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Author Details
Full Name
David G Birch
Affiliation
Retina Foundation of the Southwest
ORCID
Career Start Year
1975
Papers
288
H Index
75
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36764426
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.
Am J Ophthalmol
2023
37869030
Macular Sensitivity Endpoints in Geographic Atrophy: Exploratory Analysis of Chroma and Spectri Clinical Trials.
Ophthalmol Sci
2023
37126335
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence.
Transl Vis Sci Technol
2023
37294701
Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel.
Transl Vis Sci Technol
2023
36764427
Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17).
Am J Ophthalmol
2023
33214244
Randomised study evaluating the pharmacodynamics of emixustat hydrochloride in subjects with macular atrophy secondary to Stargardt disease.
Br J Ophthalmol
2022
35759666
The 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 A
2022
35861669
Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2.
Invest Ophthalmol Vis Sci
2022
35781068
Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical Results.
Ophthalmol Retina
2022
35865175
Performance 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
36388727
RNA-based therapies in inherited retinal diseases.
Ther Adv Ophthalmol
2022
36007554
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.
Am J Ophthalmol
2022
35332618
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Hum Mutat
2022
35174801
VALIDATION 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.
Retina
2022
35293952
The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene.
Invest Ophthalmol Vis Sci
2022
34695402
Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients With Stargardt Disease: SMART Study Report No. 2.
Am J Ophthalmol
2022
34298008
Longitudinal Changes of Fixation Stability and Location Within 24 Months in Stargardt Disease: ProgStar Report No. 16.
Am J Ophthalmol
2022
32562884
Effect of Human Central Nervous System Stem Cell Subretinal Transplantation on Progression of Geographic Atrophy Secondary to Nonneovascular Age-Related Macular Degeneration.
Ophthalmol Retina
2021
33737949
Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases.
Front Genet
2021
33595255
LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.
Retina
2021
34584045
Endpoints for Measuring Efficacy in Clinical Trials for Inherited Retinal Disease.
Int Ophthalmol Clin
2021
34751740
A Hybrid Model Composed of Two Convolutional Neural Networks (CNNs) for Automatic Retinal Layer Segmentation of OCT Images in Retinitis Pigmentosa (RP).
Transl Vis Sci Technol
2021
34326763
Unexpected Etiology in a Case of Bilateral Maculopathy.
Case Rep Ophthalmol
2021
34185059
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.
Invest Ophthalmol Vis Sci
2021
34004001
Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium.
Transl Vis Sci Technol
2021
33951446
The Progression of Stargardt Disease Using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15.
Am J Ophthalmol
2021
33465333
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene <i>CNGB1</i>.
Ophthalmic Genet
2021
32222369
Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14.
Am J Ophthalmol
2020
31953110
X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.
Ophthalmol Retina
2020
33425925
Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy.
Front Cell Dev Biol
2020
33133772
The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.
Transl Vis Sci Technol
2020
32832227
Quantification of RPE Changes in Choroideremia Using a Photoshop-Based Method.
Transl Vis Sci Technol
2020
32832209
Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.
Transl Vis Sci Technol
2020
32821486
Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1).
Transl Vis Sci Technol
2020
32818077
Application of a Deep Machine Learning Model for Automatic Measurement of EZ Width in SD-OCT Images of RP.
Transl Vis Sci Technol
2020
32422174
The Effect of Attention on Fixation Stability During Dynamic Fixation Testing in Stargardt Disease.
Am J Ophthalmol
2020
32446738
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.
Am J Ophthalmol
2020
32441177
A novel SVA retrotransposon insertion in the <i>CHM</i> gene results in loss of REP-1 causing choroideremia.
Ophthalmic Genet
2020
32463436
Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13.
JAMA Ophthalmol
2020
30582903
Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa.
Am J Ophthalmol
2019
29940588
Scotopic Microperimetric Assessment of Rod Function in Stargardt Disease (SMART) Study: Design and Baseline Characteristics (Report No. 1).
Ophthalmic Res
2019
29925512
Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
Br J Ophthalmol
2019
31589764
Retinal Sensitivity Using Microperimetry in Age-Related Macular Degeneration in an Amish Population.
Ophthalmic Surg Lasers Imaging Retina
2019
31211001
Reliability of Semiautomated Kinetic Perimetry (SKP) and Goldmann Kinetic Perimetry in Children and Adults With Retinal Dystrophies.
Transl Vis Sci Technol
2019
30703401
Microperimetry for geographic atrophy secondary to age-related macular degeneration.
Surv Ophthalmol
2019
31171998
Histopathologic Assessment of Optic Nerves and Retina From a Patient With Chronically Implanted Argus II Retinal Prosthesis System.
Transl Vis Sci Technol
2019
31021898
CHOROIDEREMIA: Retinal Degeneration With an Unmet Need.
Retina
2019
31019847
A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned.
Transl Vis Sci Technol
2019
30901388
Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations.
Invest Ophthalmol Vis Sci
2019
30297337
Macular spatial distribution of preserved autofluorescence in patients with choroideremia.
Br J Ophthalmol
2019
1 - 50 of 288
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