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Meeting Abstract (8)
Journal Articles (3)

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Investigative Ophthalmology & Visual Science (11)

Article Type

ARVO Annual Meeting Abstract (8)
Genetics (3)

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Genetics (3)
Eye Anatomy and Disorders (2)
Retina (2)

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mutation (3)
family (2)
genes (2)
homozygote (2)
retinal degeneration (2)
autosomal recessive inheritance (1)
genetic analysis (1)
mosaicism (1)
retinitis pigmentosa (1)
rhodopsin (1)

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ARVO Annual Meeting Abstract July 2019

Subretinal and Intravitreal Delivery of the Photoreceptor-Specific AAV2-7m8-hGRK1-GFP Viral Vector in Mice

Chen Matsevich; Deniz Dalkara; Alexey Obolensky; Melissa Desrosiers; Ayala Ejzenberg; Dror Sharon; Eyal Banin; Avigail Beryozkin

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2924. doi:

ARVO Annual Meeting Abstract July 2018

Ataluren-mediated read-through of a nonsense mutation in FAM161A gene which causes retinitis pigmentosa

Avigail Beryozkin; Ananya Samanta; Samer Khateb; Eyal Banin; Dror Sharon; Uwe Wolfrum; Kerstin Nagel-Wolfrum

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5324. doi:

ARVO Annual Meeting Abstract June 2017

Clinical Characteristics of a Large Cohort of Patients with Retinitis Pigmentosa due to Biallelic FAM161A Mutations

Avigail Beryozkin; Samer Khateb; Carlos Idrobo; Mor Hanany; Alexey Obolensky; Dror Sharon; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3219. doi:

ARVO Annual Meeting Abstract September 2016

Generation and characterization of Fam161a Conditional Knockout mice

Avigail Beryozkin; Alexey Obolensky; Segev Meyer; Ayala Ejzenberg; Chen Matsevich; Yvan Arsenijevic; Carlo Rivolta; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3151. doi:

Genetics March 2016

Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual

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Avigail Beryozkin; Gal Levy; Anat Blumenfeld; Segev Meyer; Prasanthi Namburi; Yair Morad; Libe Gradstein; Anand Swaroop; Eyal Banin; Dror Sharon
TAGS: genes, genetic analysis, mosaicism, mutation, retinitis pigmentosa, rhodopsin, family
Invest. Ophthalmol. Vis. Sci.. 2016; 57(3):940-947. doi: https://doi.org/10.1167/iovs.15-18702

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

Identification of Homozygous and Hemizygous Genomic Deletions that Cause Inherited Retinal Degenerations by Analyzing Whole Exome Sequencing Data

Dror Sharon; Samer Khateb; Ayat Khalailah; Avigail Beryozkin; Liliana Mizrahi-Meissonnier; Alaa Abu-diab; Fathiah Abu-Turkey; Mor Hanany; Tamar Ben-Yosef; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4346. doi:

Genetics February 2014

Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping

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Avigail Beryozkin; Lina Zelinger; Dikla Bandah-Rozenfeld; Elia Shevach; Anat Harel; Tim Storm; Michal Sagi; Dalia Eli; Saul Merin; Eyal Banin; Dror Sharon
TAGS: family, genes, homozygote, mutation, retinal degeneration
Invest. Ophthalmol. Vis. Sci.. 2014; 55(2):1149-1160. doi: https://doi.org/10.1167/iovs.13-13625

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Whole Exome Sequencing as a Tool for Identification of Genes Causing Autosomal Recessive Retinitis Pigmentosa

Dror Sharon; Lina Zelinger; Samer Khateb; Avigail Beryozkin; Liliana Mizrahi-Meissonnier; Samuel Jacobson; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3348. doi:

ARVO Annual Meeting Abstract June 2013

The farnesylated small GTPase RAB28 is mutated in autosomal recessive cone-rod dystrophy

Susanne Roosing; Klaus Rohrschneider; Avigail Beryozkin; Nicole Weisschuh; Susanne Kohl; Bernd Wissinger; Eyal Banin; Frans Cremers; Anneke Den Hollander; RAB28 Study Group

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1228. doi:

Genetics March 2013

Mutations in CRB1 are a Relatively Common Cause of Autosomal Recessive Early-Onset Retinal Degeneration in the Israeli and Palestinian Populations

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Avigail Beryozkin; Lina Zelinger; Dikla Bandah-Rozenfeld; Anat Harel; Tim A. Strom; Saul Merin; Itay Chowers; Eyal Banin; Dror Sharon
TAGS: autosomal recessive inheritance, mutation, retinal degeneration, homozygote
Invest. Ophthalmol. Vis. Sci.. 2013; 54(3):2068-2075. doi: https://doi.org/10.1167/iovs.12-11419

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2011

A Missense Mutation in the Dehydrodolichyl Diphosphate Synthase (DHDDS) Gene is Associated with Autosomal Recessive Retinitis Pigmentosa in Ashkenazi Jews

Lina Zelinger; Eyal Banin; Alex Obolensky; Liliana Mizrahi-Meissonnier; Avigail Beryozkin; Tamar Ben-Yosef; Sharon B. Schwartz; Artur V. Cideciyan; Samuel G. Jacobson; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):75. doi:

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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