Dror Sharon - Concepedia

Author

Dror Sharon

Hadassah Medical Center ORCID

Also Known As

D SHARON, D Sharon, D. Sharon, DROR SHARON, Dror Sharon, E. Banin, Sharon, D, Sharon, Daniel, Sharon, Dror, Sharon,Dror

240

Publications

7.1K

Citations

H-Index

Concepts

All Affiliations

Hadassah Medical Center Hebrew University of Jerusalem Technion – Israel Institute of Technology Radboud University Nijmegen Radboud University Medical Center

About

Dror Sharon is an author at Hadassah Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	52	3.4K
2	Natural Sciences	10	10	602
3	Engineering	4	4	284
4	Public Health	3	3	171
5	Social Sciences	1	1	37

Dror Sharon

113

Publications

6.1K

Citations

H-Index

Page 1

	Year	Citations
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases Mor Hanany, Carlo Rivolta, Dror Sharon Proceedings of the National Academy of Sciences	2020	368
RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa Dror Sharon, Michael A. Sandberg, Vivian W. Rabe, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2003	225
The olfactory receptor gene superfamily: data mining, classification, and nomenclature Gustavo Glusman, Anita Y. Bahar, Dror Sharon, Mammalian Genome BiologyBioinformaticsNeurobiological MechanismFunctional GenomicsGenetics	2000	216
Shared Mutations in NR2E3 in Enhanced S-cone Syndrome, Goldmann-Favre Syndrome, and Many Cases of Clumped Pigmentary Retinal Degeneration Dror Sharon Archives of Ophthalmology	2003	176
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE) Dror Sharon, Seth Blackshaw, Constance L. Cepko, Proceedings of the National Academy of Sciences Ocular DiseasePeripheral RetinaGeneticsGene CharacterizationMolecular Genetics	2001	169
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics Mubeen Khan, Stéphanie S. Cornelis, Marta Del Pozo‐Valero, Genetics in Medicine Functional GenomicsMedicineNatural SciencesOmics DatasetsNext-generation Sequencing	2020	139
A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews Lina Zelinger, Eyal Banin, Alexey Obolensky, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderAshkenazi JewsGeneticsMissense Mutation	2011	138
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyMendelian DisorderOphthalmologyGenetic Disorder	2012	132
BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Audrey Sénéćhal, Archives of Ophthalmology	2012	125
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and <i>NEK2</i> as a new disease gene Koji M. Nishiguchi, Richard G. Tearle, Yangfan P. Liu, Proceedings of the National Academy of Sciences Dna SequencingProgressive Retinal DegenerationWhole Genome SequencingEngineeringGenetic Disorder	2013	124

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