Tsutomu Takahashi

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

Life Sciences, Genetics, Molecular Genetics +16

De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)

Kiyoshi Hayasaka, Masato Himoro, Yukio Sawaishi et al. · Nature Genetics · 1993 · 203 citations

Medicine, Genetics, Neurology +14

Active hypothalamic-pituitary-gonadal axis in an infant with X-linked adrenal hypoplasia congenita

Tsutomu Takahashi, Yutaka Shoji, Yasuko Shoji et al. · The Journal of Pediatrics · 1997 · 87 citations

Medicine, Endocrinology, Pediatrics +14

Spread and predominance in Japan of novel G1P[8] double-reassortant rotavirus strains possessing a DS-1-like genotype constellation typical of G2P[4] strains

Yoshiki Fujii, Toyoko Nakagomi, Naoko Nishimura et al. · Infection Genetics and Evolution · 2014 · 65 citations

Life Sciences, Genetics, Microbiology +12

Thyroid dysgenesis caused by PAX8 mutation: The hypermutability with CpG dinucleotides at codon 31

Masaki Komatsu, Tsutomu Takahashi, Ikuko Takahashi et al. · The Journal of Pediatrics · 2001 · 63 citations

Life Sciences, Genetics, Molecular Genetics +11