Richard G. Weleber

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

James Bainbridge, Manjit Mehat, Venki Sundaram et al. · New England Journal of Medicine · 2015 · 713 citations · Full text

Evaluation of Grid Pattern Photocoagulation for Macular Edema in Central Vein Occlusion

John G. Clarkson, Elaine L. Chuang, DONALD J. M. GASS et al. · Ophthalmology · 1995 · 507 citations · Full text

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

Neena B. Haider, Samuel G. Jacobson, Artur V. Cideciyan et al. · Nature Genetics · 2000 · 497 citations

Ocular Disease, Developmental Biology, Signal Transduction +10

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome

Kirk Mykytyn, Darryl Nishimura, Charles Searby et al. · Nature Genetics · 2002 · 353 citations

Obesity, Metabolic Syndrome, Body Composition +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 · 349 citations

Ocular Disease, Developmental Biology, Ophthalmology +6