• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

TOMIYAMA Hiroyuki  富山 弘幸

Researcher Number 20515069
Other IDs
  • ORCIDhttps://orcid.org/0000-0001-9508-163X
Affiliation (based on the past Project Information) *help 2013 – 2014: 順天堂大学, 医学部, 准教授
2011: 順天堂大学, 医学部, 准教授
2009 – 2010: 順天堂大学, 医学研究科, 助教
2008 – 2010: 順天堂大学, 医学部, 助教
2008: 順天堂大学, 医学部・神経内科, 助教
Review Section/Research Field
Principal Investigator
Neurology
Except Principal Investigator
Neurology
Keywords
Principal Investigator
パーキンソン病 / 遺伝 / 遺伝子解析 / 国際情報交流 / 臨床的特徴 / 遺伝子変異解析 / 新規責任遺伝子同定 / 常染色体優性遺伝性パーキンソン病 / 家族性パーキソンソ病 / パーキソンソ病 … More / LRRK2 / SNCA / 変異 / 分子遺伝学 / 常染色体優性遺伝 / 家族性パーキンソン病 / 多型 / 遺伝子変異 / 遺伝子 / 常染色体優性遺伝性パーキンソン病(ADPD) / パーキンソン病(PD) … More
Except Principal Investigator
グアム島 / タウオパチー / TDP-43 / パーキンソン認知症複合 / 筋萎縮性側索硬化症 / 紀伊半島 / α-synuclein / 遺伝子解析 / 連鎖解析 / 常染色体劣性晩発性パーキンソン病 / ユビキチン化 / ATP132 / autophagy-lysosomal path& / DJ-1 / Parkin / PINK1 / ミトコンドリア機能 / 劣性遺伝性パーキンソン病 / 新規原因遺伝子 / 共通機構 / 遺伝性パーキンソン病 / パーキンソン病 / パーキンソン症候群 / 認知症 / タウ蛋白 / 酸化ストレス / アルツハイマー神経原線維変化 / 遺伝子 Less
  • Research Projects

    (5 results)
  • Research Products

    (130 results)
  • Co-Researchers

    (26 People)
  •  常染色体優性遺伝性パーキンソン病の遺伝子解析・新規原因遺伝子同定Principal Investigator

    • Principal Investigator
      富山 弘幸
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Gnentic analysis to identify new causative genes in autosomal dominant Parkinson's diseasePrincipal Investigator

    • Principal Investigator
      TOMIYAMA Hiroyuki
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  Gene analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex, Kii, Japan

    • Principal Investigator
      KOKUBO Yasumasa
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Mie University
  •  Molecular biological study on the cause and pathogenesis of amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii peninsula of Japan

    • Principal Investigator
      KUZUHARA Shigeki
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
      Mie University
  •  Identification of a common pathway among gene products for familial Parkinson's disease and screening for a novel causative gene for

    • Principal Investigator
      HATTORI Nobutaka
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University

All 2015 2014 2013 2012 2011 2010 2009 2008 2007 Other

All Journal Article Presentation Book

  • [Book] 12番染色体に連鎖する遺伝性パーキンソン病(PARK8).日本臨牀「神経症候群 II」.2014

    • Author(s)
      富山弘幸,服部信孝.
    • Total Pages
      4
    • Publisher
      日本臨牀社
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Book] 「神経症候群 II」.12番染色体に連鎖する遺伝性パーキンソン病(PARK8).2014

    • Author(s)
      富山弘幸,服部信孝.
    • Publisher
      日本臨床
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Book] パーキンソン病の基礎研究最前線:実地医家のためのminimum requirement. Modern Physician2012

    • Author(s)
      舩山学, 富山弘幸
    • Publisher
      新興医学出版社
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Book] パーキンソン病(臨床の諸問題2).遺伝的因子,遺伝学的見地からのパーキンソン病update-パーキンソン病にどこまで遺伝的要因が関与しているか?-2010

    • Author(s)
      富山弘幸
    • Total Pages
      29
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Book] 遺伝的因子,遺伝学的見地からのパーキンソン病update-パーキンソン病にどこまで遺伝的要因が関与しているか?-.パーキンソン病(臨床の諸問題2)2010

    • Author(s)
      富山弘幸
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Book] パーキンソン病の発症に遺伝子の関与はあるのか? :いきなり名医! パーキンソン病Q&A-押さえておくべきポイント332009

    • Author(s)
      富山弘幸
    • Total Pages
      6
    • Publisher
      日本医事新報
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Book] パーキンソン病の発症に遺伝子の関与はあるのか?:いきなり名医!パーキンソン病Q & A-押さえておくべきポイント2009

    • Author(s)
      富山弘幸
    • Publisher
      日本医事新報
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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] 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] Familial Parkinson's disease/parkinsonism.(Editorial)2015

    • Author(s)
      Tomiyama H, Lesage S, Tan EK, Jeon BS.
    • Journal Title

      Biomed Res Int.

      Volume: 2015 Pages: 736915-736915

    • DOI

      10.1155/2015/736915

    • Open Access
    • Data Source
      KAKENHI-PROJECT-25461292
  • [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] 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 preliminary diffusional kurtosis imaging study of Parkinson disease: comparison with conventional diffusion tensor imaging.2014

    • Author(s)
      Kamagata K, Tomiyama H, Hatano T, Motoi Y, Abe O, Shimoji K, Kamiya K, Suzuki M, Hori M, Yoshida M, Hattori N, Aoki S.
    • Journal Title

      Neuroradiology

      Volume: 56 Issue: 3 Pages: 251-258

    • DOI

      10.1007/s00234-014-1327-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24591787, KAKENHI-PROJECT-25461290, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25861126
  • [Journal Article] Diffusional kurtosis imaging of cingulate fibers in Parkinson disease: comparison with conventional diffusion tensor imaging.2013

    • Author(s)
      Kamagata K
    • Journal Title

      Magn Reson Imaging.

      Volume: 31(9) Issue: 9 Pages: 1501-1506

    • DOI

      10.1016/j.mri.2013.06.009

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-221S0003, KAKENHI-PROJECT-24591787, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25461848, KAKENHI-PROJECT-25861126
  • [Journal Article] The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.2013

    • Author(s)
      Heckman MG, Elbaz A, Soto-Ortolaza AI, Serie DJ, Aasly JO, Annesi G, Auburger G, Bacon JA, Boczarska-Jedynak M, Bozi M, Brighina L, Chartier-Harlin MC, Dardiotis E, Destée A, Ferrarese C, Ferraris A, Fiske B, Gispert S, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, ... , Tomiyama H, et al.
    • Journal Title

      Neurobiol Aging

      Volume: S0197-4580 Pages: 318-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Journal Article] Relationship between cognitive impairment and white-matter alteration in Parkinson’s disease with dementia: tract-based spatial statistics and tract-specific analysis.2013

    • Author(s)
      Kamagata K
    • Journal Title

      Eur Radiol.

      Volume: 23(7) Issue: 7 Pages: 1946-1955

    • DOI

      10.1007/s00330-013-2775-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-221S0003, KAKENHI-PROJECT-24591787, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25861126
  • [Journal Article] 運動ニューロン疾患の遺伝学:update 『わが国のALSにおけるC9ORF72』2013

    • Author(s)
      富山弘幸.
    • Journal Title

      臨床神経学 .

      Volume: 53 Pages: 1074-6

    • Data Source
      KAKENHI-PROJECT-25461292
  • [Journal Article] Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium.2013

    • Author(s)
      Heckman MG, Soto-Ortolaza AI, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Fiske B, Gibson JM, Gibson R, Hadjigeorgiou GM, Hattori N, ... , Tomiyama H, et al.
    • Journal Title

      Mov Disord

      Volume: 28 Issue: 12 Pages: 1740-4

    • DOI

      10.1002/mds.25600

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Journal Article] Intronic C9orf72 mutation expanding on neurodegenerative disorders and other diseases (Editorial).2013

    • Author(s)
      Tomiyama H.
    • Journal Title

      J Neurol Disord Stroke

      Volume: 1 Pages: 1009-1009

    • Data Source
      KAKENHI-PROJECT-25461292
  • [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] Lack of Genetic Associations of PPAR-γ and PGC-1α with Alzheimer’s Disease and Parkinson’s Disease with Dementia.2013

    • Author(s)
      Shibata N, Motoi Y, Tomiyama H, Ohnuma T, Kuerban B, Tomson K, Komatsu M, Shimazaki H, Hattori N, Arai H.
    • Journal Title

      Dement Geriatr Cogn Disord Extra

      Volume: 3 Issue: 1 Pages: 161-7

    • DOI

      10.1159/000351419

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461292
  • [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 requirement. Modern Physician2012

    • Author(s)
      舩山学, 富山弘幸
    • Journal Title

      新興医学出版社

      Volume: 32 Pages: 201-5

    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Perry症候群とDCTN1遺伝子変異2012

    • Author(s)
      富山弘幸
    • Journal Title

      Medical Science Digest (MSD)ニューサイエンス社

      Volume: 38

    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Analysis of PLA2G6 in patients with frontotemporal type of dementia2011

    • Author(s)
      Tomiyama H, Yoshino H, Hattori N
    • Journal Title

      Parkinsonism Relat Disord

      Volume: 17 Pages: 493-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease2011

    • Author(s)
      Seki N, Takahashi Y, Tomiyama H, Rogaeva E, Murayama S, Mizuno Y, Hattori N, Marras C, Lang AE, George-Hyslop PS, Goto J, Tsuji S
    • Journal Title

      J Hum Genet

      Volume: 56 Pages: 671-5

    • NAID

      10030660937

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Axon guidance pathway genes and Parkinson's disease(Commentary)2011

    • Author(s)
      Tomiyama H
    • Journal Title

      J Hum Genet

      Volume: 56 Pages: 102-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Genetic Epidemiology of Parkinson's Disease Consortium. Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease2011

    • Author(s)
      Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destee A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C, Lesage S, Lynch T, Lichtner P, Lambert JC, Lang AE, Mellick GD, Nigris FD, Opala G, Quattrone A, Riva C, Rogaeva E, Ross OA, Satake W, Silburn PA, Theuns J, Toda T, Tomiyama H, Uitti RJ, Wirdefeldt K, Wszolek Z, Gasser T, Kruger R
    • Journal Title

      Neurobiol Aging

      Volume: 32

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Association of LRRK2 exonic variants with susceptibility to Parkinson's disease : a case-control study2011

    • Author(s)
      Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Ferraris A, Fiske B, Gibson JM,Gibson R, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Jeon BS, Kim YJ, Klein C, Kruger R, Kyratzi E, Lesage S, Lin CH, Lynch T, Maraganore DM, Mellick GD, Mutez E, Nilsson C, Opala G, Park SS, Puschmann A, Quattrone A, Sharma M, Silburn PA, Sohn YH, Stefanis L, Tadic V, Theuns J, Tomiyama H, Uitti RJ, Valente EM, van de Loo S, Vassilatis DK, Vilarino-Guell C, White LR, Wirdefeldt K, Wszolek ZK, Wu RM, Farrer MJ ; on behalf of the Genetic Epidemiology Of Parkinson's Disease(GEO-PD) Consortium
    • Journal Title

      Lancet Neurol

      Volume: 10 Pages: 898-908

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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 Pages: 401-3

    • NAID

      10030659472

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Axon guidance pathway genes and Parkinson's disease (Commentary)2011

    • Author(s)
      Tomiyama H
    • Journal Title

      J Hum Genet

      Volume: 56 Pages: 102-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Visual Grasping in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 (Microtubule-Associated with Protein Tau) : A Comparison of 123 I-IMP Brain Perfusion SPECT Analysis with Progressive Supranuclear Palsy2011

    • Author(s)
      Ogaki K, Motoi Y, Li Y, Tomiyama H, et al
    • Journal Title

      Mov Disord

      Volume: 26 Pages: 561-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N.PLA2G6 variant in Parkinson's disease2011

    • Author(s)
      Tomiyama H, Yoshino H, Ogaki K, et al
    • Journal Title

      J Hum Genet

      Volume: 56 Pages: 401-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] A large-scale genetic association study to evaluate the contribution of Omi/HtrA2(PARK13) to Parkinson's disease2011

    • Author(s)
      Kruger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage S, Lin JJ, Lynch T, Mellick GD, de Nigris F, Opala G, Prigione A, Quattrone A, Ross OA, Satake W, Silburn PA, Tan EK, Toda T, Tomiyama H, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM ; for the Genetic Epidemiology of Parkinson's disease consortium
    • Journal Title

      Neurobiol Aging

      Volume: 32

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Visual Grasping in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17(Microtubule-Associated with Protein Tau): A Comparison of 123 I-IMP Brain Perfusion SPECT Analysis with Progressive Supranuclear Palsy2011

    • Author(s)
      Ogaki K, Motoi Y, Li Y, Tomiyama H, Shimizu N, Takanashi M, Nakanishi A, Yokoyama K, Hattori N
    • Journal Title

      Mov Disord

      Volume: 26 Pages: 561-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.2010

    • Author(s)
      Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, et al.
    • Journal Title

      Hum Mol Genet

      Volume: 19 Pages: 1998-2004

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism.2010

    • Author(s)
      Yoshino H, Tomiyama H, Tachibana N, Ogaki K, et al.
    • Journal Title

      Neurology

      Volume: 75 Pages: 1356-61

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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: 245-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Clinical course of the first Asian family with Parkinsonism related to SNCA triplication.2010

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

      Mov Disord

      Volume: 25 Pages: 2871-75

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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: 2434-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Clinical course of the first Asian family with Parkinsonism related to SNCA triplication2010

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

      Mov Disord

      Volume: 25 Pages: 2871-75

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters2010

    • Author(s)
      Lin Li, Manabu Funayama, Hiroyuki Tomiyama, Yuanzhe Li, Hiroyo Yoshino, Ryogen Sasaki, Yasumasa Kokubo, Shigeki Kuzuhara, Yoshikuni Mizuno, Nobutaka Hattori
    • Journal Title

      Neuroscience Letters

      Volume: 479 Pages: 245-248

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Journal Article] Axon guidance pathway genes and Parkinson's disease (Commentary).2010

    • Author(s)
      Tomiyama H.
    • Journal Title

      J Hum Genet

      Volume: 56 Pages: 102-3

    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines.2010

    • Author(s)
      Mitsui J, Takahashi Y, Goto J, Tomiyama H, et al.
    • Journal Title

      Am J Hum Genet

      Volume: 87 Pages: 75-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Nobutaka HattoriNo evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters Neuroscience2010

    • Author(s)
      Lin Li, Manabu Funayama, Hiroyuki Tomiyama, Yuanzhe Li, Hiroyo Yoshino, Ryogen Sasaki,Yasumasa Yasumasa Kokubo, Shigeki Kuzuhara, Yoshikuni Mizuno
    • Journal Title

      Letters 479

      Pages: 245-248

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Journal Article] Parkinson's disease-related LRRK2 G2019mutation results from independent mutational events in humans2010

    • Author(s)
      Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, Pirkevi C, Hamadouche T, Cazeneuve C, Basak AN, Hattori N, Durr A, Tazir M,Orr-Urtreger A, Quintana-Murci L, Brice A
    • Journal Title

      Hum Mol Genet

      Volume: 19 Pages: 1998-2004

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Rapid screening of ATP13A2 variant with high-resolution melting analysis.2010

    • Author(s)
      Funayama M, Tomiyama H, Wu RM, Ogaki K, et al.
    • Journal Title

      Mov Disord

      Volume: 25 Pages: 2434-37

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Phenotypicspectrum 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: 1356-61

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.2010

    • Author(s)
      Li L, Funayama M, Tomiyama H, et al.
    • Journal Title

      Neurosci Lett

      Volume: 479 Pages: 245-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines2010

    • Author(s)
      Mitsui J, Takahashi Y, Goto J, Tomiyama H, Ishikawa S, Yoshino H, Minami N, Smith DI, Lesage S, Aburatani H, Nishino I, Brice A, Hattori N, Tsuji S
    • Journal Title

      Am J Hum Genet

      Volume: 87 Pages: 75-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Mutation analysis for DJ-1 in sporadic and familial parkinsonism : Screening strategy in parkinsonism2009

    • Author(s)
      Tomiyama H, Li Y, Yoshino H, Mizuno Y, Kubo S, et al.
    • Journal Title

      Neuroscience Letters 455

      Pages: 159-161

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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 T, Sekiguchi Y, Funayama M, Kuwabara S, Hattori N, Hattori T.
    • Journal Title

      Movement Disorders 24

      Pages: 1403-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease : Large-scale collaborative study2009

    • Author(s)
      Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, Ferrarese C, Hadjigeorgiou GM, Krueger R, Lambert JC, Lesage S, Markopoulou K, Mellick GD, Meeus B, Pedersen NL, Quattrone A, Van Broeckhoven C, Sharma M, Silburn PA, Tan EK, Wirdefeldt K, Ioannidis JP, Sutherland GT, Siebert GA. Theuns J, Crosiers D, Pickut B, Pals P, Engelborghs S, Nuytemans K, De Deyn PP, Cras P, Agid Y, Bonnet AM, Borg M, Brice A, Broussolle E, Damier P, Destee A, Durr A, Durif F, Lesage S, Lohmann E, Pollak P, Rascol O, Tison F, Tranchant C, Viallet F, Vidailhet M, Tzourio C, Amouyel P, Loriot MA, Gasser T, Riess O, Berg D, Schulte C, Klein C, Djarmati A, Lohmann K, Xiromerisiou G, Dardiotis E, Kountra P, Hattori N, Tomiyama H, Funayama M, Yoshino H, Li Y, Valente EM, FerraBentivoglio AR, Ialongo T, Riva C, Corradi B, Opala G, Myga BJ, Duda GK, Jedynak MB, Belin AC, Galter LD, Westerlund M, Sydow O, Nilsson C, Puschmann A, Maraganore DM, Ahlskog Mariza de Andrade JE, Lesnick TG, Rocca WA, Checkoway H
    • Journal Title

      Am J Med Genet B Neuropsychiatr Genet

      Volume: 153B(1) Pages: 220-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype2009

    • Author(s)
      Pirkevi C, Lesage S, Condroyer C, Tomiyama H, Hattori N, Ertan S, Brice A, Ba. ak AN
    • Journal Title

      Neurogenetics

      Volume: 10 Pages: 271-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Mutation analysis for DJ-1 in sporadic and familial parkinsonism : Screening strategy in parkinsonism2009

    • Author(s)
      Tomiyama H, Li Y, Yoshino H, Mizuno Y, Kubo S, Toda T, Hattori N
    • Journal Title

      Neurosci Lett

      Volume: 455 Pages: 159-61

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Evaluation of the genetic contribution of Omi/HtrA2 to Parkinson disease in a large collaborative study2009

    • Author(s)
      Kruger R, Sharma M, Riess O, Gasser T, van Broeckhoven C, Aasly J, Annesi G, Bentivoglio, AR Brice A, Elbaz A, Farrer M, Ferrarese C, Ferraris A, Hadjigeorgiou GM, Hattori N, Tomiyama H, et al.
    • Journal Title

      Neurobiol Aging (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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 T, Sekiguchi Y, Funayama M, Kuwabara S, Hattori N, Hattori T
    • Journal Title

      Mov Disord

      Volume: 24 Pages: 1403-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype2009

    • Author(s)
      Pirkevi C, Lesage S, Condroyer C, Tomiyama H, et al.
    • Journal Title

      Neurogenetics 10

      Pages: 271-273

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease2009

    • Author(s)
      Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T
    • Journal Title

      Nature Genet

      Volume: 41 Pages: 1303-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease2009

    • Author(s)
      Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, et al.
    • Journal Title

      Nature Genetics (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Mutation analyses in amyotrophic lateral sclerosis/ parkinsonism-dementia complex of Kii, Japan2008

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

      Mov Disord. 23

      Pages: 2344-2348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Journal Article] Progress in the pathogenesis and genetics of Parkinson's disease2008

    • Author(s)
      Mizuno Y, Hattori N, Kubo SI, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. Review
    • Journal Title

      Philos Trans R Soc Lond B Biol Sci 27

      Pages: 2215-2227

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, 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

      Pages: 2344-2348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390239
  • [Journal Article] Mutation analysis of the PINK1 gene in 391 patients with Parkinson 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

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.2008

    • 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

      Pages: 2344-2348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390239
  • [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

      Pages: 2344-2348

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of Kii2008

    • Author(s)
      Hiroyuki Tomiyama, Yasumasa Kokubo, Ryogen Sasaki, Yuanzhe Li, Yoko Imamichi, Manabu Funayama, Yoshikuni Mizuno, Nobutaka Hattori, Shigeki Kuzuhara
    • Journal Title

      Japan Mov Disord. 23

      Pages: 2344-2348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Journal Article] PARK9-linked parkinsonism in Eastern Asia : Mutation detection in ATP13A2 andclinical 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

      Pages: 1491-1493

    • Data Source
      KAKENHI-PROJECT-19390244
  • [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

      Pages: 1012-5

    • NAID

      10025584966

    • Data Source
      KAKENHI-PROJECT-19390244
  • [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

      Pages: 802-808

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population2007

    • Author(s)
      Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N
    • Journal Title

      Neuroreport 18

      Pages: 273-5

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier2007

    • Author(s)
      Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y
    • Journal Title

      J Neurol Sci 252

      Pages: 181-4

    • Data Source
      KAKENHI-PROJECT-19390244
  • [Journal Article] PLA2G6 variant in Parkinson's disease.

    • Author(s)
      Tomiyama H, Yoshino H, Ogaki K, Li L, et al.
    • Journal Title

      J Hum Genet

      Volume: (in press)

    • NAID

      10030659472

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Visual grasping in FTDP-17 (MAPT)-A comparison of ^<123>I-IMP brain perfusion SPECT analysis with PSP-.

    • Author(s)
      Ogaki K, Motoi Y, Li Y, Tomiyama H, et al.
    • Journal Title

      Mov Disord

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Journal Article] Pseudo-heterozygous rearrangement mutation of parkin

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

      Mov Disord

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Perry症候群の診断基準案作成と疫学調査について2011

    • Author(s)
      富山弘幸, 李林, 中尾紘一, 京楽格, 栗崎玲一, 李元哲, 舩山学, 吉野浩代, 音成龍司, 坪井義夫, 服部信孝
    • Organizer
      平成23年度神経変性疾患に関する調査研究班
    • Place of Presentation
      東京
    • Year and Date
      2011-12-16
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Analysis of the FBXO7 gene in early-onset parkinsonism2011

    • Author(s)
      Y. Li, M. Funayama, H. Yoshino, H. Tomiyama, N. Hattori
    • Organizer
      The 12th International Congress of Human Genetics, ICHG and the American Society of Human Genetics, ASHG 61st Annual Meeting
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-14
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] PLA2G6 in patients with Parkinson's disease/frontotemporal type of dementia2011

    • Author(s)
      H. Tomiyama, H. Yoshino, K. Ogaki, L. Li, C. Yamashita, Y. Li, M. Funayama, R. Sasaki, Y. Kokubo, S. Kuzuhara, and N. Hattori
    • Organizer
      The 12th International Congress of Human Genetics, ICHG and the American Society of Human Genetics, ASHG 61st Annual Meeting
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-14
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 日本人パーキンソニズムにおけるDCTN1変異解析-Perry症候群について2011

    • Author(s)
      富山弘幸, 李林, 中尾紘一, 京楽格, 栗崎玲一, 李元哲, 舩山学, 吉野浩代, 音成龍司, 坪井義夫, 服部信孝
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋
    • Year and Date
      2011-05-18
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 日本人パーキンソニズム症例におけるDCTN1解析2011

    • Author(s)
      富山弘幸, 李林, 中尾紘一, 京楽格, 栗崎玲一, 李元哲, 舩山学, 吉野浩代, 音成龍司, 坪井義夫, 服部信孝
    • Organizer
      日本人類遺伝学会総会
    • Place of Presentation
      東京
    • Year and Date
      2011-11-12
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 日本人パーキンソニズムにおけるDCTN1び変異解析-Perry症候群について2011

    • Author(s)
      富山弘幸, 他
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋
    • Year and Date
      2011-05-18
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] α-synucleinopathyと遺伝子変異2011

    • Author(s)
      富山弘幸
    • Organizer
      Japanese Consortium for Age-related Neurodegenerative disorders, JCAN
    • Place of Presentation
      東京
    • Year and Date
      2011-08-27
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソニズムにおけるDCTN1解析-Perry症候群とパーキンソン病の異同について2011

    • Author(s)
      富山弘幸, 李林, 中尾紘一, 京楽格, 栗崎玲一, 李元哲, 舩山学, 吉野浩代, 音成龍司, 坪井義夫, 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
      東京
    • Year and Date
      2011-10-08
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Analyses of compound heterozygous rearrangements of parkin2011

    • Author(s)
      M. Funayama, H. Kusaka, H. Yoshino, Y. Li, K. Ogaki, H. Tomiyama, N. Hattori
    • Organizer
      The 12th International Congress of Human Genetics, ICHG and the American Society of Human Genetics, ASHG 61st Annual Meeting
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-14
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Clinicogenetic study of patients with FTDP-17(MAPT) in Japan2011

    • Author(s)
      K. Ogaki, Y. Li, M. Takanashi, K. Ishikawa, T. Kobayashi, A. Nakanishi, T. Nonaka, M. Hasegawa, M. Kishi, H. Yoshino, M. Funayama, K. Shioya, M. Yokochi, R. Sasaki, Y. Kokubo, S. Kuzuhara, Y. Motoi, H. Tomiyama, N. Hattori
    • Organizer
      The 12th International Congress of Human Genetics, ICHG and the American Society of Human Genetics, ASHG 61st Annual Meeting
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-14
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Japanese subsequent GWAS identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease2011

    • Author(s)
      W. Satake, K. Yamamoto, Y. Nakabayashi, M. Kubo, T. Morizono, T. Kawaguchi, T. Tsunoda, H. Tomiyama, M. Yamamoto, N. Hattori, M. Murata, Y. Nakamura, T. Toda
    • Organizer
      The 12th International Congress of Human Genetics, ICHG and the American Society of Human Genetics, ASHG 61st Annual Meeting
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-14
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 若年性パーキンソニズム症例におけるPLA2G6(PARK14)変異解析2010

    • Author(s)
      吉野浩代, 富山弘幸, 立花直子, 大垣光太郎, 李元哲, 舩山学, 橋本隆男, 高嶋修太郎, 服部信孝
    • Organizer
      神経変性疾患に関する調査研究班
    • Place of Presentation
      東京
    • Year and Date
      2010-12-18
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 孤発性パーキンソン病におけるPLA2G6 p. P806R2010

    • Author(s)
      富山弘幸, 吉野浩代, 大垣光太郎, 李林, 李元哲, 舩山学, 佐々木良元, 小久保康昌, 葛原茂樹, 服部信孝
    • Organizer
      第4回MDSJ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-21591098
  • [Presentation] パーキンソン病におけるPLA2G6 p.P806R.2010

    • Author(s)
      富山弘圭, 吉野浩代, 大垣光太郎, 李林, 李元哲, 舩山学, 佐々木良元, 小久保康昌, 葛原茂樹, 服部信孝
    • Organizer
      日本人類遺伝学会総会
    • Place of Presentation
      大宮
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] FTDP-17が疑われた日本人71症例におけるMAPT、PGRN遺伝子解析2010

    • Author(s)
      大垣光太郎、李元哲、高梨雅史、石川景一、小林智則、中西淳、野中隆、長谷川成人、岸雅彦、吉野浩代、舩山学、塩屋敬一、横地正之、佐々木良元、小久保康昌、葛原茂樹、本井ゆみ子、富山弘幸、服部信孝
    • Organizer
      第4回 MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] 孤発性パーキンソン病におけるPLA2G6 p.P806R.2010

    • Author(s)
      富山弘幸, 吉野浩代, 大垣光太郎, 李林, 李元哲, 舩山学, 佐々木良元, 小久保康昌, 葛原茂樹, 服部信孝
    • Organizer
      第4回MDSJ学術集会
    • Place of Presentation
      京都
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 孤発性パーキンソン病におけるPLA2G6 p.P806R2010

    • Author(s)
      富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
    • Organizer
      第4回MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] FTDP-17が疑われた日本人71症例におけるMAPT、PGRN遺伝子解析2010

    • Author(s)
      大垣光太郎、李元哲、高梨雅史、石川景一、小林智則、中西淳、野中隆、長谷川成人、岸雅彦、吉野浩代、舩山学、塩屋敬一、横地正之、佐々木良元、小久保康昌、葛原茂樹、本井ゆみ子、富山幸、服部信孝
    • Organizer
      第4回MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] パーキンソン病におけるPLA2G6p.P806R2010

    • Author(s)
      富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
    • Organizer
      日本人類遺伝学会総会
    • Place of Presentation
      大宮
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] 日本人におけるIGYF2の変異解析2010

    • Author(s)
      李林, 舩山学, 李元哲, 今道洋子, 吉野浩代, 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-21591098
  • [Presentation] 若年性パーキンソニズム症例におけるPLA2G6(PARK14)変異解析2010

    • Author(s)
      吉野浩代, 富山弘幸, 立花直子, 大垣光太郎, 李元哲, 舩山学, 橋本隆男, 高嶋修太郎, 服部信孝
    • Organizer
      平成22年度神経変性疾患に関する調査研究班
    • Place of Presentation
      東京
    • Year and Date
      2010-12-18
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソン病におけるPLA2G6 p. P806R2010

    • Author(s)
      富山弘幸, 吉野浩代, 大垣光太郎, 李林, 李元哲, 舩山学, 佐々木良元, 小久保康昌, 葛原茂樹, 服部信孝
    • Organizer
      日本人類遺伝学会総会
    • Place of Presentation
      大宮
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 日本人パーキンソン病患者におけるGIGYF2の変異解析2010

    • Author(s)
      李林、舩山学、富山弘幸、李元哲、吉野浩代、佐々木良元、小久保康昌、葛原茂樹、水野美邦、服部信孝
    • Organizer
      第4回 MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] 日本人パーキンソン病患者におけるGIGYF2の変異解析2010

    • Author(s)
      李林、舩山学、富山弘幸、李元哲、吉野浩代、佐々木良元、小久保康昌、葛原茂樹、水野美邦、服部信孝
    • Organizer
      第4回MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] パーキンソン病におけるPLA2G6 p.P806R2010

    • Author(s)
      富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
    • Organizer
      日本人類遺伝学会総会
    • Place of Presentation
      大宮
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] 孤発性パーキンソン病におけるPLA2G6 p.P806R2010

    • Author(s)
      富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
    • Organizer
      第4回 MDSJ
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20590994
  • [Presentation] 遺伝的見地から見たパーキンソン病2010

    • Author(s)
      富山弘幸
    • Organizer
      浜松パーキンソン病講演会
    • Place of Presentation
      浜松
    • Year and Date
      2010-10-26
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Parkin遺伝子とPINK1遺伝子の変異を持ちMIBG心筋シンチが正常の家族性パーキンソン病2009

    • Author(s)
      野倉一也, 清水穂高, 山本横子, 富山弘幸, 舩山学, 服部信孝
    • Organizer
      日本神経学会東海北陸地方会
    • Year and Date
      2009-04-22
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] LRRK2 P755L variant in Parkinson's disease2009

    • Author(s)
      Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo S.-I., Mizuno Y, Toda T, Hattori N
    • Organizer
      Movement Disorders
    • Place of Presentation
      Paris
    • Year and Date
      2009-06-11
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] FTDP-17の一症例2009

    • Author(s)
      塩屋敬一, 斉田和子, 杉本精一郎, 比嘉利信, 富山弘幸, 服部信孝
    • Organizer
      日本神経学会九州地方会
    • Place of Presentation
      九州
    • Year and Date
      2009-03-29
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Glucocerebrosidase(GBA)mutations and familial Parkinson's disease in Japan2009

    • Author(s)
      関根威, 李林, 李元哲, 今道洋子, 吉野浩代, 舩山学, 富山弘幸, 久保紳一郎, 服部信孝
    • Organizer
      Movement Disorders
    • Place of Presentation
      France, Paris
    • Year and Date
      2009-06-07
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソン病におけるDJ-1変異解析:常染色体劣性遺伝性パーキンソニズムにおけるスクリーニング法について2009

    • Author(s)
      富山弘幸, 李元哲, 吉野浩代, 舩山学, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      MDSJ
    • Place of Presentation
      東京
    • Year and Date
      2009-10-10
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Different origins and demographic histories of the LRK2 G2019S mutation in Parkinson's disease2009

    • Author(s)
      Lesage S, Patin E, Condroyer C, Leutenegger A.-L, Lohmann E, Pollak P, Ouvrard-Hernandez A.-M., Bardien-Kruger S, Tomiyama H, et al.
    • Organizer
      Movement Disorders
    • Place of Presentation
      France, Paris
    • Year and Date
      2009-06-07
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Preserved cardiac 123I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient2009

    • Author(s)
      Kanai K, Arai K, Asahina M, Tomiyama H, Kuwabara Y, Uchiyama T, Sekiguchi Y, Funayama M, Hattori N, Kuwabara S.
    • Organizer
      Movement Disorders
    • Place of Presentation
      France, Paris
    • Year and Date
      2009-06-07
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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
    • Place of Presentation
      東京
    • Year and Date
      2009-07-25
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Mutation analysis for DJ-1 in parkinsonism : Screening strategy in autosomal recessive parkinsonism2009

    • Author(s)
      Tomiyama H, Li Y, Funayama M, Yoshino H, Kubo S, Mizuno Y, Toda T, Hattori N
    • Organizer
      4^<th> GEO-PD meeting
    • Place of Presentation
      Germany, Tubingen
    • Year and Date
      2009-07-06
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] LRR2 P755L variant in Parkinson's disease2009

    • Author(s)
      富山弘幸, 水田依久子, 李元哲, 舩山学, 吉野浩代, 李林, 村田美穂, 山本光利, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      Movement Disorders
    • Place of Presentation
      France, Paris
    • Year and Date
      2009-06-07
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Different origins and demographic histories of the LRK2 G2019S mutation in Parkinson's disease2009

    • Author(s)
      Lesage S, Patin E, Condroyer C, Leutenegger A.-L, Lohmann E, Pollak P, Ouvrard-Hernandez A.-M., Bardien-Kruger S, Tomiyama H, Basak N, Durr A, Hattori N, Orr-Urtreger A, Tazir M, Quintana-Murci L, Brice A
    • Organizer
      Movement Disorders
    • Place of Presentation
      Paris
    • Year and Date
      2009-06-11
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソン病原因遺伝子の大規模変異解析2009

    • Author(s)
      吉野浩代, 今道洋子, 李元哲, 関根威, 李林, 西岡健弥, 大垣光太郎, 舩山学, 富山弘幸, 水野美邦, 服部信孝
    • Organizer
      日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2009-07-24
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソン病におけるDL-1変異解析:常染色体劣性遺伝性パーキンソニズムにおけるスクリーニング法について2009

    • Author(s)
      富山弘幸, 李元哲, 吉野浩代, 舩山学, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      MDSJ
    • Place of Presentation
      東京
    • Year and Date
      2009-10-08
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Park2, DMDの欠失・重複は特定の領域に独立してランダムに集中する2009

    • Author(s)
      三井純, 高橋祐二, 富山弘幸, 石川俊平, 後藤順, 油谷浩幸, Brice Alexis, Smith David, 西野一三, 服部信孝, 辻省次
    • Organizer
      日本神経学会総会
    • Place of Presentation
      仙台
    • Year and Date
      2009-05-20
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 孤発性パーキンソン病におけるLRRK2 P755L変異2009

    • Author(s)
      富山弘幸, 水田依久子, 李元哲, 舩山学, 吉野浩代, 李林, 村田美穂, 山本光利, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2009-07-24
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 孤発性パーキンソン病における LRRK2 P755L2009

    • Author(s)
      富山弘幸, 水田依久子, 李元哲, 舩山学, 吉野浩代, 李林, 村田美穂, 山本光利, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      2009日本神経学会総会
    • Place of Presentation
      宮城県仙台市
    • Year and Date
      2009-05-20
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Glucocerebrosidase(GBA) mutations and familial Parkinson's disease in Japan2009

    • Author(s)
      Sekine T, Li L., Li Y, Imamichi Y, Yoshino H, Funayama M, Tomiyama H, Kubo S, Hattoi N
    • Organizer
      Movement Disorders
    • Place of Presentation
      Paris
    • Year and Date
      2009-06-11
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Preserved cardiac 123I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient2009

    • Author(s)
      Kanai K, Arai K, Asahina M, Tomiyama H, Kuwabara Y, Uchiyama T, Sekiguchi Y, Funayama M, Hattori N, Kuwabara S
    • Organizer
      Movement Disorders
    • Place of Presentation
      Paris
    • Year and Date
      2009-06-11
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] パーキンソン病におけるLRRK2 P755L変異2009

    • Author(s)
      富山弘幸, 水田依久子, 李元哲, 舩山学, 吉野浩代, 李林, 村田美穂, 山本光利, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2009-09-24
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] Mutation analysis for DJ-1 in parkinsonism : Screening strategy in autosomal recessive parkinsonism2009

    • Author(s)
      富山弘幸, 李元哲, 舩山学, 吉野浩代, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      GEO-PD meeting
    • Place of Presentation
      Germany, Tubingen
    • Year and Date
      2009-07-06
    • Data Source
      KAKENHI-PROJECT-21591098
  • [Presentation] 孤発性パーキンソン病におけるLRRK2 P755L2009

    • Author(s)
      富山弘幸, 水田依久子, 李元哲, 舩山学, 吉野浩代, 李林, 村田美穂, 山本光利, 久保紳一郎, 水野美邦, 戸田達史, 服部信孝
    • Organizer
      日本神経学会総会
    • Place of Presentation
      仙台
    • Year and Date
      2009-05-20
    • Data Source
      KAKENHI-PROJECT-21591098
  • [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-19390244
  • [Presentation] 新たに見つかった遺伝性パーキンソン病の臨床像.

    • Author(s)
      富山弘幸.
    • Organizer
      第7回パーキンソン病・運動障害疾患コングレス(MDSJ)オープニングセミナー
    • Place of Presentation
      東京
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] ALS/FTDにおけるC9orf72遺伝子診断について

    • Author(s)
      富山弘幸,大垣光太郎,熱田直樹,李元哲,舩山学,渡辺はづき,中村亮一,吉野英夫,谷藤誠司,田村麻子,内藤寛,谷口彰,藤田浩司,和泉唯信,梶龍兒,服部信孝,祖父江元,Japanese Consortium for Amyotrophic Lateral Sclerosis research (JaCALS).
    • Organizer
      第58回日本人類遺伝学会大会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] The first case report describing the moment of sudden respiratory arrest in a patient with Perry syndrome.

    • Author(s)
      Ryoichi Kurisaki, Hiroyuki Tomiyama, Tetsuro Sakamoto, Kazutoshi Uekawa, Yoshio Tsuboi.
    • Organizer
      MDPD international congress 2013
    • Place of Presentation
      Seoul, Korea
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] 順天堂大学脳神経内科におけるパーキンソン病の遺伝子解析・遺伝子診断.

    • Author(s)
      富山弘幸.
    • Organizer
      パーキンソン病学術講演会
    • Place of Presentation
      滋賀草津
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] パーキンソン病.

    • Author(s)
      富山弘幸.
    • Organizer
      静清リハビリテーション病院セミナーシリーズ2013
    • Place of Presentation
      静岡
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] Progress in clinical genetics for patients with Parkinson's disease and related disorders - focusing on non-motor aspects.

    • Author(s)
      H. Tomiyama, N. Hattori.
    • Organizer
      MDPD international congress 2013
    • Place of Presentation
      Seoul, Korea.
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461292
  • [Presentation] 運動ニューロン疾患の遺伝学:Update わが国のALSにおけるC9ORF72.

    • Author(s)
      富山弘幸.
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461292
  • 1.  HATTORI Nobutaka (80218510)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 70 results
  • 2.  KUZUHARA Shigeki (70111383)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 14 results
  • 3.  KOKUBO Yasumasa (60263000)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 14 results
  • 4.  SASAKI Ryogen (60303723)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 5.  KUWANO Ryouzou (20111734)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  TSUJI Syouji (70150612)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  HARA Kenjyu (10377195)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 8.  MURAYAMA Shigeo (50183653)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  SAITO Yuuko (60344066)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  HASEGAWA Nmasato (10251232)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  IWATSUBO Takeshi (50223409)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  KUBO Shinitiro (20327795)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 5 results
  • 13.  SATO Shigeto (00445537)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 14.  IWAI Kazyhiro (60252459)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  伊藤 伸朗 (10362344)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  平澤 基之 (90338393)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  佐藤 健一 (00276461)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 18.  吉野 浩代 (80338417)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 10 results
  • 19.  MORIMOTO Satoru
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  AKATSUKA Naomi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  SAKATA Shinithi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 22.  SATAKE Wataru
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 23.  HORI Masaaki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 24.  KAMAGATA KOJI
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 25.  戸田 達史
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 26.  青木 茂樹
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

URL: 

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi