Dr. Vats is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals 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.
- Read the latest clinical news, personalized to your specialty.
Office
4650 W Sunset Blvd
Los Angeles, CA 90027Phone+1 323-361-2178Fax+1 323-361-1172
Education & Training
- University of California (San Francisco)Residency, Medical Genetics and Genomics, 2009 - 2011
- MercyOne Des Moines/PHC ConsortiumResidency, Family Medicine, 2007 - 2009
- Mercy St Vincent Medical Center/Mercy Health PartnersInternship, Transitional Year, 2006 - 2007
- N.H.L Municipal Medical CollegeClass of 1998
Certifications & Licensure
- CA State Medical License 2009 - 2026
- HI State Medical License 2023 - 2026
- IA State Medical License 2007 - 2010
- OH State Medical License 2006 - 2007
- American Board of Family Medicine Family Medicine
- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Phase 2 Study of Triheptanoin (UX007) for the Treatment of Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS) Start of enrollment: 2014 Feb 28
- Mucopolysaccharidosis (MPS) I, II, and VI Screening in a High-Risk Population With Previous Surgical Repair or Presence of Inguinal and/or Umbilical Hernia in Combination With Pediatric ENT Surgery (The HATT Project) Start of enrollment: 2014 May 21
Publications & Presentations
PubMed
- Biliary cirrhosis associated with WDR19-related ciliopathy in siblings.Naseem Ravanbakhsh, Yuri Genyk, Alauna Cheng, Divya Vats, George Yanni
Journal of Hepatology. 2024-12-01 - 24 citationsThe diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?Neal J Weinreb, Ozlem Goker-Alpan, Priya S Kishnani, Nicola Longo, T Andrew Burrow
Molecular Genetics and Metabolism. 2022-05-01 - 8 citationsBiochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the ABCD1 GeneStephanie I. W. van de Stadt, Petra A. W. Mooyer, Inge M. E. Dijkstra, C. Dekker, Divya Vats
Genes. 2021-11-30
Press Mentions
- Newborn Screening Uncovers Hidden Genetic DisordersSeptember 23rd, 2014
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence: