M. Korostishevsky

Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

Avital Adato, Dominique Weil, Hagar Kalinski et al. · The American Journal of Human Genetics · 1997 · 115 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +9

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Batsheva Bonné‐Tamir, Anita L. DeStefano, Christine Briggs et al. · PubMed · 1996 · 114 citations · Full text

Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel

M. Korostishevsky, I Kremer, M. Kaganovich et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · 58 citations

Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

Hagar Kalinsky, Adina Funes, Alina Zeldin et al. · Human Mutation · 1998 · 55 citations

Diverse Israeli Families, Genetics, Genetic Epidemiology +16

Association of heparanase gene (HPSE) single nucleotide polymorphisms with hematological malignancies

Olga Ostrovsky, M. Korostishevsky, Iris Levite et al. · Leukemia · 2007 · 44 citations

Medicine, Genetics, Genetic Epidemiology +9