1995 - Fellow of American Physical Society (APS) Citation For pioneering advances in gammaray astronomy, particularly his important observations of gammaray bursts that suggest a possible cosmological origin
Retinitis pigmentosa, Ophthalmology, Genetics, Visual acuity and Eye disease are his primary areas of study. His work on Usher syndrome as part of his general Retinitis pigmentosa study is frequently connected to In patient, thereby bridging the divide between different branches of science. Many of his studies involve connections with topics such as Retina and Ophthalmology.
Many of his studies on Genetics apply to Retinal as well. His Visual acuity research includes themes of Fovea centralis, Pediatrics and Contrast. His research in Eye disease intersects with topics in Dioptre and Foveal.
His primary scientific interests are in Ophthalmology, Retinitis pigmentosa, Visual acuity, Retinal and Electroretinography. His work on Retina expands to the thematically related Ophthalmology. His study on Retinitis pigmentosa is covered under Genetics.
His Visual acuity research is multidisciplinary, relying on both Optical coherence tomography and Foveal. His Retinal research includes elements of Anatomy and Pathology. Gerald A. Fishman interconnects Erg and Retinoschisis in the investigation of issues within Electroretinography.
His primary areas of investigation include Ophthalmology, Visual acuity, Stargardt disease, Retinal and Genetics. His Ophthalmology research focuses on Pupillometry and how it relates to Pupillary light reflex. The concepts of his Visual acuity study are interwoven with issues in Fovea centralis, Retinal Cone Photoreceptor Cells, Retrospective cohort study and Audiology.
His Stargardt disease research integrates issues from Optometry and Microperimetry. His research integrates issues of Histopathology, Pathology, Retina and Anatomy in his study of Retinal. Gerald A. Fishman combines subjects such as Erg and Dystrophy with his study of Electroretinography.
His main research concerns Ophthalmology, Visual acuity, Genetics, Retina and Retinal. Gerald A. Fishman undertakes multidisciplinary studies into Ophthalmology and In patient in his work. His work carried out in the field of Visual acuity brings together such families of science as Pupillometry, Electroretinography, Young adult, Ophthalmoscopy and Fovea centralis.
His work on RPE65 is typically connected to Cis-trans-Isomerases as part of general Retina study, connecting several disciplines of science. Gerald A. Fishman specializes in Retinal, namely Retinal degeneration. His biological study spans a wide range of topics, including Opsin, OPN1MW, Retinitis pigmentosa and Anatomy.
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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Artur V. Cideciyan;Tomas S. Aleman;Sanford L. Boye;Sharon B. Schwartz.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations: Safety and Efficacy in 15 Children and Adults Followed Up to 3 Years
Samuel G. Jacobson;Artur V. Cideciyan;Ramakrishna Ratnakaram;Elise Heon.
Archives of Ophthalmology (2012)
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis
Hiroyuki Morimura;Gerald A. Fishman;Sandeep A. Grover;Anne B. Fulton.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
Ching Hwa Sung;Carol M. Davenport;Jill C. Hennessey;Irene H. Maumenee.
Proceedings of the National Academy of Sciences of the United States of America (1991)
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;Ruth Swiderski.
Nature Genetics (2000)
Multiple Evanescent White Dot Syndrome: I. Clinical Findings
Lee Merrill Jampol;Paul A. Sieving;David Pugh;Gerald A. Fishman.
Archives of Ophthalmology (1984)
Molecular genetics of human blue cone monochromacy
Jeremy Nathans;Carol M. Davenport;Irene H. Maumenee;Richard Alan Lewis.
Science (1989)
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6
Thaddeus P. Dryja;Terri L. McGee;Eliot L. Berson;Gerald A. Fishman.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Retinitis Pigmentosa: Genetic Percentages
Gerald A. Fishman.
Archives of Ophthalmology (1978)
In vivo imaging of human cone photoreceptor inner segments.
Drew Scoles;Yusufu N. Sulai;Christopher S. Langlo;Gerald A. Fishman.
Investigative Ophthalmology & Visual Science (2014)
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