Dror Sharon

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Venues

Journal of medical genetics

International journal of molecular sciences

Proceedings of the National Academy of Sciences of the United States of America

Human mutation

Hadassah Medical Organization

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hadassah Medical Organization Dec 1o 2002

Israel

PI :: Ophthalmology

Publications

Tamar Hayman, Talya Millo, Karen Hendler, Itay Chowers, Menachem Gross, Eyal Banin, Dror Sharon
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 (2023)
Avigail Beryozkin, Ananya Samanta, Prakadeeswari Gopalakrishnan, Samer Khateb, Eyal Banin, Dror Sharon, Kerstin Nagel-Wolfrum
Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in FAM161A . International journal of molecular sciences 23 (7) (2022)
Martial Mbefo, Adeline Berger, Karine Schouwey, Xavier Gérard, Corinne Kostic, Avigail Beryozkin, Dror Sharon, Hélène Dolfuss, Francis Munier, Hoai Viet Tran, Maarten van Lohuizen, William A Beltran, Yvan Arsenijevic
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy. International journal of molecular sciences 22 (17) (2021)
Mor Hanany, Carlo Rivolta, Dror Sharon
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases. Proceedings of the National Academy of Sciences of the United States of America 117 (5) (2020)
Mor Hanany, Dror Sharon
Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variants. Journal of medical genetics 56 (8) (2019)
Dror Sharon, Tamar Ben-Yosef, Gokhan Gurelik, Eran Pras, Libe Gradstein, Shiri Soudry, Mezer Eedy, Dinah Zur, Anan H Abbasi, Christina Zeitz, Frans P M Cremers, Muhammad I Khan, Jaime Levy, Ygal Rotenstreich, Ohad S Birk, Miriam Ehrenberg, Rina Leibu, Hadas Newman, Noam Shomron, Eyal Banin, Ido Perlman
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC). Human mutation 41 (1) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Dror Sharon