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Retina February 2023

An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy

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Mor Hanany; Richard Rui Yang; Chun Man Lam; Avigail Beryozkin; Yogapriya Sundaresan; Dror Sharon
TAGS: crystal structure, genes, genetics, mutation, prevalence
Trans. Vis. Sci. Tech.. 2023; 12(2):27. https://doi.org/10.1167/tvst.12.2.27

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2022

Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily

Dror Sharon; Talya Millo; Jose Antonio Rivera; Alexey Obolensky; Dvorah Marks-Ohana; Enosh Wilhelm; Prakadee Gopalakrish; Menachem Gross; Boris Rosin; Mor Hanany; Anna Maria Tracewska; Ora Schueler-Furman; Susanne Roosing; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2623.

ARVO Annual Meeting Abstract July 2019

Allele Frequency Analysis of Variants Reported to cause Autosomal Dominant Retinal Diseases Revealed that 17% of Genes and 9% of Mutations are Unlikely Pathogenic

Dror Sharon; Mor Hanany

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2809.

ARVO Annual Meeting Abstract July 2019

Worldwide Carrier Frequency Analysis of Mutations Causing Autosomal Recessive Inherited Retinal Diseases

Mor Hanany; Segev Meyer; Carlo Rivolta; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):407.

ARVO Annual Meeting Abstract July 2018

Carrier Frequency Analysis of Mutations Causing Recessive Inherited Retinal Diseases in the Israeli Population

Dror Sharon; Gilad Allon; Adva Kimchi; Anat Blumenfeld; Hadas Newman; Eran Pras; Libe Gradstein; Eyal Banin; Tamar Ben-Yosef; Mor Hanany

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3494.

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 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.

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