Michael Korostishevsky

Author

Tel Aviv University

Also Known As

Michael Korostishevsky

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Tel Aviv University Sheba Medical Center Schneider Children's Medical Center Rabin Medical Center Geha Mental Health Center

About

Michael Korostishevsky is an author at Tel Aviv University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	717
2	Public Health	4	4	114
3	Health Sciences	3	3	130
4	Arts	1	1	234
5	Allergy	1	1	19

Michael Korostishevsky

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness Hamish S. Scott, Jun Kudoh, Marie Wattenhofer‐Donzé, Nature Genetics Developmental BiologyTransmembrane ProteasePediatric OtolaryngologyGenetic DisorderMendelian Disorder	2001	234
Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis Michael Korostishevsky, M. Kaganovich, Alina Cholostoy, Biological Psychiatry Risk PredictionPsychiatryPsychotic DisorderGeneticsPsychiatric Genetics	2004	184
Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high‐risk women Tair Kontorovich, Asaf Levy, Michael Korostishevsky, International Journal of Cancer	2009	122
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population Clinton T. Baldwin, Sari Weiss, Lindsay A. Farrer, Human Molecular Genetics	1995	98
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome Doron Gothelf, Elena Michaelovsky, Amos Frisch, The International Journal of Neuropsychopharmacology	2006	68
Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3 Hannah Tamary, Lea Shalmon, Hanna Shalev, The American Journal of Human Genetics CytogeneticsGenetic DisorderGeneticsHematology1-Cm Interval	1998	59
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS Elena Michaelovsky, Doron Gothelf, Michael Korostishevsky, The International Journal of Neuropsychopharmacology	2007	53
Genomics and metabolomics of muscular mass in a community-based sample of UK females Michael Korostishevsky, Claire J. Steves, Ida Malkin, European Journal of Human Genetics ObesityMetabolic SyndromeCommunity-based SampleBody CompositionMetabolic Disorder	2015	45
Ala244Val Is a Common, Probably Ancient Mutation Causing Factor VII Deficiency in Moroccan and Iranian Jews Hannah Tamary, Yonit Fromovich, Lea Shalmon, Thrombosis and Haemostasis Serine Protease DomainGeneticsImmunologyGenetic EpidemiologyPathology	1996	43
Pemphigus vulgaris in Jewish patients is associated with HLA-A region genes Elena Slomov, Ron Loewenthal, Ilan Goldberg, Human Immunology Autoimmune DiseaseGeneticsPathogenesisPathologyAutoimmunity	2003	35

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