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Author Details

Jacque L Duncan
University of California san francisco
1998
153
44
PMIDPaper TitleJournal TitlePublished Year
37660736Classification and Growth Rate of Chorioretinal Atrophy after Voretigene Neparvovec-Rzyl for RPE65-Mediated Retinal Degeneration.Ophthalmol Retina2024
36220331Adaptive Optics Imaging of Inherited Retinal Disease.Cold Spring Harb Perspect Med2023
37459066Enhanced S-Cone Syndrome: Elevated Cone Counts Confer Supernormal Visual Acuity in the S-Cone Pathway.Invest Ophthalmol Vis Sci2023
36948373Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration.Am J Ophthalmol2023
37440033Enhanced S-cone Syndrome, a Mini-review.Adv Exp Med Biol2023
37333224Neuropathy target esterase activity predicts retinopathy among <i>PNPLA6</i> disorders.bioRxiv2023
36646238Cone Structure and Function in RPGR- and USH2A-Associated Retinal Degeneration.Am J Ophthalmol2023
36909455Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with <i>RHO</i> copy number variation.medRxiv2023
36764426Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.Am J Ophthalmol2023
36420660Retinopathy and optic atrophy in a case of <i>COQ2</i>-related primary coenzyme Q<sub>10</sub> deficiency.Ophthalmic Genet2023
34437870Correlation Between Localized Choriocapillaris Perfusion and Macular Function in Eyes with Geographic Atrophy.Am J Ophthalmol2022
35365235Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.Orphanet J Rare Dis2022
35417300Chorioretinal Findings as the Initial Presentation of Chronic Granulomatous Disease.Ophthalmic Surg Lasers Imaging Retina2022
36007554Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.Am J Ophthalmol2022
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
35266249Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study.Hum Mutat2022
35201337Choriocapillaris Changes in Myopic Macular Degeneration.Transl Vis Sci Technol2022
35293952The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene.Invest Ophthalmol Vis Sci2022
30142112PRESUMED FOVEAL BACILLARY LAYER DETACHMENT IN A PATIENT WITH TOXOPLASMOSIS CHORIORETINITIS AND PACHYCHOROID DISEASE.Retin Cases Brief Rep2021
33595255LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.Retina2021
33512402Biometrics, Impact, and Significance of Basal Linear Deposit and Subretinal Drusenoid Deposit in Age-Related Macular Degeneration.Invest Ophthalmol Vis Sci2021
34940782Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10.Invest Ophthalmol Vis Sci2021
34584051Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.Int Ophthalmol Clin2021
34662339Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.PLoS Genet2021
34653402Allele-specific gene editing to rescue dominant CRX-associated LCA7 phenotypes in a retinal organoid model.Stem Cell Reports2021
34004001Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium.Transl Vis Sci Technol2021
34331386Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).Am J Med Genet A2021
33144691Response to: Comment on: Dark without pressure retinal changes in a paediatric age group.Eye (Lond)2021
33161127Promises and pitfalls of evaluating photoreceptor-based retinal disease with adaptive optics scanning light ophthalmoscopy (AOSLO).Prog Retin Eye Res2021
32690924Dark without pressure retinal changes in a paediatric age group.Eye (Lond)2021
30074570PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCY.Retin Cases Brief Rep2021
32341851Automated morphometric measurement of the retinal pigment epithelium complex and choriocapillaris using swept source OCT.Biomed Opt Express2020
33133772The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.Transl Vis Sci Technol2020
32832213OCT Angiography to Predict Geographic Atrophy Progression using Choriocapillaris Flow Void as a Biomarker.Transl Vis Sci Technol2020
32832209Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.Transl Vis Sci Technol2020
32714643Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal Degenerations.Transl Vis Sci Technol2020
32446738Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.Am J Ophthalmol2020
32504085Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness.Hum Mol Genet2020
32568988ABUNDANCE AND MULTIMODAL VISIBILITY OF SOFT DRUSEN IN EARLY AGE-RELATED MACULAR DEGENERATION: A Clinicopathologic Correlation.Retina2020
32343782Comparing Cone Structure and Function in RHO- and RPGR-Associated Retinitis Pigmentosa.Invest Ophthalmol Vis Sci2020
31021898CHOROIDEREMIA: Retinal Degeneration With an Unmet Need.Retina2019
31692580Quantifying choriocapillaris hypoperfusion in patients with choroidal neovascularization using swept-source OCT angiography.Clin Ophthalmol2019
31770433Cone Structure Persists Beyond Margins of Short-Wavelength Autofluorescence in Choroideremia.Invest Ophthalmol Vis Sci2019
31884602Multimodal Imaging in Choroideremia.Adv Exp Med Biol2019
30097992Cobalamin D Deficiency Identified Through Newborn Screening.JIMD Rep2019
31589763Quantifying Choriocapillaris Flow Voids in Patients With Geographic Atrophy Using Swept-Source OCT Angiography.Ophthalmic Surg Lasers Imaging Retina2019
31465091Gene Therapy for Choroideremia-Progress and Remaining Questions.JAMA Ophthalmol2019
31408630Influence of eye pigmentation on retinal degeneration in P23H and S334ter mutant rhodopsin transgenic rats.Exp Eye Res2019
31335944Loss of Foveal Cone Structure Precedes Loss of Visual Acuity in Patients With Rod-Cone Degeneration.Invest Ophthalmol Vis Sci2019
30924848Cone Spacing Correlates With Retinal Thickness and Microperimetry in Patients With Inherited Retinal Degenerations.Invest Ophthalmol Vis Sci2019
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Co-authored papers 13
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Wills Eye Hospital/Mid Atlantic Retina
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Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
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National Eye Institute, National Institutes of Health
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University Eye Hospital, University of Tubingen
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The State University of New Jersey
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Radboud University Medical Center
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Medical College of Wisconsin
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