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Ophthalmology|November 24, 2022
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural HistoryMichalis Georgiou, Anthony G Robson, Katarina Jovanovic, et al.Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.Translational Vision Science & Technology|August 22, 2020
Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular DegenerationKamron N Khan, Shyamanga Borooah, Leonardo Lando, et al.JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.Proceedings of the National Academy of Sciences of the United States of America|May 20, 2022
Electrical responses from human retinal cone pathways associate with a common genetic polymorphism implicated in myopiaXiaofan Jiang, Zihe Xu, Talha Soorma, et al.Journal of Neurointerventional Surgery|September 11, 2015
Endovascular treatment of ophthalmic artery aneurysms: ophthalmic artery patency following flow diversion versus coil embolizationChristopher R Durst, Robert M Starke, David Clopton, et al.Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.Translational Vision Science & Technology|December 24, 2019
Remote Tool-Based Adjudication for Grading Diabetic RetinopathyMike Schaekermann, Naama Hammel, Michael Terry, et al.Ophthalmology|February 1, 2014
Detailed phenotypic and genotypic characterization of bietti crystalline dystrophyStephanie Halford, Gerald Liew, Donna S Mackay, et al.Oecologia|June 5, 2004
Carbon and nitrogen stoichiometry and nitrogen cycling rates in streamsWalter K Dodds, Eugenia Martí, Jennifer L Tank, et al.Pageof 125