.1002/(SICI)1096-8628(19971112)72:4<422::AID-AJM.

Romitti, P. A., Burns, T. L. & Murray, J. C. (1997). Maternal interview reports of family history of birth defects: evaluation from a population-based case-control study of orofacial clefts. American journal of medical genetics, 72(4), 422-9. PMID: 9375725.

Yoshiura, K. I., Murray, J. C. (1997). Sequence and chromosomal assignment of human BAPX1, a bagpipe-related gene, to 4p16.1: a candidate gene for skeletal dysplasia. Genomics, 45(2), 425–428. PMID: 9344671.

Kavanagh, G. M., Jardine, P. E., Peachey, R. D., Murray, J. C. & DeBerker, D. (1997). The scleroatrophic syndrome of Huriez. British Journal of Dermatology, 137(1), 114–118. DOI: 10.1111/j.1365-2133.1997.tb03712.x.

Murray, J. C., Daack-Hirsch, S., Buetow, K. H., Munger, R., Espina, L., Paglinawan, N., Villanueva, E., Rary, J., Magee, K. & Magee, W. (1997). Clinical and epidemiologic studies of cleft lip and palate in the Philippines. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 34(1), 7–10. PMID: 9003905.

Zeng, S. M., Yankowitz, J., Murray, J. C., Widness, J. A. & Strauss, R. G. (1997). Association of sequence-based polymorphisms in the erythropoietin receptor and thrombopoietin genes with hematocrit. American Journal of Human Genetics, 61(4), A302–A302.

Yandava, C. N., Gastier, J. M., Pulido, J. C., Brody, T., Sheffield, V., Murray, J., Buetow, K. & Duyk, G. M. (1997). Characterization of Alu Repeats That Are Associated with Trinucleotide and Tetranucleotide Repeat Microsatellites. Genome Research, 7(7), 716–724. PMID: 9253600.

Semina, E. V., Reiter, R., Alward, W. L., Bitoun, P., Ferrell, R., Daack-Hirsch, S., Wise, M., Funkhauser, C. D., Nishimura, C. J., Ludwig, B. & Murray, J. C. (1997). Characterization of the PITX/REIG homeobox-containing gene family and its involvement in the formation of anterior eye structures. American Journal of Human Genetics, 61(4), A346–A346.

Lidral, A. C., Murray, J. C., Buetow, K. H., Basart, A. M., Schearer, H., Shiang, R., Naval, A., Layda, E., Magee, K. & Magee, W. (1997). Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 34(1), 1–6. PMID: 9003904.

Gaudelus, J., Murray, J. C. & Bitoun, P. (1997). Bilateral severe microphthalmos, pulmonary hypoplasia and diaphragmatic hernia: a non lethal case and further delineation of the MATTHEW-WOOD syndrome. American Journal of Human Genetics, 61(4), A153–A153.

Peiffer-Schneider, S., Schutte, B. C., Murray, J. C., Frees, K. L., Williamson, K., Leysens, N. J. & Schwartz, D. A. (1997). Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus. Mammalian Genome: Official Journal of the International Mammalian Genome Society, 8(10), 785–786. PMID: 9321479.

Yoshiura, K., Leysens, N. J., Chang, J., Ward, D., Murray, J. C. & Muenke, M. (1997). Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes. American Journal of Medical Genetics, 72(3), 354–362. PMID: 9332670.

Canady, J. W., Murray, J. C., Wise, M., Williamson, K. A. & Thompson, S. A. (1996). Genetic factors associated with scar formation. 53rd annual meeting of the Cleft Palate-Craniofacial Association, San Diego, CA, Apr 22-27.

Klewer, S. E., Williamson, K. A., Lauer, R. M. & Murray, J. C. (1996). Association of candidate genes with atrioventricular septal defects (AVSD’s) in trisomy 21 and non-syndromic cases. Pediatric Research, 39(4), 168–168.

Davis, P. H., Clarke, W. R., Bendixen, B. H., Adams, H. P., Woolson, R. F., Culebras, A., Jacoby, M. R., Gomez, F. J., Hughes, B., Dyken, M. E., Uc, E. Y., Wojcieszek, J. M., Kappelle, L. J., Tanna, A. B., Mitchell, V. L., King, M. K., Bruno, A., Lakind, E. D., Jeffrey, D. R., Mladinich, E. K., Iqbal, J., Reiners, M., Barrett, D. W., Shibuya, D., Williams, J. K., Russell, P., Chapin, J. E., Ahmed, W., Carter, S., Jeffries, L., Karanjia, P. M., Madden, K. P., Ruggles, K. H., Mickel, S. F., Gottschalk, P. G., Hansotia, P. L., Sorenson, R. W., Jacobson, D. M., Hiner, B. C., Mancl, K., Lukasik, E., Burch, C. M., Gomez, C. R., Malkoff, M. D., Tulyapronchote, R., Sauer, C. M., Riaz, G., Schmidt, J. G., Malik, M. M., VivesCastro, L. R., CruzFlores, S., Thompson, D. W., Banet, G. A., Jackson, C. M., Rothrock, J. F., Lyden, P. D., Brody, M. L., Zweifler, R. M., Tom, T., Forde, G., Kelly, N. M., Helgason, C. M., Hier, D. B., Shapiro, R. A., Brint, S. U., Gnutek, T., Hoff, J., OConnell, D., Fisher, M. J., Ameriso, S. F., Garabedian, M. H., Macko, R. F., Hanna, M., Yegyan, G. A., Park, S. J., Martin, A., Scicli, A., Libman, R. B., Kwiatkowski, T. G., Kanner, R. M., Wirkowski, E. J., Abrams, R., Donnaruma, R., Cullen, V., Rosenbaum, D. M., Sparr, S. A., Katz, P. M., Valencia, A. M., Klonowski, E., Gordon, D. L., Thiel, A. A., Fredericks, R. K., Singh, R., Rafique, A., Dendinger, J., Gorelick, P. B., Riskin, B. J., Mirza, D. B., Kelly, M. A., Bijari, A., Murray, J. C., Curtin, J., Bozzola, F. G., Kofman, J. C., Pajeau, A. K., Shanmugam, V., AgnelloDimitrijevic, W., Brown, N., Dollear, W. C., Weinberger, J. M., Tuhrim, S., Rudolph, S. H., Horowitz, D. R., Sheinart, K. F., Gondolo, T. M., Ali, J., Bitton, A., Feldmann, E., Wilterdink, J. L., Furie, K., Baldwin, E., Ricks, L., Carey, G. C., Martir, N. M., Kent, P. F., Rabiee, H., Guevara, R. A., Bangco, M. S., Shah, K., Attarian, H., Pastor, D., Ficarra, C., Mohr, J. P., Sacco, R. L., Clavijo, M., Biller, J., Saver, J. L., Frank, J. I., Patrick, J. T., FernandezBeer, E., Byer, J. A., White, H. H., Sundrani, S., Zafar, M. J., Arora, R., Gamboa, E. C., Stacy, M., Bonnett, A., Kelley, C., Coull, B. M., Briley, D. P., Clark, W. M., Kenny, C., Austin, T., deGarmo, P. L., Anderson, D. C., Tarrel, R. M., Nance, M. A., Bundlie, S. R., Doyle, J. J., Dierich, M., Love, B. B., Struck, L. K., Mueller, C., Hogan, E. L., Carter, T. D., Gurecki, P., Plyer, J. W., MuntzPope, B. K., Hollander, J., Honch, G. W., Lesser, H. D., Weber, C., Wrobel, C. J., Leramo, O. B., Buxton, S., Fayad, P. B., Brass, L. M., Pavalkis, F. J., Durocher, A., Pascuzzi, R. M., Pourmand, R., Reddy, V. R., Chadwick, L. R., Warach, S. J., Mayman, C. I., Darby, D. G., Dashe, J. F., Tijerina, M. L., Mandelbaum, M. A., Hassan, R. U., Abbas, D. H., Olmstead, C. G., Sedlacek, L., Miller, A. E., Keilson, M. J., Bruining, K. M., Drexler, E. E., Morgante, L., RamirezLassepas, M., Tulloch, J. W., Quinones, M. R., Clavel, A., Mendez, M. F., Zhang, S., Ala, T. A., Espinosa, C., Johnston, K. L., Hwang, T. L., Brannon, W. L., Trujillano, A. C., Frank, R. L., Kase, C. S., Wolf, P. A., Babikian, V. L., LicataGehr, E. E., Allen, N. C., Chaturvedi, S., Chappidi, P. V., Tvardek, L., Homer, D., Neely, S., Carpenter, J., Futrell, N. N., Wang, D., Davis, K. A., Korsnack, A. M., Bassam, B. A., Cunningham, S., Drinkard, R., Saver, J. L., Starkman, S., Horowitz, S. H., Lava, N. S., Manning, M., Love, B. B., Grimsman, K. J., Olson, J. D., Pennell, B. J., Johnson, K., Cornell, S. H., Crosby, D. L., Simonson, T. M., Krumbholz, V., Comine, J. A., Zalesky, C. R., Wasek, P. A., Dieleman, J. A., Paulsen, J. M., Boreen, J. P., Jones, M. F., Robb, B. M., Oberbroeckling, L. A., Hansen, M. D., Hicklin, K. M., Frankowski, R. F., Greenberg, C. S., Harker, L. A., Whisnant, J. P., Fincham, R. W., Kisker, T. C. & Wallace, R. B. (1996). Silent cerebral infarction in patients enrolled in the TOAST study. Neurology, 46(4), 942–948.

Bjork, B. C., Schutte, B. C., Leysens, N., Sander, A. & Murray, J. C. (1996). Isolation and characterization of a novel brain-specific gene from the Van der Woude syndrome critical region. (Vols. 59S). pp. A145. Am J Hum Genet.

Shaw, G. M., Wasserman, C. R., Lammer, E. J., O'Malley, C. D., Murray, J. C., Basart, A. M. & Tolarova, M. M. (1996). Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants. American journal of human genetics, 58(3), 551-61. PMID: 8644715.

Munger, R. G., Romitti, P. A., Daack-Hirsch, S., Burns, T. L., Murray, J. C. & Hanson, J. (1996). Maternal alcohol use and risk of orofacial cleft birth defects. Teratology, 54(1), 27-33. PMID: 8916367.

Sunden, S. L., Businga, T., Beck, J., McClain, A., Gastier, J. M., Pulido, J. C., Yandava, C. N., Brody, T., Ghazizadeh, J., Weber, J. L., Duyk, G. M., Murray, J. C., Buetow, K. H. & Sheffield, V. C. (1996). Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics, 32(1), 15–20. PMID: 8786107.

Sunden, S. L., Businga, T., Beck, J., McClain, A., Gastier, J. M., Pulido, J. C., Yandava, C. N., Brody, T., Ghazizadeh, J., Weber, J. L., Duyk, G. M., Murray, J. C., Buetow, K. H. & Sheffield, V. C. (1996). Chromosomal assignment of 2900 Tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics, 32(1), 15–20. DOI: 10.1006/geno.1996.0071.

Gastier, J. M., Brody, T., Pulido, J. C., Businga, T., Sunden, S., Hu, X., Maitra, S., Buetow, K. H., Murray, J. C., Sheffield, V. C., Boguski, M., Duyk, G. M. & Hudson, T. J. (1996). Development of a screening set for new (CAG/CTG)n dynamic mutations. Genomics, 32(1), 75-85. PMID: 8786123.

Sertié, A. L., Quimby, M., Moreira, E. S., Murray, J., Zatz, M., Antonarakis, S. E. & Passos-Bueno, M. R. (1996). A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3. Human Molecular Genetics, 5(6), 843–847. PMID: 8776601.

Trembath, D., Sherbondy, A., Van Dyke, D., Finnell, R., Marker, S. & Murray, J. C. (1996). Analysis of the folate pathway, human T, and PAX-3 in a midwest neural tube defect population. 46th annual meeting of the American Society of Human Genetics, San Francisco, CA, Oct 29-Nov 2.

Semina, E. V., Datson, N. A., Leysens, N. J., Zabel, B. U., Carey, J. C., Bell, G. I., Bitoun, P., Lindgren, C., Stevenson, T., Frants, R. R., van Ommen, G. & Murray, J. C. (1996). Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. American journal of human genetics, 59(6), 1288-96. PMID: 8940274.

Datson, N. A., Semina, E., van Staalduinen, A. A., Dauwerse, H. G., Meershoek, E. J., Heus, J. J., Frants, R. R., den Dunnen, J. T., Murray, J. C. & van Ommen, G. J. (1996). Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. American journal of human genetics, 59(6), 1297-305. PMID: 8940275.

Semina, E. V., Datson, N. A., Leysens, N. J., Zabel, B. U., Carey, J. C., Bell, G. I., Bitoun, P., Lindgren, C., Stevenson, T., Frants, R. R., van Ommen, G. & Murray, J. C. (1996). Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. American Journal of Human Genetics, 59(6), 1288–1296. PMID: 8940274.

Munger, R. G., Romitti, P. A., Daack-Hirsch, S., Burns, T. L., Murray, J. C. & Hanson, J. (1996). Maternal alcohol use and risk of orofacial cleft birth defects. Teratology, 54(1), 27–33. PMID: 8916367.

Semina, E. V., Reiter, R., Leysens, N. J., Alward, W. L., Small, K. W., Datson, N. A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B. U., Carey, J. C. & Murray, J. C. (1996). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature Genetics, 14(4), 392–399. PMID: 8944018.

Semina, E. V., Reiter, R., Leysens, N. J., Alward, W. L., Small, K. W., Datson, N. A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B. U., Carey, J. C. & Murray, J. C. (1996). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature genetics, 14(4), 392-9. PMID: 8944018.

Schutte, B. C., Sander, A., Malik, M. & Murray, J. C. (1996). Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41. Genomics, 36(3), 507-14. PMID: 8884274.

Semina, E. V., Murray, J. C., Reiter, B., Leysens, N. J., Datsons, N. A., Mondt, G., Alward, W., Bitoun, P., Bierke-Nelson, D., Small, K. W., Zabel, B. U. & Carey, J. C. (1996). Cloning and characterization of a novel human homeobox gene involved in the Rieger syndrome and its mouse homolog. 46th annual meeting of the American Society of Human Genetics, San Francisco, CA, Oct 29-Nov 2.

Sertié, A. L., Quimby, M., Murray, J. C., Moriera, E. S., Zatz, M. & Passos-Bueno, M. R. (1996). COL6A1 and COL6A2 as candidate genes for Knobloch syndrome. IX International Congress of Human Genetics, Sao Paulo, Brazil, Aug 18-23.

Schutte, B. C., Sander, A., Malik, M. & Murray, J. C. (1996). Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41. Genomics, 36(3), 507–514. PMID: 8884274.

Lidral, A. C., Leysens, N. J., Basart, A. M., Machida, J., Daack-Hirsch, S., Leysens, M., Romitti, P., Buetow, K. H. & Murray, J. C. (1996). Genetic evidence for an etiologic role for TGFB3 and MSX1 in nonsyndromic cleft lip and palate. 46th annual meeting of the American Society of Human Genetics, San Francisco, CA, Oct 29-Nov 2.

Yoshiura, K., Leysens, N. J., Chang, J., Ward, D., Murray, J. C. & Muenke, M. (1996). Genomic structure, sequence, and mapping of human FGF8 with exclusion of its role in craniosynostosis/limb defect syndromes. 46th annual meeting of the American Society of Human Genetics, San Francisco, CA, Oct 29-Nov 2.

Shaw, G. M., Wasserman, C. R., Lammer, E. J. & Murray, J. C. (1996). TGF-alpha genotypes, orofacial clefts, and maternal periconceptual multivitamin use. 46th annual meeting of the American Society of Human Genetics, San Francisco, CA, Oct 29-Nov 2.

Stadler, H. S., Murray, J. C., Leysens, N. J., Goodfellow, P. J. & Solursh, M. (1995). Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family. Mammalian genome : official journal of the International Mammalian Genome Society, 6(6), 383-8. PMID: 7647458.

Munger, R., Lidral, A., Basart, A., Romitti, P. & Murray, J. (1995). The MSX1 homeobox gene and risk of isolated orofacial clefts: an effect modified by maternal vitamin use?. Society for Epidemiologic Research annual meeting, Snowbird, UT, Jun 22-24.

Crosby, A. H., Edwards, S. J., Murray, J. C. & Dixon, M. J. (1995). Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Genomics, 27(1), 155-60. PMID: 7665163.

Yankowitz, J., Li, S. & Murray, J. C. (1995). Polymerase chain reaction determination of RhD blood type: an evaluation of accuracy. Obstetrics and gynecology, 86(2), 214-7. PMID: 7617351.

Mathews, K. D., Rapisarda, D., Bailey, H. L., Murray, J. C., Schelper, R. L. & Smith, R. (1995). Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy. Journal of neuropathology and experimental neurology, 54(4), 601-6. PMID: 7602333.

Mills, K. A., Mathews, K. D., Scherpbier-Heddema, T., Schelper, R. L., Schmalzel, R., Bailey, H. L., Nadeau, J. H., Buetow, K. H. & Murray, J. C. (1995). Genetic mapping near the myd locus on mouse chromosome 8. Mammalian genome : official journal of the International Mammalian Genome Society, 6(4), 278-80. PMID: 7613034.

Murray, J. C. (1995). Face facts: genes, environment, and clefts. (Vols. 57). (2), pp. 227-32. American journal of human genetics. PMID: 7668246.

Cox, D. W., Billingsley, G. D., Bale, A. E., Donis-Keller, H., Edwards, J. H., Litt, M., Mcbride, W., Persichetti, F., Spurr, N. K. & Weber, J. L. (1995). CEPH consortium map of chromosome 14. Cytogenetics and Cell Genetics, 69(3-4), 175–178. PMID: 7698005.

Klewer, S. E., Stadler, H. S., Kitten, G. T., Weeks, D. L. & Murray, J. C. (1995). Differential display of embryonic mouse endocardial cushion cDNA libraries identifies candidate cDNA clones expressed during cushion morphogenesis. Scientific Conference on the Molecular Cellular and Functional Aspects of Cardiovascular Development, New Orleans, LA, Mar 24-26.

Canady, J. W., Murray, J. C. & Thompson, S. A. (1995). Genetic factors associated with scar formation. American Society of Plastic and Reconstructive Surgeons (ASPRS) Scientific meeting.

Mears, A. J., el-Shanti, H., Murray, J. C., McDermid, H. E. & Patil, S. R. (1995). Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. American journal of human genetics, 57(3), 667-73. PMID: 7668296.

Alward, W. L., Murray, J. C. (1995). Axenfeld-Rieger Syndrome. In Molecular Genetics of Ocular Disease. pp. 31-50. Wilmington, DE: Wiley-Liss, Inc.

Mathews, K. D., Mills, K. A., Bailey, H. L., Schelper, R. L. & Murray, J. C. (1995). Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Muscle & nerve. Supplement,(2), S98-102. PMID: 23573594.

Graham, J. M., Hixon, H., Bacino, C. A., Daack-Hirsch, S., Stadler, S. & Murray, J. C. (1995). Autosomal dominant transmission of a Goldenhar-like syndrome with linkage to the Branchio-Oto-Renal syndrome locus at 8q13.3. Western Regional Meeting of the American Federation for Clinical Research, Carmel, CA, Feb 8-11.

Wijmenga, C., Dauwerse, H. G., Padberg, G. W., Meyer, N., Murray, J. C., Mills, K., van Ommen, G. B., Hofker, M. H. & Frants, R. R. (1995). Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35. Muscle & nerve. Supplement, 2, S14-8. PMID: 7739620.

Sander, A., Murray, J. C., Scherpbier-Heddema, T., Buetow, K. H., Weissenbach, J., Zingg, M., Ludwig, K. & Schmelzle, R. (1995). Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. American journal of human genetics, 56(1), 310-8. PMID: 7825592.

Sheffield, V. C., Weber, J. L., Buetow, K. H., Murray, J. C., Even, D. A., Wiles, K., Gastier, J. M., Pulido, J. C., Yandava, C. & Sunden, S. L. (1995). A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Human molecular genetics, 4(10), 1837-44. PMID: 8595404.

Schutte, B. C., Sander, A., Malik, M., Leysens, N., Basart, A., Lohman, B., Edwards, S., Dixon, M., Dixon, J., Haider, N., Bjork, B., Ding, Y. & Murray, J. C. (1995). Physical mapping of the Van der Woude critical region. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Schwartz, D. A., Freel, K. L., Leysens, N. J. & Murray, J. C. (1995). Direct sequencing excludes the 11-member type I interferon genes as etiologic for murine endotoxin (LPS) resistance. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Yoshiura, K., Stadler, S. & Murray, J. C. (1995). Identification of mouse homologs for the human H6 homeobox gene. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Datson, N. A., van Staalduinen, A. A., Semina, E., Meershoek, E. M., Heus, J. J., Hofker, M. H., van Ommen, G., den Dunnen, J. T., Murray, J. & Frants, R. R. (1995). Mapping the translocation breakpoints in Rieger syndrome. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Lidral, A., Basart, A., Romitti, P., Parnell, T., Doetschman, T., Rubenstein, J., Porteus, M., Smiga, S., Buetow, K., Lammer, E., Shaw, G., Proetzel, G., Daack-Hirsch, S. & Murray, J. (1995). Candidate gene analysis of nonsyndromic cleft lip with or without cleft palate (NS-CLP) and cleft palate only (NS-CPO) in humans. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Zittergruen, M. M., Murray, J. C., Lauer, R. M., Burns, T. L. & Sheffield, V. C. (1995). Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects. Circulation, 92(10), 2803–2810. PMID: 7586245.

Gastier, J. M., Pulido, J. C., Sunden, S., Brody, T., Buetow, K. H., Murray, J. C., Weber, J. L., Hudson, T. J., Sheffield, V. C. & Duyk, G. M. (1995). Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. Human molecular genetics, 4(10), 1829-36. PMID: 8595403.

Trembath, D., Sherbondy, A., VanDyke, D., Finnell, R. & Murray, J. (1995). Candidate gene analysis of neural tube defects (NTDs) in humans. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Zittergruen, M. M., Murray, J. C., Lauer, R. M. & Sheffield, V. C. (1995). Molecular analysis of the nondisjoined chromosomes in trisomy 21 with and without atrioventricular septal defects. 68th Scientific Sessions of the American Heart Association, Anaheim, CA, Nov 13-16.

Sheffield, V. C., Weber, J. L., Buetow, K. H., Murray, J. C., Even, D. A., Wiles, K., Gastier, J. M., Pulido, J. C., Yandava, C. & Sunden, S. L. (1995). A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Human Molecular Genetics, 4(10), 1837–1844. PMID: 8595404.

Jones, D., Lindquist, S., Malik, M., Winistorfer, S., Even, D., Murray, J. C. & Schutte, B. C. (1995). The MSS1 gene: a positive modulator of HIV Tat-mediated transactivation maps to 7q21.3-q22. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Lysaught, M. T., Murray, J. C., Hausler, W., Getchell, J. P. & Thompson, C. (1995). The use of DNA-based techniques on Guthrie cards as a method for measuring carrier and allele frequencies in the Iowa population: a pilot study on cystic fibrosis and phenylketonuria. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Crosby, A. H., Scherpbier-Heddema, T., Wijmenga, C., Altherr, M. R., Murray, J. C., Buetow, K. H. & Dixon, M. J. (1995). Genetic mapping of the dentinogenesis imperfecta type II locus. American journal of human genetics, 57(4), 832-9. PMID: 7573043.

Wiles, K., Murray, J. C., Buetow, K. H. & Sheffield, V. C. (1995). Population genetic characteristics of human short tandem repeat polymorphisms and 3’UTR variants in a human diversity panel. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Zittergruen, M. M., Murray, J. C., Lauer, R. M., Burns, T. L. & Sheffield, V. C. (1995). Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects. Circulation, 92(10), 2803-10. PMID: 7586245.

Semina, E. V., Murray, J. C., Leysens, N., Yoshiura, K. & Altherr, M. (1995). Progress in positional cloning of Rieger gene. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Nishimura, C. F., Leysens, N. J., Padanilam, B., Sutherland, L. B. & Murray, J. C. (1995). Sequencing of a human PAX-9 cDNA clone and discovery of a polymorphic PCR product homologous to PAX-9 in primer sequence. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Sheffield, V., Weber, J., Buetow, K., Murray, J., Even, D., Wiles, K., Gastier, J., Pulido, J., Yandava, C., Sunden, S., Mattes, G., Businga, T., Mcclain, A., Beck, J., Scherpier, T., Gilliam, J., Zhong, J. & Duyk, G. (1995). Progress in Trinucleotide and Tetranucleotide Development for the Cooperative Human Linkage Center. American Journal of Human Genetics, 57(4), 1169–1169.

Nishimura, C., Leysens, N., Padanilam, B., Sutherland, L. & Murray, J. (1995). Sequencing of a Human Pax-9 Cdna Clone and Discovery of a Polymorphic Pcr Product. American Journal of Human Genetics, 57(4), 1825–1825.

Williams, J. K., Murray, J. C. (1995). Psychosocial aspects of heterozygote testing. 45th annual meeting of the American Society of Human Genetics, Minneapolis, MN, Oct 24-28.

Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Duyk, G. M., Sheffield, V. C., Wang, Z. & Murray, J. C. (1994). Integrated human genome-wide maps constructed using the CEPH reference panel. Nature genetics, 6(4), 391-3. PMID: 8054980.

Basart, A. M., Qian, J. F., May, E. & Murray, J. C. (1994). A PCR method for detecting polymorphism in the TGFA gene. Human molecular genetics, 3(4), 678. PMID: 8069321.

Francomano, C. A., de Ortiz Luna, R. I., Hefferon, T. W., Bellus, G. A., Turner, C. E., Taylor, E., Meyers, D. A., Blanton, S. H., Murray, J. C. & McIntosh, I. (1994). Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p. Human molecular genetics, 3(5), 787-92. PMID: 8081365.

Winokur, S. T., Bengtsson, U., Feddersen, J., Mathews, K. D., Weiffenbach, B., Bailey, H., Markovich, R. P., Murray, J. C., Wasmuth, J. J. & Altherr, M. R. (1994). The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, 2(3), 225-34. PMID: 8069466.

Muenke, M., Gurrieri, F., Bay, C., Yi, D., Collins, A., Johnson, V., Hennekam, R., Schaefer, G., Weik, L., Lubinsky, M., Daackhirsch, S., Moore, C., Dobyns, W., Murray, J. & Price, R. (1994). Linkage of a Human Brain Malformation, Familial Holoprosencephaly, to Chromosome-7 and Evidence for Genetic-Heterogeneity. Proceedings of the National Academy of Sciences of the United States of America, 91(17), 8102–8106. DOI: 10.1073/pnas.91.17.8102.

Solursh, M., Murray, J. (1994). Craniofacial Morphogenesis Workshop Report. The Cleft Palate-Craniofacial Journal, 31(3), 230–231. DOI: 10.1597/1545-1569(1994)031<0230:CMWR>2.3.CO;2.

Sander, A., Schmelzle, R. & Murray, J. (1994). Evidence for a microdeletion in 1q32–41 involving the gene responsible for Van der Woude syndrome. Human Molecular Genetics, 3(4), 575-578.

Sunden, S., Stone, E., Beck, J., Duyk, G., Murray, J., Weber, J., Buetow, K. & Sheffield, V. (1994). Development of Tri-Nucleotide and Tetra-Nucleotide Repeat Marker Screening Sets for Efficient Linkage Mapping of Hereditary Eye Diseases. Investigative Ophthalmology & Visual Science, 35(4), 1312–1312.

Weber, J., Stephenson, M., Buetow, K., Duyk, G., Sheffield, V. & Murray, J. (1994). New Trinucleotide and Tetranucleotide Short Tandem Repeat Polymorphisms. Cytogenetics and Cell Genetics, 67(4), 275–276.

Detera-Wadleigh, S. D., Hsieh, W., Berrettini, W. H., Goldin, L. R., Rollins, D. Y., Muniec, D., Grewal, R., Guroff, J. J., Turner, G., Coffman, D., Barrick, J., Mills, K., Murray, J., Donohue, S. J., Klein, D. C., Sanders, J., Nurnberger, J. I. & Gershon, E. S. (1994). Genetic linkage mapping for a susceptibility locus to bipolar illness: Chromosomes 2,3,4,7,9,10p,11p,22, and Xpter. American Journal of Medical Genetics, 54(3), 206–218. DOI: 10.1002/ajmg.1320540307.

Mears, A., Riazi, M., Budarf, M., Emanuel, B., Murray, J., Patil, Sr & Mcdermid, H. (1994). Mapping of the Critical Region of Cat Eye Syndrome at 22q11.2. Cytogenetics and Cell Genetics, 67(4), 289–289.

Muenke, M., Gurrieri, F., Yi, D., Bay, C., Collins, A., Johnson, V., Hennekam, R., Schaefer, G., Lubinsky, M., Moore, C., Dobyns, W., Murray, J. & Price, R. (1994). Linkage of a Gene Causing Familial Holoprosencephaly (hpe) to Chromosome 7q36. Cytogenetics and Cell Genetics, 65(1-2), 70–71.

Sander, A., Kennedy, M. A., Rayner, J. C. & Murray, J. C. (1994). Dinucleotide repeat polymorphism for HLX1 gene. Human molecular genetics, 3(1), 219. PMID: 8162047.

Mathews, K., Mills, K., Bailey, H., Rapisarda, D., Schelper, R., Smith, R. & Murray, J. (1994). Characterization and mapping of the myd mouse: A possible model for facioscapulohumeral dystrophy. VIII International Congress on Neuromuscular Diseases, Tokyo, Japan.

Fan, J. B., DeYoung, J., Lagacé, R., Lina, R. A., Xu, Z., Murray, J. C., Buetow, K. H., Weissenbach, J., Goold, R. D. & Cox, D. R. (1994). Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4. Human molecular genetics, 3(2), 243-6. PMID: 8004089.

Zittergruen, M. M., Murray, J. C., Lauer, R. M. & Sheffield, V. C. (1994). Molecular analysis of the nondisjoined chromosome in trisomy 21 with and without endocardial cushion defects. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Murray, J., Duyk, J., Sheffield, V., Weber, J. & Buetow, K. (1994). High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Graham, J. M., Hixon, H., Bacino, C. A., Daack-Hirsch, S., Stadler, S. & Murray, J. C. (1994). Linkage and physical mapping approaches utilizing families and individuals with a Goldenhar phenotype. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Riazi, M. A., Mears, A. J., Bell, C., Budarf, M. L., Emanuel, B. S., Murray, J. C., Patil, S. R. & McDermid, H. E. (1994). Long-range mapping and construction of a YAC contig within the cat’s-eye syndrome critical region. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Albanese, M., Clarke, W., Adams, H., Woolson, R., Bendixen, B., Davis, P., Jacoby, M., Gomez, F., Dyken, M., Uc, E., Wojcieszek, J., Kappelle, L., Tanna, A., Mitchell, V., Gomez, C., Malkoff, M., Tulyapronchote, R., Sauer, C., Riaz, G., Schmidt, J., Malik, M., Banet, G., Karanjia, P., Madden, K., Ruggles, K., Mickel, S., Gottschalk, P., Hansotia, P., Sorenson, R., Jacobson, D., Hiner, B., Mancl, K., Lukasik, E., Bruno, A., Lakind, E., Jeffrey, D., Mladinich, E., Iqbal, J., Reiners, M., Barrett, D., Shibuya, D., Williams, J., Russell, P., King, M., Chapin, J., Carter, S., Jeffries, L., Hier, D., Shapiro, R., Brint, S., Hoff, J., Oconnell, D., Fisher, M., Ameriso, S., Garabedian, M., Macko, R., Hanna, M., Yegyan, G., Martin, A., Scicli, A., Jackson, C., Rothrock, J., Lyden, P., Brody, M., Zweifler, R., Kelly, N., Gordon, D., Thiel, A., Fredericks, R., Singh, R., Dendinger, J., Gorelick, P., Riskin, B., Mirza, D., Kelly, M., Bijari, A., Murray, J., Curtin, J., Bozzola, F., Kofman, J., Brown, N., Dollear, W., Weinberger, J., Tuhrim, S., Rudolph, S., Horowitz, D., Sheinart, K., Gondolo, T., Ali, J., Bitton, A., Biller, J., Saver, J., Frank, J., Patrick, J., Fernandezbeer, E., Chadwick, L., Feldmann, E., Wilterdink, J., Ricks, L., Mohr, J., Sacco, R., Clavijo, M., Rosenbaum, D., Sparr, S., Katz, P., Klonowski, E., Byer, J., White, H., Sundrani, S., Zafar, M., Arora, R., Gamboa, E., Stacy, M., Bonnett, A., Kelley, C., Culebras, A., Carey, G., Martir, N., Kent, P., Rabiee, H., Guevara, R., Bangco, M., Pastor, D., Ficarra, C., Coull, B., Briley, D., Clark, W., Kenny, C., Austin, T., Degarmo, P., Anderson, D., Tarrel, R., Nance, M., Bundlie, Sr, Doyle, J., Dierich, M., Love, B., Struck, L., Mueller, C., Hogan, E., Carter, T., Gurecki, P., Plyer, J., Muntzpope, B., Libman, R., Kwiatkowski, T., Kanner, R., Donnaruma, R., Cullen, V., Fayad, P., Brass, L., Pavalkis, F., Wrobel, C., Leramo, O., Buxton, S., Hollander, J., Honch, G., Weber, C., Mayman, C., Warach, S., Tijerina, M., Mandelbaum, M., Hassan, R., Abbas, D., Olmstead, C., Sedlacek, L., Miller, A., Keilson, M., Bruining, K., Drexler, E., Morgante, L., Ramirezlassepas, M., Tulloch, J., Quinones, M., Clavel, A., Mendez, M., Zhang, S., Ala, T., Espinosa, C., Johnston, K., Kase, C., Wolf, P., Babikian, V., Licatagehr, E., Allen, N., Homer, D., Neely, S., Carpenter, J., Horowitz, S., Lava, N., Manning, M., Grimsman, K., Olson, J., Pennell, B., Johnson, K., Cornell, S., Crosby, D., Simpson, T., Krumbholz, V., Zalesky, C., Wasek, P., Dieleman, J., Paulsen, J., Boreen, J., Jones, M., Robb, B., Oberbroeckling, L., Hansen, M., Hicklin, K., Dyken, M., Frankowski, R., Greenberg, C., Harker, L., Whisnant, J., Fincham, R., Kisker, T., Wallace, R., Day, H., Detre, K., Grotta, J., Haley, E., Longstreth, W. & Marler, Jr (1994). Ensuring Reliability of Outcome Measures in Multicenter Clinical-Trials. Stroke, 25(9), 1746–1751.

Stadler, H. S., Goodfellow, P. J., Solursh, M. & Murray, J. C. (1994). A variant of the H6 homeobox gene maps to the 10q25.1-q26.2 region of human chromosome 10. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Klewer, S., Stadler, H., Kitten, G., Weeks, D. & Murray, J. (1994). Differential Display of Mouse Endocardial Cushion Cdna Libraries Identifies Candidate Genes Expressed During Cushion Morphogenesis. Circulation, 90(4), 246–246.

Daack-Hirsch, S., Basart, A., Lidral, A., Dixon, M., Semina, E., Buetow, K., Frischmeyer, P., Romitti, P., Munger, R. & Murray, J. C. (1994). Candidate gene association studies in syndromic and non-syndromic cleft lip and palate. 44th annual meeting of the American Society of Human Genetics, Oct 18-22.

Businga, T., Beck, J. S., Sunden, S., Duyk, G. M., Murray, J. C., Weber, J. L., Buetow, K. H. & Sheffield, V. C. (1994). Assignment of 1000 tri- and tetranucleotide repeats to chromosomes by somatic cell hybrid analysis. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Mathews, K., Wiles, K., Scherpbier-Heddema, T., Buetow, K. H. & Murray, J. C. (1994). Genetic mapping of Borjeson-Forssman-Lehmann syndrome. Child Neurology Society and International Child Neurology Association, Oct. 2-8.

Shaw, G. M., Lammer, E. J., Wasserman, C. R., Murray, J. C. & Basart, A. (1994). TGF-alpha genotypes, oral clefts, and environmental risk factors: A population-based California study. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Buetow, K. H., Ludwigsen, S., Scherpbier-Heddema, T., Quillen, J., Murray, J. C., Sheffield, V. C., Duyk, G. M., Weber, J. L., Weissenbach, J. & Gyapay, G. (1994). Human genetic map. Genome maps V. Wall chart. Science (New York, N.Y.), 265(5181), 2055-70. PMID: 8091228.

Murray, J., Buetow, K., Weber, J., Ludwigsen, S., Scherpbierheddema, T., Manion, F., Quillen, J., Sheffield, V., Sunden, S., Duyk, G., Weissenbach, J., Gyapay, G., Dib, C., Morrissette, J., Lathrop, G., Vignal, A., White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S., Ward, D., Dausset, J., Cohen, D. & Cann, H. (1994). A Comprehensive Human Linkage with Centimorgan Density. Science, 265(5181), 2049–2054. DOI: 10.1126/science.8091227.

Yankowitz, J., Li, S. & Murray, J. (1994). PCT determination of RhD blood type: An initial evaluation of accuracy. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Murray, J. C., Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Manion, F., Quillen, J., Sheffield, V. C., Sunden, S. & Duyk, G. M. (1994). A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). Science (New York, N.Y.), 265(5181), 2049–2054. PMID: 8091227.

Leysens, N., Murray, J. C., Lindgren, C., Carey, J. & Zabel, B. (1994). Progress in positional cloning of the Rieger syndrome gene. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Padanilam, B. J., Barsel, S., Leysens, N., Solursh, M. & Murray, J. C. (1994). Sequence characterization of a human embryonic craniofacial cDNA library. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Sander, A., Schutte, B. C., Schmelzle, R. & Murray, J. (1994). Physical map of the 850 kb Van der Woude critical region. 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Mills, K. A., Bailey, H. L., Murray, J. C. & Mathews, K. D. (1994). Refined localization of myd, a candidate animal model for facioscapulohumeral dystrophy (FSHC). 44th annual meeting of the American Society of Human Genetics, Montreal, Oct 18-22.

Farrall, M., Buetow, K. H. & Murray, J. C. (1993). Resolving an apparent paradox concerning the role of TGFA in CL/P. (Vols. 52). (2), pp. 434-7. American journal of human genetics. PMID: 8094269.

Nishimura, D. Y., Purchio, A. F. & Murray, J. C. (1993). Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q. Genomics, 15(2), 357-64. PMID: 8095486.

Duyk, G., Sheffield, V., Murray, J., Weber, J. & Buetow, K. (1993). High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms. Cold Spring Harbor meetings, May 12-16.

Shiang, R., Lidral, A., Ardinger, H., Buetow, K., Romitti, P., Munger, R., Bell, G., Hanson, J. & Murray, J. (1993). Studies of Tgfa as a Candidate Gene for Cleft-Lip and Palate on Human Chromosome-2. Cytogenetics and Cell Genetics, 64(2), 91–91.

Buetow, K., Murray, J., Mills, K. & Weber, J. (1993). A Short Tandem Repeat Polymorphism Based Linkage Map of Human Chromosome-2. Cytogenetics and Cell Genetics, 64(2), 86–86.

Farrall, M., Buetow, K. H. & Murray, J. C. (1993). Resolving an apparent paradox concerning the role of TGFA in CL/P (Letter to the Editor). (Vols. 52). pp. 434-436. Am J Hum Genet.

Schutte, B. C., Saal, H. M., Goudy, S. & Leslie, E. (1993). IRF6-Related Disorders. In GeneReviews(®). Seattle (WA): University of Washington, Seattle. PMID: 20301581.

Wijmenga, C., Winokur, S. T., Padberg, G. W., Skraastad, M. I., Altherr, M. R., Wasmuth, J. J., Murray, J. C., Hofker, M. H. & Frants, R. R. (1993). The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus. Human genetics, 92(2), 198-203. PMID: 8103757.

Mills, K., Mathews, K., Buetow, K., Schmelzle, R., Bailey, H., Nichols, W., Nadeau, J. & Murray, J. (1993). Genetic mapping of myd, a possible mouse model for facioscapulohumeral muscular dystrophy. 43rd annual meeting of the American Society of Human Genetics, New Orleans, LA, Oct 5-9.

Murray, J., El-Shanti, H., Lindgren, C., Leysens, N., Patil, S., Zabel, B., Alward, W., Stevenson, T., Bitoun, P. & Buetow, K. (1993). Combined mapping approaches to Rieger syndrome. 43rd annual meeting of the American Society of Human Genetics, New Orleans, LA, OCt 5-9.

Rebbeck, T. R., Dietz, F. R., Murray, J. C. & Buetow, K. H. (1993). A single-gene explanation for the probability of having idiopathic talipes equinovarus. American journal of human genetics, 53(5), 1051-63. PMID: 8213831.

Murray, J. C., Buetow, K. H., Duyk, G., Sheffield, V. & Weber, J. (1993). High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms. Human Genome Mapping Workshop 93, Kobe, Japan, Nov 14-17.

Murray, J., Wiles, K., Mathews, K., Schlessinger, D., Ludwigsen, S., Buetow, K. & Weissenbach, J. (1993). Short tandem repeat polymorphism based map of the human X chromosome. St Louis, MO: 4th X Chromosome Workshop, Washington Univ.

Bascom, R. A., Liu, L., Humphries, P., Fishman, G. A., Murray, J. C. & McInnes, R. R. (1993). Polymorphisms and rare sequence variants at the ROM1 locus. Human molecular genetics, 2(11), 1975-7. PMID: 7904211.

Elshanti, H., Hulseberg, D., Murray, J. & Patil, Sr (1993). A 3 Generation Minute Supernumarary Ring 22 - Association with Cat-Eye Syndrome. American Journal of Human Genetics, 53(3), 126–126.

Beck, J., Powers, L., Sheffield, V. & Murray, J. (1993). Chromosomal Assignment Using an Efficient Monochromosomal Hybrid Pooling Strategy. American Journal of Human Genetics, 53(3), 974–974.

Buetow, K., Duyk, G., Sheffield, V., Weber, J. & Murray, J. (1993). High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms. 43rd annual meeting of the American Society of Human Genetics, New Orleans, LA, Oct 5-9.

Muenke, M., Gurrieri, F., Yi, D., Bay, C., Collins, A., Johnson, V., Hennekam, R., Schaefer, G., Weik, J., Lubinsky, M., Daackhersh, S., Moore, C., Dobyns, W., Murray, J. & Price, R. (1993). Linkage of Familial Holoprosencephaly to Chromosome-7q36 - Clinical and Molecular Studies. American Journal of Human Genetics, 53(3), 1048–1048.

Sander, A., Scherpbier-Heddema, T., Buetow, K., Schmelzle, R. & Murray, J. (1993). Microsatellite-based fine mapping of the Van der Woude syndrome on 1q. 43rd annual meeting of the American Society of Human Genetics, New Orleans, LA, Oct. 5-9.

Shiang, R., Lidral, A. C., Ardinger, H. H., Buetow, K. H., Romitti, P. A., Munger, R. G. & Murray, J. C. (1993). Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO). American journal of human genetics, 53(4), 836-43. PMID: 8105683.

Nishimura, D. Y., Leysens, N. J. & Murray, J. C. (1992). A dinucleotide repeat for the D1S53 locus. Nucleic acids research, 20(5), 1167. PMID: 1549502.

Murray, J., Buetow, K. (1992). The Chromosome-4 Workshop Report. Genomics, 12(4), 857–858. DOI: 10.1016/0888-7543(92)90329-Q.

Sleister, H. M., Mills, K. A., Blackwell, S. E., Killary, A. M., Murray, J. C. & Malone, R. E. (1992). Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability. Nucleic acids research, 20(13), 3419-25. PMID: 1630913.

Nishimura, D. Y., Murray, J. C. (1992). A tetranucleotide repeat for the F13B locus. Nucleic acids research, 20(5), 1167. PMID: 1549503.

Mathews, K. D., Mills, K. A., Bosch, E. P., Ionasescu, V. V., Wiles, K. R., Buetow, K. H. & Murray, J. C. (1992). Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35. American journal of human genetics, 51(2), 428-31. PMID: 1642242.

Mills, K. A., Buetow, K. H., Xu, Y., Ritty, T. M., Mathews, K. D., Bodrug, S. E., Wijmenga, C., Balazs, I. & Murray, J. C. (1992). Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD). American journal of human genetics, 51(2), 432-9. PMID: 1642243.

MacDougall, M., Zeichner-David, M., Murray, J., Crall, M., Davis, A. & Slavkin, H. (1992). Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III. American Journal of Human Genetics, 50(1), 190–194. PMID: 1729887.

Byth, B., Love, D., Murray, J. & Davies, K. (1992). Localization of 2 New Dna Markers on the Linkage Map of Human-Chromosome 6q. Cytogenetics and Cell Genetics, 60(3-4), 216–218. DOI: 10.1159/000133342.

Lidral, A., Shiang, R., Ardinger, H., Buetow, K. & Murray, J. (1992). Association of sequence based DNA polymorphisms for TGFA with cleft lip and/or palate. Portland, OR: American Cleft Palate-Craniofacial Association Meeting.

Byth, B. C., Love, D. R., Murray, J. C. & Davies, K. E. (1992). Localization of two new DNA markers on the linkage map of human chromosome 6q. Cytogenetics and cell genetics, 60(3-4), 216-8. PMID: 1354595.

Crall, M. G., Schuler, C. F., Buetow, K. H. & Murray, J. C. (1992). Genetic marker study of dentinogenesis imperfecta. Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia, 88 Suppl 1, 285-93. PMID: 1508884.

Shiang, R., Buetow, K. H. & Murray, J. C. (1992). A comparison of physical and genetic distances in human chromosomal regions 4p16.3 and 13q14.2. San Francisco, CA: 42nd annual meeting of the American Society of Human Genetics.

Murray, J. C., Buetow, K. H., Mills, K. A., Denman, S., Malone, R., Shiang, R., Xu, Y. & Jiang, O. (1992). High resolution mapping studies on chromosome 4. San Francisco, CA: 42nd annual meeting of the American Society of Human Genetics.

Buetow, K. H., Shiang, R., Yang, P. & Murray, J. C. (1992). A detailed multipoint map of human chromosome 4p16.3 provides evidence for linkage heterogeneity and position specific recombination rates. 42nd annual meeting of the American Society of Human Genetics.

Georgiou, C., Murray, J. C., Buetow, K. H., Leysens, N., Miller, B., Rarey, J., Chung, C. S. & McGee, W. (1992). Clinical and molecular studies of craniofacial anomalies in the Philippines. 42nd annual meeting of the American Society of Human Genetics.

Sarfarazi, M., Wijmenga, C., Upadhyaya, M., Weiffenbach, B., Hyser, C., Mathews, K., Murray, J., Gilbert, J., Pericak-Vance, M., Lunt, P., Frants, R. R., Jacobsen, S., Harper, P. S. & Padberg, G. W. (1992). Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: Combined analysis of an international consortium. American Journal of Human Genetics, 51(2), 396–403. PMID: 1642237.

Stadler, H. S., Padanilam, B. J., Buetow, K., Murray, J. C. & Solursh, M. (1992). Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4. Proceedings of the National Academy of Sciences of the United States of America, 89(23), 11579-83. PMID: 1360670.

Bowcock, A., Barnes, R., White, R., Kruse, T., Tsipouras, P., Sarfarazi, M., Jenkins, T., Viljoen, C., Litt, M., Kramer, P., Murray, J. & Vergnaud, G. (1992). The Ceph Consortium Linkage Map of Human Chromosome-15q. Genomics, 14(4), 833–840. DOI: 10.1016/S0888-7543(05)80101-6.

Spurr, N. K., Cox, S., Bryant, S. P., Attwood, J., Robson, E. B., Shields, D. C., Steinbrueck, T., Jenkins, T., Murray, J. C. & Kidd, K. K. (1992). The CEPH consortium linkage map of human chromosome 2. Genomics, 14(4), 1055-63. PMID: 1478647.

Mills, K. A., Even, D. & Murray, J. C. (1992). Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA). Human molecular genetics, 1(9), 779. PMID: 1302622.

Padanilam, B. J., Stadler, H. S., Mills, K. A., McLeod, L. B., Solursh, M., Lee, B., Ramirez, F., Buetow, K. H. & Murray, J. C. (1992). Characterization of the human HOX 7 cDNA and identification of polymorphic markers. Human molecular genetics, 1(6), 407-10. PMID: 1284527.

Wijmenga, C., Sandkuijl, L., Moerer, P., Vanderboorn, N., Bodrug, S., Ray, P., Brouwer, O., Murray, J., Vanommen, G., Padberg, G. & Frants, R. (1992). Genetic-Linkage Map of Facioscapulohumeral Muscular-Dystrophy and 5 Polymorphic Loci on Chromosome 4q35-Qter. American Journal of Human Genetics, 51(2), 411–415.

Nishimura, D. Y., Buetow, K. H., Lammer, E., Purchio, A. F. & Murray, J. C. (1992). Recombination analysis of markers closely linked to the Van der Woude (VWS) syndrome and examination of TGFB2 as a candidate gene. San Francisco, CA: 42nd annual meeting of the American Society of Human Genetics.

Murray, J. C., Bennett, S. R., Kwitek, A. E., Small, K. W., Schinzel, A., Alward, W. L., Weber, J. L., Bell, G. I. & Buetow, K. H. (1992). Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nature genetics, 2(1), 46-9. PMID: 1303248.

(1992). A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. Science (New York, N.Y.), 258(5079), 67–86. PMID: 1439770.

Mills, K. A., Buetow, K. H., Xu, Y., Weber, J. L., Altherr, M. R., Wasmuth, J. J. & Murray, J. C. (1992). Genetic and physical maps of human chromosome 4 based on dinucleotide repeats. Genomics, 14(2), 209-19. PMID: 1427835.

Mathews, K., Schutte, B., Ray, J., Bailey, H., Mills, K. & Murray, J. (1992). Linkage and mapping studies in facioscapulohumeral dystrophy. New Orleans, LA: Child Neurology Society meeting.

Mills, K. A., Xu, Y., Buetow, K. H. & Murray, J. C. (1991). High resolution genetic and physical mapping studies on human chromosome 4 yield a single linkage group. Washington DC: VIII International Congress of Human Genetics.

Buetow, K., Sheffield, V., Murray, J. & Mcmahon, B. (1991). Genetic-Studies of Primary Hepatocellular-Carcinoma (phc). Cytogenetics and Cell Genetics, 58(3-4), 1885–1886.

Murray, J., Mills, K., Xu, Y., Ritty, T., Leysens, N., Mathews, K. & Buetow, K. H. (1991). High resolution genetic and physical mapping sudies on human chromosome 4. Cold Spring Harbor Meetings.

Coleman, M. P., Murray, J. C., Willard, H. F., Monaco, A., Lindsay, S., Bhattacharya, S. S. & Davies, K. E. (1991). Genetic and physical mapping around the RP2 locus in Xp11.23. Washington DC: VIII International Congress of Human Genetics.

Wijmenga, C., Sandkuyl, L., Moerer, P., Ray, S., Ray, P., Murray, J., Vanommen, G., Padberg, G. & Frants, R. (1991). Linkage Map of Facioscapulohumeral Muscular-Dystrophy (fmd) and 5 Polymorphic Loci on Chromosome 4q35-Qter. Cytogenetics and Cell Genetics, 58(3-4), 1891–1891.

Mills, K. A. (1991). High resolution mapping near the locus for FMD. London: Human Gene Mapping 11.

Shiang, R., Lidral, A., Ardinger, H., Buetow, K. H. & Murray, J. C. (1991). Direct sequencing of TGFA DNA from patients with cleft lip and palate. Washington DC: VIII International Congress of Human Genetics.

Nishimura, D. Y., Buetow, K. H., Lammer, E. & Murray, J. C. (1991). Molecular analysis of Van der Woude syndrome. Washington DC: VIII International Congress of Human Genetics.

Stadler, H., Padanilam, B., Murray, J. & Solursh, M. (1991). Identification and Chromosomal Localization of a Novel Homeobox Gene from a Human Craniofacial Library. American Zoologist, 31(5), A46–A46.

Siniscalco, M., Oberlé, I., Melis, P., Alhadeff, B., Murray, J., Filippi, G., Mattioni, T., Chen, Y. T., Furneaux, H. & Old, L. J. (1991). Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. American Journal of Medical Genetics, 38(2-3), 357–362. PMID: 1708201.

Miller, B. L., Nishimura, D. Y., Wieben, E. D. & Murray, J. C. (1991). An EcoO109 RFLP for the SNRPE gene on chromosome 1. Nucleic acids research, 19(7), 1724. PMID: 1674142.

Wijmenga, C., Padberg, G., Moerer, P., Vanderboorn, N., Bodrug, S., Ray, P., Worton, R., Murray, J., Vonommen, G., Sandkuyl, L. & Frants, R. (1991). Multipoint Map Around the Facioscapulohumeral Muscular-Dystrophy Locus. American Journal of Human Genetics, 49(4), 363–363.

Murray, J. C., Lidral, A., Buetow, K. H., Stadler, S., Solursh, M. & Kwitek, A. E. (1991). Comprehensive molecular genetic approaches to human disorders of morphogenesis. Cold Spring Harbor meetings.

Nishimura, D., Buetow, K., Lammer, E. & Murray, J. (1991). Molecular Analysis of Vanderwoude Syndrome. American Journal of Human Genetics, 49(4), 415–415.

Buetow, K., Sheffield, V., Murray, J. & Mcmahon, B. (1991). Genetic-Studies of Primary Hepatocellular-Carcinoma (phc). American Journal of Human Genetics, 49(4), 401–401.

Coleman, M. P., Murray, J. C., Willard, H. F., Nolan, K. F., Reid, K. B., Blake, D. J., Lindsay, S., Bhattacharya, S. S., Wright, A. & Davies, K. E. (1991). Genetic and physical mapping around the properdin P gene. Genomics, 11(4), 991-6. PMID: 1783405.

Mathews, K., Mills, K., Leysens, N., Xu, Y., Bodrug, S., Buetow, K. & Murray, J. (1991). Characterization of the Facioscapulohumeral Dystrophy Locus on 4q35. American Journal of Human Genetics, 49(4), 350–350.

Buetow, K., Shiang, R., Yang, P., Nakamura, Y., Lathrop, G., White, R., Wasmuth, J., Wood, S., Berdahl, L., Leysens, N., Ritty, T., Wise, M. & Murray, J. (1991). A Detailed Multipoint Map of Human Chromosome-4 Provides Evidence for Linkage Heterogeneity and Position-Specific Recombination Rates. American Journal of Human Genetics, 48(5), 911–925.

Tait, J. F., Frankenberry, D. A., Shiang, R., Murray, J. C., Adler, D. A. & Disteche, C. M. (1991). Chromosomal localization of the human gene for annexin V (placental anticoagulant protein I) to 4q26----q28. Cytogenetics and cell genetics, 57(4), 187-92. PMID: 1683830.

Ritty, T. M., Jaye, M., Kaplan, R. & Murray, J. C. (1991). EcoRI and PvuII RFLPs in the endonexin II/annexin V (ANX5) gene on chromosome four. Nucleic acids research, 19(7), 1723. PMID: 1674140.

Shiang, R. (1991). Association of TGFA DNA variants with cleft lip and palate (OFC2). London: Human Gene Mapping 11.

Buetow, K., Murray, J. (1991). A Multipoint Genetic-Map of Human Chromosome-4. Cytogenetics and Cell Genetics, 58(3-4), 1885–1885.

Russo, A. F., Chamany, K., Klemish, S. W., Hall, T. M. & Murray, J. C. (1991). Characterization of the calcitonin/CGRP gene in Williams syndrome. American journal of medical genetics, 39(1), 28-33. PMID: 1867260.

Dracopoli, N. C., O’Connell, P., Elsner, T. I., Lalouel, J. M., White, R. L., Buetow, K. H., Nishimura, D. Y., Murray, J. C., Helms, C. & Mishra, S. K. (1991). The CEPH consortium linkage map of human chromosome 1. Genomics, 9(4), 686–700. PMID: 2037294.

Nishimura, D. Y., Buetow, K. H., Lammer, E., Purchio, A. F. & Murray, J. C. (1990). Recombinational analysis of markers closely linked to the Van der Woude (VWS) syndrome and examination of TGFB2 as a candidate gene. 40th annual meeting of the American Society of Human Genetics.

Murray, J. C., Buetow, K. H., Mills, K. A., Denman, S., Malone, R., Shiang, R., Xu, Y. & Jiang, O. (1990). High resolution mapping studies on chromosome 4. 40th Annual meeting of the American Society of Human Genetics.

Shiang, R., Buetow, K. H. & Murray, J. C. (1990). A comparison of physical and genetic distances in human chromosomal regions 4p16.3 and 13q14.2. 40th annual meeting of the American Society of Human Genetics.

Murray, J. C., Nishimura, D. Y., Buetow, K. H., Ardinger, H. H., Spence, M. A., Sparkes, R. S., Falk, R. E., Falk, P. M., Gardner, R. J. & Harkness, E. M. (1990). Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. American journal of human genetics, 46(3), 486-91. PMID: 2309700.

Georgiou, C., Murray, J. C., Buetow, K. H., Leysens, N., Miller, B., Rarey, J., Chung, C. S. & McGee, W. (1990). Clinical and molecular studies of craniofacial anomalies in the Philippines. 40th annual meeting of the American Society of Human Genetics.

Murray, J. C., van Ommen, G. B. (1990). Report of the committee on the genetic constitution of chromosome 4. Cytogenetics and cell genetics, 55(1-4), 97-110. PMID: 2073850.

White, R., Lalouel, J., Nakamura, Y., Doniskeller, H., Green, P., Bowden, D., Mathew, C., Easton, D., Robson, E., Morton, N., Gusella, J., Haines, J., Retief, A., Kidd, K., Murray, J., Lathrop, G. & Cann, H. (1990). The Ceph Consortium Primary Linkage Map of Human Chromosome-10. Genomics, 6(3), 393–412. DOI: 10.1016/0888-7543(90)90469-B.

Buetow, K. H., Shiang, R., Yang, P. & Murray, J. C. (1990). A detailed multipoint map of human chromosome 4p16.3 provides evidence for linkage heterogeneity and position specific recombination rates. 40th annual meeting of the American Society of Human Genetics.

Buetow, K. H., Nishimura, D., Nakamura, Y., Jiang, O. & Murray, J. C. (1990). A detailed multipoint gene map of chromosome 1q. Genomics, 8(1), 13-21. PMID: 1981991.

Nishimura, D., Buetow, K., Spence, M., Gardner, R., Pauli, R., Nakamura, Y., Green, P., Schinzel, A. & Murray, J. (1989). Linkage of Vanderwoude Syndrome (lps) to Renin on 1q. Cytogenetics and Cell Genetics, 51(1-4), 1053–1053.

Nishimura, D. Y., Buetow, K. H., Spence, M. A., Gardner, R., Pauli, R., Nakamura, Y., Green, P., Schnizel, A. & Murray, J. C. (1989). Linkage of Van der Woude syndrome (LPS) to Renin on 1q. Human Gene Mapping 10.

Siniscalco, M., Alhadeff, B., Kekish, O., Melis, P., Maltioni, T., Filippi, G., Murray, J., Oberle, I., Chen, Y., Old, L. & Posner, J. (1989). The Cdr Gene, Located at the Upper Boundary of the Fraxa, Is Tightly Linked to Dxs98 and Dxs105 Rflps, Moderately to the Fra(x)-Syndrome and Loosely to the Cluster of Dxs15-Dxs52 Rflps. Cytogenetics and Cell Genetics, 51(1-4), 1081–1081.

Kittur, S. D., Bagdon, M. M., Lubs, M. L., Phillips, 3rd, J. A., Murray, J. C., Slaugenhaupt, S. A., Chakravarti, A. & Adler, W. H. (1989). Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers. American journal of human genetics, 44(1), 48-50. PMID: 2491782.

(1989). The CEPH consortium linkage map of human chromosome 1. Genomics, 4, 12-20. PMID: 2037294.

Cox, D. R., Murray, J. C. & Buetow, K. H. (1989). Report of the committee on the genetic constitution of chromosome 4. Cytogenetics and cell genetics, 51(1-4), 121-36. PMID: 2676366.

Shiang, R., Murray, J. C., Morton, C. C., Buetow, K. H., Wasmuth, J. J., Olney, A. H., Sanger, W. G. & Goldberger, G. (1989). Mapping of the human complement factor I gene to 4q25. Genomics, 4(1), 82-6. PMID: 2563353.

Shiang, R., Buetow, K. & Murray, J. (1989). Linkage Disequilibrium on Chromosome-4. Cytogenetics and Cell Genetics, 51(1-4), 1077–1078.

Disteche, C., Plowman, G., Gronwald, R., Kelly, J., Bowenpope, D., Adler, D. & Murray, J. (1989). Mapping of the Amphiregulin and the Platelet-Growth Factor Receptor a Genes to the Proximal Long Arm of Chromosome-4. Cytogenetics and Cell Genetics, 51(1-4), 990–990.

Theilmann, J., Kanani, S., Shiang, R., Robbins, C., Quarrell, O., Huggins, M., Hedrick, A., Weber, B., Collins, C. & Wasmuth, J. J. (1989). Non-random association between alleles detected at D4S95 and D4S98 and the Huntington’s disease gene. Journal of Medical Genetics, 26(11), 676–681. PMID: 2531224.

Buetow, K. H., Murray, J. C., Israel, J. L., London, W. T., Smith, M., Kew, M., Blanquet, V., Brechot, C., Redeker, A. & Govindarajah, S. (1989). Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proceedings of the National Academy of Sciences of the United States of America, 86(22), 8852-6. PMID: 2573067.

Georgiou, C., Shull, M., Lane, L. K., Lingrel, J. B. & Murray, J. C. (1989). RFLPs for ATP1BL1 (beta subunit Na+/K+ ATPase pseudogene) on chromosome 4. Nucleic acids research, 17(21), 8894. PMID: 2573880.

Buetow, K., Shiang, R., Nakamura, Y., Brechot, C., Evans, R., Fukuda, M., Schull, M., Hulsebos, T., Wallner, B. & Murray, J. (1989). A Multipoint Genetic-Map and New Rflps for Human Chromosome-4. Cytogenetics and Cell Genetics, 51(1-4), 973–973.

Mathews, K. D., Ardinger, H. H., Nishimura, D. Y., Buetow, K. H., Murray, J. C. & Bartley, J. A. (1989). Linkage localization of Börjeson-Forssman-Lehmann syndrome. American journal of medical genetics, 34(4), 470-4. PMID: 2624254.

Beck, J. S., Sager, R. & Murray, J. C. (1989). A ScaI RFLP demonstrated for the GRO gene on chromosome 4. Nucleic acids research, 17(21), 8895. PMID: 2573881.

Nishimura, D. Y., Wieben, E. D., Stanford, D. R. & Murray, J. C. (1989). MspI RFLP for SNRNPE gene on 1q. Nucleic acids research, 17(21), 8896. PMID: 2479914.

Leysens, N., Murray, J. C. & Bell, G. I. (1989). A KpnI polymorphism for the human insulin-responsive glucose transporter gene (GLUT4) on chromosome 17. Nucleic acids research, 17(9), 3621. PMID: 2566978.

Ardinger, H. H., Buetow, K. H., Bell, G. I., Bardach, J., VanDemark, D. R. & Murray, J. C. (1989). Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. American journal of human genetics, 45(3), 348-53. PMID: 2570526.

O’Connell, P., Lathrop, G. M., Nakamura, Y., Leppert, M. L., Ardinger, R. H., Murray, J. L., Lalouel, J. M. & White, R. (1989). Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. Genomics, 4(1), 12–20. PMID: 2914706.

Leysens, N. J., Newkirk, N. G. & Murray, J. C. (1989). SacI and XbaI polymorphisms detected by lipocortin 2A (LPC2A). Nucleic acids research, 17(13), 5417. PMID: 2569714.

Bell, G. I., Murray, J. C., Nakamura, Y., Kayano, T., Eddy, R. L., Fan, Y. S., Byers, M. G. & Shows, T. B. (1989). Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13. Diabetes, 38(8), 1072-5. PMID: 2568955.

Ritty, T. M., Murray, J. C. (1989). A new HincII RFLP for epidermal growth factor (EGF) on chromosome 4. Nucleic acids research, 17(14), 5870. PMID: 2569722.

Berdahl, L., Murray, J. & Besmer, P. (1988). A Hindiii Rflp Demonstrated for the Kit Oncogene on Chromosome-4. Nucleic Acids Research, 16(10), 4740–4740. PMID: 2898128.

Berdahl, L. D., Smith, R. F., Murray, J. C. & Buetow, K. H. (1988). A TaqI RFLP demonstrated for pIBS17 [D4S123], a single copy sequence on chromosome 4. Nucleic acids research, 16(6), 2743. PMID: 2896340.

Murray, J. C., Buetow, K. H., Ferrell, R. E., Sieberg, P. D. & Fukuda, M. (1988). An RFLP for glycoprotein A (MN) is in linkage disequilibrium with MN and Ss. Cytogenetics and cell genetics, 47(3), 149-51. PMID: 2897896.

Murray, J. C., Buetow, K. H., Smith, M., Carlock, L., Chakravarti, A., Ferrell, R. F., Gedamu, L., Gilliam, C., Shiang, R. & DeHaven, C. R. (1988). Pairwise linkage analysis of 11 loci on human chromosome 4. American journal of human genetics, 42(3), 490-7. PMID: 2894759.

Murray, J., Buetow, K., Ferrell, R., Sieberg, P. & Fukuda, M. (1988). An Rflp for Glycophorin-a (mn) Is in Linkage Disequilibrium with Mn and Ss. Cytogenetics and Cell Genetics, 47(3), 149–151. DOI: 10.1159/000132534.

Smith, M., Weiss, M. J., Griffin, C. A., Murray, J. C., Buetow, K. H., Emanuel, B. S., Henthorn, P. S. & Harris, H. (1988). Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34. Genomics, 2(2), 139-43. PMID: 3410475.

Williamson, R. A., Murray, J. C. (1988). Molecular Analysis of Genetic Disorders. (2) Clinical Obstetrics and Gynecology.

Shiang, R., Murray, J. C., Wiggs, J. & Dryja, T. (1988). A TaqI RFLP identified at the retinoblastoma locus on chromosome 13. Nucleic acids research, 16(18), 9069. PMID: 2902570.

Williamson, R. A., Murray, J. C. (1988). Molecular analysis of genetic disorders. Clinical obstetrics and gynecology, 31(2), 270-84. PMID: 3042217.

Murray, J. C., Nishimura, D., Ardinger, H. A., Buetow, K. H., Spence, A., Falk, R., Falk, P., Sparkes, R., Gardner, R., Glinski, L., Pauli, R., Nakamura, Y., Green, P. & Yamada, Y. (1988). Linkage of Van der Woude syndrome to markers on chromosome 1q and exclusion of lamanin B2 as a candidate gene. 38th annual meeting of the American Society of Human Genetics.

Ardinger, H. H., Buetow, K. H., Bell, G. I. & Murray, J. C. (1988). Excess of a particular TGFA haplotype in individuals with cleft lip +/- cleft palate and a positive family history. 38th annual meeting of the American Society of Human Genetics.

Shiang, R., Buetow, K. H., Nakamura, Y., Wasmuth, J. & Murray, J. C. (1988). Conservation of human VNTRs in nonhuman primates. 38th annual meeting of the American Society of Human Genetics.

Nishimura, D., Buetow, K. H., Yamada, Y. & Murray, J. C. (1988). RFLPs and linkage relationships of the human laminin B2 gene. Genomics, 3(4), 393-5. PMID: 2907506.

Crowe, R. R., Tsai, L. Y., Murray, J. C., Patil, S. R. & Quinn, J. (1988). A study of autism using X chromosome DNA probes. Biological psychiatry, 24(4), 473-9. PMID: 3408765.

Ardinger, H. H., Rose, K. M., Murray, J. C. & Yamada, Y. (1988). HincII and KpnI RFLPs for laminin B1 (LAMB1) gene on chromosome 7. Nucleic acids research, 16(17), 8742. PMID: 2901729.

Ardinger, R. H., Murray, J. C. (1988). A Bgii Polymorphism for the Interleukin-2 Receptor Gene (il2r) on Chromosome-10. Nucleic Acids Research, 16(16), 8201–8201. DOI: 10.1093/nar/16.16.8201.

Ardinger, H. H., Ardinger, R. H., Bell, G. I. & Murray, J. C. (1988). RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19. Nucleic acids research, 16(16), 8202. PMID: 2901721.

Ardinger, R., Murray, J., Bell, G. & Lauer, R. (1988). Endocardial Cushion Defects Are Associated with Allele of Transforming Growth Factor-Alpha. American Journal of Cardiology, 62(7), 500–500.

Shiang, R., Murray, J., Divelbiss, J., Patil, S., Overhauser, J., Wasmuth, J. & Buetow, K. (1987). A Physical Map for the Long Arm of Chromosome-4 Using D4s35, D4s1, Mt2p1, Alb, Afp, Gc, Inp10, Adh3, Egf, Il2, Fgg, Fgb, and Mns, If, Fgfb. Cytogenetics and Cell Genetics, 46(1-4), 691–691.

Chance, P. F., Murray, J. C., Bird, T. D. & Kochin, R. S. (1987). Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markers. Neurology, 37(2), 325-9. PMID: 3468376.

Carlock, L. R., Vo, T. D., DeHaven, C. R. & Murray, J. C. (1987). An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease. Nucleic acids research, 15(1), 377. PMID: 2881254.

Mueller, O., Wasmuth, J., Murray, J., Lozzio, C., Lovrien, E. & Shows, T. (1987). Chromosomal Assignment of N-Acetylglucosaminyl Phosphotransferase, the Lysosomal Hydrolase Targeting Enzyme Deficient in Mucolipidosis-Ii and Mucolipidosis-Iii. Cytogenetics and Cell Genetics, 46(1-4), 664–665.

Crall, M., Murray, J., Buetow, K. & Ferrell, R. (1987). Multipoint Linkage Analysis of Dentinogenesis Imperfecta (dgi1) on 4q. Cytogenetics and Cell Genetics, 46(1-4), 600–600.

Buetow, K., Murray, J., Dehaven, C., Ardinger, R., Weiss, M. & Nemer, M. (1987). Linkage Analysis of 7 Markers on Human Chromosome-1. Cytogenetics and Cell Genetics, 46(1-4), 588–588.

Shows, T. B., Eddy, R. L., Byers, M. G., Fukushima, Y., Dehaven, C. R., Murray, J. C. & Bell, G. I. (1987). Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35. Diabetes, 36(4), 546-9. PMID: 3028891.

Smith, R., Ardinger, H., Dehaven, C., Murray, J. & Buetow, K. (1987). Rflps for the Glucocorticoid Receptor (grl) on Chromosome-5 and the Epidermal Growth-Factor Receptor (egfr) on Chromosome-7. Cytogenetics and Cell Genetics, 46(1-4), 695–695.

Murray, J., Buetow, K., Siebert, P. & Fukuda, M. (1987). Rflp for Glycophorin-a (gypa) and Linkage Disequilibrium with Mns on Chromosome-4. Cytogenetics and Cell Genetics, 46(1-4), 666–666.

Murray, J. C., Shiang, R., Carlock, L. R., Smith, M. & Buetow, K. H. (1987). Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci. Human genetics, 76(3), 274-7. PMID: 2885257.

Murray, J. C., Buetow, K. H., Donovan, M., Hornung, S., Motulsky, A. G., Disteche, C., Dyer, K., Swisshelm, K., Anderson, J. & Giblett, E. (1987). Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. American journal of human genetics, 40(4), 338-50. PMID: 2883890.

Buetow, K. H., Murray, J. C., Redeker, A., Govindarajan, S. & London, W. T. (1987). Loss of heterozygosity in primary hepatocellular carcinoma (PHC) suggests recessive oncogenes on chromosome 4q. 37th annual meeting of the American Society of Human Genetics.

Ionasescu, V., Anderson, R., Ginns, E., Ferrell, R., Murray, J. C., Burns, T., Searby, C. H. & Ionasescu, R. (1987). Linkage between autosomal dominant Charcot-Marie-tooth (CMT) neuropathy type l and long arm chromosome 1 markers. 37th annual meeting of the American Society of Human Genetics.

Ardinger, H. H., Bardach, J., Bell, G. I., Buetow, K. H., Maxey, S. S., Murray, J. C. & Van Denmark, D. R. (1987). Growth factors associated with nonsyndromic cleft lip +/- cleft palate. 37th annual meeting of the American Society of Human Genetics.

Mueller, O. T., Wasmuth, J. J., Murray, J. C., Lozzio, C. B., Lovrien, E. W. & Shows, T. B. (1987). Chromosomal assignment of N-acetylglucosaminylphospho-transferase, the lysosomal hydrolase targeting enzyme deficient in mucolipidosis II and III. 37th annual meeting of the American Society of Human Genetics.

Steele, M. W., Wenger, S. L., Chorazy, A., Huff, F., Dyer, K., Shiang, R. & Murray, J. C. (1987). Chromosome site 4q2l and Huntington Like Disease. 37th annual meeting of the American Society of Human Genetics.

Shiang, R., Bell, G., Divelbiss, J. E., Haskins-Olney, A., Overhauser, J., Wasmuth, J. & Murray, J. C. (1987). Mapping of ADH3, EGF and IL2 in a patient with Riegers-like phenotype and 4q23-q27 deletion. 37th annual meeting of the American Society of Human Genetics.

Murray, J. C., Smith, R. F., Ardinger, H. A. & Weinberger, C. (1987). RFLP for the glucocorticoid receptor (GRL) located at 5q11-5q13. Nucleic acids research, 15(16), 6765. PMID: 2888091.

Ardinger, R. H., Buetow, K. H., Weiss, J. H., Nemer, M., DeHaven, C. R. & Murray, J. C. (1987). Multipoint linkage relationships of 6 loci on 1p (ALPL, GLUT, PGD, PGM1, PND, RH). 37th annual meeting of the American Society of Human Genetics.

Ionasescu, V., Murray, J. C., Burns, T. L., Ionasescu, R., Ferrell, R., Searby, C. & Chirgwin, J. (1987). Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I). Journal of the neurological sciences, 80(1), 73-8. PMID: 3302118.

Smith, R. F., Ardinger, H. A. & Murray, J. C. (1987). Multiple RFLPs demonstrated for epidermal growth factor receptor (EGFR) on chromosome 7. Nucleic acids research, 15(16), 6764. PMID: 2888090.

Cox, T. K., Chakravarti, A. & Murray, J. C. (1987). Phylogenetic relationships between humans and other primates based on albumin/-fetoprotein DNA fragments. 37th annual meeting of the American Society of Human Genetics.

Ferrell, R., Buetow, K., Darby, J., Eichner, J., Murray, J., Smith, R., Waziri, M., Huson, S. & Riccardi, V. (1987). Vonrecklinghausen Neurofibromatosis - a Linkage Study of Candidate and Random Marker Genes. Journal of Medical Genetics, 24(9), 522–524. DOI: 10.1136/jmg.24.9.522.

Murph, Jr, Bale, J., Murray, J. & Stinski, M. (1986). Age-Related Transmission of Cytomegalovirus in Day-Care. Pediatric Research, 20(4), A229–A229.

Chakravarti, A., Cox, T., Buetow, K. & Murray, J. C. (1986). A catarrhini phylogeny based on albumin and alpha-fetoprotein DNA fragments. American Association of Physical Anthropologists.

Williamson, R. A., Weiner, C. P. & Murray, J. C. (1986). Maternal serum fetoprotein in presence of both neural tube defects and chromosome anomalies. pp. 757. Lancet.

Murray, J. C., Buetow, K., Shiang, R., Chakravarti, A., Ferrell, R., Carlock, L., Smith, M., Gilliam, C. & Leppert, M. (1986). Multipoint linkage map of chromosome 4 with ten markers. 36th annual meeting of the American Society of Human Genetics.

Smith, M., HIroshige, S. & Murray, J. C. (1986). Evidence in human hepatomas for structural chromosome changes and alteration in the expression of genes in the region 4q2l-4q27. 36th annual meeting of the American Society of Human Genetics.

Murray, J. C., Buetow, K. H. & Bell, G. I. (1986). RFLPs for transforming growth factor alpha (TGFA) gene at 2p13. Nucleic acids research, 14(17), 7136. PMID: 2876411.

Murray, J. C., DeHaven, C. R. & Bell, G. I. (1986). RFLPs for epidermal growth factor (EGF), a single copy sequence at 4q25-4q27. Nucleic acids research, 14(12), 5117. PMID: 3014442.

Shiang, R., Ferrell, R., Patil, S., Divelbiss, J., Olney, A. & Murray, J. C. (1986). Physical map of markers on the long arm of chromosome 4. l. 36th annual meeting of the American Society of Human Genetics.

Murph, J. R., Bale, Jr, J. F., Murray, J. C., Stinski, M. F. & Perlman, S. (1986). Cytomegalovirus transmission in a Midwest day care center: possible relationship to child care practices. The Journal of pediatrics, 109(1), 35-9. PMID: 3014103.

Murray, J. C. (1986). Identifying genetic risks. Iowa medicine : journal of the Iowa Medical Society, 76(9), 409-11. PMID: 3771163.

Bartley, J. A., Murray, J. C., Ionasescu, V. V. & Pearson, P. L. (1985). X-linked glycerol kinase, adrenal hypoplasia and myopathy maps at Xp2l. Helsinki, Finland: Eighth Human Gene Mapping Workshop.

Murray, J., Buetow, K., Tamaoki, T., Watanabe, K. & Motulsky, A. (1985). Linkage Disequilibrium of Alb and Afp Rflps Predicts 5’ to 3’ Orientation. Cytogenetics and Cell Genetics, 40(1-4), 708–708.

Patil, Sr, Bartley, J., Murray, J., Ionasescu, V. & Pearson, P. (1985). X-Linked Glycerol Kinase, Adrenal Hypoplasia and Myopathy Maps at Xp21. Cytogenetics and Cell Genetics, 40(1-4), 720–720.

Murray, J., Buetow, K., Chung, D. & Aschbacher, A. (1985). Linkage Disequilibrium of Rflps at the Beta-Fibrinogen (fgb) and Gamma-Fibrinogen (fgg) Loci on Chromosome-4. Cytogenetics and Cell Genetics, 40(1-4), 707–708.

Buetow, K., Murray, J. & Ferrell, R. (1985). Linkage Relationship of Plg, Gc and Alb. Cytogenetics and Cell Genetics, 40(1-4), 595–596.

Murray, J. C., Buetow, K., Chung, D. & Aschbacher, A. (1985). Linkage disequilibrium of RFLPs at the beta fibrinogen (FGB) locus on chromosome 4. Helsinki, Finland: Eighth Human Gene Mapping Workshop.

Murray, J. C., Waziri, M., Buetow, K., Ferrell, R. & Aschbacher, A. (1985). No tight linkage between neurofibromatosis and Gc/ALB/AFP/PLG. Eighth Human Gene Mapping Workshop.

Buetow, K., Chakravarti, A., Murray, J. & Ferrell, R. (1985). Multipoint mapping using seriation. 35th annual meeting of the American Society of Human Genetics.

Aschbacher, A., Buetow, K., Chung, D., Walsh, S. & Murray, J. C. (1985). Linkage disequilibrium of RFLPs associated with fibrinogen predict gene order on chromosome 4. 35th annual meeting of the American Society of Human Genetics.

Murray, J. C., Patil, S., Fatemi, C., Aschbacher, A., Buetow, K., Ferrell, R., Miles, J., Smith, M. & Carlock, L. (1985). Effect of a large pericentric inversion of chromosome 4 on meiotic recombination. 35th annual meeting of the American Society of Human Genetics.

Murray, J. C., Buetow, K. H., Aschbacher, A. & Veith, R. (1985). RFLPs and nucleotide heterozygosity in nonhuman primates at the albumin/alpha fetoprotein locus. 35th annual meeting of the American Society of Human Genetics.

Carlock, L., Murray, J. C. & Smith, M. (1985). Use of somatic cell hybrids to generate a genetic and physical linkage map to human chromosome 4. 35th annual meeting of the American Society of Human Genetics.

Murray, J. C., Buetow, K., Tamaoki, T., Watanabe, K. & Motulsky, A. (1985). Linkage disequilibrium of ALB RFLPs predicts 5' to 3' orientation. Helsinki, Finland: Eighth Human Gene Mapping Workshop.

Murray, J. C., Sadler, E., Eddy, R. L. & Shows, T. B. (1985). Evidence for assignment of plasminogen (PLG) to chromosome 6, not chromosome 4. Helsinki, Finland: Eighth Human Gene Mapping Workshop.

Murray, J. C., Watanabe, K., Tamaoki, T., Hornung, S. & Motulsky, A. (1985). RFLPs for the human alphafetoprotein (AFP), at 4q11-4q13. Nucleic acids research, 13(18), 6794. PMID: 2414731.

Murray, J. C., Johnson, J. A. & Bird, T. D. (1985). Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks. Clinical genetics, 28(4), 272-83. PMID: 4064366.

Murray, J. C., Pagon, R. A. (1984). Informed consent for research publication of patient-related data. Clinical research, 32(4), 404-8. PMID: 6509867.

Murray, J. C., Mills, K. A., Demopulos, C. M., Hornung, S. & Motulsky, A. G. (1984). Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. Proceedings of the National Academy of Sciences of the United States of America, 81(11), 3486-90. PMID: 6328518.

Silver, M. H., Murray, J. C. & Pratt, R. M. (1984). Epidermal growth factor stimulates type-V collagen synthesis in cultured murine palatal shelves. Differentiation; research in biological diversity, 27(3), 205-8. PMID: 6334002.

Murray, J. C., Donovan, M., Sadler, E., Homung, S., Anderson, J., Buetow, K., Giblett, E. & Motulsky, A. (1984). Association of DNA and protein polymorphisms at the human plasminogen locus. 34th annual meeting of the American Society of Human Genetics.

Motulsky, A. G., Murray, J. C. (1983). Will Prenatal Diagnosis with Selective Abortion Affect Society's Attitude Toward the Handicapped. In Res Ethics. New York, NY .

Murray, J. C., Karp, L. E., Williamson, R. A., Cheng, E. Y. & Luthy, D. A. (1983). Rh isoimmunization related to amniocentesis. American journal of medical genetics, 16(4), 527-34. PMID: 6419606.

Murray, J. C., Demopulos, C., Mills, K. & Motulsky, A. (1983). Allelic frequencies and linkage disequilibrium of DNA polymorphisms at the albumin locus. 33rd annual meeting of the American Society of Human Genetics.

Mueller, R. F., Murray, J. C., Gelinas, R., Farquhar, M. & Papayannopulous, T. (1983). Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line. Hemoglobin, 7(3), 245-56. PMID: 6307930.

Farquhar, M., Gelinas, R., Tatsis, B., Murray, J. C., Yagi, M., Mueller, R. & Stamatoyannopoulos, G. (1983). Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant. Am J Hum Genet, 35(4), 611-20. PMID: 6192712.

Murray, J. C., Demopulos, C. M., Lawn, R. M. & Motulsky, A. G. (1983). Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. Proceedings of the National Academy of Sciences of the United States of America, 80(19), 5951-5. PMID: 6310605.

Murray, J. C., Johnson, J. & Bird, T. (1983). Etiologic heterogeneity and empiric recurrence risks in Dandy-Walker Malformation (DWM). 33rd annual meeting of the American Society of Human Genetics.

Murray, J. C., Demopulos, C., Lawn, R. & Motulsky, A. (1983). Restriction endonuclease study of analbuminemia and polymorphisms at the human albumin locus. Society for Pediatric Research.

(1983). PMID: 6307930.

Motulsky, A. G., Murray, J. C. (1983). Current Concepts in Hemoglobin Genetics. In Proceedings of 1982 Conference on Hemoglobins in Evolution.

(1983). PMID: 6307930.

Murray, J. C., et al (1982). Risk of Rh sensitization following amniocentesis. (Vols. 34). pp. 103A. Am J Hum Genet.