Available to mentor
Wendy R. Uhlmann, MS, LCGC, is the director/senior genetic counselor of the Medical Genetics Clinic (adults). She is a Clinical Professor in the Departments of Internal Medicine and Human Genetics and notably was the first faculty member to achieve this rank in the medical school with a master’s degree. She is an executive faculty member of the Genetic Counseling Program and an executive committee member of University of Michigan’s ELSI (ethical, legal and social implications) Research Training Program, member of the IMPOWER Council (addressing issues of DEI and Wellness) and Adult Ethics Committee.
Wendy Uhlmann is a Past President of the National Society of Genetic Counselors (NSGC) and previously served on the Board of Directors of the Genetic Alliance, NSGC’s liaison to the National Advisory Council for Human Genome Research and on the ELSI Congress Organizing Committee. Currently she serves on the Board of Directors of the American Society of Human Genetics, the Editorial Board of the Journal of Genetic Counseling and the Scientific Advisory Board of the Michigan Biotrust.
Wendy Uhlmann co-edited the first two editions of the book “A Guide to Genetic Counseling,” which is used internationally in genetic counseling graduate programs. She teaches in courses in the genetic counseling program, medical school and School of Public health in addition to providing clinical supervision for trainees and serving as a research mentor. Wendy Uhlmann was the recipient of NSGC’s Regional Leadership Award (1996), the Outstanding Volunteer Award (2009), the Natalie Weissberger Paul Lifetime Achievement Award (2011) and University of Michigan’s Basic Sciences Teaching Award in Human Genetics (2013).
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Center MemberCenter for Bioethics and Social Sciences in Medicine
Predictive genetic testing
Ethical issues and genetics
Return of results (research and clinical)
Genetics policy issues
Integration of genetics into healthcare
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Charnysh E, Pal S, Reader JM, Uhlmann WR, McCain S, Sanghavi K, Blasco D, Brandt R, Feero WG, Ferber R, Giri VN, Hendy K, Prince AER, Lee C, Roberts JS, INSIGHT @ Work Consortium . Genet Med, 2024 Aug; 26 (8): 101160Journal ArticleHealth care utilization and behavior changes after workplace genetic testing at a large US health care system.
DOI:10.1016/j.gim.2024.101160 PMID: 38733246 -
Trachtman H, Desmond H, Williams AL, Mariani LH, Eddy S, Ju W, Barisoni L, Ascani HK, Uhlmann WR, Spino C, Holzman LB, Sedor JR, Gadegbeku C, Subramanian L, Lienczewski CC, Manieri T, Roberts SJ, Gipson DS, Kretzler M, NEPTUNE investigators . Kidney Int, 2024 Feb; 105 (2): 218 - 230.Journal ArticleRationale and design of the Nephrotic Syndrome Study Network (NEPTUNE) Match in glomerular diseases: designing the right trial for the right patient, today.
DOI:10.1016/j.kint.2023.11.018 PMID: 38245210 -
Charnysh E, Pal S, Reader J, McCain S, Hendy K, Sanghavi K, Uhlmann W, Feero W, Prince A, Brandt R, Ferber R, Giri V, Lee C, Roberts JS. Genetics in Medicine Open, 2024 2: 101778Journal ArticleP864: Employees’ views and healthcare utilization following employer-sponsored pharmacogenomic testing at a large US healthcare system
DOI:10.1016/j.gimo.2024.101778 -
Dratch L, Kinnamon DD, Harrington EA, Goldman J, Fong JC, Jones T, Uhlmann WR, Roggenbuck J. Amyotroph Lateral Scler Frontotemporal Degener, 2024 Nov; 25 (7-8): 797 - 799.Journal ArticleResponse to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion".
DOI:10.1080/21678421.2024.2362854 PMID: 38902980 -
Willard L, Uhlmann W, Prince AER, Blasco D, Pal S, Roberts JS, INSIGHT @ Work Consortium . J Genet Couns, 2024 Jul 22;Journal ArticleThe Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States.
DOI:10.1002/jgc4.1945 PMID: 39037108 -
Goldman JS, Uhlmann WR, Naini AB, Klitzman RL, Marder KS. Mov Disord, 2023 Dec; 38 (12): 2151 - 2154.Journal ArticleGenetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines.
DOI:10.1002/mds.29650 PMID: 37975739 -
Gerido LH, Griggs JJ, Resnicow K, Kidwell KM, Delacroix E, Austin S, Hanson EN, Bacon E, Koeppe E, Goodall S, Demerath M, Rizzo EA, Weiner S, Hawley ST, Uhlmann WR, Roberts JS, Stoffel EM. Trials, 2023 Feb 10; 24 (1): 105Journal ArticleThe Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial.
DOI:10.1186/s13063-023-07125-2 PMID: 36765432 -
Cohn B, Ryan KA, Hendy K, Callahan K, Roberts JS, Spector-Bagdady K, Mathews DJH, INSIGHT @ Work Consortium . Mol Genet Genomic Med, 2023 Nov; 11 (11): e2245Journal ArticleGenomic testing in voluntary workplace wellness programs in the US: Evidence and challenges.
DOI:10.1002/mgg3.2245 PMID: 37592452