RichardGordonWeleberMD
Ophthalmology • Portland, ORRetinal Disease
Professor, Ophthalmology, Oregon Health and Science University School of Medicine
Dr. Weleber 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
3181 SW Sam Jackson Park Rd
Portland, OR 97239Phone+1 503-494-8311
Education & Training
University of ColoradoFellowship, Medical Genetics and Genomics, 1975 - 1977
Oregon Health & Science University (OHSU Health)Residency, Ophthalmology, 1971 - 1975- Oregon Health Science University HospitalFellowship, Clinical Biochemical Genetics, 1971 - 1972
- Oregon Health & Science UniversityFellowship, Medical Genetics and Genomics, 1971 - 1972
University of Vermont Medical CenterInternship, Transitional Year, 1967 - 1968
Oregon Health and Science University School of MedicineClass of 1967
Certifications & Licensure
OR State Medical License 1972 - 2023
CO State Medical License 1975 - 1977- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Ophthalmology Ophthalmology
Awards, Honors, & Recognition
- Fellow (FAAO) American Academy of Ophthalmology
- Fellow American College of Medical Genetics, 1993
- Diplomate American Board of Medical Genetids, 1981
- Join now to see all
Clinical Trials
- Phase I/IIA Study of SAR422459 in Participants With Stargardt's Macular Degeneration Start of enrollment: 2011 Jun 08
- Study of SAR421869 in Participants With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B Start of enrollment: 2012 Mar 26
- Clinical and Genetic Characterization of Individuals With Achromatopsia Start of enrollment: 2013 Jun 01
- Join now to see all
Publications & Presentations
PubMed
- 45 citationsREPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.Christopher S Langlo, Laura R Erker, Maria Parker, Emily J. Patterson, Brian P. Higgins
Retina. 2017-10-01 - 201 citationsLeber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventionsNeruban Kumaran, Anthony T. Moore, Richard G. Weleber, Michel Michaelides
The British Journal of Ophthalmology. 2017-07-08 - 59 citationsQuantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.Amir H Hariri, Hong Yang Zhang, Alexander Ho, Peter J. Francis, Richard G. Weleber
JAMA Ophthalmology. 2016-06-01
Journal Articles
- Strategies for Treating Inherited Retinal Degeneration with Large Genes That Are Not Amenable to Adeno-Associated Virus–Based Gene Replacement TherapyMark E Pennesi, Richard G Weleber, JAMA Ophthalmology
- Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients with Autosomal Dominant Retinitis PigmentosaDavid G Birch, Michael P Teske, Richard G Weleber, Robert Lindblad, Byron L Lam, Judith Warner, Gary Edd Fish, Neal L Sklaver, Mark E Pennesi, John Heckenlively, Paul ..., JAMA
Press Mentions
In Surprise Result, Gene Therapy Reverses Blinding Eye DiseaseMarch 15th, 2018
New Study Shows Children Benefited Most from Gene Therapy for LCA, a Rare Eye DiseaseApril 15th, 2016
Professional Memberships
- Fellow
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
