Gerald A. Fishman - Concepedia

Author

Gerald A. Fishman

Also Known As

Fishman, G. J., G A Fishman, G Fishman, G. A Fishman, G. A. Fishman, G. Fishman, G.A. Fishman, GERALD A. FISHMAN, GERALD FISHMAN, Gerald A Fishman

475

Publications

19.8K

Citations

H-Index

167

Concepts

All Affiliations

University of Illinois Chicago New York Eye and Ear Infirmary University of Iowa University of Pennsylvania Oregon Health & Science University

About

Gerald A. Fishman is an author at University of Illinois Chicago specializing in ophthalmology, medicine, and glaucoma.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	50	121	8.7K
2	Health Sciences	5	5	137
3	Engineering	4	4	123
4	Arts	1	1	54
5	Education	1	1	63

Gerald A. Fishman

275

Publications

18.8K

Citations

H-Index

Page 1

	Year	Citations
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, Proceedings of the National Academy of Sciences Slow Rod KineticsGene TherapiesOcular DiseaseHuman Gene TherapyRpe65 Gene	2008	660
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, Nature Genetics Ocular DiseaseDevelopmental BiologySignal TransductionOphthalmologyRetina	2000	497
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis Hiroyuki Morimura, Gerald A. Fishman, Sandeep Grover, Proceedings of the National Academy of Sciences	1998	482
Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Ching‐Hwa Sung, Carol Davenport, Jill C. Hennessey, Proceedings of the National Academy of Sciences Ocular DiseasePhotoreceptor CellRhodopsin MutationsOphthalmologyPoint Mutations	1991	466
In Vivo Imaging of Human Cone Photoreceptor Inner Segments Drew Scoles, Yusufu N. Sulai, Christopher S. Langlo, Investigative Ophthalmology & Visual Science	2014	370
Molecular Genetics of Human Blue Cone Monochromacy Jeremy Nathans, Carol Davenport, Irene H. Maumenee, Science BiologyBlue Cone MonochromacyRed Pigment GeneMolecular EcologyGenetic Disorder	1989	319
Mutations in the Cone-Rod Homeobox Gene Are Associated with the Cone-Rod Dystrophy Photoreceptor Degeneration Prabodha K. Swain, Shiming Chen, Qing-liang Wang, Neuron	1997	280
A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa Debra K. Breuer, Beverly M. Yashar, Elena V. Filippova, The American Journal of Human Genetics North American CohortMendelian DisorderGenetic DisorderMedicineGenetics	2002	245
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the <i>GRM6</i> gene encoding mGluR6 Thaddeus P. Dryja, Terri L. McGee, Eliot L. Berson, Proceedings of the National Academy of Sciences Glutamate Receptor Mglur6Unrelated PatientsOcular DiseaseGeneticsSynaptic Transmission	2005	244
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older Sandeep Grover, Gerald A. Fishman, Robert J. Anderson, Ophthalmology Ocular DiseaseRetinaOphthalmologyRetinitis PigmentosaMedicine	1999	231

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