Gerald A. Fishman

Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics

Artur V. Cideciyan, Tomás S. Alemán, Sanford L. Boye et al. · Proceedings of the National Academy of Sciences · 2008 · 660 citations · Full text

Slow Rod Kinetics, Gene Therapies, Ocular Disease +12

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

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

Hiroyuki Morimura, Gerald A. Fishman, Sandeep Grover et al. · Proceedings of the National Academy of Sciences · 1998 · 482 citations

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Ching‐Hwa Sung, Carol Davenport, Jill C. Hennessey et al. · Proceedings of the National Academy of Sciences · 1991 · 466 citations · Full text

Ocular Disease, Photoreceptor Cell, Rhodopsin Mutations +15

In Vivo Imaging of Human Cone Photoreceptor Inner Segments

Drew Scoles, Yusufu N. Sulai, Christopher S. Langlo et al. · Investigative Ophthalmology & Visual Science · 2014 · 370 citations · Full text