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Funayama Manabu  舩山 学

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FUNAYAMA Manabu  舩山 学

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Researcher Number 70468578
Other IDs
Affiliation (Current) 2025: 順天堂大学, 医学部, 先任准教授
Affiliation (based on the past Project Information) *help 2019 – 2024: 順天堂大学, 医学部, 先任准教授
2011 – 2020: 順天堂大学, 医学部, 准教授
2011: 順天堂大学, 医学研究科, 准教授
2009 – 2010: Juntendo University, 大学院・医学研究科, 助教
2009: 医学部, 助教 … More
2009: 順天堂大学, 医学部, 助教
2009: 順天堂大学, 医学部・神経学, 助教
2008: Juntendo University, 医学部, 研究員 Less
Review Section/Research Field
Principal Investigator
Neurology / Basic Section 52020:Neurology-related / Biological Sciences
Except Principal Investigator
Neurology / Basic Section 52020:Neurology-related / Complex Systems Disease Theory / Biological Sciences / Biological Sciences
Keywords
Principal Investigator
パーキンソン病 / 遺伝子 / ミトコンドリア / iPS細胞 / 電子伝達系 / エクソーム / 変異 / 次世代シーケンサー / 酸化ストレス / ATP … More / ノックアウト細胞 / 解糖系 / 複合体IV / CHCHD2 / 呼吸鎖複合体 / 感受性遺伝子 / 遺伝 / ゲノム / exome / 多型 / 連鎖 / ゲノムワイド / ロングリードシーケンサー / 神経細胞死 / 神経細胞変性 / ドーパミン / オートファジー / 原因遺伝子 / 網膜色素変性症 / エネルギー代謝 / 細胞モデル / 機能喪失 / メタボロミクス / 分化 / ドーパミン神経細胞 / iPS / 酸素呼吸 / 活性酸素 / 神経分化 / モデル動物 / iTRAQ / MPTP / NDUFV2 / ノックインマウス / CRSPR/Cas9 / 全ゲノム / 次世代 / マイクロアレイ / 連鎖解析 / ハプロタイプ / SNPs … More
Except Principal Investigator
パーキンソン病 / ミトコンドリア / オートファジー / 神経変性疾患 / リソソーム / 蛋白分解系 / Mitophagy / PINK1 / Parkin / 遠隔効果 / miRNA / スペルミジン / スペルミン / ジアセチルスペルミジン / ポリアミン / バイオマーカー / PLA2G6 / 封入体 / 脂質代謝 / GBA / CHCHD2 / ATP13A2 / 小分子化合物 / 蛋白分解 / 創薬シーズ / 脳・神経 / 内科 / マイトファジー / ケミカルバイオロジー / 神経内科学 / SNCS / 重複 / 変異 / duplication / Gene chip / 二倍体 / DNA / 遺伝子 / 認知症 / びまん性レビー小体病 / 遺伝子重複 / SNCA / alpha-synuclein / ドーパミントランスポーター / slip rod test / PINk1 / TIRF / インスリン / IRP2 / パーキンソン病(PD) / ATP / MEF / ミトコンドリア膜電位 / 呼吸能 / parkin / MPTP / NDUFV2 / ミトファジー / モデルマウス / 共通機構 / DJ-1 / 学習能力 / 遺伝性パーキンソン病 / 品質管理 / CCCP Less
  • Research Projects

    (17 results)
  • Research Products

    (183 results)
  • Co-Researchers

    (38 People)
  •  Understanding the complete picture of familial Parkinson's disease using comprehensive genetic analysis.Principal Investigator

    • Principal Investigator
      舩山 学
    • Project Period (FY)
      2024 – 2026
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Juntendo University
  •  ミトコンドリア呼吸鎖障害によるパーキンソン病ドパミン神経特異的変性の分子機構

    • Principal Investigator
      天羽 拓
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      防衛大学校(総合教育学群、人文社会科学群、応用科学群、電気情報学群及びシステム工学群)
  •  Mitochondrial dysfunction by loss of CHCHD8

    • Principal Investigator
      Amo Taku
    • Project Period (FY)
      2020 – 2023
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      防衛大学校(総合教育学群、人文社会科学群、応用科学群、電気情報学群及びシステム工学群)
  •  Elucidation of the molecular mechanisms of dopaminergic neurodegenerative disorders using a large genome resourcePrincipal Investigator

    • Principal Investigator
      Funayama Manabu
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Juntendo University
  •  Research on PD pathogenesis based on polyamine metabolism using multiomics analysis

    • Principal Investigator
      Saiki Shinji
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Complex Systems Disease Theory
    • Research Institution
      Juntendo University
  •  Development of novel cellular models for Parkinson's disease focusing on energy-homeostasisPrincipal Investigator

    • Principal Investigator
      FUNAYAMA Manabu
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Generation of new mouse model for Parkinson's disease(Fostering Joint International Research)Principal Investigator

    • Principal Investigator
      FUNAYAMA Manabu
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Fund for the Promotion of Joint International Research (Fostering Joint International Research)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Analysis of lipid composition in hereditary Parkinson's Disease and the association with the pathology

    • Principal Investigator
      Hattori Nobutaka
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  新規パーキンソン病・本態性振戦原因遺伝子のゲノム解析と分子病態解析Principal Investigator

    • Principal Investigator
      舩山 学
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
    • Review Section
      Biological Sciences
    • Research Institution
      Juntendo University
  •  Generation of the novel mouse model for Parkinson's disease derived from two-hit hypothesisPrincipal Investigator

    • Principal Investigator
      Funayama Manabu
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  The detection of modifier gens in alpha-synuclein multiplications

    • Principal Investigator
      Nishioka Kenya
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Development of autophagy enhancing chemicals based on Parkinson's disease pathogenesis.

    • Principal Investigator
      SAIKI Shinji
    • Project Period (FY)
      2013 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
    • Review Section
      Biological Sciences
    • Research Institution
      Juntendo University
  •  エクソーム解析による新規パーキンソン病原因遺伝子の単離Principal Investigator

    • Principal Investigator
      舩山 学
    • Project Period (FY)
      2011 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
    • Review Section
      Biological Sciences
    • Research Institution
      Juntendo University
  •  Identification of new gene for familial parkinsonismPrincipal Investigator

    • Principal Investigator
      FUNAYAMA Manabu
    • Project Period (FY)
      2010 – 2011
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Generation of pathological models for Parkinson's disease

    • Principal Investigator
      HATTORI Nobutaka
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  To elucidate the pathogenesis of Parkinson' s disease and to develop a new therapy for the disease

    • Principal Investigator
      HATTORI Nobutaka
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Juntendo University
  •  Identification of the new gene for familial parkinsonism and its functional analysesPrincipal Investigator

    • Principal Investigator
      FUNAYAMA Manabu
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University

All 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 Other

All Journal Article Presentation Book Patent Other

  • [Book] 順天堂大脳神経内科ではこうしている 最新 パーキンソン病診療【電子版付】2021

    • Author(s)
      服部信孝(編著)、舩山学(分担執筆)
    • Total Pages
      224
    • Publisher
      日本医事新報社
    • ISBN
      9784784949502
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Book] 別冊 日本臨床 新領域別症候群シリーズ No.27、神経症候群(第2版)(II) -その他の神経疾患を含めて-2014

    • Author(s)
      舩山 学、安藤真矢、服部信孝
    • Total Pages
      903
    • Publisher
      日本臨床社
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Journal Article] Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort2023

    • Author(s)
      Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Bruggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L, Ferreira JJ, Nishioka K, Funayama M, et. al.
    • Journal Title

      Movement Disorders

      Volume: 38 Issue: 2 Pages: 286-303

    • DOI

      10.1002/mds.29288

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K07878
  • [Journal Article] A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene2022

    • Author(s)
      Daida Kensuke、Nishioka Yosuke、Li Yuanzhe、Yoshino Hiroyo、Funayama Manabu、Hattori Nobutaka、Nishioka Kenya
    • Journal Title

      eNeurologicalSci

      Volume: 26 Pages: 100391-100391

    • DOI

      10.1016/j.ensci.2021.100391

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-21H04820
  • [Journal Article] Loss of <i>Atg2b</i> and <i>Gskip</i> Impairs the Maintenance of the Hematopoietic Stem Cell Pool Size2022

    • Author(s)
      Sakai Shun-suke、Hasegawa Atsushi、Ishimura Ryosuke、Tamura Naoki、Kageyama Shun、Komatsu-Hirota Satoko、Abe Manabu、Ling Yiwei、Okuda Shujiro、Funayama Manabu、Kikkawa Mika、Miura Yoshiki、Sakimura Kenji、Narita Ichiei、Waguri Satoshi、Shimizu Ritsuko、Komatsu Masaaki
    • Journal Title

      Molecular and Cellular Biology

      Volume: 42 Issue: 1 Pages: 1-17

    • DOI

      10.1128/mcb.00024-21

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K01972, KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-19K16478, KAKENHI-PROJECT-20K16161, KAKENHI-PLANNED-19H05706, KAKENHI-PROJECT-21H04771, KAKENHI-PROJECT-19H03555, KAKENHI-PROJECT-20H03415, KAKENHI-PROJECT-21H04163, KAKENHI-PROJECT-18KK0458, KAKENHI-PROJECT-21K17850
  • [Journal Article] Deep Brain Stimulation for a Patient with Familial Parkinson's Disease Harboring CHCHD2 p.T61I.2022

    • Author(s)
      Kamo Hikaru、Oyama Genko、Nishioka Kenya、Funayama Manabu、Hattori Nobutaka
    • Journal Title

      Movement Disorders Clinical Practice

      Volume: 9 Issue: 3 Pages: 407-409

    • DOI

      10.1002/mdc3.13428

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07878
  • [Journal Article] The East Asian Parkinson Disease Genomics Consortium2021

    • Author(s)
      Mok Kin Y、、、Funayama Manabu、、et al.
    • Journal Title

      The Lancet Neurology

      Volume: 20 Issue: 12 Pages: 982-982

    • DOI

      10.1016/s1474-4422(21)00373-2

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-19K17047
  • [Journal Article] Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p.D620N with long-term follow-up2021

    • Author(s)
      Ishiguro Mayu、Li Yuanzhe、Yoshino Hiroyo、Daida Kensuke、Ishiguro Yuta、Oyama Genko、Saiki Shinji、Funayama Manabu、Hattori Nobutaka、Nishioka Kenya
    • Journal Title

      Parkinsonism & Related Disorders

      Volume: 84 Pages: 139-143

    • DOI

      10.1016/j.parkreldis.2021.02.014

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21H04820
  • [Journal Article] Genetic analysis of ATP10B for Parkinson's disease in Japan2021

    • Author(s)
      Ishiguro Mayu、Yoshino Hiroyo、Li Yuanzhe、Ikeda Aya、Funayama Manabu、Nishioka Kenya、Hattori Nobutaka
    • Journal Title

      Parkinsonism and Related Disorders

      Volume: 88 Pages: 10-12

    • DOI

      10.1016/j.parkreldis.2021.05.020

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283
  • [Journal Article] Homeostatic p62 levels and inclusion body formation in CHCHD2 knockout mice2021

    • Author(s)
      Sato Shigeto、Noda Sachiko、Torii Satoru、Amo Taku、Ikeda Aya、Funayama Manabu、Yamaguchi Junji、Fukuda Takahiro、Kondo Hiromi、Tada Norihiro、Arakawa Satoko、Watanabe Masahiko、Uchiyama Yasuo、Shimizu Shigeomi、Hattori Nobutaka
    • Journal Title

      Human Molecular Genetics

      Volume: 30 Issue: 6 Pages: 443-453

    • DOI

      10.1093/hmg/ddab057

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K07878, KAKENHI-PROJECT-19K22603, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-17K09769, KAKENHI-PROJECT-18K06210, KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K22744, KAKENHI-PLANNED-17H06414, KAKENHI-PUBLICLY-20H05314, KAKENHI-PROJECT-18K05691, KAKENHI-PROJECT-20K07353, KAKENHI-PROJECT-21K15198, KAKENHI-PROJECT-20H00467
  • [Journal Article] Variants in saposin D domain of prosaposin gene linked to Parkinson’s disease2020

    • Author(s)
      Oji Y, Hatano T, Ueno SI, Funayama M, Ishikawa KI, Okuzumi A, Noda S, Sato S, Satake W, Toda T, Li Y, Hino-Takai T, Kakuta S, Tsunemi T, Yoshino H, Nishioka K, Hattori T, Mizutani Y, Mutoh T, Yokochi F, et al.
    • Journal Title

      Brain

      Volume: 143 Issue: 4 Pages: 1190-1205

    • DOI

      10.1093/brain/awaa064

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-19K22603, KAKENHI-PROJECT-19K16928, KAKENHI-PROJECT-19K17019, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-18K15463, KAKENHI-PROJECT-19K08288, KAKENHI-PROJECT-18K07510, KAKENHI-PROJECT-19K23782
  • [Journal Article] Shared Metabolic Profile of Caffeine in Parkinsonian Disorders2020

    • Author(s)
      Takeshige‐Amano Haruka、Saiki Shinji、Fujimaki Motoki、Ueno Shin‐Ichi、Li Yuanzhe、Hatano Taku、Ishikawa Kei‐Ichi、Oji Yutaka、Mori Akio、Okuzumi Ayami、Tsunemi Taiji、Daida Kensuke、Ishiguro Yuta、Imamichi Yoko、Nanmo Hisayoshi、Nojiri Shuko、Funayama Manabu、Hattori Nobutaka
    • Journal Title

      Movement Disorders

      Volume: 35 Issue: 8 Pages: 1438-1447

    • DOI

      10.1002/mds.28068

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-19K16928, KAKENHI-PROJECT-18H02744, KAKENHI-PROJECT-18K07510, KAKENHI-PROJECT-18KT0027
  • [Journal Article] Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease2020

    • Author(s)
      Daida Kensuke、Funayama Manabu、Li Yuanzhe、Yoshino Hiroyo、Hayashida Arisa、Ikeda Aya、Ogaki Kotaro、Nishioka Kenya、Hattori Nobutaka
    • Journal Title

      Frontiers in Neurology

      Volume: 11 Pages: 576465-576465

    • DOI

      10.3389/fneur.2020.576465

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-19K17047, KAKENHI-PROJECT-18H04043
  • [Journal Article] Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy2020

    • Author(s)
      Lin Chin-Hsien、Tsai Pei-I、Lin Han-Yi、Hattori Nobutaka、Funayama Manabu、Jeon Beomseok、et al.
    • Journal Title

      Brain

      Volume: 143 Issue: 11 Pages: 3352-3373

    • DOI

      10.1093/brain/awaa279

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893
  • [Journal Article] Identifying Therapeutic Agents for Amelioration of Mitochondrial Clearance Disorder in Neurons of Familial Parkinson Disease2020

    • Author(s)
      Yamaguchi Akihiro、Ishikawa Kei-ichi、Inoshita Tsuyoshi、Shiba-Fukushima Kahori、Saiki Shinji、Hatano Taku、Mori Akio、Oji Yutaka、Okuzumi Ayami、Li Yuanzhe、Funayama Manabu、Imai Yuzuru、Hattori Nobutaka、Akamatsu Wado
    • Journal Title

      Stem Cell Reports

      Volume: 14 Issue: 6 Pages: 1060-1075

    • DOI

      10.1016/j.stemcr.2020.04.011

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07873, KAKENHI-PROJECT-20K07910, KAKENHI-PROJECT-17H04049, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-17K09765
  • [Journal Article] Mutation analysis of LRP10 in Japanese patients with familial Parkinson’s disease, progressive supranuclear palsy, and fronto-temporal dementia2019

    • Author(s)
      Daida K, Nishioka K, Li Y, Yoshino H, Kikuchi A, Hasegawa T, Funayama M, Hattori N
    • Journal Title

      Neurobiol Aging

      Volume: 84 Pages: 235.e11-235.e16

    • DOI

      10.1016/j.neurobiolaging.2019.08.030

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K09789, KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-17K09744
  • [Journal Article] Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperone.2019

    • Author(s)
      J. S. Lee, K. Kanai, M. Suzuki, W. S. Kim, H. S. Yoo, Y. Fu, D-K. Kim, B. C. Jung, M. Choi, K. W. Oh, Y. Li, M. Nakatani, T. Nakazato, S. Sekimoto, M. Furuyama, H. Yoshino, S. Kubo, K. Nishioka, R. Sakai, M. Ueyama, H. Mochizuki, H-J. Lee, S. P. Sardi, G. M. Halliday, Y. Nagai, P. H. Lee, N. Hattori, S-J. Lee
    • Journal Title

      Brain

      Volume: 142 Issue: 9 Pages: 2845-59

    • DOI

      10.1093/brain/awz205

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K07823, KAKENHI-PROJECT-19K07987, KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-17K09811, KAKENHI-PROJECT-17K19658, KAKENHI-PUBLICLY-17H05699, KAKENHI-PROJECT-16H05325
  • [Journal Article] Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features2019

    • Author(s)
      Ikeda Aya、Shimada Hitoshi、Nishioka Kenya、Takanashi Masashi、Hayashida Arisa、Li Yuanzhe、Yoshino Hiroyo、Funayama Manabu、Ueno Yuji、Hatano Taku、Sahara Naruhiko、Suhara Tetsuya、Higuchi Makoto、Hattori Nobutaka
    • Journal Title

      Movement Disorders

      Volume: 34 Issue: 4 Pages: 568-574

    • DOI

      10.1002/mds.27623

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-26117008, KAKENHI-PROJECT-16H05324, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-19K08003, KAKENHI-PUBLICLY-19H05437, KAKENHI-PROJECT-18H04043
  • [Journal Article] A metabolic profile of polyamines in parkinson disease: A promising biomarker2019

    • Author(s)
      Saiki Shinji、Sasazawa Yukiko、Fujimaki Motoki、Kamagata Koji、Kaga Naoko、Taka Hikari、Li Yuanzhe、Souma Sanae、Hatano Taku、Imamichi Yoko、Furuya Norihiko、Mori Akio、Oji Yutaka、Ueno Shin‐Ichi、Nojiri Shuko、Miura Yoshiki、Ueno Takashi、Funayama Manabu、Aoki Shigeki、Hattori Nobutaka
    • Journal Title

      Annals of Neurology

      Volume: 86 Issue: 2 Pages: 251-263

    • DOI

      10.1002/ana.25516

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KT0027, KAKENHI-PROJECT-17K07797, KAKENHI-PROJECT-18K07829, KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-19K11752, KAKENHI-PROJECT-19K22603, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-18H02744, KAKENHI-PROJECT-18K15464
  • [Journal Article] Serum caffeine and metabolites are reliable biomarkers of early Parkinson disease2018

    • Author(s)
      Motoki Fujimaki, Shinji Saiki, Yuanzhe Li, Naoko Kaga, Taku Hatano, Kei-Ichi Ishikawa, Yutaka Oji, Akio Mori, Ayami Okuzumi, Takahiro Koinuma, Shin-Ichi Ueno, Yoko Imamichi, Takashi Ueno, Yoshiki Miura, Manabu Funayama
    • Journal Title

      Neurology

      Volume: 90

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-25111007
  • [Journal Article] GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.2018

    • Author(s)
      Yoshino H, Nishioka K, Li Y, Oji Y, Oyama G, Hatano T, Machida Y, Shimo Y, Hayashida A, Ikeda A, Mogushi K, Shibagaki Y, Hosaka A, Iwanaga H, Fujitake J, Ohi T, Miyazaki D, Sekijima Y, Oki M, Kusaka H, Fujimoto KI Ugawa Y, Funayama M, Hattori N.
    • Journal Title

      Journal of Neurology

      Volume: 265(8) Issue: 8 Pages: 1860-1870

    • DOI

      10.1007/s00415-018-8930-8

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K10552, KAKENHI-PROJECT-17K07797, KAKENHI-PROJECT-18K08798, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
  • [Journal Article] Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations2018

    • Author(s)
      Takanashi M, Funayama M (Contributed equally), Matsuura E, Yoshino H, Li Y, Tsuyama S, Takashima H, Nishioka K, Hattori N
    • Journal Title

      Acta Neuropathologica Communications

      Volume: 6 Issue: 1 Pages: 105-105

    • DOI

      10.1186/s40478-018-0617-y

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
  • [Journal Article] Serum caffeine and metabolites are reliable biomarkers of early Parkinson disease.2018

    • Author(s)
      Fujimaki M, Saiki S, Li Y, Kaga N, Taka H, Hatano T, Ishikawa KI, Oji Y, Mori A, Okuzumi A, Koinuma T, Ueno SI, Imamichi Y, Ueno T, Miura Y, Funayama M, Hattori N.
    • Journal Title

      Neurology.

      Volume: 90 Issue: 5 Pages: 1-8

    • DOI

      10.1212/wnl.0000000000004888

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K01834, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-17K07797, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-18K07829, KAKENHI-PROJECT-18H04043
  • [Journal Article] COQ2 variants in Parkinson's disease and multiple system atrophy.2018

    • Author(s)
      Mikasa M, Kanai K, Li Y, Yoshino H, Mogushi K, Hayashida A, Ikeda A, Kawajiri S, Okuma Y, Kashihara K, Sato T, Kondo H, Funayama M, Nishioka K, Hattori N.
    • Journal Title

      J Neural Transm (Vienna)

      Volume: - Issue: 6 Pages: 938-944

    • DOI

      10.1007/s00702-018-1885-1

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-26461319, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-16K10476, KAKENHI-PROJECT-16K10552, KAKENHI-PROJECT-17K09811, KAKENHI-PROJECT-17K10652, KAKENHI-PROJECT-18K08798, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-20K18340
  • [Journal Article] Genetic analysis of TMEM230 in Japanese patients with familial Parkinson’s disease.2018

    • Author(s)
      Conedera SA, Li Y, Funayama M, Yoshino H, Nishioka K, Hattori N.
    • Journal Title

      Parkinsonism Relat Disord

      Volume: 48 Pages: 107-108

    • DOI

      10.1016/j.parkreldis.2017.12.020

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-16K09678
  • [Journal Article] A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease2017

    • Author(s)
      Ikeda, Aya; Matsushima, Takashi; Daida, Kensuke; Nakajima, Sho; Conedera, Silvio; Li, Yuanzhe; Yoshino, Hiroyo; Oyama, Genko; Funayama, Manabu; Nishioka, Kenya; Hattori, Nobutaka
    • Journal Title

      PARKINSONISM & RELATED DISORDERS

      Volume: 34 Pages: 66-68

    • DOI

      10.1016/j.parkreldis.2016.10.018

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-15K19498, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-15KK0354
  • [Journal Article] Loss of Parkinson's disease-associated protein CHCHD2 affects mitochondrial crista structure and destabilizes cytochrome c.2017

    • Author(s)
      Meng H, Yamashita C, Shiba-Fukushima K, Inoshita T, Funayama M, Sato S, Hatta T, Natsume T, Umitsu M, Takagi J, Imai Y, Hattori N.
    • Journal Title

      Nat Commun

      Volume: 8 Issue: 1 Pages: 15500-15500

    • DOI

      10.1038/ncomms15500

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K19525, KAKENHI-PROJECT-26293070, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-17H01420
  • [Journal Article] Genotype-phenotype correlations of cysteine replacement in CADASIL2017

    • Author(s)
      Matsushima, Takashi; Conedera, Silvio; Tanaka, Ryota; Li, Yuanzhe; Yoshino, Hiroyo; Funayama, Manabu; Ikeda, Aya; Hosaka, Yuka; Okuzumi, Ayame; Shimada, Yoshiaki; Yamashiro, Kazuo; Motoi, Yumiko; Nishioka, Kenya; Hattori, Nobutaka
    • Journal Title

      NEUROBIOLOGY OF AGING

      Volume: 50 Pages: 169.e7-169.e14

    • DOI

      10.1016/j.neurobiolaging.2016.10.026

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09678
  • [Journal Article] Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism.2017

    • Author(s)
      Yamashita C, Funayama M, Li Y, Yoshino H, Yamada H, Seino Y, Tomiyama H, Hattori N.
    • Journal Title

      J Neural Transm

      Volume: 4 Issue: 4 Pages: 431-435

    • DOI

      10.1007/s00702-016-1658-7

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-15KK0354
  • [Journal Article] Schizophrenia as a prodromal symptom in a&nbsp;patient harboring SNCA duplication.2016

    • Author(s)
      Takamura S, Ikeda A, Nishioka K, Furuya H, Tashiro M, Matsushima T, Li Y, Yoshino H, Funayama M, Morinobu S, Hattori N.
    • Journal Title

      Parkinsonism Relat Disord.

      Volume: S1353-8020 Pages: 30028-1

    • DOI

      10.1016/j.parkreldis.2016.01.028

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-26461311, KAKENHI-PROJECT-15KK0354
  • [Journal Article] Lysosomal storage of subunit c of mitochondrial ATP synthase in brain-specific ATP13a2-deficient mice2016

    • Author(s)
      Sato, S., Koike, M., Funayama, M., Ezaki, J., Fukuda, T., Ueno, T., Uchiyama, Y., Hattori, N
    • Journal Title

      Am. J. Pathol.

      Volume: 186 Issue: 12 Pages: 3074-3082

    • DOI

      10.1016/j.ajpath.2016.08.006

    • Peer Reviewed
    • Data Source
      KAKENHI-PUBLICLY-15H01388, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-15KK0354
  • [Journal Article] Genotype-phenotype correlations of cysteine replacement in CADASIL.2016

    • Author(s)
      Matsushima T, Conedera S, Tanaka R, Li Y, Yoshino H, Funayama M, Ikeda A, Hosaka Y, Okuzumi A, Shimada Y, Yamashiro K, Motoi Y, Nishioka K, Hattori N
    • Journal Title

      Neurobiology of Aging

      Volume: 50

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Journal Article] FBXO7 mutations in Parkinson's disease and multiple system atrophy.2016

    • Author(s)
      Conedera S, Apaydin H, Li Y, et al.
    • Journal Title

      Neurobiol Aging.

      Volume: 40 Pages: 192.e1-192.e5

    • DOI

      10.1016/j.neurobiolaging.2016.01.003

    • Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25860726, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-15KK0354
  • [Journal Article] Genotype-phenotype correlations of cysteine replacement in CADASIL.2016

    • Author(s)
      Matsushima T, Conedera S, Tanaka R, Li Y, Yoshino H, Funayama M, Ikeda A, Hosaka Y, Okuzumi A, Shimada Y, Yamashiro K, Motoi Y, Nishioka K, Hattori N
    • Journal Title

      Neurobiology of Aging

      Volume: 50

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15KK0354
  • [Journal Article] ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.2015

    • Author(s)
      Matsuo H, Tomiyama H, Satake W, Chiba T, Onoue H, Kawamura Y, Nakayama A, ShimizuS, Sakiyama M, Funayama M, Nishioka K, Shimizu T, Kaida K, Kamakura K, Toda T, Hattori N, ShinomiyaN.
    • Journal Title

      Ann Clin Transl Neurol

      Volume: 2 Issue: 3 Pages: 302-306

    • DOI

      10.1002/acn3.167

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25110720, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25293145, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25670307, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-15H04315, KAKENHI-PROJECT-25713015
  • [Journal Article] Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.2015

    • Author(s)
      Ogaki K, Koga S, Heckman MG, et al.
    • Journal Title

      Neurology

      Volume: 85 Issue: 23 Pages: 2016-2025

    • DOI

      10.1212/wnl.0000000000002170

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25860726, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25461291
  • [Journal Article] CHCHD2 mutations in autosomal dominant late-onset Parkinson’s disease: a genome-wide linkage and sequencing study.2015

    • Author(s)
      Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Yuanzhe L, Ogaki K, Ando M, Yoshinon H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N.
    • Journal Title

      Lancet Neurol

      Volume: 14 Issue: 3 Pages: 274-282

    • DOI

      10.1016/s1474-4422(14)70266-2

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24500868, KAKENHI-PROJECT-24790903, KAKENHI-PUBLICLY-25110720, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26870175, KAKENHI-PROJECT-15K10050, KAKENHI-ORGANIZER-23111001, KAKENHI-PLANNED-23111003, KAKENHI-PLANNED-23111004, KAKENHI-PROJECT-25257507, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25305030
  • [Journal Article] High frequency of beta-propeller protein-associated neurodegeneration (BPAN) among patients with intellectual disability and young-onset parkinsonism.2015

    • Author(s)
      Nishioka K, Oyama G, Yoshino H, Li Y, Matsushima T, Takeuchi C, Mochizuki Y, Mori-Yoshimura M, Murata M, Yamasita C, Nakamura N, Konishi Y, Ohi K, Ichikawa K, Terada T, Obi T, Funayama M, Saiki S, Hattori N.
    • Journal Title

      Neurobiol Aging.

      Volume: S0197 Issue: 5 Pages: 54-58

    • DOI

      10.1016/j.neurobiolaging.2015.01.020

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-15K19498, KAKENHI-PROJECT-15H04842
  • [Journal Article] Target- and input-dependent organization of AMPA and NMDA receptors in synaptic connections of the cochlear nucleus2015

    • Author(s)
      Rubio ME, Fukazawa Y, Kamasawa N, Clarkson C, Molnar E, Shigemoto R
    • Journal Title

      J Comp Neurol

      Volume: 588 Pages: 29-35

    • DOI

      10.1016/j.neulet.2014.12.052

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-221S0003, KAKENHI-PLANNED-23111003, KAKENHI-PLANNED-24108008, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24659431, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25460276, KAKENHI-PROJECT-25461290, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860711, KAKENHI-PUBLICLY-26111519, KAKENHI-PROJECT-25461279, KAKENHI-PROJECT-26860188
  • [Journal Article] CHCHD2 and Parkinson's disease-Authors' reply.2015

    • Author(s)
      Funayama M, Hattori N.
    • Journal Title

      Lancet Neurology

      Volume: 14 Issue: 7 Pages: 682-683

    • DOI

      10.1016/s1474-4422(15)00097-6

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Journal Article] EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population2014

    • Author(s)
      Nishioka K, Funayama M, Vilarino-GuellC, Ogaki K, Li Y, Sasaki R, Kokubo Y, Kuzuhara S, Kachergus JM, Cobb SA, Takahashi H, Mizuno Y, Farrer MJ, Ross OA, Hattori N
    • Journal Title

      Parkinsonism Relat Disord.

      Volume: 20 Issue: 6 Pages: 659-61

    • DOI

      10.1016/j.parkreldis.2014.03.004

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25257507, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726
  • [Journal Article] Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.2014

    • Author(s)
      Li Y, Sekine T, Funayama M, Li L, Yoshino H, Nishioka K, Tomiyama H, Hattori N
    • Journal Title

      Neurobiol Aging.

      Volume: 35 Issue: 4 Pages: 935.e3-935.e8

    • DOI

      10.1016/j.neurobiolaging.2013.09.019

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726
  • [Journal Article] Identification of a Japanese family with LRRK2 p.R1441G-related Parkinson's disease.2014

    • Author(s)
      Hatano T, Funayama M, Kubo S, Mata IF, Oji Y, Mori A, Zabetian CP, Waldherr SM, Yoshino H, Oyama G, Shimo Y, Fujimoto K, Oshima H, Kunii Y, Yabe H, Mizuno Y, Hattori N.
    • Journal Title

      Neurobiol Aging.

      Volume: Nov;35(11) Issue: 11 Pages: 2656.e17-2656.e23

    • DOI

      10.1016/j.neurobiolaging.2014.05.025

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461290, KAKENHI-PROJECT-25461291
  • [Journal Article] Juvenile-onset parkinsonism with digenic parkin and PINK1 mutations treated with subthalamic nucleus stimulation at 45 years after disease onset.2014

    • Author(s)
      Nakahara K, Ueda M, Yamada K, Koide T, Yoshimochi G, Funayama M, Kim JH, Yamakawa S, Mori A, Misumi Y, Uyama E, Hattori N, Ando Y.
    • Journal Title

      J Neurol Sci.

      Volume: 15 Issue: 1-2 Pages: 276-277

    • DOI

      10.1016/j.jns.2014.07.053

    • Peer Reviewed
    • Data Source
      KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25870541
  • [Journal Article] The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease.2014

    • Author(s)
      Yamashita C, Tomiyama H, Funayama M, Inamizu S, Ando M, Li Y, Yoshino H, Araki T, Ichikawa T, Ehara Y, Ishikawa K, Mizusawa H, Hattori N.
    • Journal Title

      Neurobiol Aging.

      Volume: 35 Issue: 7 Pages: 1779.e17-1779.e21

    • DOI

      10.1016/j.neurobiolaging.2014.01.022

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25860725
  • [Journal Article] A case of α-synuclein gene duplication presenting with head-shaking movements.2013

    • Author(s)
      Itokawa K, Sekine T, Funayama M, Tomiyama H, Fukui M, Yamamoto T, Tamura N, Matsuda H, Hattori N, Araki N.
    • Journal Title

      Mov Disord.

      Volume: 28 Issue: 3 Pages: 384-387

    • DOI

      10.1002/mds.25243

    • Peer Reviewed
    • Data Source
      KAKENHI-PUBLICLY-25129707, KAKENHI-PUBLICLY-23129506
  • [Journal Article] Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, andCBS2013

    • Author(s)
      Ogaki K
    • Journal Title

      Parkinsonism & Related Disorders

      Volume: 19 Issue: 1 Pages: 15-20

    • DOI

      10.1016/j.parkreldis.2012.06.019

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23240050, KAKENHI-PROJECT-23791003, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PUBLICLY-23110526, KAKENHI-PUBLICLY-23129506
  • [Journal Article] ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons.2013

    • Author(s)
      Matsui H, Sato F, Sato S, Koike M, Taruno Y, Saiki S, Funayama M, Ito H, Taniguchi Y, Uemura N, Toyoda A, Sakaki Y, Takeda S, Uchiyama Y, Hattori N, Takahashi R.
    • Journal Title

      FEBS Lett

      Volume: 587(9) Issue: 9 Pages: 1316-1325

    • DOI

      10.1016/j.febslet.2013.02.046

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-ORGANIZER-23111001, KAKENHI-PLANNED-23111002, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-23390232, KAKENHI-PROJECT-23590244, KAKENHI-PROJECT-23689046, KAKENHI-PROJECT-23790238, KAKENHI-PROJECT-24300132, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24659435, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PUBLICLY-23129506
  • [Journal Article] パーキンソン病の基礎研究最前線:実地医家のためのminimum requirement2012

    • Author(s)
      舩山学, 他
    • Journal Title

      モダンフィジシャン

      Volume: 32 Pages: 201-205

    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Journal Article] Pseudo-heterozygous rearrangement mutation of parkin2012

    • Author(s)
      Fumayama M, et al
    • Journal Title

      Movement Disorders

      Volume: vol.27 Issue: 4 Pages: 552-555

    • DOI

      10.1002/mds.24906

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829, KAKENHI-PROJECT-23791003, KAKENHI-PUBLICLY-23129506
  • [Journal Article] 遺伝子工学からの恩恵-2〓連鎖解析,疾患遺伝子の探索:パーキン遺伝子発見の経緯2012

    • Author(s)
      舩山学, 他
    • Journal Title

      BIO Clinica

      Volume: 27 Pages: 90-93

    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Journal Article] 遺伝子工学からの恩恵-2□連鎖解析,疾患遺伝子の探索:パーキン遺伝子発見の経緯2012

    • Author(s)
      舩山学, 他
    • Journal Title

      BIO Clinica

      Volume: 27 Pages: 90-93

    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] パーキンソン病の基礎研究最前線:実地医家のためのminimum requirement2012

    • Author(s)
      舩山学, 他
    • Journal Title

      モダンフィジシャン

      Volume: 32 Pages: 201-205

    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] Pseudo-heterozygous rearrangement mutation of parkin2012

    • Author(s)
      Funayama M, Yoshino H, Li Y, Kusaka H, Tomiyama H, Hattori N
    • Journal Title

      Mov Disord

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] PLA2G6 variant in Parkinson's disease2011

    • Author(s)
      Tomiyama H, Yoshino H, Ogaki K, Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N
    • Journal Title

      J Hum Genet

      Volume: 56(5) Pages: 401-3

    • NAID

      10030659472

    • Data Source
      KAKENHI-PROJECT-21390272
  • [Journal Article] DJ-1 associates with synaptic membranes2011

    • Author(s)
      Usami Y, Hatano T, Imai S, Kubo S, Sato S, Saiki S, Fujioka Y, Ohba Y, Sato F, Funayama M, Eguchi H, Shiba K, Ariga H, Shen J, Hattori N
    • Journal Title

      Neurobiol Dis

      Volume: 43 Pages: 651-62

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] PLA2G6 variant in Parkinson's disease2011

    • Author(s)
      Tomiyama H, Yoshino H, Ogaki K, Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N
    • Journal Title

      Hum Genet

      Volume: 56 Pages: 401-403

    • NAID

      10030659472

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] DJ-1 associates with synaptic membranes2011

    • Author(s)
      Usami Y, Hatano T, Imai S, Kubo S, Sato S, Saiki S, Fujioka Y, Ohba Y, Sato F, Funayama M, Eguchi H, Shiba K, Ariga H, Shen J, Hattori N
    • Journal Title

      Neurobiol Dis

      Volume: 43(3) Pages: 651-651

    • Data Source
      KAKENHI-PROJECT-21390272
  • [Journal Article] Prevalence of GJB2 Causing Recessive Profound Non-Syndromic Deafness in Japanese Children2011

    • Author(s)
      Hayashi C, Funayama M, Li Y, Kawano A, Suzuki M, Hattori N, Ikeda K
    • Journal Title

      Int J Pediatr Otorhinolaryngol

      Volume: 75 Pages: 211-214

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] A rotarod test for evaluation of motor skill learning2010

    • Author(s)
      Hiromi Shiotsuki, Kenji Yoshimi, Yasushi Shimo, Manabu Funayama, Yukio Takamatsu, Kazutaka Ikeda, Ryosuke Takahashi, Shigeru Kitazawa, Nobutaka Hattori
    • Journal Title

      Journal Of Neuroscience Methods (In press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390272
  • [Journal Article] Impaired in vivo dopamine release in parkin knockout mice.2010

    • Author(s)
      Oyama G, Yoshimi K, Natori S, Chikaoka Y, Ren YR, Funayama M, Shimo Y, Takahashi R, Nakazato T, Kitazawa S, Hattori N.
    • Journal Title

      Brain Res.

      Volume: 1352 Pages: 214-22

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390272
  • [Journal Article] Rapid screening of ATP13A2 variant with high-resolution melting analysis.2010

    • Author(s)
      Funayama M, et al.
    • Journal Title

      Movement Disorders

      Volume: 25 Pages: 2434-2437

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients2010

    • Author(s)
      Li L, Funayama M, Tomiyama H, Li Y, Yoshino H, Sasaki R, Kokubo Y, Kuzuhara S, Mizuno Y, Hattori N
    • Journal Title

      Neurosci Lett

      Volume: 479 Pages: 245-248

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism2010

    • Author(s)
      Yoshino H, Tomiyama H, Tachibana N, Ogaki K, Li Y, Funayama M, Hashimoto T, Takashima S, Hattori N
    • Journal Title

      Neurology

      Volume: 75 Pages: 1356-1361

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] Rapid screening of ATP13A2 variant with high-resolution melting analysis.2010

    • Author(s)
      Funayama M
    • Journal Title

      Movement Disorders. (In press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Impaired in vivo dopamine release in parkin knockout mice2010

    • Author(s)
      Oyama G, Yoshimi K, Natori S, Chikaoka Y, Ren YR, Funayama M, Shimo Y, Takahashi R, Nakazato N, Kitazawa S, Hattori N
    • Journal Title

      Brain Research

      Volume: 1352 Pages: 214-222

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] Rapid screening of ATP13A2 variant with high-resolution melting analysis2010

    • Author(s)
      Funayama M, Tomiyama H, Wu RM, Ogaki K, Yoshino H, Mizuno Y, Hattori N
    • Journal Title

      Mov Disord

      Volume: 25 Pages: 2434-2437

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] Clinical course of the first Asian family with parkinsonism related to SNCA triplication2010

    • Author(s)
      Sekine T, Kagata H, Funayama M, Li Y, Yoshino H, Tomiyama H, Hattori N
    • Journal Title

      Mov Disord

      Volume: 25 Pages: 2871-2875

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Journal Article] A rotarod test for evaluation of motor skill learning2010

    • Author(s)
      Shiotsuki H, Yoshimi K, Shimo Y, Funayama M, Takamatsu Y, Ikeda K, Takahashi R, Kitazawa S, Hattori N.
    • Journal Title

      J Neurosci Methods.

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Preserved cardiac 123I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient2009

    • Author(s)
      Kanai K, Asahina M, Arai K, Tomiyama H, Kuwabara Y, Uchiyama U, Sekiguchi Y, Funayama M, Kuwabara S, Hattori N, Hattori T.
    • Journal Title

      Mov Disord 24(9)

      Pages: 1403-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Screening PARK Genes for Mutations in Early Onset Parkinson's Disease Patients from Queensland, Australia2009

    • Author(s)
      Mellick GD, Siebert GA, Funayama M, Buchanan DD, Li Y, Imamichi Y, Yoshino H, Silburn PA, Hattori N
    • Journal Title

      Parkinsonism & Related Disorders 15

      Pages: 105-109

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20023028
  • [Journal Article] Screening PARK Genes for Mutations in Early Onset Parkinson ' s Disease Patients from Queensland, Australia.2009

    • Author(s)
      Mellick GD, Siebert GA, Funayama M, Buchanan DD, Li Y, Imamichi Y, Yoshino H, Silburn PA, Hattori N.
    • Journal Title

      Parkinsonism Relat Disord 15(2)

      Pages: 105-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] A new mutation in the GCH1 gene presents as early-onset Parkinsonism2009

    • Author(s)
      Momma K, Funayama M, Li Y, Ichinose H, Motoyoshi K, Hattori N, Mizuno Y, Kamakura K.
    • Journal Title

      Parkinsonism Relat Disord. 15(2)

      Pages: 160-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] A new mutation in the GCH1 gene presents as early-onset Parkinsonism2009

    • Author(s)
      Momma K, Funayama M, Li Y, Ichinose H, Motoyoshi K, Hattori N, Mizuno Y, Kamakura K
    • Journal Title

      Parkinsonism & Related Disorders 15

      Pages: 160-161

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20023028
  • [Journal Article] Analysis of Lrrk2 R1628P as a risk factor for Parkinson' s disease2008

    • Author(s)
      Ross OA, Wu YR, Lee MC, Funayama M, Chen ML, Soto AI, Mata IF, Lee-Chen GJ, Chen CM, Tang M, Zhao Y, Hattori N, Farrer MJ, Tan EK, Wu RM.
    • Journal Title

      Ann Neurol. 64(1)

      Pages: 88-92

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Familial parkinsonism with digenic parkin and PINK1 mutations2008

    • Author(s)
      Funayama M, et.al.
    • Journal Title

      MOVEMENT DISORDERS 65

      Pages: 802-808

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Familial narkinsonism with dieenic narkin and PINK1 mutations2008

    • Author(s)
      Funayama M, et.al.
    • Journal Title

      Mov Disord 65

      Pages: 802-808

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20023028
  • [Journal Article] PARK9-linked parkinsonism in Eastern Asia: Mutation detection in ATP13A2 and clinical phenotype2008

    • Author(s)
      Ning Y, Kanai K, Tomiyama H, Li Y, Funayama M, Yoshino H, Sato S, Asahina M, Kuwabara S, Takeda A, Hattori T, Mizuno Y, Hattori N
    • Journal Title

      Neurology 70(162)

      Pages: 1491-1493

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Mutation analysis of the PINK1 gene in 391 patients with Parkinson's disease2008

    • Author(s)
      Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N.
    • Journal Title

      Arch Neurol 65(6)

      Pages: 802-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of Kii, Japan2008

    • Author(s)
      Tomiyama H, Kokubo Y, Sasaki R, Li Y, Imamichi Y, Funayama M, Mizuno Y, Hattori N, Kuzuhara S.
    • Journal Title

      Mov Disord. 23(16)

      Pages: 2344-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease.2008

    • Author(s)
      Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N
    • Journal Title

      Arch Neurol 65

      Pages: 802-808

    • Data Source
      KAKENHI-PROJECT-20023028
  • [Journal Article] Familial parkinsonism with digenic parkin and PINK1 mutations2008

    • Author(s)
      Funayama M, Li Y, Tsoi TH, Lam CW, Ohi T, Yazawa S, Uyama E, Djaldetti R, Melamed E, Yoshino H, Imamichi Y, Takashima H, Nishioka K, Sato K, Tomiyama H, Kubo S, MD, Mizuno Y, Hattori N.
    • Journal Title

      Mov Disord 65(6)

      Pages: 802-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] LRRK2 P755L variant in sporadic Parkinson's disease2008

    • Author(s)
      Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo S, Mizuno Y, Toda T, Hattori N.
    • Journal Title

      J Hum Genet. 53(11-12)

      Pages: 1012-5

    • NAID

      10025584966

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Journal Article] PARK9-linked parkinsonism in Eastern Asia: Mutation detection in ATP13A2 and clinical phenotype.2008

    • Author(s)
      Ning Y, Kanai K, Tomiyama H, Li Y, Funayama M, Yoshino H, Sato S, Asahina M, Kuwabara S, Takeda A, Hattori T, Mizuno Y, Hattori N
    • Journal Title

      Neurology 70

      Pages: 1491-1493

    • Data Source
      KAKENHI-PROJECT-20023028
  • [Journal Article] Rapid screening of ATP13A2 variant with high-resolution melting analysis

    • Author(s)
      Funayama M, Tomiyama H, Wu RM, Ogaki K, Yoshino H, Mizuno Y, Hattori N.
    • Journal Title

      Mov Disord (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Patent] パーキンソン病の診断2014

    • Inventor(s)
      服部信孝、舩山学
    • Industrial Property Rights Holder
      服部信孝、舩山学
    • Industrial Property Rights Type
      特許
    • Industrial Property Number
      2014-228827
    • Filing Date
      2014-11-11
    • Data Source
      KAKENHI-PUBLICLY-25129707
  • [Presentation] Characterization of CHCHD2 variants linked to amyotrophic lateral sclerosis and Parkinson's disease.2023

    • Author(s)
      A. Ikeda, M. Funayama, M. Yoshida, Y. Li, T. Inoshita, K. Shiba-Fukushima, H. Meng, T. Amo, I. Aiba, Y. Saito, N. Atsuta, R. Nakamura, G. Tohnai, J. Sone, Y. Izumi, R. Kaji, M. Morita, A. Taniguchi, K. Nishioka, Y. Imai, G. Sobue, N. Hattori, JaCALS
    • Organizer
      第64回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-23K06958
  • [Presentation] Characterization of CHCHD2 variants linked to amyotrophic lateral sclerosis and Parkinson's disease2023

    • Author(s)
      A. Ikeda, M. Funayama, M. Yoshida, Y. Li, T. Inoshita, K. Shiba-Fukushima, H. Meng, T. Amo, I. Aiba, Y. Saito, N. Atsuta, R. Nakamura, G. Tohnai, J. Sone, Y. Izumi, R. Kaji, M. Morita, A. Taniguchi, K. Nishioka, Y. Imai, G. Sobue, N. Hattori, JaCALS
    • Organizer
      第64回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-20K07878
  • [Presentation] Causative gene finding for families with Parkinson's disease and Retinitis pigmentosa by whole exome sequencing.2021

    • Author(s)
      舩山学, 斉木臣二, 代田健祐, 吉野浩代, 李元哲, 西岡健弥, 服部信孝
    • Organizer
      日本人類遺伝学会第66回大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] The frequency of 22q11.2 deletion among the patients with early-onset Parkinson's disease.2021

    • Author(s)
      Yuki Mangyoku, Manabu Funayama, Yuanzhe Li, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori
    • Organizer
      日本人類遺伝学会第66回大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] SH-SY5YにおけるCHCHD8欠損によるミトコンドリア呼吸鎖複合体IVの機能不全2021

    • Author(s)
      日景 勇賀, 永沼 陸, 古本 菜々子, 舩山 学, 服部 信孝, 天羽 拓
    • Organizer
      第20回 日本ミトコンドリア学会年会
    • Data Source
      KAKENHI-PROJECT-20K07878
  • [Presentation] SH-SY5YにおけるCHCHD8欠損によるミトコンドリア呼吸鎖複合体IVの機能不全2021

    • Author(s)
      日景 勇賀, 永沼 陸, 古本 菜々子, 舩山 学, 服部 信孝, 天羽 拓
    • Organizer
      第44回 日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-20K07878
  • [Presentation] 22q11.2 deletion syndrome among the patients with early-onset Parkinson's disease.2021

    • Author(s)
      Yuki Mangyoku, Manabu Funayama, Yuanzhe Li, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori
    • Organizer
      第62回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Identification of common molecular mechanism between Parkinson’s disease and Retinitis pigmentosa.2021

    • Author(s)
      舩山学,斉木臣二,吉野浩代,李元哲,西岡健弥,服部信孝
    • Organizer
      第62回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] パーキンソン病の分子遺伝学―近年の解析の動向―2021

    • Author(s)
      舩山学
    • Organizer
      高松国際パーキンソン病シンポジウム in Tokyo 2022
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] SH-SY5YにおけるCHCHD8欠損によるミトコンドリア呼吸鎖複合体IVの機能不全2021

    • Author(s)
      日景勇賀, 永沼陸, 古本菜々子, 舩山学, 服部信孝, 天羽拓
    • Organizer
      第20回日本ミトコンドリア学会 年会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Analysis of genetic testing for spinocerebellar ataxia2020

    • Author(s)
      櫻井麻由、土屋浩二、吉野浩代、舩山 学、田部陽子、西岡健弥、服部信孝
    • Organizer
      第61回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Mutational and functional analysis of the CHCHD2 gene in amyotrophic lateral sclerosis2020

    • Author(s)
      池田 彩、舩山 学、吉田眞理、李 元哲、饗場郁子、齋藤由扶子、熱田直樹、中村亮一、藤内玄規、曽根 淳、和泉唯信、梶 龍兒、森田光哉、谷口 彰、祖父江 元、服部信孝、JaCALS
    • Organizer
      第61回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Identifying a novel causative gene associated with familial Parkinson's disease2020

    • Author(s)
      代田健祐、舩山 学、李 元哲、吉野浩代、林田有紗、池田 彩、大垣光太郎、西岡健弥、服部信孝
    • Organizer
      第61回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Next-generation sequencing expand the possibilities to detect more variants in Parkinson's disease2020

    • Author(s)
      李 元哲、吉野浩代、舩山 学、戸田達史、西岡健弥、服部信孝
    • Organizer
      第61回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] PINK1 heterozygote変異はalpha-synucleinopathyに部分的に関与する2020

    • Author(s)
      西岡健弥、李 元哲、林田有紗、代田健祐、池田 彩、大垣光太郎、吉野浩代、舩山 学、服部信孝
    • Organizer
      第61回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Clinicogenetic study on mono-allelic and bi-allelic mutation of PLA2G6 in Parkinson’s disease2019

    • Author(s)
      Manabu Funayama, Hiroyo Yoshino, Yuanzhe Li, Yasushi Shimo, Kenya Nishioka, Nobutaka Hattori
    • Organizer
      第60回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] Comparison of clinical phenotype between mono-allelic and bi-allelic mutation of PLA2G6 in Parkinson’s disease.2019

    • Author(s)
      舩山学、吉野浩代、李元哲、下泰司、西岡健弥、服部信孝
    • Organizer
      第13回パーキンソン病・運動障害疾患コングレス
    • Data Source
      KAKENHI-PROJECT-19K08003
  • [Presentation] パーキンソン病の分子遺伝学研究2018

    • Author(s)
      舩山学
    • Organizer
      第59回日本神経学会学術大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] A novel mutation of LRRK2 p.V1447M in familial Parkinson's disease2018

    • Author(s)
      池田彩, 吉野浩代, 大山彦光, 吉田亘佑, 木村隆, 木谷光博, 沼尾文香, 鈴木圭輔, 卜部貴夫, 中山宜昭, 伊東秀文, 菅野直人, 河野智, 宮嶋裕明, 木村活生, 上田直久, 田中 章景, 舩山 学, 西岡 健弥, 服部信孝
    • Organizer
      第59回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] Brain pathology, functional analysis and fly models of CHCHD2 p.T61I2018

    • Author(s)
      Nishioka K, Ikeda A, Meng H, Takanashi M, Yoshino H, Li Y, Imai Y, Funayama M, Hattori N
    • Organizer
      Genetic Epidemiology of Parkinson's Disease 2018
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] Novel Parkinson’s disease families with LRRK2 p.R1441H homozygous and heterozygous mutation in Makurazaki region2018

    • Author(s)
      Yoshino H, Takanashi M, Funayama M, Matsuura E, Li Y, Tsuyama S, Takashima T, Nishioka K, Hattori N
    • Organizer
      日本人類遺伝学会 第63回大会
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] A novel variant of CHCHD2 in a patient with sporadic Parkinson's disease.2017

    • Author(s)
      Funayama M, Ikeda A, Matsushima T, Daida S, Nakajima S, Conedera S, Li Y, Yoshino H, Oyama G, Nishioka K, Hattori N.
    • Organizer
      日本人類遺伝学会第62階大会
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] CHCHD2 DEFICIENCY LEADS TO MITOCHONDRIAL DYSFUNCTION AND INCREASING OXIDATIVE STRESS IN HUMAN NEUROBLASTOMA SH-SY5Y CELLS.2017

    • Author(s)
      unayama M, Park JS, Amo T, Funayama T, Akamatsu W, Sue CM, Hattori N.
    • Organizer
      XXIII World Congress of Neurology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] A novel variant of CHCHD2 in a patient with sporadic Parkinson's disease.2017

    • Author(s)
      Funayama M, Ikeda A, Matsushima T, Daida S, Nakajima S, Conedera S, Li Y, Yoshino H, Oyama G, Nishioka K, Hattori N
    • Organizer
      日本人類遺伝学会第62階大会
    • Data Source
      KAKENHI-PROJECT-15KK0354
  • [Presentation] CHCHD2 DEFICIENCY LEADS TO MITOCHONDRIAL DYSFUNCTION AND INCREASING OXIDATIVE STRESS IN HUMAN NEUROBLASTOMA SH-SY5Y CELLS.2017

    • Author(s)
      Funayama M, Park JS, Amo T, Funayama T, Akamatsu W, Sue CM, Hattori N
    • Organizer
      XXIII World Congress of Neurology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15KK0354
  • [Presentation] CHCHD2 is novel gene for autosomal dominant Parkinson’s disease2016

    • Author(s)
      Funayama M, Hattori N
    • Organizer
      The 13th International Congress of Human Genetics
    • Place of Presentation
      京都国際会館 (京都府京都市)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] CHCHD2 is Novel Causative Gene for Autosomal Dominant Parkinson’s Disease2016

    • Author(s)
      舩山学, 服部信孝
    • Organizer
      第39回日本神経科学大会
    • Place of Presentation
      パシフィコ横浜 (神奈川県横浜市)
    • Invited
    • Data Source
      KAKENHI-PROJECT-15KK0354
  • [Presentation] Analysis of GCH1 mutations in the patients with Parkinson’s disease in Japanese population2016

    • Author(s)
      Kenya Nishioka, Hiroyo Yoshino, Takashi Matsushima, Aya Ikeda, Manabu Funayama, Nobutaka Hattori
    • Organizer
      11th Annual Meeting of the Genetic Epidemiology of Parkinson’s disease (GEOPD) Consortium
    • Place of Presentation
      Campus Belval, Luxembourg
    • Year and Date
      2016-10-06
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] 遺伝性パーキンソン病PARK9(ATP13A2)の分子病態とリソソームの障害、シンポジウム1AS19-42016

    • Author(s)
      佐藤栄人、小池正人、舩山 学、野田幸子、江崎淳二、福田隆浩、上野 隆、内山安男、服部信孝
    • Organizer
      パシフィコ横浜、横浜
    • Place of Presentation
      パシフィコ横浜、横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] CHCHD2 is Novel Causative Gene for Autosomal Dominant Parkinson’s Disease2016

    • Author(s)
      舩山学, 服部信孝
    • Organizer
      第39回日本神経科学大会
    • Place of Presentation
      パシフィコ横浜 (神奈川県横浜市)
    • Invited
    • Data Source
      KAKENHI-PROJECT-16K09676
  • [Presentation] Analysis of GCH1 mutations in the patients with Parkinson’s disease in Japanese population2016

    • Author(s)
      Hiroyo Yoshino, Kenya Nishioka, Aya Ikeda, Takashi Matsushima, Mitsuaki Oki, Daigo Miyazaki, Yoshiki Sekijima, Ai Hosaka, Takekazu Ohi, Hiroshi Iwanaga, Yuanzhe Li, Manabu Funayama, Nobutaka Hattori
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸ポートピアホテル
    • Year and Date
      2016-05-18
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] CHCHD2 is novel gene for autosomal dominant Parkinson’s disease2016

    • Author(s)
      Funayama M, Hattori N
    • Organizer
      The 13th International Congress of Human Genetics
    • Place of Presentation
      京都国際会館 (京都府京都市)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15KK0354
  • [Presentation] Mutations of mitochondrial protein CHCHD2 lead to parkinson’s disease-like phenotypes inDrosophil. ポスター発表2016

    • Author(s)
      Meng H, Yamashita C, Shiba-Fukushima K, Inoshita T, Funayama M, Sato S, Imai Y, Hattori N
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸コンベンションホール他、神戸
    • Year and Date
      2016-05-18
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] CHCHD2 is Novel Causative Gene for Autosomal Dominant Parkinson's Disease, Symposium S1-B-3, Emerging genes for neurodegenerative diseases: a perspective on pathomechanisms2016

    • Author(s)
      Funayama M, Hattori N.
    • Organizer
      The 39th Annual Meeting of the Japan Neuroscience Society
    • Place of Presentation
      Pacifico Yokohama, Yokohama
    • Year and Date
      2016-07-20
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] .The function of CHCHD2, the novel gene responsible for a familial form of Parkinson's disease, Symposium S1-D-3, Pathogenetic mechanisms underlying Parkinson's disease -On the roles of alpha-synuclein, mitochondria and lysosomes2016

    • Author(s)
      Hattori N, Funayama M, Imai Y, Sato S
    • Organizer
      The 39th Annual Meeting of the Japan Neuroscience Society
    • Place of Presentation
      Pacifico Yokohama, Yokohama
    • Year and Date
      2016-07-20
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] Schizophrenia as a prodromal symptom in a patient harboring SNCA duplication2016

    • Author(s)
      Silvio Conedera, Aya Ikeda, Kenya Nishioka, Shogo Takamura, Takashi Matsushima, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Shigeru Morinobu, Nobutaka Hattori
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸ポートピアホテル
    • Year and Date
      2016-05-18
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] The analyze of four pedigrees with MAPT N279K mutation accompanying DAT scan and Tau imaging2016

    • Author(s)
      Aya Ikeda (Manabe), Kenya Nishioka, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Takashi Matsushima, Shinichi Ueno, Naohide Kurita, Hitoshi Shimada, Naruhiko Sahara, Makoto Higuchi, Tetsuya Suhara, Yuji Ueno, Masashi Takanashi, Yumiko Motoi, Nobutaka Hattori
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸ポートピアホテル
    • Year and Date
      2016-05-18
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] The Loss of Parkinson's Disease-Associated Protein CHCHD2 Affects Mitochondrial Cristae Structure and Destabilizes Cytochrome c, Symposium 2PS9-42016

    • Author(s)
      Meng H, Yamashita C, Shiba K, Inoshita T, Funayama M, Sato S, Imai Y, Hattori N.
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜、横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] Keeping Up with New Genetic Predispositions and Mutations in Parkinson’s Disease2016

    • Author(s)
      Funayama M, Hattori N
    • Organizer
      5th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress
    • Place of Presentation
      マニラ、フィリピン
    • Year and Date
      2016-03-12
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] CHCHD2 is novel gene for autosomal dominant Parkinson's disease2015

    • Author(s)
      Funayama M, Hattori N
    • Organizer
      10th Annual GEoPD Meeting in Tokyo
    • Place of Presentation
      東京都港区
    • Year and Date
      2015-10-02
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] ミトコンドリア呼吸鎖遺伝子改変マウスにおけるMPTP感受性の検討(ポスター)2015

    • Author(s)
      舩山 学、服部 信孝
    • Organizer
      第9回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル、東京
    • Year and Date
      2015-10-15
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] CHCHD2は家族性パーキンソン病の新規原因遺伝子である2015

    • Author(s)
      舩山 学、服部 信孝
    • Organizer
      第9回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      東京都品川区
    • Year and Date
      2015-10-15
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] CHCHD2は家族性パーキンソン病の新規原因遺伝子である2015

    • Author(s)
      舩山 学、服部 信孝
    • Organizer
      第9回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル、東京
    • Year and Date
      2015-10-15
    • Data Source
      KAKENHI-PROJECT-15H04842
  • [Presentation] CHCHD2は家族性パーキンソン病の新規原因遺伝子である2015

    • Author(s)
      舩山 学
    • Organizer
      第56回日本神経学会学術大会
    • Place of Presentation
      新潟県新潟市
    • Year and Date
      2015-05-23
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] Genetics of PD2015

    • Author(s)
      Funayama M
    • Organizer
      Basic Scientists Summer School, Tokyo, Japan
    • Place of Presentation
      東京都千代田区
    • Year and Date
      2015-08-02
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] ミトコンドリア呼吸鎖複合体に着目した新規パーキンソン病モデルマウスの解析.2014

    • Author(s)
      舩山 学, 服部 信孝.
    • Organizer
      第55回日本神経病理学会総会学術研究会
    • Place of Presentation
      東京
    • Year and Date
      2014-06-06
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] 日本人パーキンソン病におけるEIF4G1遺伝子変異の頻度.2014

    • Author(s)
      舩山 学, 西岡 健弥, 大垣 光太郎, 李 元哲, 佐々木 良元, 小久保 康昌, 葛原 茂樹, 高橋 裕秀, 富山 弘幸, 水野 美邦, 服部 信孝.
    • Organizer
      第55回日本神経学会学術大会
    • Place of Presentation
      福岡国際センター
    • Year and Date
      2014-05-23
    • Data Source
      KAKENHI-PUBLICLY-25129707
  • [Presentation] 日本人パーキンソン病におけるVPS35 D620N変異の同定.2013

    • Author(s)
      舩山学、安藤真矢、李元哲、柏原健一、村上善勇、石津暢隆、豊田千純子、野口克彦、橋本貴司、中野直樹、佐々木良元、小久保康昌、葛原茂樹、大垣光太郎、山下力、吉野浩代、波田野琢、富山弘幸、服部信孝.
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PUBLICLY-25129707
  • [Presentation] 日本人パーキンソン病におけるVPS35 D620N変異の同定.2013

    • Author(s)
      舩山学、安藤真矢、李元哲、柏原健一、村上善勇、石津暢隆、豊田千純子、野口克彦、橋本貴司、中野直樹、佐々木良元、小久保康昌、葛原茂樹、大垣光太郎、山下力、吉野浩代、波田野琢、富山弘幸、服部信孝.
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] A screening of neuroprotective compounds for Parkinson’s disease from herbal medicines.2013

    • Author(s)
      Yamada D, Fujimaki T, Saiki S, Tashiro E, Funayama M, Imoto M, Hattori N.
    • Organizer
      International Symposium on Mitochondria 2013
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-25461291
  • [Presentation] 常染色体劣性遺伝性パーキンソン病家系の連鎖解析2012

    • Author(s)
      舩山学, 他
    • Organizer
      第53回日本神経学会学術大会
    • Place of Presentation
      東京国際フォーラム(東京)
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] 常染色体劣性遺伝性パーキンソン病の連鎖解析2011

    • Author(s)
      舩山学, 李元哲, 佐竹渉, 吉野浩代, 今道洋子, 富山弘幸, 松浦英治, 野元三治, 有村公良, 戸田達史, 高嶋博, 服部信孝
    • Organizer
      第5回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル(東京)
    • Year and Date
      2011-10-07
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] 常染色体劣性遺伝性パーキンソン病の連鎖解析2011

    • Author(s)
      舩山学, 他
    • Organizer
      第5回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル
    • Year and Date
      2011-10-07
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Genetic Analysis for Parkinson's Disease in Juntendo University Tokyo, Japan2011

    • Author(s)
      Funayama M, Tomiyama H, Hattori N
    • Organizer
      2011 Meeting of the Genetic Epidemiology of Parkinson's Disease Consortium
    • Place of Presentation
      ノースショア大学(シカゴ,アメリカ合衆国)
    • Year and Date
      2011-09-19
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Parkin遺伝子のpseudo-heterozygous rearrangement変異2011

    • Author(s)
      舩山学, 他
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
    • Place of Presentation
      幕張メッセ
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] Genetic Analysis for Parkinson's Disease in Juntendo University, Tokyo, Japan2011

    • Author(s)
      舩山学, 他
    • Organizer
      2011 Meeting of the Genetic Epidemiology of Parkinson's Disease Consortium
    • Place of Presentation
      ノースショア大学
    • Year and Date
      2011-09-19
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Parkin遺伝子のpseudo-heterozygous rearrangement変異2011

    • Author(s)
      舩山学, 日下弘道, 吉野浩代, 李元哲, 富山弘幸, 服部信孝
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
    • Place of Presentation
      幕張メッセ(千葉)
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Parkin遺伝子のpseudo-heterozygous rearrangement変異2011

    • Author(s)
      舩山学, 他
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
    • Place of Presentation
      幕張メッセ
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Analyses of compound heterozygous rearrangements of parkin2011

    • Author(s)
      Funayama M, Kusaka H, Yoshino H, Li Y, Ogaki K, Tomiyama H, Hattori N
    • Organizer
      ASHG/ICHG 2011 Meeting
    • Place of Presentation
      モントリオールコンベンションセンター(モントリオール,カナダ)
    • Year and Date
      2011-10-13
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] 常染色体劣性遺伝性パーキンソン病の連鎖解析2011

    • Author(s)
      舩山学, 他
    • Organizer
      第5回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル
    • Year and Date
      2011-10-07
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] Clinicogenetic study of patients with FTDP-17(MAPT) in Japan2011

    • Author(s)
      Ogaki K, Li Y, Takanashi1 M, Ishikawa1 K, Kobayashi T, Nakanishi A, Nonaka T, Hasegawa M, Kishi M, Yoshino H, Funayama M, Shioya K, Yokochi M, Sasaki R, Kokubo Y, Kuzuhara S, Motoi Y, Tomiyama H, Hattori N
    • Organizer
      ASHG/ICHG 2011 Meeting
    • Place of Presentation
      モントリオールコンベンションセンター(モントリオール,カナダ)
    • Year and Date
      2011-10-13
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病の連鎖解析と新規原因遺伝子探索2011

    • Author(s)
      舩山学, 李元哲, 佐竹渉, 吉野浩代, 今道洋子, 富山弘幸, 松浦英治, 野元三治, 有村公良, 高嶋博, 戸田達史, 水野美邦, 服部信孝
    • Organizer
      第52回日本神経学会総会
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2011-05-20
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病の連鎖解析と新規原因遺伝子探索2011

    • Author(s)
      舩山学, 他
    • Organizer
      第52回日本神経学会総会
    • Place of Presentation
      名古屋国際会議場
    • Year and Date
      2011-05-20
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Genetic Analysis for Parkinson's Disease in Juntendo University, Tokyo, Japan2011

    • Author(s)
      舩山学, 他
    • Organizer
      2011 Meeting of the Genetic Epidemiology of Parkinson's Disease Consortium
    • Place of Presentation
      ノースショア大学
    • Year and Date
      2011-09-19
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] Analyses of compound heterozygous rearrangements of parkin2011

    • Author(s)
      舩山学, 他
    • Organizer
      ASHG/ICHG 2011 Meeting
    • Place of Presentation
      モントリオールコンベンションセンター
    • Year and Date
      2011-10-13
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] Analyses of compound heterozygous rearrangements of parkin2011

    • Author(s)
      舩山学, 他
    • Organizer
      ASHG/ICHG 2011 Meeting
    • Place of Presentation
      モントリオールコンベンションセンター
    • Year and Date
      2011-10-13
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病の連鎖解析と新規原因遺伝子探索2011

    • Author(s)
      舩山学, 他
    • Organizer
      第52回日本神経学会総会
    • Place of Presentation
      名古屋国際会議場
    • Year and Date
      2011-05-20
    • Data Source
      KAKENHI-PUBLICLY-23129506
  • [Presentation] SNCA三重複変異の同定2010

    • Author(s)
      舩山学、関根威、加賀谷肇、李元哲、吉野浩代、富山弘幸、服部信孝
    • Organizer
      第4回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      京都
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-21390272
  • [Presentation] SNCA三重複変異の同定2010

    • Author(s)
      舩山学, ら
    • Organizer
      第4回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      京都ホテルオークラ
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] アジア初のα-synuclein遺伝子三重複変異2010

    • Author(s)
      舩山学、関根威、加賀谷肇、李元哲、吉野浩代、富山弘幸、服部信孝
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      大宮ソニックシティ(大宮)
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] アジア初のα-synuclein遺伝子三重複変異2010

    • Author(s)
      舩山学, ら
    • Organizer
      日本人類遺伝学会 第55回大会
    • Place of Presentation
      大宮ソニックシティ
    • Year and Date
      2010-10-22
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病のlinkage解析(続報)2010

    • Author(s)
      舩山学, 吉野浩代, 今道洋子, 李元哲, 松浦英治, 有村公良, 高嶋博, 野元三治, 富山弘幸, 水野美邦, 服部信孝
    • Organizer
      第51回日本神経学会総会
    • Place of Presentation
      東京国際フォーラム(東京)
    • Year and Date
      2010-05-20
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病のlinkage解析(続報)2010

    • Author(s)
      舩山学, ら
    • Organizer
      第51回日本神経学会総会
    • Place of Presentation
      東京国際フォーラム
    • Year and Date
      2010-05-20
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] SNP chipによる家族性パーキンソン病のlinkage解析(続報)2010

    • Author(s)
      舩山学, 吉野浩代, 今道洋子, 李元哲, 松浦英治, 有村公良, 高嶋博, 野元三治, 富山弘幸, 水野美邦, 服部信孝
    • Organizer
      第51回日本神経学会総会
    • Place of Presentation
      東京
    • Year and Date
      2010-05-20
    • Data Source
      KAKENHI-PROJECT-21390272
  • [Presentation] アジア初のα-synuclein遺伝子三重複変異2010

    • Author(s)
      舩山学、関根威、加賀谷肇、李元哲、吉野浩代、富山弘幸、服部信孝
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      大宮
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PROJECT-21390272
  • [Presentation] SNCA三重複変異の同定2010

    • Author(s)
      舩山学、関根威、加賀谷肇、李元哲、吉野浩代、富山弘幸、服部信孝
    • Organizer
      第4回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      京都ホテルオークラ(京都)
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-22790829
  • [Presentation] Rapid screening of ATP13A2 variant with high-resolution melting analysis2009

    • Author(s)
      Funayama M, Tomiyama H, Wu RM, Yoshino H, Ogaki K, Mizuno Y, Hattori N.
    • Organizer
      Genetic Epidemiology of Parkinson's Disease 4th annual meeting
    • Place of Presentation
      Tubingen, Germany
    • Year and Date
      2009-07-08
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] 高分解能融解曲線分析法をもちいたATP13A2 A746T多型の大規模解析2009

    • Author(s)
      舩山学, 富山弘幸, 柳瀬貴章, Ruey-Meei Wu, 大垣光太郎, 吉野浩代, 水野美邦, 服部信孝
    • Organizer
      第3回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      東京
    • Year and Date
      2009-10-10
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] SNP chipによる家族性パーキンソン病のlinkage解析2009

    • Author(s)
      舩山学, 吉野浩代, 今道洋子, 李元 哲, 高嶋博, 松浦英治, 有村公良, 野元三治, 富山弘幸, 久保紳一郎, 水野美邦, 服部信孝
    • Organizer
      第50回日本神経学会総会
    • Place of Presentation
      仙台
    • Year and Date
      2009-05-22
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] 高分解能融解曲線分析法をもちいたATP13A2 A746T多型の大規模解析.2009

    • Author(s)
      舩山学
    • Organizer
      第3回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      品川プリンスホテル(東京都)
    • Year and Date
      2009-10-10
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Hi-Res Melting法をもちいたATP13A2 A746T多型の高速解析.2009

    • Author(s)
      舩山学
    • Organizer
      日本人類遺伝学会第54回大会
    • Place of Presentation
      グランドプリンスホテル高輪(東京都)
    • Year and Date
      2009-09-25
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Rapid screening of ATP13A2 variant with high-resolution melting analysis.2009

    • Author(s)
      Funayama M
    • Organizer
      Genetic Epidemiology of Parkinson's Disease 4th annual meeting.
    • Place of Presentation
      Tubingen, Germany
    • Year and Date
      2009-07-08
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Hi-Res Melting法をもちいたATP13A2 A746T多型の高速解析2009

    • Author(s)
      舩山学, 富山弘幸, 柳瀬貴章, 吉野浩代, 水野美邦, 服部信孝
    • Organizer
      日本人類遺伝学会第54回大会
    • Place of Presentation
      東京
    • Year and Date
      2009-09-25
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] SNP chipによる家族性パーキンソン病のlinkage解析.2009

    • Author(s)
      舩山学
    • Organizer
      第50回日本神経学会総会
    • Place of Presentation
      仙台国際センター(宮城県)
    • Year and Date
      2009-05-22
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Autosomal recessive late onset parkinsonismの原因遺伝子探索2008

    • Author(s)
      舩山学
    • Organizer
      第49回日本神経学会総会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2008-05-16
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] NDUFV2+/-マウスにおけるMPTP感受性の検討2008

    • Author(s)
      舩山学, 大橋聡, 市川直樹, 今井哲司, 山本庄司, 日下弘道, 板谷昌子, 平澤恵理, 水野美邦, 服部信孝
    • Organizer
      第8回日本ミトコンドリア学会年会
    • Place of Presentation
      東京
    • Year and Date
      2008-12-20
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Autosomal recessive late onset parkinsonismの原因遺伝子探索2008

    • Author(s)
      舩山学, 吉野浩代, 今道洋子, 李元哲, 李林, 増田浩美, 板谷昌子, 高梨雅史, 高嶋博, 松浦英治, 有村公良, 野元三治, 水野美邦, 服部信孝
    • Organizer
      第49回日本神経学会総会
    • Place of Presentation
      横浜
    • Year and Date
      2008-05-16
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] Autosomal recessive late onset parkinsonismの原因遺伝子探索2008

    • Author(s)
      舩山学, 吉野浩代, 今道洋子, 李元哲, 李林, 増田浩美, 板谷昌子, 高梨雅史, 高嶋博, 松浦英治, 有村公良, 野元三治, 富山弘幸, 久保紳一郎, 水野美邦, 服部信孝
    • Organizer
      第2回Movement Disorder Society, Japan学術集会
    • Place of Presentation
      京都
    • Year and Date
      2008-10-04
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] NDUFV2+/-マウスにおけるMPTP感受性の検討2008

    • Author(s)
      舩山学, 大橋聡, 市川直樹, 今井哲司, 山本庄司, 日下弘道, 板谷昌子, 平澤恵理, 水野美邦, 服部信孝
    • Organizer
      生体機能と創薬シンポジウム
    • Place of Presentation
      東京
    • Year and Date
      2008-09-05
    • Data Source
      KAKENHI-PROJECT-20790625
  • [Presentation] 日本人パーキンソン病患者におけるαシヌクレイン遺伝子新規変異の解析

    • Author(s)
      吉野浩代、西岡健弥、李元哲、舩山学、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] 日本人パーキンソン病におけるEIF4G1遺伝子変異の頻度

    • Author(s)
      舩山学、西岡健弥、大垣光太郎、李元哲、佐々木良元、小久保康昌、葛原茂樹、高橋裕秀、富山弘幸、水野美邦、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] GBA遺伝子変異を伴う家族性パーキンソン病の臨床遺伝学的検討

    • Author(s)
      李元哲、舩山学、李林、吉野浩代、西岡健弥、富山弘幸、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] 異染性白質ジストロフィー患者の家族に発症したパーキンソン病2症例の検討

    • Author(s)
      金井数明、李元哲、中谷光良、藤巻基紀、舩山学、西岡健弥、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] Parkinノックアウトマウスにおける細胞骨格蛋白異常による機能障害

    • Author(s)
      江口博人、今泉美佳、塚口ケネス、舩山学、西岡健弥、波田野琢、斉木臣二、佐藤栄人、久保紳一郎、今井譲、永松信哉、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] パーキンソン病の家族歴を有する多系統萎縮症患者におけるCOQ2変異解析

    • Author(s)
      三笠道太、金井数明、李元哲、西岡健弥、舩山学、富山弘幸、服部信孝
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25860726
  • [Presentation] High frequency of WDR45 mutation in Japanese patients with beta- propeller protein-associated neurodegeneration (BPAN)

    • Author(s)
      Nishioka K, Oyama G, Yoshino H, Li Y, Matsushima T, Takeuchi C, Mochizuki Y, Mori-Yoshimura M, Murata M, Yamasita C, Nakamura N, Konishi Y, Ohi K, Ichikawa K, Terada T, Obi T, Funayama M, Saiki S, Hattori N.
    • Organizer
      9th Annual Genetics Epidemiology of Parkinson's Disease Consortium
    • Place of Presentation
      Vancouver, British Columbia
    • Year and Date
      2014-09-10 – 2014-09-13
    • Data Source
      KAKENHI-PROJECT-25860726
  • []

  • 1.  HATTORI Nobutaka (80218510)
    # of Collaborated Projects: 5 results
    # of Collaborated Products: 38 results
  • 2.  SATO Shigeto (00445537)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 6 results
  • 3.  AMO Taku (40453922)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 6 results
  • 4.  SAIKI Shinji (00339996)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 7 results
  • 5.  SHIOMO Yashushi (70286714)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 2 results
  • 6.  HATANO Taku (60338390)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 7.  ISHIKAWA Kei-ichi (90733973)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 1 results
  • 8.  SASAZAWA Yukiko (20594922)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 1 results
  • 9.  赤松 和土 (60338184)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 1 results
  • 10.  Nishioka Kenya (40348933)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 11 results
  • 11.  LI Yuanzhe (40549292)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 11 results
  • 12.  TODA Tatsushi (30262025)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 13.  IMOTO Masaya (60213253)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  FURUYA Norihiko (50401188)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  YAMADA Daisuke (30757539)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  IMAI Yuzuru (30321730)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 17.  久保 紳一郎 (20327795)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  村上 晶 (90157743)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  北川 光洋 (10528566)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  小松 雅明 (90356254)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  Sue Carolyn M
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 22.  Farrer Matthew J
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 23.  Ross Owen A.
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 24.  Kruger Rejko Kruger
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 25.  SATAKE Wataru
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 26.  KIKUCHI Akio
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 27.  Higuchi Makoto
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 28.  MOGUSHI Kaoru
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 29.  TAKA Hikari
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 30.  KAGA Naoko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 31.  上山 盛夫
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 32.  佐原 成彦
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 33.  小池 正人
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 34.  阿部 学
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 35.  内山 安男
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 36.  高橋 良輔
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 37.  重本 隆一
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 38.  深澤 有吾
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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