Michael Korostishevsky

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 et al. · Nature Genetics · 2001 · 234 citations · Full text

Developmental Biology, Transmembrane Protease, Pediatric Otolaryngology +11

Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis

Michael Korostishevsky, M. Kaganovich, Alina Cholostoy et al. · Biological Psychiatry · 2004 · 184 citations

Risk Prediction, Psychiatry, Psychotic Disorder +11

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 et al. · International Journal of Cancer · 2009 · 122 citations

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 et al. · Human Molecular Genetics · 1995 · 98 citations

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

Doron Gothelf, Elena Michaelovsky, Amos Frisch et al. · The International Journal of Neuropsychopharmacology · 2006 · 68 citations