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ARVO Annual Meeting Abstract June 2024

PRPH2 Gene Mutations and Associated Phenotypes in IRD patients with diverse genetic background.

Christopher Hallock; Riccardo Sangermano; Elfride De Baere; Siying Lin; Jennifer Thompson; Pascal Escher; Andrea L Vincent; Kaylie D Webb-Jones; Monika Grudzinska Pechhacker; Jacque L Duncan; Samer Khateb; Tamar Ben-Yosef; David G Birch; Andrew Webster; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5297.

ARVO Annual Meeting Abstract June 2024

An intronic REEP6 variant affecting the splicing of a retina-specific exon causes autosomal recessive retinitis pigmentosa in Palestinian patients

Manar Ismail Salameh; Daan Panneman; Susanne Roosing; Frans Cremers; Samer Khateb; Yahya Swaiti; Wissam Saleh; Eyal Banin; Alaa Talbishi; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):6036.

Genetics February 2024

Best Disease: Global Mutations Review, Genotype–Phenotype Correlation, and Prevalence Analysis in the Israeli Population

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Avigail Beryozkin; Ifat Sher; Miriam Ehrenberg; Dinah Zur; Hadas Newman; Libe Gradstein; Francis Simaan; Ygal Rotenstreich; Nitza Goldenberg-Cohen; Irit Bahar; Anat Blumenfeld; Antonio Rivera; Boris Rosin; Iris Deitch-Harel; Ido Perlman; Hadas Mechoulam; Itay Chowers; Rina Leibu; Tamar Ben-Yosef; Eran Pras; Eyal Banin; Dror Sharon; Samer Khateb
TAGS: best1 gene, genetic analysis, genotype-phenotype associations, mutation, prevalence, vitelliform dystrophy, proteins
Invest. Ophthalmol. Vis. Sci.. 2024; 65(2):39. https://doi.org/10.1167/iovs.65.2.39

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2023

Worldwide multicenter ocular imaging study (EyeConic) to identify patients eligible for cone-based optogenetics therapy

Lucas Janeschitz-Kriegl; Zoltán Zsolt Nagy; Boris Rosin; Jacque L Duncan; Michel Michaelides; Byron L Lam; Samer Khateb; Katarina Stingl; Kaoru Fujinami; Giacomo Calzetti; Zi-Bing Jin; Karsten Borgwardt; Michael Adamer; Botond Roska; Bence Gyorgy; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5517.

ARVO Annual Meeting Abstract June 2023

Prospective evaluation of vitreous traction on retinal lattice degeneration and atrophic holes by swept-source optical coherence tomography.

Brice Nguedia Vofo; Yair Bet Yosef; Samer Khateb; Liran Tiosano; Jaime Levy; Itay Chowers

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5007.

ARVO Annual Meeting Abstract June 2023

Best Disease: Review of reported causing mutations, genotype-phenotype correlation, and prevalence analysis in the Israeli population

Samer Khateb; Ygal Rotenstreich; Nitza Goldenberg-Cohen; Libe Gradstein; Boris Rosin; Itay Chowers; Rina Leibu; Hadas Newman; Miriam Ehrenberg; Tamar Ben-Yosef; Eran Pras; Dina Zur; Eyal Banin; Dror Sharon; Avigail Beryozkin

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1528.

Retina March 2023

Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice

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Alaa Abu-Diab; Prakadeeswari Gopalakrishnan; Chen Matsevich; Marije de Jong; Alexey Obolensky; Ayat Khalaileh; Manar Salameh; Ayala Ejzenberg; Menachem Gross; Eyal Banin; Dror Sharon; Samer Khateb
TAGS: homozygote, mice, retinal degeneration, sensorineural hearing loss, mice, knockout, retina
Trans. Vis. Sci. Tech.. 2023; 12(3):3. https://doi.org/10.1167/tvst.12.3.3

Includes: Supplemental Content

Retina August 2021

Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular Degeneration

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Batya Rinsky; Gala Beykin; Michelle Grunin; Radgonde Amer; Samer Khateb; Liran Tiosano; Diego Almeida; Shira Hagbi-Levi; Sarah Elbaz-Hayoun; Itay Chowers
TAGS: age-related macular degeneration, aqueous humor, hypertension, proteins, proteome, enzyme-linked immunosorbent assay
Invest. Ophthalmol. Vis. Sci.. 2021; 62(10):18. https://doi.org/10.1167/iovs.62.10.18

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2021

Clinical characterization and genotype-phenotype correlation in RPGRIP1 patients with autosomal recessive early onset retinal degeneration

Avigail Beryozkin; Hamzah Aweidah; Roque Daniel Carrero-Valenzuela; Manar Salameh; Myriam Berman; Oscar Iguzquiza; Samer Khateb; Tamar Ben-Yosef; Dror Sharon; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3218.

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.

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.

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.

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.

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. 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.

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.

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.

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.

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.

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.

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PRPH2 Gene Mutations and Associated Phenotypes in IRD patients with diverse genetic background.

An intronic REEP6 variant affecting the splicing of a retina-specific exon causes autosomal recessive retinitis pigmentosa in Palestinian patients

Best Disease: Global Mutations Review, Genotype–Phenotype Correlation, and Prevalence Analysis in the Israeli Population

Worldwide multicenter ocular imaging study (EyeConic) to identify patients eligible for cone-based optogenetics therapy

Prospective evaluation of vitreous traction on retinal lattice degeneration and atrophic holes by swept-source optical coherence tomography.

Best Disease: Review of reported causing mutations, genotype-phenotype correlation, and prevalence analysis in the Israeli population

Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice

Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular Degeneration

Clinical characterization and genotype-phenotype correlation in RPGRIP1 patients with autosomal recessive early onset retinal degeneration

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

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

Analysis of CEP78 knockout in zebrafish generated by CRISPR-Cas9

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

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations

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

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

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

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations

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

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

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