Shunji Yamamori

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

Masayo Kagami, Yoichi Sekita, Gen Nishimura et al. · Nature Genetics · 2008 · 288 citations

Developmental Biology, Genetic Disorder, Genetics +7

Detection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma

Hitoshi Tsuda, Futoshi Akiyama, Hiroshi Terasaki et al. · Cancer · 2001 · 105 citations

Increase of deoxycholate in supersaturated bile of patients with cholesterol gallstone disease and its correlation with de novo syntheses of cholesterol and bile acids in liver, gallbladder emptying, and small intestinal transit

Junichi Shoda, Bingfang He, Naomi Tanaka et al. · Hepatology · 1995 · 98 citations

Two cases of partial trisomy 21 (pter‐q22.1) without the major features of Down syndrome

Yoko Kondo, Seiji Mizuno, Kei Ohara et al. · American Journal of Medical Genetics Part A · 2006 · 85 citations

Homozygous deletions of p16/MTS1 gene are frequent but mutations are infrequent in childhood T-cell acute lymphoblastic leukemia

H. Ohnìshì, M Kawamura, Kohmei Ida et al. · Blood · 1995 · 85 citations · Full text