Rchr
J-GLOBAL ID：201801011951118702
Update date: Jan. 30, 2024
Aritoshi Iida
イイダ アリトシ | Aritoshi Iida
Affiliation and department：
Research field (3)：
Genetics
, Medical biochemistry
, Genomics
Research keywords (2)：
遺伝医学
, ゲノム科学
Research theme for competitive and other funds (5)：
- 2013 - 2016 Searching for factors associated with progression and prognosis in patients with sporadic amyotrophic lateral sclerosis
- 2011 - 2013 Elucidation of molecular pathogenesis of amyotrophic lateral sclerosis based on genome analysis
- 2007 - 2008 Large-scale genome association study of amyotrophic lateral sclerosis in Japanese
- 1998 - 1999 ポジショナルクローニング法を用いた多脾症/左右内臓逆位原因遺伝子の検索
- 1996 - 1999 乳癌の遺伝子診断法の確立
Papers (143)：
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Yosuke Kawai, Yusuke Watanabe, Yosuke Omae, Reiko Miyahara, Seik-Soon Khor, Eisei Noiri, Koji Kitajima, Hideyuki Shimanuki, Hiroyuki Gatanaga, Kenichiro Hata, et al. Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis. PLoS genetics. 2023. 19. 12. e1010625
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Akiko Hida, Aritoshi Iida, Motoki Ukai, Hiroshi Kadotani, Makoto Uchiyama, Takashi Ebisawa, Yuichi Inoue, Shingo Kitamura, Kazuo Mishima. Novel CLOCK and NR1D2 variants in 64 sighted Japanese individuals with non-24-hour sleep-wake rhythm disorder. Sleep. 2023. 46. 6
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Wakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, Kazuki Yamamoto, Yasushi Oya, Madoka Mori-Yoshimura, Takashi Kurashige, Mariko Okubo, Megumu Ogawa, Fumihiko Matsuda, et al. Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy. Scientific Reports. 2022. 12. 1
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Michio Inoue, Satoru Noguchi, Yukiko U. Inoue, Aritoshi Iida, Megumu Ogawa, Rocio Bengoechea, Sara K. Pittman, Shinichiro Hayashi, Kazuki Watanabe, Yasushi Hosoi, et al. Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4. Acta Neuropathologica. 2022
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Masashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, Theerawat Kumutpongpanich, Narihiro Minami, Ikuya Nonaka, Shinichiro Hayashi, Satoru Noguchi, Ichizo Nishino. Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy. Acta neuropathologica communications. 2022. 10. 1. 176-176
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MISC (83)：
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中川栄二, 橋本和彦, 馬場信平, 竹下絵里, 阿部ちひろ, 飯田有俊, 井上健, 後藤雄一, 後藤雄一. 後頭蓋窩くも膜嚢胞を伴い発達性てんかん性脳症を認めたSMC1A遺伝子変異例. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th (CD-ROM)
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小笠原真志, 小笠原真志, 飯田有俊, THEERAWAT Kumutpongpanich, 尾崎文美, 林晋一郎, 林晋一郎, 野口悟, 野口悟, 西野一三, et al. 遺伝学的診断が確定した眼咽頭遠位型ミオパチーの臨床病理学的特徴. 日本神経学会学術大会プログラム・抄録集. 2021. 62nd
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田畑 健士郎, 飯田 有俊, 竹下 絵里, 住友 典子, 本橋 裕子, 石山 昭彦, 齋藤 貴志, 小牧 宏文, 中川 栄二, 佐藤 典子, et al. Chiari奇形I型様のMRI所見を呈したMalan症候群の1例. 脳と発達. 2021. 53. 1. 73-73
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松村 剛, 井上 貴美子, 井上 道雄, 飯田 有俊, 西川 達哉, 西野 一三, 藤村 晴俊. 肥大型心筋症とミオパチー、多発性腫瘍を認めたfilaminopathyの1例. 日本筋学会学術集会プログラム・抄録集. 2020. 6回. 79-79
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飯田有俊, 西野一三, 西野一三. Comprehensive genomic analysis of inherited muscular diseases. 生体の科学. 2020. 71. 2. 158-163
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Patents (14)：
Professional career (1)：
Association Membership(s) (1)：
THE JAPAN SOCIETY OF HUMAN GENETICS
