Colleen Campbell, PhD, MS, LGC
Clinical Associate Professor of Internal Medicine-Cardiovascular Medicine
Current Positions
- Clinical Associate Professor of Internal Medicine-Cardiovascular Medicine
- Director, Genetic Counseling Operations, University of Iowa Hospitals & Clinics
- Assistant Director, Iowa Institute of Human Genetics
Education
- MS, Human Genetics, Sarah Lawrence College, Bronxville, New York
- PhD, Genetics, University of Iowa, Iowa City, Iowa
Center, Program and Institute Affiliations
Licenses & Certifications
- Licensed Genetic Counselor, Iowa Board of Medicine
- Certified Genetic Counselor, American Board of Genetic Counseling
Selected Publications
- Berkovic, S. F., Goldstein, D. B., Heinzen, E. L., Laughlin, B. L., Lowenstein, D. H., Lubbers, L., Stewart, R., Whittemore, V., Angione, K., Bazil, C. W., Bier, L., Bluvstein, J., Brimble, E., Campbell, C., Cavalleri, G., Chambers, C., Choi, H., Cilio, M. R., Ciliberto, M., Cornes, S., Delanty, N., Demarest, S., Devinsky, O., Dlugos, D., Dubbs, H., Dugan, P., Ernst, M. E., Gibbons, M., Goodkin, H. P., Helbig, I., Jansen, L., Johnson, K., Joshi, C., Lippa, N. C., Marsh, E., Martinez, A., Millichap, J., Mulhern, M. S., Numis, A., Park, K., Pippucci, T., Poduri, A., Porter, B., Regan, B., Sands, T. T., Scheffer, I. E., Schreiber, J. M., Sheidley, B., Singhal, N., Smith, L., Sullivan, J., Taylor, A., Tolete, P., Afgani, T. M., Aggarwal, V., Burgess, R., Dixon-Salazar, T., Hemati, P., Milder, J., Petrovski, S., Revah-Politi, A. & Stong, N. (2019). The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield. Epilepsia 60 (5) 797-806. DOI: 10.1111/epi.14698.
- Berkovic, S. F., Grinton, B., Dixon-Salazar, T., Laughlin, B. L., Lubbers, L., Milder, J., Goldstein, D. B., Heinzen, E. L., Bier, L., Ernst, M. E., Lippa, N. C., Mulhern, M. S., Afgani, T. M., Aggarwal, V., Stong, N., Lowenstein, D. H., Cornes, S., Johnson, K., Stewart, R., Whittemore, V., Angione, K., Demarest, S., Gibbons, M., Joshi, C., Park, K., Bazil, C. W., Choi, H., Bluvstein, J., Devinsky, O., Dugan, P., Tolete, P., Brimble, E., Campbell, C., Chambers, C., Goodkin, H., Jansen, L., Cilio, M. R., Numis, A., Singhal, N., Sullivan, J., Ciliberto, M., Delanty, N., Delanty, N., Dlugos, D., Dubbs, H., Helbig, I., Marsh, E., Martinez, A., Gallentine, W., Makati, M. A., Millichap, J., Moskovich, Y., Millichap, J., Poduri, A., Sheidley, B., Smith, L., Taylor, A., Porter, B., Sands, T. T., Riviello, J. J., Scheffer, I. E., Allen, A. S., Hamid, R., Helbig, K. L., Tang, S., Meisler, M. H., Petrovski, S. & Pfotenhauer, J. (2018). De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy. Genetics in Medicine 20 (2) 275-281. DOI: 10.1038/gim.2017.100.
- Zierhut, H. A., Campbell, C. A., Mitchell, A. G., Lemke, A. A., Mills, R. & Bishop, J. R. (2017). Collaborative Counseling Considerations for Pharmacogenomic Tests. Pharmacotherapy 37 (9) 990-999. PMID: 28672074.
- Kirsch, H., Slavotinek, A., Cilio, M. R., Cervenka, M. C., Cohen, J. S., McClellan, R., Fatemi, A., Yuen, A., Sagawa, Y., Littlejohn, R., McLean, S. D., Hernandez-Hernandez, L., Maher, B., Møller, R. S., Palmer, E., Lawson, J. A., Campbell, C. A., Joshi, C. N., Kolbe, D. L., Hollingsworth, G., Neubauer, B. A., Muhle, H., Stephani, U., Scheffer, I. E., Pena SDJ, Sisodiya, S. M., Helbig, I., von Spiczak, S., Helbig, K. L., Shinde, D. N., Huether, R., Pendziwiat, M., Lourenço, C., Nunes, M. E., Sarco, D. P., Kaplan, R. A. & Dlugos, D. J. (2017). DNM1 encephalopathy: A new disease of vesicle fission. Neurology 89 (4) 385-394. PMID: 28667181.
- Thomas, C. P., Mansilla, M. A., Sompallae, R., Mason, S. O., Nishimura, C. J., Kimble, M. J., Campbell, C. A., Kwitek, A. E., Darbro, B. W., Stewart, Z. A. & Smith, R. J. (2017). Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing Strategy. American Journal of Transplantation : Official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 17 (2) 401-410. PMCID: PMC5297870.
- Joshi, C., Kolbe, D. L., Mansilla, M. A., Mason, S., Smith, R. J. & Campbell, C. A. (2016). Ketogenic diet - A novel treatment for early epileptic encephalopathy due to PIGA deficiency. Brain and Development 38 (9) 848-51. PMID: 27126216.
- Sloan-Heggen, C. M., Bierer, A. O., Shearer, A. E., Kolbe, D. L., Nishimura, C. J., Frees, K. L., Ephraim, S. S., Shibata, S. B., Booth, K. T., Campbell, C. A., Ranum, P. T., Weaver, A. E., Black-Ziegelbein, E. A., Wang, D., Azaiez, H. & Smith, R. J. (2016). Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Human Genetics 135 (4) 441-50. PMID: 26969326.
- Joshi, C., Kolbe, D. L., Mansilla, M. A., Mason, S. O., Smith, R. J. & Campbell, C. A. (2016). Reducing the Cost of the Diagnostic Odyssey in Early Onset Epileptic Encephalopathies. BioMed Research International 2016 6421039. PMCID: PMC4875968.
- Zong, L., Guan, J., Ealy, M., Zhang, Q., Wang, D., Wang, H., Zhao, Y., Shen, Z., Campbell, C. A., Wang, F., Yang, J., Sun, W., Lan, L., Ding, D., Xie, L., Qi, Y., Lou, X., Huang, X., Shi, Q., Chang, S., Xiong, W., Yin, Z., Yu, N., Zhao, H., Petit, C., Smith, R. J., Wang, Q., Wang, J., Wang, J. & Salvi, R. J. (2015). Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder. Journal of Medical Genetics 52 (8) 523-31. PMID: 25986071.
- Supper, J., Gugenmus, C., Klocke, B., Hahn, A., Schubach, M., Menzel, M., Biskup, S., Freisinger, P., Deng, M., Braun, M., Perner, S., Smith, R. J., Andorf, J. L., Huang, J., Ryckman, K., Sheffield, V. C., Stone, E. M., Bair, T., Black-Ziegelbein, E. A., Braun, T. A., Darbro, B., DeLuca, A. P., Kolbe, D. L., Scheetz, T. E., Shearer, A. E., Sompallae, R., Wang, K., Bassuk, A. G., Edens, E., Mathews, K., Moore, S. A., Shchelochkov, O. A., Trapane, P., Bossler, A., Campbell, C. A., Heusel, J. W., Kwitek, A., Maga, T., Panzer, K., Wassink, T., Van Daele, D., Azaiez, H., Booth, K., Meyer, N., Segal, M. M., Williams, M. S., Tromp, G., White, P., Corsmeier, D., Fitzgerald-Butt, S., Herman, G., Lamb-Thrush, D., McBride, K. L., Newsom, D., Pierson, C. R., Rakowsky, A. T., Maver, A., Lovrečić, L., Palandačić, A., Peterlin, B., Torkamani, A., Wedell, A., Huss, M., Alexeyenko, A., Lindvall, J. M., Magnusson, M., Nilsson, D., Stranneheim, H., Taylan, F., Gilissen, C., Hoischen, A., van Bon, B., Yntema, H., Nelen, M., Zhang, W., Sager, J., Zhang, L., Blair, K., Kural, D., Cariaso, M., Lennon, G. G., Javed, A., Agrawal, S., Ng, P. C., Sandhu, K. S., Krishna, S., Veeramachaneni, V., Isakov, O., Halperin, E., Friedman, E., Shomron, N., Glusman, G., Roach, J. C., Caballero, J., Cox, H. C., Mauldin, D., Ament, S. A., Rowen, L., Richards, D. R., San Lucas, F. A., Gonzalez-Garay, M. L., Caskey, C. T., Bai, Y., Huang, Y., Fang, F., Zhang, Y., Wang, Z., Barrera, J., Garcia-Lobo, J. M., González-Lamuño, D., Llorca, J., Rodriguez, M. C., Varela, I., Reese, M. G., De La Vega, F. M., Kiruluta, E., Cargill, M., Hart, R. K., Sorenson, J. M., Lyon, G. J., Stevenson, D. A., Bray, B. E., Moore, B. M., Eilbeck, K., Yandell, M., Zhao, H., Hou, L., Chen, X., Yan, X., Chen, M., Li, C., Yang, C., Gunel, M., Li, P., Kong, Y., Alexander, A. C., Albertyn, Z. I., Boycott, K. M., Bulman, D. E., Gordon, P. M., Innes, A. M., Knoppers, B. M., Majewski, J., Marshall, C. R., Parboosingh, J. S., Sawyer, S. L., Samuels, M. E., Schwartzentruber, J., Kohane, I. S., Margulies, D. M., Brownstein, C. A., Beggs, A. H., Homer, N., Merriman, B., Yu, T. W., Flannery, K. C., DeChene, E. T., Towne, M. C., Savage, S. K., Price, E. N., Holm, I. A., Luquette, L. J., Lyon, E., Majzoub, J., Neupert, P., McCallie, Jr, D., Szolovits, P., Willard, H. F., Mendelsohn, N. J., Temme, R., Finkel, R. S., Yum, S. W., Medne, L., Sunyaev, S. R., Adzhubey, I., Cassa, C. A., de Bakker, P. I., Duzkale, H., Dworzyński, P., Fairbrother, W., Francioli, L., Funke, B. H., Giovanni, M. A., Handsaker, R. E., Lage, K., Lebo, M. S., Lek, M., Leshchiner, I., MacArthur, D. G., McLaughlin, H. M., Murray, M. F., Pers, T. H., Polak, P. P., Raychaudhuri, S., Rehm, H. L., Soemedi, R., Stitziel, N. O. & Vestecka, S. (2014). An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biology 15 (3) R53. PMID: 24667040.