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Plos One|March 7, 2014
Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerationsWilliam A Beltran, Artur V Cideciyan, Karina E Guziewicz, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
Experimental Eye Research|May 10, 2026
PRCD-associated retinitis pigmentosa in dogs and humansValerie L Dufour, Yu Sato, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
Iscience|November 14, 2024
Erratum: Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Ophthalmology|January 25, 2015
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene TherapyLina Zelinger, Artur V Cideciyan, Susanne Kohl, et al.
Retinal Cases & Brief Reports|January 27, 2026
A Spectrum of Severity of a Unifying Retinal Phenotype in TUBB4B-Associated Inherited Retinal DegenerationSophia Zhang, Robert A Avery, Vivian Wu, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5Randa T H Li, Alejandro J Roman, Alexander Sumaroka, et al.
Human Gene Therapy|July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 yearArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
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