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ARVO Annual Meeting Abstract June 2020

Rapid onset post-operative pre-retinal fibrosis is Macular Proliferative Vitreoretinopathy (PVR) rather than Epiretinal Membrane (ERM) – A case series

Hamzah Aweidah; Samer Khateb; Shahar Frenkel; Tareq Jaouni

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4246. doi:

ARVO Annual Meeting Abstract July 2018

Analysis of the Aqueous Humor Proteome in Patients with Age-related Macular Degeneration

Itay Chowers; Gala Beykin; Liran Tiosano; Samer Khateb; Sarah Hayoun; Michelle Grunin; Shira Levi; Batya Rinsky

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):356. doi:

ARVO Annual Meeting Abstract July 2018

Analysis of CEP78 knockout in zebrafish generated by CRISPR-Cas9

Yael Kinarty; Samer Khateb; Dror Sharon; Adi Inbal

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):375. 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:

Genetics February 2018

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations

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Ayat Khalaileh; Alaa Abu-Diab; Tamar Ben-Yosef; Annick Raas-Rothschild; Israela Lerer; Yahya Alswaiti; Itay Chowers; Eyal Banin; Dror Sharon; Samer Khateb
TAGS: genetics, mutation, usher syndrome, family
Invest. Ophthalmol. Vis. Sci.. 2018; 59(2):1095-1104. doi: https://doi.org/10.1167/iovs.17-22817

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2017

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects

Adva Kimchi; Samer Khateb; Rong Wen; Ziqiang Guan; Eran Pras; Shoshi Kurtzman; Samuel G Jacobson; Hadas Newman; Tamar Ben-Yosef; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):570. doi:

ARVO Annual Meeting Abstract June 2017

Whole-Genome Association Study of Age-Related Macular Degeneration in the Israeli Population

Itay Chowers; Gala Beykin; Elior Rahmani; Regev Schweiger; Liran Tiosano; Samer Khateb; Shira Levi; Batya Rinsky; Shai Carmi; Eran Halperin; Michelle Grunin

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1834. 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

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations

Samer Khateb; Ayat Khalaileh; Tamar Ben-Yosef; Annick Raas-Rothschild; Itay Chowers; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3154. doi:

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:

ARVO Annual Meeting Abstract April 2014

A Nonsense Mutation in CEP250, a Mammalian-Specific Homolog of Rootletin, Causes Usher Syndrome

Samer Khateb; Lina Zelinger; Liliana Mizrahi-Meissonnier; Carmen Ayuso; Robert K Koenekoop; Uri Laxer; Menachem Gross; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1712. doi:

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:

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