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Nobuko Moriyama
Nobuko Moriyama
Hitachi
Genetics
Biology
Exome sequencing
Noonan like syndrome
Mutation testing
4
Papers
98
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Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies.
2021
Journal of Human Genetics
Sachiko Miyamoto
Mitsuhiro Kato
Takuya Hiraide
Tadashi Shiohama
Tomohide Goto
Akira Hojo
Akio Ebata
Manabu Suzuki
Kozue Kobayashi
Pin Fee Chong
Ryutaro Kira
Hiroko Baber Matsushita
Hiroko Ikeda
Kyoko Hoshino
Mayumi Matsufuji
Nobuko Moriyama
Masayuki Furuyama
Tatsuya Yamamoto
Mitsuko Nakashima
Hirotomo Saitsu
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Bardet-Biedl syndrome and related disorders in Japan.
2020
Journal of Human Genetics
Makito Hirano
W. Satake
Nobuko Moriyama
Ken Saida
Nobuhiko Okamoto
Pei-Chieng Cha
Yutaka Suzuki
Susumu Kusunoki
Tatsushi Toda
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Citations (2)
CASK aberrations in male patients with Ohtahara syndrome and cerebellar hypoplasia.
2012
Epilepsia
Hirotomo Saitsu
Mitsuhiro Kato
Hitoshi Osaka
Nobuko Moriyama
Hideki Horita
Kiyomi Nishiyama
Yuriko Yoneda
Yukiko Kondo
Yoshinori Tsurusaki
Hiroshi Doi
Noriko Miyake
Kiyoshi Hayasaka
Naomichi Matsumoto
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Citations (58)
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies.
2010
Journal of Human Genetics
Shoko Komatsuzaki
Yoko Aoki
Tetsuya Niihori
Nobuhiko Okamoto
Raoul C. M. Hennekam
Saskia M.J. Hopman
Hirofumi Ohashi
Seiji Mizuno
Yoriko Watanabe
Hotaka Kamasaki
Ikuko Kondo
Nobuko Moriyama
Kenji Kurosawa
Hiroshi Kawame
Ryuhei Okuyama
Masue Imaizumi
Takeshi Rikiishi
Shigeru Tsuchiya
Shigeo Kure
Yoichi Matsubara
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Citations (38)
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