David G Birch

发表

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.

Hatice Duzkale, Hope Northrup, R. Lewis, 2006, Investigative ophthalmology & visual science.

Normative reference ranges for the retinal nerve fiber layer, macula, and retinal layer thicknesses in children.

Yuquan Wen, Jingyun Wang, E. Birch, 2013, American journal of ophthalmology.

Leveraging splice‐affecting variant predictors and a minigene validation system to identify Mendelian disease‐causing variants among exon‐captured variants of uncertain significance

Hui Li, Rui Chen, Yumei Li, 2017, Human mutation.

The transition zone between healthy and diseased retina in patients with retinitis pigmentosa.

Donald C Hood, Vivienne C Greenstein, V. Greenstein, 2011, Investigative ophthalmology & visual science.

Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography.

Xian Zhang, Donald C Hood, D. Hood, 2009, Investigative ophthalmology & visual science.

Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease, and test-retest variability.

Donald C Hood, D. Hood, D. Birch, 2002, Archives of ophthalmology.

A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT.

Donald C Hood, Rithambara Ramachandran, Lisa Zhou, 2013, Translational vision science & technology.

Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease

Mark E Pennesi, Byron L Lam, S. Tsang, 2019, Pharmaceutical Research.

A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa.

Donald C Hood, D. Hood, D. Birch, 2010, Investigative ophthalmology & visual science.

A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa.

R. Spencer, G. Fish, D. Birch, 2004, American journal of ophthalmology.

Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.

Donald C Hood, Yuquan Wen, D. Hood, 2011, Investigative ophthalmology & visual science.

Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.

Austin Roorda, Kavitha Ratnam, Jacque L Duncan, 2011, Investigative ophthalmology & visual science.

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.

Seth Blackshaw, C. Cepko, S. Daiger, 2002, Human molecular genetics.

Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.

Richard G Weleber, SriniVas R Sadda, Frederick L Ferris, 2016, JAMA ophthalmology.

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

Jian Zuo, A. Kennan, S. Daiger, 2003, Molecular vision.

Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa.

Glenn J Jaffe, Richard G Weleber, Weng Tao, 2013, American journal of ophthalmology.