Funayama Manabu 舩山学

… Alternative Names

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

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

[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 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

Funayama Manabu 舩山 学

FUNAYAMA Manabu 舩山 学

Research Projects

Research Products

Co-Researchers

Understanding the complete picture of familial Parkinson's disease using comprehensive genetic analysis.Principal Investigator

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Elucidation of the molecular mechanisms of dopaminergic neurodegenerative disorders using a large genome resourcePrincipal Investigator

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Development of novel cellular models for Parkinson's disease focusing on energy-homeostasisPrincipal Investigator

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Generation of new mouse model for Parkinson's disease(Fostering Joint International Research)Principal Investigator

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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

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Generation of the novel mouse model for Parkinson's disease derived from two-hit hypothesisPrincipal Investigator

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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

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Identification of new gene for familial parkinsonismPrincipal Investigator

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Funayama Manabu 舩山学

FUNAYAMA Manabu 舩山学

[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

[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