Professor, Ophthalmology, Oregon Health and Science University School of Medicine
Ophthalmology
Dr. Richard G. Weleber, MD
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Richard Weleber practices Ophthalmology. He went to Oregon Health & Science University School of Medicine. He has 3 awards "CMS Meaningful Use Stage 1 Certification", "Top MD" and "Fellow (FAAO)". Richard G. Weleber has written publications. He has 52 publications published with PubMed. The lastest publication is: 'Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa.' He is registered with Medicare.
Publications
- Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
- Advancing therapeutic strategies for inherited retinal Degeneration: recommendations from the Monaciano Symposium.
- Retinal Morphology of Patients With Achromatopsia During Early Childhood: Implications for Gene Therapy.
- Randomized Trial of Ciliary Neurotrophic Factor Delivered by Encapsulated Cell Intraocular Implants for Retinitis Pigmentosa.
- Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis.
- Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies.
- Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database.
- Variability in Isopter Position and Fatigue during Semi-Automated Kinetic Perimetry.
- Autosomal Recessive Retinitis Pigmentosa caused by Mutations in the MAK Gene.
- Residual Electroretinograms in Young Leber Congenital Amaurosis Patients with Mutations of AIPL1.
- Acute Macular outer retinopathy (AMOR): a reappraisal of acute Macular neuroretinopathy using multimodality diagnostic testing.
- The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.
- Retinal toxicity associated with hydroxychloroquine and chloroquine: risk factors, screening, and progression despite cessation of therapy.
- Mutations in FLVCR1 cause posterior column ataxia and retinitis pigmentosa.
- Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children.
- Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.
- High-resolution optical coherence tomography shows new aspects of Bietti crystalline retinopathy.
- Molecular biomarkers for autoimmune retinopathies: significance of anti-transducin-alpha autoantibodies.
- Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best Macular dystrophy.
- Comparison of the new perimetric GATE strategy with conventional full-threshold and SITA standard strategies.
- Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene.
- Conorenal dysplasia: a syndrome of cone-shaped epiphysis, renal disease in childhood, retinitis pigmentosa and abnormality of the proximal femur.
- Microcephaly with chorioretinopathy in a brOther-sister pair: evidence for germ line mosaicism and further delineation of the ocular phenotype.
- Molecular testing for hereditary retinal disease as part of clinical care.
- Joubert syndrome surviving to adulthood associated with a progressive movement disorder.
- Haplotypes in the complement factor H (CFH) gene: associations with drusen and advanced age-related Macular degeneration.
- Expanded genome scan in extended families with age-related Macular degeneration.
- Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups.
- A network of patients with orphan retinal diseases for clinical trials: goals, structure, challenges.
- Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene.
- Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.
- Outcome measures and their application in clinical trials for retinal Degenerative diseases: outline, review, and perspective.
- Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neuroDegeneration (formerly Hallervorden-Spatz syndrome).
- Stop mutations in exon 6 of the Choroideremia gene, CHM, associated with preservation of the electroretinogram.
- Clinical and electrophysiologic characterization of paraneoplastic and autoimmune retinopathies associated with antienolase antibodies.
- Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes.
- Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatus.
- Distal arthrogryposis 5: a dominant syndrome of peripheral contractures and ophthalmoplegia.
- Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease).
- MultiFocal electroretinographic evaluation of long-term hydroxychloroquine users.
- Bietti crystalline corneoretinal Dystrophy is caused by mutations in the novel gene CYP4V2.
- Clinical phenotype as a prognostic factor in Stargardt disease.
- Treatment of retinal and choroidal Degenerations and dystrophies: current status and prospects for gene-based therapy.
- Age-related Macular degeneration--a genome scan in extended families.
- Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23.
- Lack of an association of apolipoprotein E gene polymorphisms with familial age-related Macular degeneration.
- Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
- Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.
- Electronegative electroretinogram in mucolipidosis IV.
- Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa.
- Choroideremia associated with Choroidal neovascularization treated with intravitreal bevacizumab.
Schools
Oregon Health And Science University School Of Medicine
Fletcher Allen Health Care
Or Health Science University Hospital
Conditions Treated
- Age-Related Macular Degeneration
- Aphakia and Other Disorders of Lens
- Astigmatism
- Benign Neoplasm of Choroid
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Doctors Specialties
- Clinical Genetics
- Ophthalmology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- Top MD
- Fellow (FAAO)
Education
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Oregon Health & Science University -
University of Vermont - Fletcher Allen Health Care -
Oregon Health & Science University School of Medicine
Drug Facts
| NPI NUMBER | 1134171465 | |
| NPPES Provider LastName | WELEBER | |
| NPPES Provider FirstName | RICHARD | |
| NPPES Provider ZIPCode | 97239 | |
| NPPES Provider State | OR | |
| Specialty Description | Ophthalmology | |
| Total Claim Count | 12.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1134171465 |
| Last Name Of The Provider | WELEBER |
| First Name Of The Provider | RICHARD |
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