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Research.com Recognitions

  • 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

Overview

Gerald A. Fishman is affiliated with the University of Illinois at Chicago in the United States. Their research primarily spans the field of medicine, with a significant focus on ophthalmology, radiology, nuclear medicine and imaging, molecular biology, pulmonary and respiratory medicine, and rheumatology.

Fishman's work largely concentrates on retinal diseases and treatments, with extensive publications involving multiple aspects of retinal and macular surgery, retinal imaging and analysis, intraocular surgery and lenses, and retinopathy of prematurity studies. Additionally, their research covers retinal development and disorders as well as glaucoma and retinal disorders.

Several frequent coauthors collaborate with Fishman:

  • Acy Lo
  • Nicholas Fung
  • Ming Yang
  • Kwok-Fai So
  • Linda L. D. Zhong

The most common venues for Fishman's publications include:

  • Advanced Science
  • International Journal of Retina and Vitreous
  • British Journal of Ophthalmology
  • Research Square
  • Nutrients

Representative recent papers authored or coauthored by Gerald A. Fishman include:

  • Lutein Supplementation for Eye Diseases, 2020, Nutrients
  • Effect of Intravitreal Aflibercept vs Laser Photocoagulation on Treatment Success of Retinopathy of Prematurity, 2022, JAMA
  • Involvement of FSP1-CoQ10-NADH and GSH-GPx-4 pathways in retinal pigment epithelium ferroptosis, 2022, Cell Death and Disease
  • Silicone oil in vitreoretinal surgery: indications, complications, new developments and alternative long-term tamponade agents, 2020, Acta Ophthalmologica
  • Green Light-Triggered Intraocular Drug Release for Intravenous Chemotherapy of Retinoblastoma, 2021, Advanced Science

Throughout their career, Fishman has been recognized with awards, notably becoming a Fellow of the American Physical Society in 1995 for pioneering advances in gamma-ray astronomy and observations related to gamma-ray bursts suggesting a cosmological origin.

Best Publications

  • 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

  • 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

  • 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

  • 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

  • Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

    Ching Hwa Sung;Carol M. Davenport;Jill C. Hennessey;Irene H. Maumenee

  • Multiple Evanescent White Dot Syndrome: I. Clinical Findings

    Lee Merrill Jampol;Paul A. Sieving;David Pugh;Gerald A. Fishman

  • Molecular Genetics of Human Blue Cone Monochromacy

    Jeremy Nathans;Carol M. Davenport;Irene H. Maumenee;Richard Alan Lewis

  • In vivo imaging of human cone photoreceptor inner segments.

    Drew Scoles;Yusufu N. Sulai;Christopher S. Langlo;Gerald A. Fishman

  • 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

  • Mutations in the Cone-Rod Homeobox Gene Are Associated with the Cone-Rod Dystrophy Photoreceptor Degeneration

    Prabodha K. Swain;Shiming Chen;Qing Liang Wang;Louisa M. Affatigato

  • Fundus flavimaculatus. A clinical classification.

    Gerald A. Fishman

  • 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 Filippova;Suja Hiriyanna

  • Retinitis Pigmentosa: Genetic Percentages

    Gerald A. Fishman

  • Mutations in the CRB1 Gene Cause Leber Congenital Amaurosis

    Andrew J. Lotery;Samuel G. Jacobson;Gerald A. Fishman;Richard G. Weleber

  • Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

    J Ott;S Bhattacharya;J D Chen;M J Denton

  • Acetazolamide for treatment of chronic macular edema in retinitis pigmentosa.

    Gerald A. Fishman;Leonardo D. Gilbert;Richard G. Fiscella;Alan E. Kimura

  • An analysis of allelic variation in the ABCA4 gene

    Andrew R. Webster;Elise Heon;Andrew J. Lotery;Kimberlie Vandenburgh

  • iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration

    Ruchira Singh;Wei Shen;David Kuai;Jessica M. Martin

  • Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.

    Ygal Rotenstreich;Gerald A Fishman;Robert J Anderson

  • Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older.

    Sandeep Grover;Gerald A Fishman;Robert J Anderson;Marcia S.V Tozatti

Frequent Co-Authors

Edwin M. Stone
Edwin M. Stone University of Iowa
Samuel G. Jacobson
Samuel G. Jacobson University of Pennsylvania
Richard G. Weleber
Richard G. Weleber Oregon Health & Science University
Rando Allikmets
Rando Allikmets Columbia University
Robert K. Koenekoop
Robert K. Koenekoop McGill University Health Centre
Neal S. Peachey
Neal S. Peachey Cleveland Clinic
Artur V. Cideciyan
Artur V. Cideciyan University of Pennsylvania
David G. Birch
David G. Birch The University of Texas Southwestern Medical Center
Paul A. Sieving
Paul A. Sieving University of California, Davis
Val C. Sheffield
Val C. Sheffield University of Iowa

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