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 · 737 citations · Full text

Medicine, Genetics, Ophthalmology +17

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 · 510 citations · Full text

Medicine, Ophthalmology, Vision Science +15

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 · 508 citations

Medicine, Genetics, Molecular Genetics +16

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 · 354 citations

Life Sciences, Genetics, Molecular Genetics +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