David Wargowski, MD
Position title: Clinical Geneticist
Profile
Dr. Wargowski has received the Madison Magazine Top Docs awards in 2012, 2014 and 2016. He has also received 2015 Physician Excellence Award from the UW Health system. Click here to view a video profile.
Clinics
Professional Certifications and Education
- Board Certification, Clinical Genetics
- MD, University of Wisconsin-Madison
Department Affiliation
- UW School of Medicine and Public Health – Department of Pediatrics
Selected Publications
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Brunet, T., McWalter, K., Mayerhanser, K., Anbouba, G. M., Armstrong-Javors, A., Bader, I., Baugh, E., Begtrup, A., Bupp, C. P., Callewaert, B. L., Cereda, A., Cousin, M. A., Del Rey Jimenez, J. C., Demmer, L., Dsouza, N. R., Fleischer, N., Gavrilova, R. H., Ghate, S., Graf, E., Green, A., … Wagner, M. (2021). Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder. Genetics in Medicine, 23(2), 384–395. https://doi.org/10.1038/s41436-020-00993-y
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Dyment, D. A., O’Donnell-Luria, A., Agrawal, P. B., Coban Akdemir, Z., Aleck, K. A., Antaki, D., Al Sharhan, H., Au, P. B., Aydin, H., Beggs, A. H., Bilguvar, K., Boerwinkle, E., Brand, H., Brownstein, C. A., Buyske, S., Chodirker, B., Choi, J., Chudley, A. E., Clericuzio, C. L., Cox, G. F., … Innes, A. M. (2021). Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome. American Journal of Medical Genetics. Part A, 185(1), 119–133. https://doi.org/10.1002/ajmg.a.61926
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Brin Hermans L, Shields BE, Garland CB, Aagaard-Kienitz B, Wargowski D, Kovarik C, Arkin LM. (2019). Increasing Access to High Value Care: Preventing Complications in Common Disorders. Telemedicine Journal and E-Health, 25(5):423-424. doi: 10.1089/tmj.2018.0003.
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Williams K, Wargowski D, Eickhoff J, Wald E. (2017). Disparities in Health Supervision for Children With Down Syndrome. Clinical Pediatrics, 56(14):1319-1327. doi: 10.1177/0009922816685817.
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Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, et al. (2014). Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. American Journal of Human Genetics, 95(6):729-35. doi: 10.1016/j.ajhg.2014.10.015.
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Werts RL, Van Calcar SC, Wargowski DS, Smith SM. (2014). Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure. Alcoholism: Clinical and Experimental Research, 38(3):871-8. doi: 10.1111/acer.12284.