Publications by authors named "Gerald A Fishman"

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Longitudinal Imaging of the Parafoveal Cone Mosaic in Congenital Achromatopsia.
Nickolas Chen, Katie M Litts, Danica Nikezic, Christopher S Langlo, Brian P Higgins, Gerald A Fishman

Ophthalmol Sci· March 2025

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Spatial and Temporal Integration Abnormalities in X-Linked Retinoschisis.
J Jason McAnany, Jason C Park, Gerald A Fishman, Robert A Hyde

Invest Ophthalmol Vis Sci· August 2022

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Contrast Sensitivity and Equivalent Intrinsic Noise in X-Linked Retinoschisis.
J Jason McAnany, Jason C Park, Gerald A Fishman, Robert A Hyde

Transl Vis Sci Technol· March 2022

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Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease.
Jana Zernant, Winston Lee, Jun Wang, Kerry Goetz, Ehsan Ullah, Gerald A Fishman

PLoS Genet· March 2022

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Noncoding mutation in contributes to inherited retinal degenerations.
Gang Zou, Tao Zhang, Xuesen Cheng, Austin D Igelman, Jun Wang, Gerald A Fishman

Mol Vis· November 2021

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Pathognomonic macular ripples are revealed by polarized infrared retinal imaging.
Darius Ansari, Poulami P Borkar, Patricia L Davis, Frederick T Collison, Niamh Wynne, Gerald A Fishman

Exp Biol Med (Maywood)· October 2021

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Luminance Thresholds and Their Correlation With Retinal Structure in X-Linked Retinoschisis.
J Jason McAnany, Jason C Park, Gerald A Fishman, Robert A Hyde

Invest Ophthalmol Vis Sci· October 2021

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Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease.
Winston Lee, Jana Zernant, Takayuki Nagasaki, Laurie L Molday, Pei-Yin Su, Gerald A Fishman

Hum Mol Genet· June 2021

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Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure.
Katie M Litts, Erica N Woertz, Niamh Wynne, Brian P Brooks, Alicia Chacon, Gerald A Fishman

Transl Vis Sci Technol· May 2021

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Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia.
Katie M Litts, Erica N Woertz, Michalis Georgiou, Emily J Patterson, Byron L Lam, Gerald A Fishman

Transl Vis Sci Technol· January 2021

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Gene dosage manipulation alleviates manifestations of hereditary haploinsufficiency in mice.
Behnam Rabiee, Khandaker N Anwar, Xiang Shen, Ilham Putra, Mingna Liu, Gerald A Fishman

Sci Transl Med· December 2020

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Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia.
Katie M Litts, Michalis Georgiou, Christopher S Langlo, Emily J Patterson, Rebecca R Mastey, Gerald A Fishman

Curr Eye Res· October 2020

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Simplex Crumbs Homologue 1 Maculopathy Masquerading as Juvenile X-Linked Retinoschisis in Male Patients.
Daniel J Oh, Veeral Sheth, Gerald A Fishman, Michael A Grassi

J Vitreoretin Dis· October 2020

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Cellular Changes in Retinas From Patients With Mutations.
Vera L Bonilha, Brent A Bell, Meghan J DeBenedictis, Stephanie A Hagstrom, Gerald A Fishman

Front Cell Dev Biol· October 2020

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VISUAL IMPAIRMENT IN RETINITIS PIGMENTOSA.
Chloe M Vezinaw, Gerald A Fishman, J Jason McAnany

Retina· August 2020

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Electrophysiological and Pupillometric Abnormalities in PROM1 Cone-Rod Dystrophy.
Jason C Park, Frederick T Collison, Gerald A Fishman, J Jason McAnany

Transl Vis Sci Technol· August 2020

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Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis.
J Jason McAnany, Jason C Park, Gerald A Fishman, Frederick T Collison

Invest Ophthalmol Vis Sci· June 2020

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CLINICAL CHARACTERIZATION OF STARGARDT DISEASE PATIENTS WITH THE p.N1868I ABCA4 MUTATION.
Frederick T Collison, Winston Lee, Gerald A Fishman, Jason C Park, Jana Zernant

Retina· December 2019

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Two-color pupillometry in KCNV2 retinopathy.
Frederick T Collison, Jason C Park, Gerald A Fishman, Edwin M Stone, J Jason McAnany

Doc Ophthalmol· August 2019

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Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy.
Frederick T Collison, Gerald A Fishman, Takayuki Nagasaki, Jana Zernant, J Jason McAnany

Invest Ophthalmol Vis Sci· May 2019

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Unanticipated prognosis for a patient with type 2 Usher syndrome.
Chloe M Vezinaw, Gerald A Fishman, John Chiang

Doc Ophthalmol· April 2019

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VISUAL ACUITY IN PATIENTS WITH STARGARDT DISEASE AFTER AGE 40.
Frederick T Collison, Gerald A Fishman

Retina· December 2018

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Extremely hypomorphic and severe deep intronic variants in the locus result in varying Stargardt disease phenotypes.
Jana Zernant, Winston Lee, Takayuki Nagasaki, Frederick T Collison, Gerald A Fishman

Cold Spring Harb Mol Case Stud· August 2018

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Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration.
Jana Zernant, Winston Lee, Frederick T Collison, Gerald A Fishman, Yuri V Sergeev

J Med Genet· June 2017

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Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene.
Samuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, Alejandro J Roman, Jason Charng, Gerald A Fishman

Invest Ophthalmol Vis Sci· May 2017

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