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Michael Korostishevsky

Research Profile

Physiology

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Israel

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Genes & Molecular Sequences

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Chromosomes, Human, Pair 11

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Michael Korostishevsky; Ida Malkin; Yufang Pei; Svetlana Trofimov; Hong-Wen Deng; Gregory Livshits
Significant association between body composition phenotypes and the osteocalcin genomic region in normative human population.
Victor Belkin; Michael Korostishevsky; Oleg Pavlovsky; Vladimir Volkov-Dubrovin; Valery Batsevich; eugene kobyliansky
Morpho-physiological features of human populations in the context of climatic--geographical conditions.
Michael Korostishevsky; Orit Blumenfeld; Deborah Hart; Timothy Spector; Frances Williams; Gregory Livshits
Implementation of the simplified stochastic model of ageing for longitudinal osteoarthritis data assessment.

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All Publications

2012: Michael Korostishevsky; Ida Malkin; Yufang Pei; Svetlana Trofimov; Hong-Wen Deng; Gregory Livshits
Significant association between body composition phenotypes and the osteocalcin genomic region in normative human population.
Bone 2012;51(4):688-94.
2012: Victor Belkin; Michael Korostishevsky; Oleg Pavlovsky; Vladimir Volkov-Dubrovin; Valery Batsevich; eugene kobyliansky
Morpho-physiological features of human populations in the context of climatic--geographical conditions.
Collegium antropologicum 2012;36(3):729-43.
2012: Michael Korostishevsky; Orit Blumenfeld; Deborah Hart; Timothy Spector; Frances Williams; Gregory Livshits
Implementation of the simplified stochastic model of ageing for longitudinal osteoarthritis data assessment.
Annals of human biology 2012;39(3):214-22.
2011: Leonid Kalichman; Valery Batsevich; Michael Korostishevsky; eugene kobyliansky
Hand osteoarthritis in longevity populations.
Aging clinical and experimental research 2011;23(5-6):457-62.
2010: Michael Korostishevsky; Zvi R Cohen; Ida Malkin; Sergey Ermakov; O Yarenchuk; Gregory Livshits
Morphological and biochemical features of obesity are associated with mineralization genes' polymorphisms.
International journal of obesity (2005) 2010;34(8):1308-18.
2010: Tair Kontorovich; Asaf Levy; Michael Korostishevsky; Uri Nir; Eitan Friedman
Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high-risk women.
International journal of cancer. Journal international du cancer 2010;127(3):589-97.
2010: Michael Korostishevsky; Ida Malkin; Tim Spector; Gregory Livshits
Parametric model-based statistics for possible genotyping errors and sample stratification in sibling-pair SNP data.
Genetic epidemiology 2010;34(1):26-33.
2009: Olga Ostrovsky; Michael Korostishevsky; Itay Shafat; Margarita Mayorov; Neta Ilan; Israel Vlodavsky; Arnon Nagler
Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation.
Journal of leukocyte biology 2009;86(2):445-55.
2008: Leonid Kalichman; Michael Korostishevsky; eugene kobyliansky
Laterality indices in the Chuvashian population.
Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur 2008;66(4):409-18.
2008: Michael Korostishevsky; Yulia Vistoropsky; Ida Malkin; eugene kobyliansky; Gregory Livshits
Anthropometric and bone-related biochemical factors are associated with different haplotypes of ANKH locus.
Annals of human biology 2008;35(5):535-46.
2008: Elena Michaelovsky; Doron Gothelf; Michael Korostishevsky; Amos Frisch; Merav Burg; Miri Carmel; Tamar Steinberg; Dov Inbar; Alan Apter; Abraham Weizman
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2008;11(3):351-63.
2007: Olga Ostrovsky; Michael Korostishevsky; I Levite; M Leiba; Hanan Galski; Israel Vlodavsky; Arnon Nagler
Association of heparanase gene (HPSE) single nucleotide polymorphisms with hematological malignancies.
Leukemia 2007;21(11):2296-303.
2007: Doron Gothelf; Elena Michaelovsky; Amos Frisch; Ada H Zohar; Gadi Presburger; Merav Burg; Ayala Aviram-Goldring; Moshe Frydman; Josepha Yeshaya; Mordechai Shohat; Michael Korostishevsky; Alan Apter; Abraham Weizman
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2007;10(3):301-8.
2007: Olga Ostrovsky; Michael Korostishevsky; Iris Levite; Merav Leiba; Hanan Galski; Ephraim Gazit; Israel Vlodavsky; Arnon Nagler
Characterization of HPSE gene single nucleotide polymorphisms in Jewish populations of Israel.
Acta haematologica 2007;117(1):57-64.
2006: Michael Korostishevsky; Ilana Kremer; Miryam Kaganovich; Alina Cholostoy; Ibrahim Murad; M Muhaheed; Isaam Bannoura; Marcella Rietschel; Michael Dobrusin; Ullrike Bening-Abu-Shach; Robert H Belmaker; Wolfgang Maier; Richard P Ebstein; Ruth Navon
Transmission disequilibrium and haplotype analyses of the G72/G30 locus: suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(1):91-5.
2005: Elena Slomov; Ron Loewenthal; Michael Korostishevsky; Ilan Goldberg; Sarah Brenner; Ephraim Gazit
Pemphigus vulgaris is associated with the transporter associated with antigen processing (TAP) system.
Human immunology 2005;66(12):1213-22.
2004: Olga Ostrovsky; Arnon Nagler; Michael Korostishevsky; Ephraim Gazit; Hanan Galski
Genotype and allele frequencies of C3435T polymorphism of the MDR1 gene in various Jewish populations of Israel.
Therapeutic drug monitoring 2004;26(6):679-84.
2004: Michael Korostishevsky; Miryam Kaganovich; Alina Cholostoy; Maya Ashkenazi; Yael Ratner; Dvir Dahary; Jeanne Bernstein; Ullrike Bening-Abu-Shach; Edna Ben-Asher; Doron Lancet; Michael Ritsner; Ruth Navon
Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis.
Biological psychiatry 2004;56(3):169-76.
2004: Ron Loewenthal; Yelena Slomov; María Francisca González-Escribano; Iris Goldberg; Michael Korostishevsky; Sarah Brenner; A Nunez-Roldan; J S Conejo-Mir; Ephraim Gazit
Common ancestral origin of pemphigus vulgaris in Jews and Spaniards: a study using microsatellite markers.
Tissue antigens 2004;63(4):326-34.
2004: Michael Korostishevsky; Ron Loewenthal; Yelena Slomov; Ephraim Gazit
Erroneous identification in a mixed population: simulation using Israeli STR data.
International journal of legal medicine 2004;118(2):111-4.
2004: Michael Korostishevsky; Zeev Zaslavsky; Solomon Stavrov
Temperature dependence of the iron-histidine resonance Raman band of deoxyheme proteins: anharmonic coupling versus distribution over taxonomic conformational substates.
Biophysical journal 2004;86(1 Pt 1):656-9; author reply 660-1.
2003: Elena Slomov; Ron Loewenthal; Ilan Goldberg; Michael Korostishevsky; Sarah Brenner; Ephraim Gazit
Pemphigus vulgaris in Jewish patients is associated with HLA-A region genes: mapping by microsatellite markers.
Human immunology 2003;64(8):771-9.
2003: B Bonné-Tamir; Michael Korostishevsky; Alan J Redd; Y Pel-Or; M E Kaplan; Michael F Hammer
Maternal and paternal lineages of the Samaritan isolate: mutation rates and time to most recent common male ancestor.
Annals of human genetics 2003;67(Pt 2):153-64.
2001: Hamish Scott; Jun Kudoh; Marie Wattenhofer; Kazunori Shibuya; A Berry; R Chrast; Michel Guipponi; J Wang; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; F Younus; S Qasim Mehdi; Uppala Radhakrishna; MP Papasavvas; Corinne Gehrig; Colette Rossier; Michael Korostishevsky; A Gal; Nobuyoshi Shimizu; Batsheva Bonne-Tamir; Stylianos E Antonarakis
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
Nature genetics 2001;27(1):59-63.
2000: A Berry; Hamish Scott; Jun Kudoh; Ilana Talior; Michael Korostishevsky; Marie Wattenhofer; Michel Guipponi; C Barras; Colette Rossier; Kazunori Shibuya; J Wang; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; Nobuyoshi Shimizu; Stylianos E Antonarakis; B Bonné-Tamir
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region.
Genomics 2000;68(1):22-9.
1999: Avital Adato; H Kalinski; Dominique Weil; Hassan Chaib; Michael Korostishevsky; Batsheva Bonne-Tamir
Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.
American journal of human genetics 1999;65(1):261-5.
1998: Hannah Tamary; Lea Shalmon; Hanna Shalev; A Halil; D Dobrushin; N Ashkenazi; Meira Zoldan; Peretz Resnitzky; Michael Korostishevsky; Batsheva Bonne-Tamir; Rina Zaizov
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.
American journal of human genetics 1998;62(5):1062-9.
1998: H Kalinsky; A Funes; A Zeldin; Y Pel-Or; Michael Korostishevsky; Ruth Gershoni-Baruch; Lindsay A Farrer; Batsheva Bonne-Tamir
Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups.
Human mutation 1998;11(2):145-51.
1997: B Bonné-Tamir; AM Nystuen; E Seroussi; H Kalinsky; A E Kwitek-Black; Michael Korostishevsky; Avital Adato; Val C Sheffield
Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.
American journal of physical anthropology 1997;104(2):193-200.
1997: Avital Adato; Dominique Weil; H Kalinski; Y Pel-Or; Hammadi Ayadi; Christine Petit; Michael Korostishevsky; Batsheva Bonne-Tamir
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
American journal of human genetics 1997;61(4):813-21.
1997: S Iyengar; H Kalinsky; S Weiss; Michael Korostishevsky; M Sadeh; Y Zhao; Kenneth K Kidd; Batsheva Bonne-Tamir
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Journal of medical genetics 1997;34(5):391-4.
1996: Hannah Tamary; Y Fromovich; Lea Shalmon; Z Reich; O Dym; N Lanir; B Brenner; M Paz; A S Luder; O Blau; Michael Korostishevsky; Rina Zaizov; Uri Seligsohn
Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.
Thrombosis and haemostasis 1996;76(3):283-91.
1996: B Bonné-Tamir; Anita L DeStefano; C E Briggs; R Adair; B Franklyn; S Weiss; Michael Korostishevsky; Moshe Frydman; Clinton T Baldwin; Lindsay A Farrer
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
American journal of human genetics 1996;58(6):1254-9.
1995: Clinton T Baldwin; S Weiss; Lindsay A Farrer; A L De Stefano; R Adair; B Franklyn; Kenneth K Kidd; Michael Korostishevsky; B Bonné-Tamir
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
Human molecular genetics 1995;4(9):1637-42.
1994: B Bonné-Tamir; Michael Korostishevsky; H Kalinsky; E Seroussi; R Beker; S Weiss; V Godel
Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.
Genomics 1994;20(1):36-42.