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Nature Medicine|April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case reportArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retinaArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Human Molecular Genetics|January 8, 2004
Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequenceArtur V Cideciyan, Tomas S Aleman, Malgorzata Swider, et al.
Investigative Ophthalmology & Visual Science|December 13, 2022
Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 MutationsArtur V Cideciyan, Samuel G Jacobson, Malgorzata Swider, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 13, 2019
Long-Term Structural Outcomes of Late-Stage RPE65 Gene TherapyKristin L Gardiner, Artur V Cideciyan, Malgorzata Swider, et al.
American Journal of Ophthalmology Case Reports|June 30, 2023
Durable vision improvement after a single intravitreal treatment with antisense oligonucleotide in <i>CEP2</i>90-LCA: Replication in two eyesArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 30, 2021
Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosisGustavo D Aguirre, Artur V Cideciyan, Valérie L Dufour, et al.
Human Molecular Genetics|February 26, 2015
Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerationsNing Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, et al.
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