Gerald A. Fishman

University of Illinois Chicago — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

77h-index19.8kcitations475works0.02yr avg
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Research Topics

Retinal Development and Disorders(302), Retinal Diseases and Treatments(175), Glaucoma and retinal disorders(57), Photoreceptor and optogenetics research(49), Visual perception and processing mechanisms(43)

Publications474 total

Longitudinal Imaging of the Parafoveal Cone Mosaic in Congenital Achromatopsia
Ophthalmology Science·2025Open Access
Rapid progression of vision loss in a child with pigmentary retinopathy
Elsevier eBooks·2024
Contributors
Elsevier eBooks·2024Open Access
The effect of mechanical ventilation compared to high flow nasal cannulas on gastro residual volume and reflux events using novel automated technology
Clinical Nutrition ESPEN·2023Open Access
Spatial and Temporal Integration Abnormalities in X-Linked Retinoschisis
Investigative Ophthalmology & Visual Science·2022· 1 citedOpen Access
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease
PLoS Genetics·2022· 15 citedOpen Access
Contrast Sensitivity and Equivalent Intrinsic Noise in X-Linked Retinoschisis
Translational Vision Science & Technology·2022· 5 citedOpen Access
Correlation between nutrition, phosphate level and length of ventilation in critically ill patients who need renal replacement therapy
Clinical Nutrition ESPEN·2021
Luminance Thresholds and Their Correlation With Retinal Structure in X-Linked Retinoschisis
Investigative Ophthalmology & Visual Science·2021· 4 citedOpen Access
Pathognomonic macular ripples are revealed by polarized infrared retinal imaging
Experimental Biology and Medicine·2021· 4 citedOpen Access
Clinical and Genetics Characterization of Hypomorphic Variants in Stargardt disease
Investigative Ophthalmology & Visual Science·2021Open Access
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure
Translational Vision Science & Technology·2021· 10 citedOpen Access
<i>Cis</i>-acting modifiers in the <i>ABCA4</i> locus contribute to the penetrance of the major disease-causing variant in Stargardt disease
Human Molecular Genetics·2021· 54 citedOpen Access
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia
Translational Vision Science & Technology·2021· 13 citedOpen Access
Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerations.
PubMed·2021· 9 citedOpen Access
Gene dosage manipulation alleviates manifestations of hereditary <i>PAX6</i> haploinsufficiency in mice
Science Translational Medicine·2020· 28 cited
Cellular Changes in Retinas From Patients With BEST1 Mutations
Frontiers in Cell and Developmental Biology·2020· 4 citedOpen Access
Electrophysiological and Pupillometric Abnormalities in PROM1 Cone–Rod Dystrophy
Translational Vision Science & Technology·2020· 3 citedOpen Access
Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis
Investigative Ophthalmology & Visual Science·2020· 18 citedOpen Access
Optical coherence tomography artifacts predict adaptive optics scanning light ophthalmoscopy success in achromatopsia
Investigative Ophthalmology & Visual Science·2020Open Access
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Frequent Co-authors

Samuel G. Jacobson(13), Edwin M. Stone(11), Richard G. Weleber(11), John R. Heckenlively(6), Elise Héon(5), Val C. Sheffield(5), Sandeep Grover(5), Artur V. Cideciyan(4), Peter Gouras(4), Paul A. Sieving(4), Alessandro Iannaccone(4), David G. Birch(4), Kenneth R. Alexander(4), Elias I. Traboulsi(4), Byron L. Lam(4), Rando Allikmets(4), Jean Bennett(3), Eliot L. Berson(3), Joseph Carroll(3), Alfredo Dubra(3)