Dror Sharon

15PUBLICATIONS
193CO-AUTHORS
NeurogeneticsSensory systemsGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesCell and nuclear division
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (15)

|Sep 30, 2026
A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Jul 29, 2025
Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Sofia Kulyamzin, Rina Leibu, Hadas Newman

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Nov 27, 2024
A Leaky Deep Intronic Splice Variant in CLRN1 Is Associated with Non-Syndromic Retinitis Pigmentosa.

Maria Abu Elasal, Samer Khateb, Daan M Panneman

|Jul 27, 2024
Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes.

Maria Abu Elasal, Samira Mousa, Manar Salameh

Pageof 3

Frequent Collaborators

5 joint publications

Susanne Roosing

4 joint publications

Carlo Rivolta

3 joint publications

Mor Hanany

3 joint publications

Lisa Roberts