SamanthaAlexandraVerganoMDFAAP, FACMG

Clinical Genetics

Associate Medical Director, Outpatient Services, Division of Genetic Medicine, Seattle Children's Hospital Professor, Pediatrics, University of Washington

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Office
4800 Sand Point Way NE
Seattle, WA 98105
Phone+1 206-987-2000

Summary

Dr. Samantha Vergano is a medical geneticist currently practicing at Seattle Children's Hospital. She received her medical degree from Eastern Virginia Medical School and has been in practice 12 years. She specializes in clinical genetics and is experienced in intellectual disability, multiple congenital anomalies, dysmorphology, and inborn errors of metabolism. Her research interests include disability ethics and Coffin-Siris Syndrome.

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

Different, Not Less.
Samantha A Schrier Vergano
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2024-11-01
ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals.
Samantha A Schrier Vergano
American Journal of Medical Genetics. Part A. 2024-06-01
4 citations
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Francesca Peluso, Stefano G Caraffi, Gianluca Contrò, Lara Valeri, Manuela Napoli
Journal of Medical Genetics. 2023-11-27

Journal Articles

The ARID1B Spectrum in 143 Patients: From Nonsyndromic Intellectual Disability to Coffin–Siris Syndrome
Ellen 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