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Author Details
Full Name
Jacque L Duncan
Affiliation
University of California san francisco
ORCID
Career Start Year
1998
Papers
153
H Index
44
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37660736
Classification and Growth Rate of Chorioretinal Atrophy after Voretigene Neparvovec-Rzyl for RPE65-Mediated Retinal Degeneration.
Ophthalmol Retina
2024
36220331
Adaptive Optics Imaging of Inherited Retinal Disease.
Cold Spring Harb Perspect Med
2023
37459066
Enhanced S-Cone Syndrome: Elevated Cone Counts Confer Supernormal Visual Acuity in the S-Cone Pathway.
Invest Ophthalmol Vis Sci
2023
36948373
Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration.
Am J Ophthalmol
2023
37440033
Enhanced S-cone Syndrome, a Mini-review.
Adv Exp Med Biol
2023
37333224
Neuropathy target esterase activity predicts retinopathy among <i>PNPLA6</i> disorders.
bioRxiv
2023
36646238
Cone Structure and Function in RPGR- and USH2A-Associated Retinal Degeneration.
Am J Ophthalmol
2023
36909455
Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with <i>RHO</i> copy number variation.
medRxiv
2023
36764426
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.
Am J Ophthalmol
2023
36420660
Retinopathy and optic atrophy in a case of <i>COQ2</i>-related primary coenzyme Q<sub>10</sub> deficiency.
Ophthalmic Genet
2023
34437870
Correlation Between Localized Choriocapillaris Perfusion and Macular Function in Eyes with Geographic Atrophy.
Am J Ophthalmol
2022
35365235
Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.
Orphanet J Rare Dis
2022
35417300
Chorioretinal Findings as the Initial Presentation of Chronic Granulomatous Disease.
Ophthalmic Surg Lasers Imaging Retina
2022
36007554
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.
Am J Ophthalmol
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
35266249
Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study.
Hum Mutat
2022
35201337
Choriocapillaris Changes in Myopic Macular Degeneration.
Transl Vis Sci Technol
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
30142112
PRESUMED FOVEAL BACILLARY LAYER DETACHMENT IN A PATIENT WITH TOXOPLASMOSIS CHORIORETINITIS AND PACHYCHOROID DISEASE.
Retin Cases Brief Rep
2021
33595255
LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.
Retina
2021
33512402
Biometrics, Impact, and Significance of Basal Linear Deposit and Subretinal Drusenoid Deposit in Age-Related Macular Degeneration.
Invest Ophthalmol Vis Sci
2021
34940782
Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10.
Invest Ophthalmol Vis Sci
2021
34584051
Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.
Int Ophthalmol Clin
2021
34662339
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
PLoS Genet
2021
34653402
Allele-specific gene editing to rescue dominant CRX-associated LCA7 phenotypes in a retinal organoid model.
Stem Cell Reports
2021
34004001
Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium.
Transl Vis Sci Technol
2021
34331386
Auditory 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 A
2021
33144691
Response to: Comment on: Dark without pressure retinal changes in a paediatric age group.
Eye (Lond)
2021
33161127
Promises and pitfalls of evaluating photoreceptor-based retinal disease with adaptive optics scanning light ophthalmoscopy (AOSLO).
Prog Retin Eye Res
2021
32690924
Dark without pressure retinal changes in a paediatric age group.
Eye (Lond)
2021
30074570
PHENOTYPIC 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 Rep
2021
32341851
Automated morphometric measurement of the retinal pigment epithelium complex and choriocapillaris using swept source OCT.
Biomed Opt Express
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
32832213
OCT Angiography to Predict Geographic Atrophy Progression using Choriocapillaris Flow Void as a Biomarker.
Transl Vis Sci Technol
2020
32832209
Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.
Transl Vis Sci Technol
2020
32714643
Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal Degenerations.
Transl Vis Sci Technol
2020
32446738
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.
Am J Ophthalmol
2020
32504085
Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness.
Hum Mol Genet
2020
32568988
ABUNDANCE AND MULTIMODAL VISIBILITY OF SOFT DRUSEN IN EARLY AGE-RELATED MACULAR DEGENERATION: A Clinicopathologic Correlation.
Retina
2020
32343782
Comparing Cone Structure and Function in RHO- and RPGR-Associated Retinitis Pigmentosa.
Invest Ophthalmol Vis Sci
2020
31021898
CHOROIDEREMIA: Retinal Degeneration With an Unmet Need.
Retina
2019
31692580
Quantifying choriocapillaris hypoperfusion in patients with choroidal neovascularization using swept-source OCT angiography.
Clin Ophthalmol
2019
31770433
Cone Structure Persists Beyond Margins of Short-Wavelength Autofluorescence in Choroideremia.
Invest Ophthalmol Vis Sci
2019
31884602
Multimodal Imaging in Choroideremia.
Adv Exp Med Biol
2019
30097992
Cobalamin D Deficiency Identified Through Newborn Screening.
JIMD Rep
2019
31589763
Quantifying Choriocapillaris Flow Voids in Patients With Geographic Atrophy Using Swept-Source OCT Angiography.
Ophthalmic Surg Lasers Imaging Retina
2019
31465091
Gene Therapy for Choroideremia-Progress and Remaining Questions.
JAMA Ophthalmol
2019
31408630
Influence of eye pigmentation on retinal degeneration in P23H and S334ter mutant rhodopsin transgenic rats.
Exp Eye Res
2019
31335944
Loss of Foveal Cone Structure Precedes Loss of Visual Acuity in Patients With Rod-Cone Degeneration.
Invest Ophthalmol Vis Sci
2019
30924848
Cone Spacing Correlates With Retinal Thickness and Microperimetry in Patients With Inherited Retinal Degenerations.
Invest Ophthalmol Vis Sci
2019
1 - 50 of 153
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