Angela Sun MD
Clinical Biochemical Genetics, Clinical Genetics, Medical Biochemical Genetics
Assistant Professor, Pediatrics, University of Washington School of Medicine
Join to view full profile
3333 Burnet Ave# 4006Cincinnati, OH 45229
Phone+1 513-636-4760
Fax+1 513-636-7297
Join Doximity
As a Doximity member, you’ll join more than three million U.S. healthcare professionals—including 85+% of physicians, and 2/3 of all NPs and PAs—in a private, secure network.
- Gain access to free telehealth tools, such as our "call shielding" and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
You already have 3 invites waiting! - Read the latest clinical news, personalized to your specialty.
Summary
- Dr. Angela Sun, MD is a board certified medical geneticist in Cincinnati, Ohio. She is currently licensed to practice medicine in Ohio, Kentucky, and Washington. She is affiliated with Cincinnati Children's Hospital Medical Center and is an Assistant Professor at University of Washington School of Medicine.
Education & Training
Cedars-Sinai Medical CenterFellowship, Medical Biochemical Genetics, 2011 - 2012- Cedars-Sinai Medical CenterResidency, Medical Genetics and Genomics, 2009 - 2011
University of California (Irvine)/Children's Hospital of Orange CountyResidency, Pediatrics, 2006 - 2009
Saint Louis University School of MedicineClass of 2006
Certifications & Licensure
CA State Medical License 2007 - 2027
KY State Medical License 2025 - 2027
OH State Medical License 2025 - 2027
WA State Medical License 2012 - 2027
American Board of Medical Genetics and Genomics Medical Biochemical Genetics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 1 citationsDisease characteristics, effectiveness, and safety of vestronidase alfa for the treatment of patients with mucopolysaccharidosis VII in a novel, longitudinal, multicen...Roberto Giugliani, Antonio Gonzalez-Meneses, Maurizio Scarpa, Barbara Burton, Raymond Wang
Orphanet Journal of Rare Diseases. 2024-05-07 - 26 citationsDelineating the molecular and phenotypic spectrum of the SETD1B-related syndromeMarjolein J.A. Weerts, Kristina Lanko, Francisco J. Guzmán-Vega, Adam Jackson, Reshmi Ramakrishnan
Genetics in Medicine. 2021-08-03 - 16 citationsHeterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.Thomas A. Ravenscroft, Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy L. Peirce
Genetics in Medicine. 2021-06-10
Press Mentions
The Use of Technology for Communicating with Clinicians or Seeking Health Information in a Multilingual Urban Cohort: Cross-Sectional SurveyApril 6th, 2020
