Nakamura Ryoichi

ナカムラリョウイチ | Nakamura Ryoichi

Affiliation and department：
Research theme for competitive and other funds (5)：

2022 - 2025 Elucidating the heterogeneity of amyotrophic lateral sclerosis by neuropathological analysis linked to clinical genomic information
2022 - 2025 筋萎縮性側索硬化症のmissing heritabilityに関わる遺伝子の探索
2019 - 2022 候補遺伝子アプローチによる筋萎縮性側索硬化症病態関連遺伝子の探索
2017 - 2019 Analysis of genes affecting cognitive function in sporadic ALS
2015 - 2017 Comprehensive genetic analysis of ALS-related genes in Japanese sporadic ALS patients

Papers (111)：

Satoshi Yamashita, Yuji Takahashi, Jun Hashimoto, Ayuka Murakami, Ryoichi Nakamura, Masahisa Katsuno, Rumiko Izumi, Naoki Suzuki, Hitoshi Warita, Masashi Aoki. Nationwide survey of patients with multisystem proteinopathy in Japan. Annals of Clinical and Translational Neurology. 2024
Ryoichi Nakamura, Genki Tohnai, Masahiro Nakatochi, Naoki Atsuta, Hirohisa Watanabe, Daisuke Ito, Masahisa Katsuno, Akihiro Hirakawa, Yuishin Izumi, Mitsuya Morita, et al. Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients. Journal of neurology, neurosurgery, and psychiatry. 2023. 94. 10. 816-824
Reiko Ohdake, Hirohisa Watanabe, Kazuya Kawabata, Aya Ogura, Maki Sato, Yasuhiro Tanaka, Kazunori Imai, Michihito Masuda, Toshiyasu Kato, Takamasa Yokoi, et al. Convenient Auditory-Based Language and Executive Function Test for Patients With Amyotrophic Lateral Sclerosis: A Pilot Study. Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists. 2023. 38. 1. 57-71
熱田直樹, 中村亮一, 藤内玄規, 祖父江元. 【患者レジストリ】筋萎縮性硬化症患者のレジストリJapanese Consortium for Amyotrophic Lateral Sclerosis research(JaCALS). 神経治療学. 2023. 40. 1. 12-16
Satoshi Yokoi, Takuji Ito, Kentaro Sahashi, Masahiro Nakatochi, Ryoichi Nakamura, Genki Tohnai, Yusuke Fujioka, Shinsuke Ishigaki, Tsuyoshi Udagawa, Yuishin Izumi, et al. The SYNGAP1 3'UTR variant in ALS patients causes aberrant SYNGAP1 splicing and dendritic spine loss by recruiting HNRNPK. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022. 42. 47. 8881-8896

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MISC (21)：

中村亮一, 熱田直樹, 祖父江元. 【全ゲノム解析に基づく難病のゲノム医学】多因子性神経難病の全ゲノム解析筋萎縮性側索硬化症. 医学のあゆみ. 2023. 285. 1. 103-109
中村亮一, 熱田直樹, 祖父江元. 【神経疾患とゲノム医療】個別病態・疾患のゲノム医療筋萎縮性側索硬化症. Clinical Neuroscience. 2022. 40. 9. 1138-1142
安藤孝志, 中村亮一, 吉田眞理, 勝野雅央. 【多系統蛋白質症に関する最近の進歩】多系統蛋白質症の概念. 脳神経内科. 2021. 95. 1. 94-103
村尾厚徳, 辻河高陽, 小倉礼, 中村亮一, 勝野雅央. 発症13ヶ月で人工呼吸器管理を要し,SOD1遺伝子Ser134Asn変異を認めた筋萎縮性側索硬化症の1例. 神経治療学(Web). 2021. 38. 6
村尾厚徳, 辻河高陽, 中村亮一, 勝野雅央. 発症13か月で人工呼吸器管理を要し,SOD1遺伝子Ser134Asn変異を認めた筋萎縮性側索硬化症の1例. 臨床神経学(Web). 2021. 61. 11

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Professional career (1)：

医学博士 (名古屋大学)

Awards (3)：

2023/10 - 2023年度日本人類遺伝学会奨励賞筋萎縮性側索硬化症の臨床遺伝学的研究
2021/12 - 第5回せりか基金賞
2013/12 - 24th International Symposium on ALS/MND Clinical Poster Prize 2013 Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients

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