Dror Sharon
Hebrew University of Jerusalem
H-index: 50
Asia-Israel
Top articles of Dror Sharon
Fine-tuning FAM161A gene augmentation therapy to restore retinal function
EMBO Molecular Medicine
2024/4/15
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis
JAMA ophthalmology
2024/4/11
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Biomolecules
2024/3/19
A pipeline for identifying guide RNA sequences that promote RNA editing of nonsense mutations that cause inherited retinal diseases
Molecular Therapy-Nucleic Acids
2024/3/12
Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes
Journal of Medical Genetics
2024/3/1
Dror Sharon
H-Index: 31
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration
Genetics in Medicine
2024/2/28
Yumei Li
H-Index: 9
Rui Chen
H-Index: 7
Viktória Szabó
H-Index: 2
Dror Sharon
H-Index: 31
Susanne Roosing
H-Index: 23
Best Disease: Global Mutations Review, Genotype–Phenotype Correlation, and Prevalence Analysis in the Israeli Population
Investigative Ophthalmology & Visual Science
2024/2/1
Antonio Rivera
H-Index: 17
Dror Sharon
H-Index: 31
Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations
2024/2/1
Mor Hanany
H-Index: 4
Dror Sharon
H-Index: 31
Best Disease: Review of reported causing mutations, genotype-phenotype correlation, and prevalence analysis in the Israeli population
2023/6/1
Dror Sharon
H-Index: 31
RNA editing of mutations causing inherited retinal diseases using the cellular deaminase acting on RNA (ADAR) enzyme
Investigative Ophthalmology & Visual Science
2023/6/1
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
Human Genetics and Genomics Advances
2023/4/13
Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice
Translational Vision Science & Technology
2023/3/1
Dror Sharon
H-Index: 31
Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease− associated genes
Genetics in Medicine
2023/3/1
Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophies
European Journal of Ophthalmology
2023/3
Antonio Rivera
H-Index: 17
Dror Sharon
H-Index: 31
Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p. Arg523∗ Human Nonsense Pathogenic Variant
Ophthalmology Science
2023/3/1
Dror Sharon
H-Index: 31
An in-depth single-gene worldwide carrier frequency and genetic prevalence analysis of CYP4V2 as the cause of Bietti crystalline dystrophy
Translational Vision Science & Technology
2023/2/1
Mor Hanany
H-Index: 4
Dror Sharon
H-Index: 31
Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry
Molecular Vision
2023
KCNV2-associated retinopathy: genotype–phenotype correlations–KCNV2 study group report 3
British Journal of Ophthalmology
2023/10/18
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability
Human Genetics and Genomics Advances
2023/10/12
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa
Molecular Therapy
2023/10/4
Corinne Kostic
H-Index: 15
Dror Sharon
H-Index: 31
Co-Authors
