AlaMoshiriMD

Ophthalmology • Sacramento, CA

Cataract Related, Retinal Disease

Assistant Professor, Ophthalmology, University of California, Davis, School of Medicin

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Office
4860 Y St
Sacramento, CA 95817
Phone+1 916-734-6074

Fax+1 916-734-6197

Education & Training

Johns Hopkins UniversityResidency, Ophthalmology, 2007 - 2010
University of Texas Health Science Center at HoustonInternship, Transitional Year, 2006 - 2007
University of Washington School of MedicineClass of 2006

Certifications & Licensure

CA State Medical License 2012 - 2025
MD State Medical License 2010 - 2015
American Board of Ophthalmology Ophthalmology

Awards, Honors, & Recognition

CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2013

Clinical Trials

Ocriplasmin Research to Better Inform Treatment (ORBIT) Start of enrollment: 2014 May 01
Completed

Publications & Presentations

PubMed

Stimulating the regenerative capacity of the human retina with proneural transcription factors in 3D cultures.
Juliette Wohlschlegel, Faith Kierney, Kayla L Arakelian, Guillaume Luxardi, Naran Suvarnpradip
Proceedings of the National Academy of Sciences of the United States of America. 2025-01-21
Onset and Progression of Disease in Nonhuman Primates With PDE6C Cone Disorder.
Monica Ardon, Lily Nguyen, Rui Chen, Jeffrey Rogers, Tim Stout
Investigative Ophthalmology & Visual Science. 2024-12-02
VEGF inhibition increases expression of HIF-regulated angiogenic genes by the RPE limiting the response of wet AMD eyes to aflibercept.
Deepti Sharma, Evan Lau, Yu Qin, Kathleen Jee, Murilo Rodrigues
Proceedings of the National Academy of Sciences of the United States of America. 2024-11-12

Journal Articles

A Population Study of Common Ocular Abnormalities in C57BL/6N
Ala Moshiri, MD, Investigative Ophthalmology and Visual Science

Press Mentions

Managing Retinal Complications of KProMarch 10th, 2023
Patterns and Predictors of Successful Treatment Discontinuation in Retinal Vein Occlusions with Macular Edema in the Real WorldFebruary 24th, 2021
Biallelic UBE4A Loss-of-Function Variants Cause Intellectual Disability and Global Developmental DelayJanuary 8th, 2021
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