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Office
601 Childrens Ln
Division Of Medical Genetics And Metabolism
Norfolk, VA 23507Phone+1 757-668-9723Fax+1 757-668-9724
Summary
- Dr. Samantha Vergano is a medical geneticist in Norfolk, VA and is affiliated with multiple hospitals in the area, including Children's Hospital of The King’s Daughters and Sentara Norfolk General. She received her medical degree from Eastern Virginia Medical School and has been in practice 11 years. She specializes in clinical genetics and is experienced in intellectual disability, multiple congenital anomalies, dysmorphology, and inborn errors of metabolism.
Education & Training
- Children's Hospital of PhiladelphiaResidency, Medical Genetics and Genomics, 2009 - 2012
- Atlantic Health System/Goryeb Children's HospitalResidency, Pediatrics, 2006 - 2009
- Eastern Virginia Medical SchoolClass of 2006
Certifications & Licensure
- VA State Medical License 2012 - 2026
- WA State Medical License 2023 - 2026
- NC State Medical License 2020 - 2022
- PA State Medical License 2009 - 2012
- NJ State Medical License 2007 - 2011
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 35 citationsMolecular and clinical spectra of FBXL4 deficiencyAyman W. El-Hattab, Hongzheng Dai, Mohammed Almannai, Julia Wang, Eissa Faqeih
Human Mutation. 2017-12-01 - 31 citationsMutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.Joery den Hoed, Elke de Boer, Norine Voisin, Alexander J. M. Dingemans, Nicolas Guex
American Journal of Human Genetics. 2021-02-04 - 14 citationsParental Perception and Participation in Genetic Testing Among Children With Autism Spectrum Disorders.John W. Harrington, Leonard Emuren, Kathryn M. Restaino, Samantha A. Schrier Vergano
Clinical Pediatrics. 2018-09-28
Journal Articles
- The ARID1B Spectrum in 143 Patients: From Nonsyndromic Intellectual Disability to Coffin–Siris SyndromeEllen R Elias, Kylin Lammers, Samantha A Vergano, John B Moeschler, Nature
Press Mentions
- De Novo Loss-of-Function Variants in X-linked MED12 Are Associated with Hardikar Syndrome in FemalesNovember 27th, 2020
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