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Vision Research|March 9, 2024
Retinal response to light exposure in BEST1-mutant dogs evaluated with ultra-high resolution OCTVivian Wu, Malgorzata Swider, Alexander Sumaroka, et al.
Molecular Vision|June 9, 2009
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganizationSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Scientific Reports|July 30, 2020
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutationsArtur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, et al.
International Journal of Molecular Sciences|January 23, 2024
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier VariantElisha Monson, Artur V Cideciyan, Alejandro J Roman, et al.
Ophthalmic Genetics|February 9, 2016
SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosaRodrigo Matsui, David B McGuigan Iii, Michaela L Gruzensky, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
International Journal of Molecular Sciences|May 24, 2019
Short-Wavelength Sensitive Cone (S-cone) Testing as an Outcome Measure for NR2E3 Clinical Treatment TrialsAlejandro J Roman, Christian A Powers, Evelyn P Semenov, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 6, 2018
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion MutationsAlexander Sumaroka, Alexandra V Garafalo, Artur V Cideciyan, et al.
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