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Genes|July 15, 2017
EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease ProgressionDavid B McGuigan, Elise Heon, Artur V Cideciyan, et al.
Human Gene Therapy|July 7, 2026
Evaluation of the Toxicity and Efficacy of an Adeno-Associated Viral Vector Expressing BEST1 Delivered by Subretinal Injection in a Canine Model of Human BestrophinopathyAlexa Gray, Jennifer C Kwok, Yu Sato, et al.
Human Mutation|June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosisArtur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Vision Research|November 30, 2022
Photoreceptor function and structure in retinal degenerations caused by biallelic BEST1 mutationsArtur V Cideciyan, Samuel G Jacobson, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
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