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ARVO Annual Meeting Abstract June 2022

A common haplotype in the PRPH2 gene modifies Stargardt/ABCA4 disease.

Jana Zernant; Winston Lee; Jun Wang; KERRY GOETZ; Ehsan Ullah; Takayuki Nagasaki; PEI-YIN SU; Gerald A Fishman; Stephen H Tsang; Santa J Tumminia; Brian Brooks; Robert B Hufnagel; Rui Chen; Rando Allikmets

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1596 – A0385. doi:

Articles March 2022

Contrast Sensitivity and Equivalent Intrinsic Noise in X-Linked Retinoschisis

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J. Jason McAnany; Jason C. Park; Gerald A. Fishman; Robert A. Hyde
TAGS: contrast sensitivity, noise, x-linked retinoschisis
Trans. Vis. Sci. Tech.. 2022; 11(3):7. doi: https://doi.org/10.1167/tvst.11.3.7

Visual Psychophysics and Physiological Optics October 2021

Luminance Thresholds and Their Correlation With Retinal Structure in X-Linked Retinoschisis

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J. Jason McAnany; Jason C. Park; Gerald A. Fishman; Robert A. Hyde
TAGS: luminance, retina, visual fields, visual thresholds, x-linked retinoschisis
Invest. Ophthalmol. Vis. Sci.. 2021; 62(13):25. doi: https://doi.org/10.1167/iovs.62.13.25

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2021

Clinical and Genetics Characterization of Hypomorphic Variants in Stargardt disease

Winston Lee; Jana Zernant; Takayuki Nagasaki; Gerald A Fishman; Stephen H Tsang; Rando Allikmets

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):2171. doi:

Articles May 2021

Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure

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Katie M. Litts; Erica N. Woertz; Niamh Wynne; Brian P. Brooks; Alicia Chacon; Thomas B. Connor, Jr.; Deborah Costakos; Alina Dumitrescu; Arlene V. Drack; Gerald A. Fishman; William W. Hauswirth; Christine N. Kay; Byron L. Lam; Michel Michaelides; Mark E. Pennesi; Kimberly E. Stepien; Sasha Strul; C. Gail Summers; Joseph Carroll
TAGS: achromatopsia, albinism, retinal cone, diagnostic imaging, mosaicism
Trans. Vis. Sci. Tech.. 2021; 10(6):22. doi: https://doi.org/10.1167/tvst.10.6.22

Includes: Supplemental Content

Articles January 2021

Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia

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Katie M. Litts; Erica N. Woertz; Michalis Georgiou; Emily J. Patterson; Byron L. Lam; Gerald A. Fishman; Mark E. Pennesi; Christine N. Kay; William W. Hauswirth; Michel Michaelides; Joseph Carroll
TAGS: achromatopsia, artifacts, diagnostic imaging, ophthalmoscopy, optical coherence tomography, optics
Trans. Vis. Sci. Tech.. 2021; 10(1):11. doi: https://doi.org/10.1167/tvst.10.1.11

Includes: Supplemental Content

Articles August 2020

Electrophysiological and Pupillometric Abnormalities in PROM1 Cone–Rod Dystrophy

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Jason C. Park; Frederick T. Collison; Gerald A. Fishman; J. Jason McAnany
TAGS: electroretinography, passive leg raising, progressive cone-rod dystrophy, retinitis pigmentosa, luminance
Trans. Vis. Sci. Tech.. 2020; 9(9):26. doi: https://doi.org/10.1167/tvst.9.9.26

Visual Neuroscience June 2020

Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis

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J. Jason McAnany; Jason C. Park; Gerald A. Fishman; Frederick T. Collison
TAGS: electroretinography, luminance, x-linked retinoschisis, pupillometry, passive leg raising
Invest. Ophthalmol. Vis. Sci.. 2020; 61(6):53. doi: https://doi.org/10.1167/iovs.61.6.53

ARVO Annual Meeting Abstract June 2020

Optical coherence tomography artifacts predict adaptive optics scanning light ophthalmoscopy success in achromatopsia

Katie M Litts; Erica N. Woertz; Rachel E Linderman; Byron L Lam; Gerald A Fishman; Mark E Pennesi; Christine N Kay; William W Hauswirth; Joseph Carroll

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):5271. doi:

ARVO Annual Meeting Abstract July 2019

Characteristic ocular features in cases of autosomal recessive PROM1 cone-rod dystrophy

Frederick T Collison; Gerald A. Fishman; Takayuki Nagasaki; J Jason McAnany; Jason C Park; Rando Allikmets

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4512. doi:

ARVO Annual Meeting Abstract July 2019

Analysis of ABCA4 mutation spectrum in Stargardt/ABCA4 disease

Jana Zernant; Winston Lee; Fred Collison; Gerald A Fishman; Stephen Tsang; Rando Allikmets

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5016. doi:

ARVO Annual Meeting Abstract July 2019

Pathognomonic macular ripples in fovea plana are revealed by polarized infrared reflectance imaging

Darius Ansari; Xincheng Yao; Frederick T Collison; Gerald A Fishman; Michael A Grassi

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1563. doi:

Genetics May 2019

Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy

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Frederick T. Collison; Gerald A. Fishman; Takayuki Nagasaki; Jana Zernant; J. Jason McAnany; Jason C. Park; Rando Allikmets
TAGS: autosomal recessive inheritance, diagnostic imaging, electroretinography, progressive cone-rod dystrophy, retinitis pigmentosa, family, spectral domain-optical coherence tomography, autofluorescence, color, genetic analysis
Invest. Ophthalmol. Vis. Sci.. 2019; 60(6):2347-2356. doi: https://doi.org/10.1167/iovs.19-26993

ARVO Annual Meeting Abstract July 2018

Interocular symmetry of foveal cone topography in achromatopsia (ACHM)

Katie M Litts; Christopher S Langlo; Emily J Patterson; Rebecca Mastey; Jenna A Cava; Patrick May; Byron L Lam; Gerald A Fishman; Mark E Pennesi; Christine N. Kay; Alfredo Dubra; William W Hauswirth; Kathleen N Beasley; Jeffrey D Chulay; Joseph Carroll

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4992. doi:

ARVO Annual Meeting Abstract June 2017

Frequent hypomorphic alleles solve 80% of late-onset ABCA4 disease and distinguish it from age-related macular degeneration

Rando Allikmets; Jana Zernant; Frederick T Collison; Gerald A Fishman; Yuri V Sergeev; Kaspar Schuerch; Janet R Sparrow; Stephen Tsang; Winston Lee

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1240. doi:

ARVO Annual Meeting Abstract June 2017

Full-field measures of visual function in X-linked retinoschisis: comparison of ERGs, luminance thresholds, and pupil responses

J Jason McAnany; Jason C Park; Frederick T Collison; Gerald A Fishman

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4279. doi:

ARVO Annual Meeting Abstract June 2017

North Carolina macular dystrophy: mutations found in 12 additional families

Kent W Small; Fadi Shaya; Svetlana Yelchits; Adam P DeLuca; Richard Alan Lewis; Monique J Leys; Nitin Udar; Benjamin Bakall; Klaus Rohrschneider; Bernard Puech; Virginie Puech; Elise Heon; James C Folk; Gerald A Fishman; Christine Garabetian; Edwin M Stone

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2779. doi:

ARVO Annual Meeting Abstract June 2017

Visual acuity in Stargardt disease patients after age 40

Frederick T Collison; Gerald A Fishman

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4667. doi:

Retina May 2017

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene

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Samuel G. Jacobson; Artur V. Cideciyan; Alexander Sumaroka; Alejandro J. Roman; Jason Charng; Monica Lu; Windy Choi; Rebecca Sheplock; Malgorzata Swider; Mychajlo S. Kosyk; Sharon B. Schwartz; Edwin M. Stone; Gerald A. Fishman
TAGS: cohort studies, eye, genes, introns, leber's amaurosis, mutation, outcome measures, questionnaires, vision, diagnostic imaging
Invest. Ophthalmol. Vis. Sci.. 2017; 58(5):2609-2622. doi: https://doi.org/10.1167/iovs.17-21560

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

Assessing color vision in congenital achromatopsia

Emily J Patterson; Christopher S Langlo; Byron L Lam; Christine Nichols Kay; Mark E Pennesi; Richard G Weleber; Gerald A Fishman; William W Hauswirth; Joseph Carroll

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

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A common haplotype in the PRPH2 gene modifies Stargardt/ABCA4 disease.

Contrast Sensitivity and Equivalent Intrinsic Noise in X-Linked Retinoschisis

Luminance Thresholds and Their Correlation With Retinal Structure in X-Linked Retinoschisis

Clinical and Genetics Characterization of Hypomorphic Variants in Stargardt disease

Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure

Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia

Electrophysiological and Pupillometric Abnormalities in PROM1 Cone–Rod Dystrophy

Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis

Optical coherence tomography artifacts predict adaptive optics scanning light ophthalmoscopy success in achromatopsia

Characteristic ocular features in cases of autosomal recessive PROM1 cone-rod dystrophy

Analysis of ABCA4 mutation spectrum in Stargardt/ABCA4 disease

Pathognomonic macular ripples in fovea plana are revealed by polarized infrared reflectance imaging

Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy

Interocular symmetry of foveal cone topography in achromatopsia (ACHM)

Frequent hypomorphic alleles solve 80% of late-onset ABCA4 disease and distinguish it from age-related macular degeneration

Full-field measures of visual function in X-linked retinoschisis: comparison of ERGs, luminance thresholds, and pupil responses

North Carolina macular dystrophy: mutations found in 12 additional families

Visual acuity in Stargardt disease patients after age 40

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene

Assessing color vision in congenital achromatopsia

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