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Author Details

David G Birch
Retina Foundation of the Southwest
1975
288
75
PMIDPaper TitleJournal TitlePublished Year
36764426Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.Am J Ophthalmol2023
37869030Macular Sensitivity Endpoints in Geographic Atrophy: Exploratory Analysis of Chroma and Spectri Clinical Trials.Ophthalmol Sci2023
37126335Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence.Transl Vis Sci Technol2023
37294701Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel.Transl Vis Sci Technol2023
36764427Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17).Am J Ophthalmol2023
33214244Randomised study evaluating the pharmacodynamics of emixustat hydrochloride in subjects with macular atrophy secondary to Stargardt disease.Br J Ophthalmol2022
35759666The landscape of submicroscopic structural variants at the <i>OPN1LW/OPN1MW</i> gene cluster on Xq28 underlying blue cone monochromacy.Proc Natl Acad Sci U S A2022
35861669Delineating the Clinical Phenotype of Patients With the c.629C&gt;G, p.Pro210Arg Mutation in Peripherin-2.Invest Ophthalmol Vis Sci2022
35781068Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical Results.Ophthalmol Retina2022
35865175Performance of Deep Learning Models in Automatic Measurement of Ellipsoid Zone Area on Baseline Optical Coherence Tomography (OCT) Images From the Rate of Progression of USH2A-Related Retinal Degeneration (RUSH2A) Study.Front Med (Lausanne)2022
36388727RNA-based therapies in inherited retinal diseases.Ther Adv Ophthalmol2022
36007554Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.Am J Ophthalmol2022
35332618Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.Hum Mutat2022
35174801VALIDATION OF A DEEP LEARNING-BASED ALGORITHM FOR SEGMENTATION OF THE ELLIPSOID ZONE ON OPTICAL COHERENCE TOMOGRAPHY IMAGES OF AN USH2A-RELATED RETINAL DEGENERATION CLINICAL TRIAL.Retina2022
35293952The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene.Invest Ophthalmol Vis Sci2022
34695402Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients With Stargardt Disease: SMART Study Report No. 2.Am J Ophthalmol2022
34298008Longitudinal Changes of Fixation Stability and Location Within 24 Months in Stargardt Disease: ProgStar Report No. 16.Am J Ophthalmol2022
32562884Effect of Human Central Nervous System Stem Cell Subretinal Transplantation on Progression of Geographic Atrophy Secondary to Nonneovascular Age-Related Macular Degeneration.Ophthalmol Retina2021
33737949Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases.Front Genet2021
33595255LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.Retina2021
34584045Endpoints for Measuring Efficacy in Clinical Trials for Inherited Retinal Disease.Int Ophthalmol Clin2021
34751740A Hybrid Model Composed of Two Convolutional Neural Networks (CNNs) for Automatic Retinal Layer Segmentation of OCT Images in Retinitis Pigmentosa (RP).Transl Vis Sci Technol2021
34326763Unexpected Etiology in a Case of Bilateral Maculopathy.Case Rep Ophthalmol2021
34185059Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.Invest Ophthalmol Vis Sci2021
34004001Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium.Transl Vis Sci Technol2021
33951446The Progression of Stargardt Disease Using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15.Am J Ophthalmol2021
33465333Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene <i>CNGB1</i>.Ophthalmic Genet2021
32222369Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14.Am J Ophthalmol2020
31953110X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.Ophthalmol Retina2020
33425925Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy.Front Cell Dev Biol2020
33133772The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.Transl Vis Sci Technol2020
32832227Quantification of RPE Changes in Choroideremia Using a Photoshop-Based Method.Transl Vis Sci Technol2020
32832209Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.Transl Vis Sci Technol2020
32821486Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1).Transl Vis Sci Technol2020
32818077Application of a Deep Machine Learning Model for Automatic Measurement of EZ Width in SD-OCT Images of RP.Transl Vis Sci Technol2020
32422174The Effect of Attention on Fixation Stability During Dynamic Fixation Testing in Stargardt Disease.Am J Ophthalmol2020
32446738Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.Am J Ophthalmol2020
32441177A novel SVA retrotransposon insertion in the <i>CHM</i> gene results in loss of REP-1 causing choroideremia.Ophthalmic Genet2020
32463436Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13.JAMA Ophthalmol2020
30582903Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa.Am J Ophthalmol2019
29940588Scotopic Microperimetric Assessment of Rod Function in Stargardt Disease (SMART) Study: Design and Baseline Characteristics (Report No. 1).Ophthalmic Res2019
29925512Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.Br J Ophthalmol2019
31589764Retinal Sensitivity Using Microperimetry in Age-Related Macular Degeneration in an Amish Population.Ophthalmic Surg Lasers Imaging Retina2019
31211001Reliability of Semiautomated Kinetic Perimetry (SKP) and Goldmann Kinetic Perimetry in Children and Adults With Retinal Dystrophies.Transl Vis Sci Technol2019
30703401Microperimetry for geographic atrophy secondary to age-related macular degeneration.Surv Ophthalmol2019
31171998Histopathologic Assessment of Optic Nerves and Retina From a Patient With Chronically Implanted Argus II Retinal Prosthesis System.Transl Vis Sci Technol2019
31021898CHOROIDEREMIA: Retinal Degeneration With an Unmet Need.Retina2019
31019847A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned.Transl Vis Sci Technol2019
30901388Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations.Invest Ophthalmol Vis Sci2019
30297337Macular spatial distribution of preserved autofluorescence in patients with choroideremia.Br J Ophthalmol2019
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Collaborators

Doheny Eye Institute, University of California Los Angeles
Co-authored papers 21
Casey Eye Institute at Oregon Health & Science University (OHSU)
Co-authored papers 20
Institute of Molecular and Clinical Ophthalmology Basel
Co-authored papers 20
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
Co-authored papers 19
University of California san francisco
Co-authored papers 18
Institute of Ophthalmology, University College London
Co-authored papers 16
Wilmer Eye Institute, Johns Hopkins University (S.W.
Co-authored papers 13
Casey Eye Institute, Oregon Health & Science University
Co-authored papers 12
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
Co-authored papers 11
University of Illinois at Chicago
Co-authored papers 10
Bascom Palmer Eye Institute
Co-authored papers 10
University of Michigan (A.T.F.) ann arbor
Co-authored papers 8
Foundation Fighting Blindness
Co-authored papers 8
Co-authored papers 7
Foundation Fighting Blindness
Co-authored papers 6
University Eye Hospital, University of Tubingen
Co-authored papers 6
College of Animal Science and Technology, Guangxi University
Co-authored papers 6
National Eye Institute, National Institutes of Health
Co-authored papers 6
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 5
National Eye Institute, National Institutes of Health
Co-authored papers 5
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 5
Radboud University Medical Center
Co-authored papers 5
Wills Eye Hospital/Mid Atlantic Retina
Co-authored papers 5
University of Utah
Co-authored papers 5
Cullen Eye Institute, Baylor College of Medicine
Co-authored papers 4
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 4
Institute of Ophthalmology, University College London
Co-authored papers 4
The Genome Center at Washington University, Washington University School of Medicine
Co-authored papers 4
University of Washington
Co-authored papers 3
Institut de Genetique Medicale d'Alsace, Hopitaux Universitaires de Strasbourg
Co-authored papers 3