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Ophthalmology|May 28, 2013
Incidence of choroidal neovascularization in the fellow eye in the comparison of age-related macular degeneration treatments trialsMaureen G Maguire, Ebenezer Daniel, Ankoor R Shah, et al.
Translational Vision Science & Technology|December 30, 2021
Conversion of Central Subfield Thickness Measurements of Diabetic Macular Edema Across Cirrus and Spectralis Optical Coherence Tomography InstrumentsJennifer K Sun, Kristin Josic, Michele Melia, et al.
Ophthalmology Science|March 18, 2026
Simultaneous Segmentation of Geographic Atrophy in Longitudinally Acquired Fundus Autofluorescence ImagesSouvick Mukherjee, Emily Chew, Tiarnán D L Keenan, et al.
Retina (Philadelphia, Pa.)|December 29, 2017
COLORADO AGE-RELATED MACULAR DEGENERATION REGISTRY: Design and Clinical Risk Factors of the CohortAnne M Lynch, Jennifer L Patnaik, Jennifer N Cathcart, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2018
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal DeliveryCatherine Cukras, Henry E Wiley, Brett G Jeffrey, et al.
Communications Biology|December 10, 2021
AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degenerationKiyoharu J Miyagishima, Ruchi Sharma, Malika Nimmagadda, et al.
American Journal of Human Genetics|November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis PigmentosaGavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: HTRA1 /lncRNA BX842242.1 dominates, with no evidence for Complement Cascade involvementSamaneh Farashi, Carla J Abbott, Brendan Re Ansell, et al.
Nature Communications|December 8, 2025
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvementSamaneh Farashi, Carla J Abbott, Brendan R E Ansell, et al.
NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.
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