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Vision Sciences Society Annual Meeting Abstract September 2018

Conservative Criterion Explains The Non-Conscious Perception of Facial Expression Under Continuous Flash Suppression

Ali Pournaghdali; Bennett Schwartz

Journal of Vision. 2018; 18(10):945. https://doi.org/10.1167/18.10.945

ARVO Annual Meeting Abstract June 2017

Interocular Symmetry of Rod and Cone Topography in Human ORF15-RPGR -XLRP Disease Despite Large Intraretinal, Intrafamilial and Interfamilial Variation

Artur V Cideciyan; Jason Charng; Samuel G Jacobson; Alexander Sumaroka; Sharon B. Schwartz; Malgorzata Swider; Alejandro J Roman; Rebecca Sheplock; Manisha Anand; Marc C. Peden; Hemant Khanna; Elise Heon; Alan F. Wright; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3232.

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. https://doi.org/10.1167/iovs.17-21560

Includes: Supplemental Content

Visual Neuroscience February 2017

Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene

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Geoffrey K. Aguirre; Omar H. Butt; Ritobrato Datta; Alejandro J. Roman; Alexander Sumaroka; Sharon B. Schwartz; Artur V. Cideciyan; Samuel G. Jacobson
TAGS: blindness, functional magnetic resonance imaging, genes, mutation, photoreceptors, primary visual cortex, vision, white matter, blood oxygen level dependent, retina
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):959-973. https://doi.org/10.1167/iovs.16-20413

ARVO Annual Meeting Abstract September 2016

Comparative Measurements of Rod Function in Retinal Degenerations with Two-color Dark-adapted Perimetry

Artur V Cideciyan; Jason Charng; Malgorzata Swider; Rebecca Sheplock; David B McGuigan; Rodrigo Matsui; Alejandro J Roman; Sharon B Schwartz; Samuel G Jacobson

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):131.

ARVO Annual Meeting Abstract September 2016

Fragile Maculas in Patients with Retinal Degeneration due to RPGR - ORF15 Mutations: Spatio-temporal Models of Disease Progression

Jason Charng; Malgorzata Swider; Rebecca Sheplock; Alexander Sumaroka; Alejandro J Roman; Marc Christopher Peden; Elise Heon; Sharon B Schwartz; Samuel G Jacobson; Artur V Cideciyan

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):156.

Retina September 2016

Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations

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Samuel G. Jacobson; David B. McGuigan, III; Alexander Sumaroka; Alejandro J. Roman; Michaela L. Gruzensky; Rebecca Sheplock; Judy Palma; Sharon B. Schwartz; Tomas S. Aleman; Artur V. Cideciyan
TAGS: family, mutation, pathophysiology, phenotype, retina, retinitis pigmentosa, rhodopsin, rod photoreceptors, retinal cone, visual fields
Invest. Ophthalmol. Vis. Sci.. 2016; 57(11):4847-4858. https://doi.org/10.1167/iovs.16-19890

Articles July 2016

Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations

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Alexander Sumaroka; Rodrigo Matsui; Artur V. Cideciyan; David B. McGuigan, III; Rebecca Sheplock; Sharon B. Schwartz; Samuel G. Jacobson
TAGS: mutation, optical coherence tomography, retina, usher syndrome, vision, rod photoreceptors, fovea centralis
Invest. Ophthalmol. Vis. Sci.. 2016; 57(9):OCT253-OCT261. https://doi.org/10.1167/iovs.15-18860

Retina September 2015

Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration

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Rodrigo Matsui; Artur V. Cideciyan; Sharon B. Schwartz; Alexander Sumaroka; Alejandro J. Roman; Malgorzata Swider; Wei Chieh Huang; Rebecca Sheplock; Samuel G. Jacobson
TAGS: cohort studies, heterogeneity, pathophysiology, retinal degeneration, rod photoreceptors, scotoma, vision, retinal cone
Invest. Ophthalmol. Vis. Sci.. 2015; 56(10):6007-6018. https://doi.org/10.1167/iovs.15-17174

Includes: Supplemental Content

Retina September 2015

Predicting Progression of ABCA4 -Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front

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Artur V. Cideciyan; Malgorzata Swider; Sharon B. Schwartz; Edwin M. Stone; Samuel G. Jacobson
TAGS: laplace transform damping factor for arterial velocity waveform, laser-doppler flowmetry, meridians, nose, retina, retinal degeneration, follow-up, disease progression, diagnostic imaging
Invest. Ophthalmol. Vis. Sci.. 2015; 56(10):5946-5955. https://doi.org/10.1167/iovs.15-17698

Includes: Supplemental Content

Retina January 2015

Pseudo-Fovea Formation After Gene Therapy for RPE65 -LCA

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Artur V. Cideciyan; Geoffrey K. Aguirre; Samuel G. Jacobson; Omar H. Butt; Sharon B. Schwartz; Malgorzata Swider; Alejandro J. Roman; Sam Sadigh; William W. Hauswirth
TAGS: eye, fovea centralis, gene therapy, pathologic nystagmus, retina
Invest. Ophthalmol. Vis. Sci.. 2015; 56(1):526-537. https://doi.org/10.1167/iovs.14-15895

Includes: Multimedia, Supplemental Content

Retina August 2014

TULP1 Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

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Samuel G. Jacobson; Artur V. Cideciyan; Wei Chieh Huang; Alexander Sumaroka; Alejandro J. Roman; Sharon B. Schwartz; Xunda Luo; Rebecca Sheplock; Joanna M. Dauber; Malgorzata Swider; Edwin M. Stone
TAGS: ciliopathies, diagnostic imaging, mutation, retinal cone, retinal degeneration, vision, photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2014; 55(8):5354-5364. https://doi.org/10.1167/iovs.14-14570

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2014

Genomewide search for genetic modifiers in patients with Leber congenital amaurosis using whole exome sequencing

Rinki Ratna Priya; David Zipprer; Xiaowei Zhan; James S Friedman; Sharon B Schwartz; Dror Sharon; Eyal Banin; Goncalo Abecasis; Samuel G Jacobson; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3282.

Retina March 2014

Inner and Outer Retinal Changes in Retinal Degenerations Associated With ABCA4 Mutations

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Wei Chieh Huang; Artur V. Cideciyan; Alejandro J. Roman; Alexander Sumaroka; Rebecca Sheplock; Sharon B. Schwartz; Edwin M. Stone; Samuel G. Jacobson
TAGS: mutation, photoreceptors, retina, retinal degeneration, vision, retinal diseases, fovea centralis
Invest. Ophthalmol. Vis. Sci.. 2014; 55(3):1810-1822. https://doi.org/10.1167/iovs.13-13768

Retina February 2013

Intervisit Variability of Visual Parameters in Leber Congenital Amaurosis Caused by RPE65 Mutations

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Alejandro J. Roman; Artur V. Cideciyan; Sharon B. Schwartz; Melani B. Olivares; Elise Heon; Samuel G. Jacobson
TAGS: kinetics, leber's amaurosis, mutation, vision, visual fields, perimetry
Invest. Ophthalmol. Vis. Sci.. 2013; 54(2):1378-1383. https://doi.org/10.1167/iovs.12-11341

Genetics December 2012

Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease

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Kari Branham; Mohammad Othman; Matthew Brumm; Athanasios J. Karoukis; Pelin Atmaca-Sonmez; Beverly M. Yashar; Sharon B. Schwartz; Niamh B. Stover; Karmen Trzupek; Dianna Wheaton; Barbara Jennings; Maria Laura Ciccarelli; K. Thiran Jayasundera; Richard A. Lewis; David Birch; Jean Bennett; Paul A. Sieving; Sten Andreasson; Jacque L. Duncan; Gerald A. Fishman; Alessandro Iannaccone; Richard G. Weleber; Samuel G. Jacobson; John R. Heckenlively; Anand Swaroop
TAGS: degenerative disorders, mutation, x-linked inheritance, screening, genes
Invest. Ophthalmol. Vis. Sci.. 2012; 53(13):8232-8237. https://doi.org/10.1167/iovs.12-11025

Retina August 2012

RPGR- Associated Retinal Degeneration in Human X-Linked RP and a Murine Model

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Wei Chieh Huang; Alan F. Wright; Alejandro J. Roman; Artur V. Cideciyan; Forbes D. Manson; Dina Y. Gewaily; Sharon B. Schwartz; Sam Sadigh; Maria P. Limberis; Peter Bell; James M. Wilson; Anand Swaroop; Samuel G. Jacobson
TAGS: mice, retinal cone, retinal degeneration, retinal diseases, rod photoreceptors, x-linked inheritance, electroretinography, retina, histopathology tests, phenotype
Invest. Ophthalmol. Vis. Sci.. 2012; 53(9):5594-5608. https://doi.org/10.1167/iovs.12-10070

Includes: Supplemental Content

ARVO Annual Meeting Abstract March 2012

Retinal Structure and Visual Function in Patients with Blue Cone Monochromatism

Xunda Luo; Artur V. Cideciyan; Alexander Sumaroka; Sharon B. Schwartz; Alejandro J. Roman; Jacqueline B. Goldberg; Britta Bauman; Bernd Wissinger; Susanne Kohl; Samuel G. Jacobson

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):5671.

Retina February 2012

Macular Function in Macular Degenerations: Repeatability of Microperimetry as a Potential Outcome Measure for ABCA4 -Associated Retinopathy Trials

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Artur V. Cideciyan; Malgorzata Swider; Tomas S. Aleman; Willam J. Feuer; Sharon B. Schwartz; Robert C. Russell; Janet D. Steinberg; Edwin M. Stone; Samuel G. Jacobson
TAGS: macular degeneration, macular function, outcome measures, perimetry, retina, retinal diseases, vision, scotoma
Invest. Ophthalmol. Vis. Sci.. 2012; 53(2):841-852. https://doi.org/10.1167/iovs.11-8415

Includes: Supplemental Content

Genetics December 2011

Autosomal Recessive Retinitis Pigmentosa Caused by Mutations in the MAK Gene

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Edwin M. Stone; Xunda Luo; Elise Héon; Byron L. Lam; Richard G. Weleber; Jennifer A. Halder; Louisa M. Affatigato; Jacqueline B. Goldberg; Alexander Sumaroka; Sharon B. Schwartz; Artur V. Cideciyan; Samuel G. Jacobson
TAGS: autosomal recessive inheritance, genes, mutation, retinitis pigmentosa, rod photoreceptors, perimetry, retinal cone, vision
Invest. Ophthalmol. Vis. Sci.. 2011; 52(13):9665-9673. https://doi.org/10.1167/iovs.11-8527

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Conservative Criterion Explains The Non-Conscious Perception of Facial Expression Under Continuous Flash Suppression

Interocular Symmetry of Rod and Cone Topography in Human ORF15-RPGR -XLRP Disease Despite Large Intraretinal, Intrafamilial and Interfamilial Variation

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

Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene

Comparative Measurements of Rod Function in Retinal Degenerations with Two-color Dark-adapted Perimetry

Fragile Maculas in Patients with Retinal Degeneration due to RPGR - ORF15 Mutations: Spatio-temporal Models of Disease Progression

Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations

Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations

Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration

Predicting Progression of ABCA4 -Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front

Pseudo-Fovea Formation After Gene Therapy for RPE65 -LCA

TULP1 Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

Genomewide search for genetic modifiers in patients with Leber congenital amaurosis using whole exome sequencing

Inner and Outer Retinal Changes in Retinal Degenerations Associated With ABCA4 Mutations

Intervisit Variability of Visual Parameters in Leber Congenital Amaurosis Caused by RPE65 Mutations

Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease

RPGR- Associated Retinal Degeneration in Human X-Linked RP and a Murine Model

Retinal Structure and Visual Function in Patients with Blue Cone Monochromatism

Macular Function in Macular Degenerations: Repeatability of Microperimetry as a Potential Outcome Measure for ABCA4 -Associated Retinopathy Trials

Autosomal Recessive Retinitis Pigmentosa Caused by Mutations in the MAK Gene

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