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Translational Vision Science & Technology|August 5, 2025
Photoreceptor Disease at Ambiguous Transition Zones in Inherited Retinal DegenerationsAlexander Sumaroka, Malgorzata Swider, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|April 27, 2016
Retinal Structure Measurements as Inclusion Criteria for Stem Cell-Based Therapies of Retinal DegenerationsSamuel G Jacobson, Rodrigo Matsui, Alexander Sumaroka, et al.
Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.
Frontiers in Neuroscience|August 28, 2020
Foveal Therapy in Blue Cone Monochromacy: Predictions of Visual Potential From Artificial IntelligenceAlexander Sumaroka, Artur V Cideciyan, Rebecca Sheplock, et al.
Annual Review of Vision Science|July 13, 2021
Measures of Function and Structure to Determine Phenotypic Features, Natural History, and Treatment Outcomes in Inherited Retinal DiseasesArtur V Cideciyan, Arun K Krishnan, Alejandro J Roman, et al.
Cell Death & Disease|September 18, 2024
Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerationsRaghavi Sudharsan, Jennifer Kwok, Malgorzata Swider, et al.
Investigative Ophthalmology & Visual Science|July 14, 2016
Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A MutationsAlexander Sumaroka, Rodrigo Matsui, Artur V Cideciyan, et al.
The New England Journal of Medicine|May 5, 2015
Improvement and decline in vision with gene therapy in childhood blindnessSamuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, et al.
Expert Opinion on Orphan Drugs|August 7, 2015
Improvement in vision: a new goal for treatment of hereditary retinal degenerationsSamuel G Jacobson, Artur V Cideciyan, Gustavo D Aguirre, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
Leber Congenital Amaurosis: Genotypes and Retinal Structure PhenotypesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
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