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Article December 2016

The risk of pedestrian collisions with peripheral visual field loss

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Eli Peli; Henry Apfelbaum; Eliot L. Berson; Robert B. Goldstein
TAGS: blindness, pedestrian, gait, prisms, vision
Journal of Vision. 2016; 16(15):5. https://doi.org/10.1167/16.15.5

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

Residual Peripheral Fields in RP and the Risk for Pedestrian Collisions

Eli Peli; Henry Apfelbaum; Eliot L Berson; Robert B Goldstein

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4776.

Biochemistry and Molecular Biology December 2014

Targeted Exon Sequencing in Usher Syndrome Type I

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Kinga M. Bujakowska; Mark Consugar; Emily Place; Shyana Harper; Jaclyn Lena; Daniel G. Taub; Joseph White; Daniel Navarro-Gomez; Carol Weigel DiFranco; Michael H. Farkas; Xiaowu Gai; Eliot L. Berson; Eric A. Pierce
TAGS: exons, genes, mutation, usher syndrome, cohort studies, massively-parallel genome sequencing
Invest. Ophthalmol. Vis. Sci.. 2014; 55(12):8488-8496. https://doi.org/10.1167/iovs.14-15169

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2014

Long-term Vision Changes in Carriers of X-linked Retinitis Pigmentosa

Jason Comander; Carol Weigel-DiFranco; Eliot L Berson

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1393.

ARVO Annual Meeting Abstract April 2014

The Relationship of Cystoid Macular Edema to Urinary Iodine Concentration in Retinitis Pigmentosa

Michael A. Sandberg; Elizabeth N Pearce; Shyana Harper; Carol Weigel-DiFranco; Lois Hart; Bernard Rosner; Eliot L Berson

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1404.

ARVO Annual Meeting Abstract April 2014

Molecular characterization of SNRNP200 mutations causing autosomal dominant retinitis pigmentosa with incomplete penetrance and phenotypic variability

Carlo Rivolta; Paola Benaglio; Tremeur Guillaumie; Gael Manes; Shyana Harper; Eliot L Berson; Isabelle Meunier; Christian P Hamel

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3264.

ARVO Annual Meeting Abstract March 2012

FAM161A Mutations In Patients With Early-onset Retinitis Pigmentosa In The United States

Adriana Ransijn; Giulia Venturini; Silvio Alessandro Di Gioia; Shyana Harper; Carol Weigel-DiFranco; Carlo Rivolta; Eliot L. Berson

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4545.

ARVO Annual Meeting Abstract March 2012

Whole Genome Analysis Of 16 Unrelated Patients With Autosomal Recessive Retinitis Pigmentosa Reveals Novel Single-Base And Large Structural Genomic Mutations

Koji M. Nishiguchi; Makoto Nakamura; Mineo Kondo; Shinji Ueno; Tetsuhiro R. Yasuma; Rick Tearle; Jacques Beckmann; Hiroko Terasaki; Eliot L. Berson; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4524.

Retina November 2011

Disease Course of Patients with Unilateral Pigmentary Retinopathy

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Emorfily Potsidis; Eliot L. Berson; Michael A. Sandberg
TAGS: disease progression, eye, retinitis pigmentosa, electroretinography, visual fields
Invest. Ophthalmol. Vis. Sci.. 2011; 52(12):9244-9249. https://doi.org/10.1167/iovs.11-7892

Retinal Cell Biology October 2011

Histopathology and Functional Correlations in a Patient with a Mutation in RPE65 , the Gene for Retinol Isomerase

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Vera L. Bonilha; Mary E. Rayborn; Yong Li; Gregory H. Grossman; Eliot L. Berson; Joe G. Hollyfield
TAGS: autopsy, donors, eye, genes, histopathology tests, isomerase, macula densa, macula lutea, mutation, retina
Invest. Ophthalmol. Vis. Sci.. 2011; 52(11):8381-8392. https://doi.org/10.1167/iovs.11-7973

Includes: Supplemental Content

Biochemistry and Molecular Biology July 2011

Molecular Analysis of Bardet-Biedl Syndrome Families: Report of 21 Novel Mutations in 10 Genes

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Jianjun Chen; Nizar Smaoui; Monia Ben Hamed Hammer; Xiaodong Jiao; S. Amer Riazuddin; Shyana Harper; Nicholas Katsanis; Sheikh Riazuddin; Habiba Chaabouni; Eliot L. Berson; J. Fielding Hejtmancik
TAGS: mutation, family, genes
Invest. Ophthalmol. Vis. Sci.. 2011; 52(8):5317-5324. https://doi.org/10.1167/iovs.11-7554

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2011

Next Generation Sequencing Of Pooled DNA From A Large Cohort Of Patients Reveals New SNRNP200 Mutations Associated With Retinitis Pigmentosa

Paola Benaglio; Leonardo P. Capelli; Shyana Harper; Eliot L. Berson; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3316.

ARVO Annual Meeting Abstract April 2011

Mutation Screening Of The FAM161A Gene (RP28) In An Autosomal Recessive Retinitis Pigmentosa Cohort

Silvio Alessandro Di Gioia; Giulia Venturini; Shyana Harper; Eliot L. Berson; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5371.

ARVO Annual Meeting Abstract April 2011

Generalized Defects In Spliceosome Composition And Pre-mRNA Splicing Are Associated With Retinitis Pigmentosa In Humans

Goranka Tanackovic; Adriana Ransijn; Philippe Thibault; Sherif Abou Elela; Roscoe Klinck; Eliot L. Berson; Benoit Chabot; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):1639.

ARVO Annual Meeting Abstract April 2010

Genotype-Phenotype Correlations in the Bardet-Biedl Syndrome

A. B. Daniels; J. Chen; T. L. McGee; C. Wiegel-DiFranco; M. A. Sandberg; J. F. Hejtmancik; E. L. Berson

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):1382.

ARVO Annual Meeting Abstract April 2010

Histopathology of the Retina in an Eye Donation From a Patient With an RPE65 Mutation

M. E. Rayborn; V. L. Bonilha; Y. Li; G. H. Grossman; J. G. Hollyfield; E. L. Berson

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):4029.

ARVO Annual Meeting Abstract April 2010

Histologic Study of Autopsy Eyes From a Male With X-Linked Stationary Night Blindness With Myopia and a Novel Mutation in the NYX Gene, Leu202Pro

M. Adamian; T. L. McGee; E. L. Berson

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):4062.

ARVO Annual Meeting Abstract April 2010

Replacement Gene Therapy With a Human RPGRIP1 Sequence Slows Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis

B. S. Pawlyk; O. V. Bulgakov; X. Liu; X. Xu; M. Adamian; X. Sun; S. C. Khani; E. L. Berson; M. A. Sandberg; T. Li

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):4497.

Retina February 2010

The Relationship of Macular Pigment Optical Density to Serum Lutein in Retinitis Pigmentosa

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Michael A. Sandberg; Elizabeth J. Johnson; Eliot L. Berson
TAGS: lutein, optics, pigment, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2010; 51(2):1086-1091. https://doi.org/10.1167/iovs.09-3396

ARVO Annual Meeting Abstract April 2009

A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance

C. Rivolta; T. L. McGee; N. M. Wade; C. Iseli; J. S. Beckmann; E. L. Berson; T. Rio Frio

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2318.

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The risk of pedestrian collisions with peripheral visual field loss

Residual Peripheral Fields in RP and the Risk for Pedestrian Collisions

Targeted Exon Sequencing in Usher Syndrome Type I

Long-term Vision Changes in Carriers of X-linked Retinitis Pigmentosa

The Relationship of Cystoid Macular Edema to Urinary Iodine Concentration in Retinitis Pigmentosa

Molecular characterization of SNRNP200 mutations causing autosomal dominant retinitis pigmentosa with incomplete penetrance and phenotypic variability

FAM161A Mutations In Patients With Early-onset Retinitis Pigmentosa In The United States

Whole Genome Analysis Of 16 Unrelated Patients With Autosomal Recessive Retinitis Pigmentosa Reveals Novel Single-Base And Large Structural Genomic Mutations

Disease Course of Patients with Unilateral Pigmentary Retinopathy

Histopathology and Functional Correlations in a Patient with a Mutation in RPE65 , the Gene for Retinol Isomerase

Molecular Analysis of Bardet-Biedl Syndrome Families: Report of 21 Novel Mutations in 10 Genes

Next Generation Sequencing Of Pooled DNA From A Large Cohort Of Patients Reveals New SNRNP200 Mutations Associated With Retinitis Pigmentosa

Mutation Screening Of The FAM161A Gene (RP28) In An Autosomal Recessive Retinitis Pigmentosa Cohort

Generalized Defects In Spliceosome Composition And Pre-mRNA Splicing Are Associated With Retinitis Pigmentosa In Humans

Genotype-Phenotype Correlations in the Bardet-Biedl Syndrome

Histopathology of the Retina in an Eye Donation From a Patient With an RPE65 Mutation

Histologic Study of Autopsy Eyes From a Male With X-Linked Stationary Night Blindness With Myopia and a Novel Mutation in the NYX Gene, Leu202Pro

Replacement Gene Therapy With a Human RPGRIP1 Sequence Slows Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis

The Relationship of Macular Pigment Optical Density to Serum Lutein in Retinitis Pigmentosa

A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance

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