RobertS.WildinMD
Medical Genetics • Burlington, VTClinical Genetics, Pediatric Medical Genetics
Associate Professor of Pathology and Laboratory Medicine and Pediatrics; Associate Medical Director of the Genomic Medicine Program, University of Vermont Health Network, University of Vermont Larner College of Medicine
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Office
111 Colchester Ave
Burlington, VT 05401Phone+1 802-847-0000
Summary
- Dr. Robert Wildin is a clinical and laboratory geneticist in Burlington, VT and is affiliated with University of Vermont Medical Center. He received his medical degree from University of California San Francisco School of Medicine, trained in Pediatrics and Genetics at the University of Washington, and has been in practice more than 30 years. His special interests are medical informatics (vis a vis genetics) and genomic population health.
Clinical Expertise
- Diagnosis and management of inherited disorders, Somatic tumor NGS results interpretation, Genomic population health testing, Germline genetic test interpretation, Healthcare data solutions design
Education & Training
University of WashingtonResidency, Medical Genetics and Genomics, 1988 - 1992- University of WashingtonResidency, Pediatrics, 1985 - 1988
University of California San Francisco School of MedicineClass of 1985
Massachusetts Institute of Technology (MIT)BS, Biology, Phi Beta Kappa, 1977 - 1981
Certifications & Licensure
VT State Medical License 2017 - 2026
OR State Medical License 1997 - 2019
VA State Medical License 2015 - 2018
ID State Medical License 2003 - 2017
TX State Medical License 1994 - 1999- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 202 citationsLoss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculatureJan Kazenwadel, Genevieve A. Secker, Yajuan J. Liu, Jill A. Rosenfeld, Robert S. Wildin
Blood. 2012-02-02 - 31 citationsCorrelation of linkage data with phenotype in eight families with Stickler syndrome.Douglas J. Wilkin, Geert Mortier, Carey L. Johnson, Marilyn C. Jones, Anne De Paepe
American Journal of Medical Genetics. 1998-11-02 - 45 citationsHeterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus.R. S. Wildin, M. J. Antush, R. L. Bennett, J. M. Schoof, C. R. Scott
American Journal of Human Genetics. 1994-08-01
Press Mentions
Care Board Approves OneCare Budget with Eye on Administrative SpendingDecember 17th, 2018
G2C2 Expands Genomic Resources for Health ProfessionalsMay 12th, 2017
Professional Memberships
- American Society of Human GeneticsMember
- European Society of Human GeneticsMember
- American College of Medical Genetics and GenomicsMember
External Links
- NHGRI Profilehttps://www.genome.gov/27562112/
- UVM Med Ctrhttps://www.uvmhealth.org/medcenter/provider/robert-s-wildin-md
- Larner College of Medicinehttps://www.med.uvm.edu/pediatrics/bio?BioID=32761
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