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International Journal of Molecular Sciences|November 14, 2019
Autosomal Dominant Retinitis Pigmentosa Due to Class B Rhodopsin Mutations: An Objective Outcome for Future Treatment TrialsAlexander Sumaroka, Artur V Cideciyan, Jason Charng, et al.
The Journal of Biological Chemistry|January 13, 2011
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutationsSanae Sakami, Tadao Maeda, Grzegorz Bereta, et al.
Ophthalmic Genetics|March 27, 2025
Detailed structural abnormalities associated with a novel VCAN variant in a family with versican vitreoretinopathyAnny Zhong, Alexander Sumaroka, Jonathan C Tsui, et al.
American Journal of Ophthalmology|June 29, 2018
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG MutationGiacomo Calzetti, Richard A Levy, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|September 23, 2015
Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal DegenerationRodrigo Matsui, Artur V Cideciyan, Sharon B Schwartz, et al.
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to GUCY2D Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
Ophthalmic Genetics|July 3, 2024
Detailed phenotype and long-term follow-up of RAB28-associated cone-rod dystrophyNitya T Rao, Alexander Sumaroka, Arlene J Santos, et al.
Investigative Ophthalmology & Visual Science|August 13, 2010
Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remainingSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
The Journal of Biological Chemistry|January 10, 2019
A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degenerationIgor V Peshenko, Artur V Cideciyan, Alexander Sumaroka, et al.
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