Leah Rizel - Concepedia

Author

Leah Rizel

Rappaport Family Institute for Research in the Medical Sciences

Also Known As

L. Rizel, Leah Rizel

Publications

369

Citations

H-Index

Concepts

All Affiliations

Rappaport Family Institute for Research in the Medical Sciences Technion – Israel Institute of Technology Rambam Health Care Campus Emek Medical Center Hadassah Medical Center

About

Leah Rizel is an author at Rappaport Family Institute for Research in the Medical Sciences specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	231
2	Public Health	2	2	69
3	Cell Biology	1	1	87
4	Epidemiology	1	1	36
5	Molecular Biology	1	1	75

Leah Rizel

Publications

348

Citations

H-Index

Page 1

	Year	Citations
Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa Rob W.J. Collin, Christine Safieh, Karin W. Littink, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	2010	87
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT) Lonneke Haer‐Wigman, Horatio Hackett Newman, Rina Leibu, Human Molecular Genetics Ocular DiseaseGeneticsGlycobiologyMolecular BiologyPathology	2015	75
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping Liat Benayoun, Ronen Spiegel, Noa Auslender, American Journal of Medical Genetics Part A	2009	39
Abetalipoproteinemia in Israel: Evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient Liat Benayoun, Esther Granot, Leah Rizel, Molecular Genetics and Metabolism Founder MutationContiguous Gene DeletionGenetic DisorderGeneticsGenetic Epidemiology	2007	36
Four <i>USH2A</i> Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews Noa Auslender, Dikla Bandah, Leah Rizel, Genetic Testing GeneticsGenetic EpidemiologyPathologyUsh2a MutationsMolecular Genetics	2008	33
An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy. Osnat Eidinger, Rina Leibu, Hadas Newman, PubMed	2015	27
Genetic heterogeneity and consanguinity lead to a "double hit": homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa. Nitza Goldenberg‐Cohen, Eyal Banin, Yael Zalzstein, PubMed	2013	21
PRCD is Concentrated at the Base of Photoreceptor Outer Segments and is Involved in Outer Segment Disc Formation Gilad Allon, Irit Mann, Lital Remez, Human Molecular Genetics	2019	17
Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1. Leah Rizel, Christine Safieh, Stavit Shalev, PubMed Central	2011	13

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