
Anne V Hing MD
Clinical Genetics
Associate Professor, Pediatrics, University of Washington School of Medicine
Join to View Full Profile
4800 Sand Point Way NESeattle, WA 98105
Phone+1 206-987-2000
Are you Dr. Hing?
Join over one million U.S. Physicians, Nurse Practitioners and PAs, already on Doximity.
- 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.
- Read the latest clinical news, personalized to your specialty.
Summary
- Dr. Anne Hing, MD is a board certified medical geneticist in Seattle, Washington. She is currently licensed to practice medicine in Washington, Alaska, and Idaho. She is an Associate Professor at University of Washington School of Medicine.
Education & Training
- Washington University in St. Louis School of MedicineClass of 1985
- Washington University/B-JH/SLCH ConsortiumResidency, Pediatrics
Certifications & Licensure
- WA State Medical License 1999 - 2027
- AK State Medical License 2021 - 2026
- ID State Medical License 2021 - 2025
- MT State Medical License 2021 - 2025
- IL State Medical License 1994 - 1999
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and Craniosynostosis.Emily R Gallagher, Penny Chow, Maria R Mills, Hazel Perry, Allison C Tam
The Cleft Palate-Craniofacial Journal. 2024-08-18 - Isolated frontosphenoidal craniosynostosis: An argument for genetic testing.Matthew Hodapp, Anne V Hing, Emily Gallagher, Matthew Blessing, Michael L Cunningham
American Journal of Medical Genetics. Part A. 2023-10-01 - 2 citationsDominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.Jonai Pujol-Giménez, Ghayda Mirzaa, Elizabeth E Blue, Giuseppe Albano, Danny E Miller
Annals of Clinical and Translational Neurology. 2023-06-01
Press Mentions
- De Novo Loss-of-Function Variants in X-linked MED12 Are Associated with Hardikar Syndrome in FemalesNovember 27th, 2020