Dror Sharon

Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 124 publications

The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population.

The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population.

Journal: Investigative ophthalmology & visual science

Published: April 13, 2026

PRCD-associated retinitis pigmentosa in dogs and humans.

PRCD-associated retinitis pigmentosa in dogs and humans.

Journal: Experimental eye research

Published: December 01, 2025

RNA editing of pathogenic variants causing inherited retinal diseases using endogenous ADAR-current and future perspectives.

RNA editing of pathogenic variants causing inherited retinal diseases using endogenous ADAR-current and future perspectives.

Journal: Molecular aspects of medicine

Published: October 06, 2025

The potential use of anti-codon engineered tRNAs (ACE-tRNAs) to treat nonsense variants causing inherited retinal diseases.

The potential use of anti-codon engineered tRNAs (ACE-tRNAs) to treat nonsense variants causing inherited retinal diseases.

Journal: Molecular aspects of medicine

Published: October 05, 2025

Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration.

Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration.

Journal: JAMA ophthalmology

Published: July 17, 2025

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs).

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs).

Journal: bioRxiv : the preprint server for biology

Published: July 15, 2025

RetiGene, a comprehensive gene atlas for inherited retinal diseases.

RetiGene, a comprehensive gene atlas for inherited retinal diseases.

Journal: American journal of human genetics

Published: June 10, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics

Published: June 02, 2025

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Journal: Genes

Published: May 25, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Journal: NPJ genomic medicine

Published: April 22, 2025

Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll.

Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll.

Journal: Investigative ophthalmology & visual science

Published: February 05, 2025

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Journal: medRxiv : the preprint server for health sciences

Published: January 20, 2025

Showing 1-12 of 124

Last Updated: 09/26/2026