Arlene V. Drack

Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65 -mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial

Stephen R. Russell, Jean Bennett, Jennifer Wellman et al. · The Lancet · 2017 · 1.9K citations

Medicine, Ophthalmology, Vision Science +14

Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31

Val C. Sheffield, Edwin M. Stone, Wallace L.M. Alward et al. · Nature Genetics · 1993 · 439 citations

Life Sciences, Genetics, Ophthalmology +13

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

N. Torben Bech‐Hansen, Margaret J. Naylor, Tracy A. Maybaum et al. · Nature Genetics · 2000 · 352 citations

Medicine, Genetics, Ophthalmology +12

Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

Brian E. Nichols, Val C. Sheffield, Kimberlie Vandenburgh et al. · Nature Genetics · 1993 · 278 citations

Life Sciences, Genetics, Molecular Genetics +12

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

Artur V. Cideciyan, Samuel G. Jacobson, Arlene V. Drack et al. · Nature Medicine · 2018 · 216 citations · Full text

Medicine, Ophthalmology, Vision Science +15