Satake Wataru 佐竹渉

… Alternative Names

SATAKE Wataru 佐竹渉

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Researcher Number	50467594
Other IDs
Affiliation (Current)	2025: 東京大学, 医学部附属病院, 准教授
Affiliation (based on the past Project Information) *help	2018 – 2024: 東京大学, 医学部附属病院, 准教授 2017: 神戸大学, 医学研究科, 助教 2013 – 2016: 神戸大学, 医学(系)研究科(研究院), 助教 2014: 神戸大学, 大学院医学研究科, 助教
Review Section/Research Field	Principal Investigator Human genetics / Basic Section 52020:Neurology-related / Medium-sized Section 52:General internal medicine and related fields / Neurology / Biological Sciences Except Principal Investigator Biological Sciences
Keywords	Principal Investigator 神経遺伝 / パーキンソン病 / 神経変性疾患 / ゲノム医科学 / 人類遺伝学 / 神経内科学 / エクソーム / 孤発性神経疾患 / ゲノム創薬 / 個別化医療 / 遺伝性神経疾患 / ゲノム … More Except Principal Investigator … More 次世代シークエンサー / 次世代シーケンサー / 多型 / 認知機能 / パーキンソン病 / パーソナルゲノム Less

複数の神経変性疾患患者が多発する大家系の萌芽的先端ゲノム解析による疾患概念の提唱Principal Investigator
- Principal Investigator
  
  佐竹渉
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  The University of Tokyo
Genomic Medical Research as a basis for for Parkinson's DiseasePrincipal Investigator
- Principal Investigator
  
  佐竹渉
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  The University of Tokyo
Comprehensive genome analysis to elucidate the genetic background of Parkinson's diseaseand and the clinical applicationsPrincipal Investigator
- Principal Investigator
  
  SATAKE WATARU
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  The University of Tokyo
  Kobe University
ゲノム解読によるパーキンソン病の選択的神経変性の解明Principal Investigator
- Principal Investigator
  
  佐竹渉
- 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
  Kobe University
Identification of causative genes and development of a new analytical method for familial neurological diseasesPrincipal Investigator
- Principal Investigator
  
  SATAKE WATARU
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Neurology
- Research Institution
  Kobe University
Identification of Parkinson's disease genes and development of the personalized medicinePrincipal Investigator
- Principal Investigator
  
  SATAKE Wataru
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (A)
- Research Field
  
  Human genetics
- Research Institution
  Kobe University
Personal genome analysis of genes for Parkinson's disease and cognitive function
- Principal Investigator
  
  TODA Tatsushi
- Project Period (FY)
  2010 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Biological Sciences
- Research Institution
  Kobe University

All 2018 2017 2016 2015 2014 2013 2012 2011 2010 Other

All Journal Article Presentation Other

[Journal Article] In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson’s disease2018
- Author(s)
  Uenaka Takeshi、Satake Wataru、Cha Pei-Chieng、Hayakawa Hideki、Baba Kousuke、Jiang Shiying、Kobayashi Kazuhiro、Kanagawa Motoi、Okada Yukinori、Mochizuki Hideki、Toda Tatsushi
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 27 Pages: 3974-3985
- DOI
  10.1093/hmg/ddy279
- NAID
  120006549191
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K19512, KAKENHI-PUBLICLY-17H05700, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-17H04056
[Journal Article] Treatment of a case of severe insulin resistance due to a PIK3R1 mutation with a sodium-glucose cotransporter-2 inhibitor.2018
- Author(s)
  Hamaguchi T, Hirota Y, Takeuchi T, Nakagawa Y, Matsuoka A, Matsumoto M, Awano H, Iijima K, Cha PC, Satake W, Toda T, Ogawa W.
- Journal Title
  
  J Diabetes Investig.
  
  Volume: 9 Issue: 5 Pages: 1224-1227
- DOI
  10.1111/jdi.12825
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09750, KAKENHI-PROJECT-17H04056
[Journal Article] Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.2017
- Author(s)
  Wang L, Heckman MG, Aasly JO,.., Satake W,.., Farrer MJ, Ross OA, Sharma M
- Journal Title
  
  Neurobiol Aging.
  
  Volume: 49 Pages: 217.e1-217.e4
- DOI
  10.1016/j.neurobiolaging.2016.09.022
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-17H04056
[Journal Article] Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report.2017
- Author(s)
  Endo H, Uenaka T, Satake W, Suzuki Y, Tachibana H, Chihara N, Ueda T, Sekiguchi K, Mariko TI, Kowa H, Kanda F, Toda T
- Journal Title
  
  Neurol Clin Neurosci
  
  Volume: 5 Issue: 4 Pages: 131-133
- DOI
  10.1111/ncn3.12132
- NAID
  120006644121
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H04056
[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] The first nationwide survey and genetic analyses of Bardet-Biedl syndrome in Japan2015
- Author(s)
  Hirano M, Satake W, Ihara K, Tsug I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T
- Journal Title
  
  PLOS ONE
  
  Volume: 10 Issue: 9 Pages: e0136317-e0136317
- DOI
  10.1371/journal.pone.0136317
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591515, KAKENHI-PROJECT-26461613, KAKENHI-PROJECT-25461297, KAKENHI-PROJECT-25713015
[Journal Article] A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy2015
- Author(s)
  Oda T, Xiong H, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Cha PC, Hayashi Y, Nishino I, Suzuki Y, Sugano S, Wu X, Toda T.
- Journal Title
  
  Human Genome Variation
  
  Volume: 2 Issue: 1 Pages: 15022-15022
- DOI
  10.1038/hgv.2015.22
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-12F02422, KAKENHI-PROJECT-26670499, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26253057
[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] Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.2015
- Author(s)
  Shigemizu D, Aiba T, Nakagawa H, Ozaki K, Miya F, Satake W, Toda T, Miyamoto Y, Fujimoto A, Suzuki Y, Kubo M, Tsunoda T, Shimizu W, Tanaka T.
- Journal Title
  
  PLoS One.
  
  Volume: 10 (7) Issue: 7 Pages: e0130329-e0130329
- DOI
  10.1371/journal.pone.0130329
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-26430196, KAKENHI-PUBLICLY-25136727, KAKENHI-PUBLICLY-26114721, KAKENHI-PROJECT-25713015
[Journal Article] A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency.2015
- Author(s)
  Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K.
- Journal Title
  
  American Journal of Medical Genetics PartA
  
  Volume: 170 Issue: 1 Pages: 183-188
- DOI
  10.1002/ajmg.a.37397
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25713015
[Journal Article] Novel calmodulin mutations associated with congenital arrhythmia susceptibility.2014
- Author(s)
  Makita N, Tsuji Y（39人中21番目）et al
- Journal Title
  
  Circ Cardiovasc Genet.
  
  Volume: 7 Issue: 4 Pages: 466-474
- DOI
  10.1161/circgenetics.113.000459
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PROJECT-24591086, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-221S0002
[Journal Article] A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.2014
- Author(s)
  Saida K, Inaba Y, Hirano M, Satake W, Toda T, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K.
- Journal Title
  
  Brain Dev
  
  Volume: 印刷中 Issue: 8 Pages: 721-724
- DOI
  10.1016/j.braindev.2013.10.013
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015
[Journal Article] 【遺伝子・再生医療研究から学ぶパーキンソン病】 PARK遺伝子研究の現状　【RAB7L1(PARK16)】　ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013
- Author(s)
  佐竹渉, 戸田達史
- Journal Title
  
  医学のあゆみ
  
  Volume: 247 Pages: 1075-1082
- Data Source
  KAKENHI-PLANNED-22129006
[Journal Article] 神経・精神疾患の動向神経疾患と遺伝子2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  日本医師会雑誌神経・精神疾患診療マニュアル
  
  Volume: 142
- Data Source
  KAKENHI-PROJECT-25670420
[Journal Article] ゲノム多様性と神経変性疾患2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  細胞
  
  Volume: 45 Pages: 120-123
- Data Source
  KAKENHI-PROJECT-25670420
[Journal Article] ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  医学のあゆみ
  
  Volume: 247 Pages: 1075-1078
- Data Source
  KAKENHI-PROJECT-25713015
[Journal Article] YY1 binds to α-synuclein 3'-flanking region SNP and stimulates antisense noncoding RNA expression.2013
- Author(s)
  Mizuta I, Takafuji K, Ando Y, Satake W, Kanagawa M, Kobayashi K, Nagamori S, Shinohara T, Ito C, Yamamoto M, Hattori N, Murata M, Kanai Y, Murayama S, Nakagawa M, Toda T.
- Journal Title
  
  J Hum Genet
  
  Volume: 58 Issue: 11 Pages: 711-719
- DOI
  10.1038/jhg.2013.90
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-24110508, KAKENHI-PROJECT-24591198, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015
[Journal Article] ゲノム多様性と神経変性疾患2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  細胞
  
  Volume: 45 Pages: 120-123
- Data Source
  KAKENHI-PUBLICLY-25110720
[Journal Article] 神経・精神疾患の動向神経疾患と遺伝子2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  日本医師会雑誌神経・精神疾患診療マニュアル
  
  Volume: 142
- Data Source
  KAKENHI-PROJECT-25713015
[Journal Article] ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  医学のあゆみ
  
  Volume: 247 Pages: 1075-1078
- Data Source
  KAKENHI-PROJECT-25670420
[Journal Article] 遺伝性疾患の遺伝子検査2013
- Author(s)
  佐竹渉
- Journal Title
  
  Modern Physician
  
  Volume: 33 Pages: 625-628
- Data Source
  KAKENHI-PROJECT-25713015
[Journal Article] 遺伝性疾患の遺伝子検査2013
- Author(s)
  佐竹渉
- Journal Title
  
  Modern Physician
  
  Volume: 33 Pages: 625-628
- Data Source
  KAKENHI-PUBLICLY-25110720
[Journal Article] ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  医学のあゆみ
  
  Volume: 247 Pages: 1075-1078
- Data Source
  KAKENHI-PUBLICLY-25110720
[Journal Article] 神経・精神疾患の動向神経疾患と遺伝子2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  日本医師会雑誌神経・精神疾患診療マニュアル
  
  Volume: 142
- Data Source
  KAKENHI-PUBLICLY-25110720
[Journal Article] ゲノム多様性と神経変性疾患2013
- Author(s)
  佐竹渉ら
- Journal Title
  
  細胞
  
  Volume: 45 Pages: 120-123
- Data Source
  KAKENHI-PROJECT-25713015
[Journal Article] 【神経・精神疾患診療マニュアル】　神経・精神疾患の動向神経疾患と遺伝子2013
- Author(s)
  佐竹渉, 戸田達史
- Journal Title
  
  日本医師会雑誌
  
  Volume: 142
- Data Source
  KAKENHI-PLANNED-22129006
[Journal Article] 遺伝性疾患の遺伝子検査2013
- Author(s)
  佐竹渉
- Journal Title
  
  Modern Physician
  
  Volume: 33 Pages: 625-628
- Data Source
  KAKENHI-PROJECT-25670420
[Journal Article] 【神経変性疾患のゲノム・遺伝学研究】孤発性パーキンソン病のリスク遺伝子2012
- Author(s)
  佐竹渉, 戸田達史
- Journal Title
  
  Dementia Japan
  
  Volume: 26 Pages: 155-162
- Data Source
  KAKENHI-PLANNED-22129006
[Journal Article] Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.2012
- Author(s)
  Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake W, Toda T, Shang HF.
- Journal Title
  
  Neurol Res
  
  Volume: 34 Issue: 7 Pages: 725-729
- DOI
  10.1179/1743132812y.0000000075
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
[Journal Article] Large-scale replication and heterogeneity in Parkinson disease genetic loci.2012
- Author(s)
  Sharma M, Ioannidis JPA, Aasly JO, Brice A, ..., Satake W, ..., Toda T,..., Kruger R.
- Journal Title
  
  Neurology
  
  Volume: 79 Issue: 7 Pages: 659-667
- DOI
  10.1212/wnl.0b013e318264e353
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
[Journal Article] A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.2012
- Author(s)
  Sharma M, Ioannidis JP, Aasly JO, ..., Satake W, ..., Toda T, ..., GEOPD consortium.
- Journal Title
  
  J Med Genet
  
  Volume: 49 Issue: 11 Pages: 721-726
- DOI
  10.1136/jmedgenet-2012-101155
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
[Journal Article] パーキンソン病の遺伝的背景2010
- Author(s)
  佐竹渉
- Journal Title
  
  綜合臨牀
  
  Volume: 59 Pages: 2388-2391
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] パーキンソン病の遺伝背景解明とその応用2016
- Author(s)
  Satake W, Toda T.
- Organizer
  兵庫医科大学インテンシブコースセミナー
- Place of Presentation
  西宮
- Invited
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] パーキンソン病のゲノム解析研究2016
- Author(s)
  佐竹渉
- Organizer
  ニューロサイエンスネットワーク
- Place of Presentation
  神戸
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Genetics-based approach for understanding Parkinson's disease2016
- Author(s)
  Satake W, Toda T.
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸
- Year and Date
  2016-05-18
- Invited
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome Association study and 2nd SNP-GWAS of Parkinson’s disease in Japan2016
- Author(s)
  Satake W, Suzuki Y, Shigemizu D, .., Kubo M, Sugano S, Matsumoto N, Toda T.
- Organizer
  The 13th International Congress of human Genetics
- Place of Presentation
  Kyoto
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Parkinson’s disease Genomics and its Application2016
- Author(s)
  Satake W, Toda T.
- Organizer
  第4回これからのパーキンソン病治療を考える会
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Genomic study and subsequent in silico drug discovery for Parkinson’s disease2016
- Author(s)
  Satake W, Uenaka T, Cha PC, Okada Y, Kashihara K, Murayama S, Hasegawa K, Mochizuki H, Takeda A, Yamamoto M, Murata M, Hattori N, Toda T
- Organizer
  5th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress
- Place of Presentation
  Manila
- Year and Date
  2016-03-11
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Genome-wide association study (GWAS) in neurodegenerative disorders2015
- Author(s)
  Satake W
- Organizer
  International Parkinson and Movement Disorder Society Basic Summer School
- Place of Presentation
  Tokyo
- Year and Date
  2015-08-06
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome Association Study and 2nd SNP-GWAS of Parkinson's disease2015
- Author(s)
  Satake W， Ando Y， Suzuki M， Tomiyama H， Nagai Y， Murayama S， Mochizuki H， Nakashima K， Obata F， Hasegawa K， Takeda A， Wada K， Tsuji S， Yamamoto M， Murata M， Hattori N， Toda T
- Organizer
  第56回日本神経学会学術大会
- Place of Presentation
  新潟
- Year and Date
  2015-05-20
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Next step of GWAS and Exome study for Parkinson’s disease2015
- Author(s)
  Satake W, Takeda A, Mochizuki H, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda T
- Organizer
  10th Annual Meeting Genetic Epidemiology of Parkinson's disease
- Place of Presentation
  Tokyo
- Year and Date
  2015-10-01
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome Association study and SNP-GWAS of Parkinson’s disease2015
- Author(s)
  Satake W, Suzuki Y, Shigemizu D, Cha PC, Tsuji S, Tsunoda T, Kubo M, Sugano S, Matsumoto N, Toda T
- Organizer
  The 11th International workshop on Advanced Genomics; 国際ゲノム会議
- Place of Presentation
  Tokyo
- Year and Date
  2015-05-20
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson's disease2015
- Author(s)
  Satake W, Ando Y, Suzuki M, Tomiyama H, Nagai Y, Kashihara K, Murayama S, Mochizuki H, Nakashima K, Hasegawa K, Takeda A, Wada K, Tsuji S, Yamamoto M, Murata M, Hattori N, and Toda T.
- Organizer
  19th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  San Diego
- Year and Date
  2015-06-14
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2014
- Author(s)
  Satake W et al
- Organizer
  New Frontier of Molecular Neuropathology
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Risk genes and genome research of sporadic Parkinson’s disease2014
- Author(s)
  Satake W, Toda T
- Organizer
  The 20th International Congress of Personalized Medicine
- Place of Presentation
  Tokyo
- Year and Date
  2014-11-15
- Invited
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Risk genes and genome research of sporadic Parkinson’s disease2014
- Author(s)
  Satake W, Toda T
- Organizer
  The 20th International Congress of Personalized Medicine
- Place of Presentation
  Tokyo
- Year and Date
  2014-11-15
- Invited
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Risk genes and genome research of sporadic Parkinson’s disease2014
- Author(s)
  Satake W, Toda T
- Organizer
  The 20th International Congress of Personalized Medicine
- Place of Presentation
  Tokyo
- Year and Date
  2014-11-15
- Invited
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2014
- Author(s)
  Satake W et al
- Organizer
  New Frontier of Molecular Neuropathology
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2014
- Author(s)
  Satake W et al
- Organizer
  New Frontier of Molecular Neuropathology
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing2013
- Author(s)
  Satake W et al
- Organizer
  The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Sydney, Australia
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2013
- Author(s)
  Satake W et al
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing2013
- Author(s)
  Satake W, Ando Y, Tomiyama H, Takeda A, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda T
- Organizer
  The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Sydney Convention and Exhibition Centre, Sydney, Australia
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing.2013
- Author(s)
  Satake W, Ando Y, Tomiyama H, Takeda A, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda T.
- Organizer
  The MDS 17th International Congress of Parkinson's Disease and Movement Disorders.
- Place of Presentation
  Sydney Convention and Exhibition Centre, Sydney, Australia
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2013
- Author(s)
  Satake W et al
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing2013
- Author(s)
  Satake W et al
- Organizer
  The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Sydney, Australia
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Japanese 2nd GWAS Identifies Strong Association at a Novel Risk Locus and MCCC1 for Parkinson's Disease.2013
- Author(s)
  Toda T, Satake W, Yamamoto M, Hattori N, Murata M, Japanese PD Gene Consortium.
- Organizer
  he 11th international conference on alzheimer’s and parkinson’s diseases
- Place of Presentation
  Firenze Fiera, Florence, Italy,
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing2013
- Author(s)
  Satake W et al
- Organizer
  The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Sydney, Australia
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk.2013
- Author(s)
  Satake W, Suzuki Y, Ando Y, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsuji S, Sugano S, Toda T.
- Organizer
  American Society of Human Genetics Annual meeting 2013.
- Place of Presentation
  Boston Convention & Exhibition Center (BCEC), Boston, U.S.A.
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] エクソーム解読・一塩基多型解析によるパーキンソン病の遺伝背景の解明2013
- Author(s)
  佐竹渉ら
- Organizer
  2013年度包括脳ネットワーク夏のワークショップ
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] エクソーム解読・一塩基多型解析によるパーキンソン病の遺伝背景の解明2013
- Author(s)
  佐竹渉ら
- Organizer
  2013年度包括脳ネットワーク夏のワークショップ
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk2013
- Author(s)
  Satake W et al
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] エクソーム解読・一塩基多型解析によるパーキンソン病の遺伝背景の解明2013
- Author(s)
  佐竹渉ら
- Organizer
  2013年度包括脳ネットワーク夏のワークショップ
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Japanese 2nd GWAS identifies a novel risk locus and detects a strong association at MCCC1 for Parkinson's disease2011
- Author(s)
  Satake W
- Organizer
  Genetic Epidemiology of Parkinson's Disease Consortium 6th annual meeting
- Place of Presentation
  NorthShore University HealthSystem,(アメリカ)(招待講演)
- Year and Date
  2011-09-19
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] PD GWAS in Asian Cohort2011
- Author(s)
  Satake W
- Organizer
  Genetics of Neurodegenerative Disease Neurochip and Beyond
- Place of Presentation
  Omni Shoreham Hotel(ワシントンD.C.)(招待講演)
- Year and Date
  2011-04-20
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Japanese subsequent GWAS identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease2011
- Author(s)
  Satake W
- Organizer
  The American society of Human Genetics 61st Annual Meeting
- Place of Presentation
  Montreal Convention Center(カナダ)
- Year and Date
  2011-10-13
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Genome-wide association study identifies variants at four loci as genetic risk factors for Parkinson's disease2010
- Author(s)
  Satake W
- Organizer
  American Society of Human Genetics 60th Annual Meeting
- Place of Presentation
  Washington Convention Center (Washington DC,米国)
- Year and Date
  2010-11-03
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] ゲノムワイド関連解析は、4つのパーキンソン病感受性遺伝子座を同定した2010
- Author(s)
  佐竹渉
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京国際フォーラム(東京都)
- Year and Date
  2010-05-20
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] ゲノムワイド関連解析は、4つのパーキンソン病感受性遺伝子座を同定した2010
- Author(s)
  佐竹渉
- Organizer
  第33回日本分子生物学会年会第83回日本生化学会大会合同大会
- Place of Presentation
  神戸ポートアイランド(兵庫県)
- Year and Date
  2010-12-07
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease2010
- Author(s)
  Satake W
- Organizer
  14th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Sheraton Buenos Aires Hotel and Convention Center (Buenos Aires,アルゼンチン)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] ゲノムワイド関連解析は、4つのパーキンソン病感受性遺伝子座を同定した2010
- Author(s)
  佐竹渉
- 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(埼玉県)
- Year and Date
  2010-10-28
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] ゲノムワイド関連解析は、4つのパーキンソン病感受性遺伝子座を同定した2010
- Author(s)
  佐竹渉
- 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(京都府)
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Genome-wide association study identifies variants at four loci as genetic risk factors for Parkinson's disease2010
- Author(s)
  Satake W
- Organizer
  第33回日本神経科学会大会、第53回日本神経化学会大会、第20回日本神経回路学会大会合同大会
- Place of Presentation
  神戸コンベンションセンター(兵庫県)
- Year and Date
  2010-09-02
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W, Hasegawa K, Murata M, Hattori N, Toda T.
- Organizer
  Genetic Epidemiology of Parkinson's disease Annual meeting
- Place of Presentation
  Vancouver
- Year and Date
  2014-09-10 – 2014-09-12
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk
- Author(s)
  Satake W, Ando Y, Tomiyama H, Kashihara K, Mochizuki H, Murayama S, Takeda A, Hasegawa K, Tsuji S, Yamamoto M, Murata M, Hattori N, Toda T.
- Organizer
  The MDS 18th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Stockholm
- Year and Date
  2014-06-08 – 2014-06-12
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] EXOME SEQUENCING AND 2ND SNP-GWAS OF PD.
- Author(s)
  Toda T, Satake W, Hattori N, Murata M.
- Organizer
  The 12th International Conference on Alzheimer's and Parkinson's Diseases and Related Neurological Disorders.
- Place of Presentation
  Nice, France
- Year and Date
  2015-03-18 – 2015-03-22
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease.
- Author(s)
  Satake W, Shigemizu D, Suzuki Y, Yamamoto K,Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
- Organizer
  American Society of Human Genetics Annual meeting 2014.
- Place of Presentation
  San Diego U.S.A.
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W, Shigemizu D, Suzuki Y, Yamamoto K, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  San Diego
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] 孤発性パーキンソン病のエクソーム関連解析と第2期SNP-GWAS
- Author(s)
  佐竹渉、重水大智、鈴木穣、山本健、富山弘幸、高橋篤、村田美穂、服部信孝、田中敏博、角田達彦、久保充明、辻省次、松本直通、菅野純夫、戸田達史
- Organizer
  日本人類伝学会第59回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W, Hasegawa K, Murata M, Hattori N, Toda T.
- Organizer
  Genetic Epidemiology of Parkinson's disease Annual meeting
- Place of Presentation
  Vancouver
- Year and Date
  2014-09-10 – 2014-09-12
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] パーキンソン病感受性遺伝子α-synuiclein SNPとnoncoding RNA
- Author(s)
  水田依久子、佐竹渉、村山繁雄、金川基、小林千浩、高藤和輝、永森収志、山本光利、服部信孝、村田美穂、金井好克、水野敏樹、中川正法、戸田達史
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk
- Author(s)
  Satake W, Ando Y, Tomiyama H, Kashihara K, Mochizuki H, Murayama S, Takeda A, Hasegawa K, Tsuji S, Yamamoto M, Murata M, Hattori N, Toda T.
- Organizer
  The MDS 18th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Stockholm
- Year and Date
  2014-06-08 – 2014-06-12
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W et al1.Satake W, Shigemizu D, Suzuki Y, Yamamoto K, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  San Diego
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W, Hasegawa K, Murata M, Hattori N, Toda T.
- Organizer
  Genetic Epidemiology of Parkinson's disease Annual meeting
- Place of Presentation
  Vancouver
- Year and Date
  2014-09-10 – 2014-09-12
- Data Source
  KAKENHI-PUBLICLY-25110720
[Presentation] パーキンソン病感受性遺伝子α-synuiclein SNPとnoncoding RNA
- Author(s)
  水田依久子、佐竹渉、村山繁雄、金川基、小林千浩、高藤和輝、永森収志、山本光利、服部信孝、村田美穂、金井好克、水野敏樹、中川正法、戸田達史
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] 孤発性パーキンソン病のエクソーム関連解析と第2期SNP-GWAS
- Author(s)
  佐竹渉、重水大智、鈴木穣、山本健、富山弘幸、高橋篤、村田美穂、服部信孝、田中敏博、角田達彦、久保充明、辻省次、松本直通、菅野純夫、戸田達史
- Organizer
  日本人類伝学会第59回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome sequencing and 2nd SNP-GWAS of Japanese Parkinson’s disease.
- Author(s)
  Toda T, Satake W, Yamamoto M, Murata M, Hattori N, Sugano S.
- Organizer
  4th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress.
- Place of Presentation
  Pattaya, Thailand
- Year and Date
  2014-11-28 – 2014-11-30
- Data Source
  KAKENHI-PLANNED-22129006
[Presentation] 孤発性パーキンソン病のエクソーム関連解析と第2期SNP-GWAS
- Author(s)
  佐竹渉、重水大智、鈴木穣、山本健、富山弘幸、高橋篤、村田美穂、服部信孝、田中敏博、角田達彦、久保充明、辻省次、松本直通、菅野純夫、戸田達史
- Organizer
  日本人類伝学会第59回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] パーキンソン病感受性遺伝子α-synuiclein SNPとnoncoding RNA
- Author(s)
  水田依久子、佐竹渉、村山繁雄、金川基、小林千浩、高藤和輝、永森収志、山本光利、服部信孝、村田美穂、金井好克、水野敏樹、中川正法、戸田達史
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25670420
[Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk
- Author(s)
  Satake W, Ando Y, Tomiyama H, Kashihara K, Mochizuki H, Murayama S, Takeda A, Hasegawa K, Tsuji S, Yamamoto M, Murata M, Hattori N, Toda T.
- Organizer
  The MDS 18th International Congress of Parkinson's Disease and Movement Disorders
- Place of Presentation
  Stockholm
- Year and Date
  2014-06-08 – 2014-06-12
- Data Source
  KAKENHI-PROJECT-25713015
[Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease
- Author(s)
  Satake W, Shigemizu D, Suzuki Y, Yamamoto K, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
- Organizer
  American Society of Human Genetics Annual meeting
- Place of Presentation
  San Diego
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-25713015
[]
[]

1. TODA Tatsushi (30262025)

# of Collaborated Projects: 2 results

# of Collaborated Products: 24 results
2. 永井義隆 (60335354)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
3. KOBAYASHI Kazuhiro (90324780)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. HIROTA Yushi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. Ogawa Wataru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. AIBA Takeshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. TANIGUCHI Mariko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 蒔田直昌

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
9. 辻幸臣

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. 早川英規

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 井原健二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. CHA PeiChieng

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. CHA Pei Chieng

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Satake Wataru 佐竹 渉

SATAKE Wataru 佐竹 渉

Research Projects

Research Products

Co-Researchers

複数の神経変性疾患患者が多発する大家系の萌芽的先端ゲノム解析による疾患概念の提唱Principal Investigator

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Genomic Medical Research as a basis for for Parkinson's DiseasePrincipal Investigator

Principal Investigator

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Comprehensive genome analysis to elucidate the genetic background of Parkinson's diseaseand and the clinical applicationsPrincipal Investigator

Principal Investigator

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Research Institution

ゲノム解読によるパーキンソン病の選択的神経変性の解明Principal Investigator

Principal Investigator

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Review Section

Research Institution

Identification of causative genes and development of a new analytical method for familial neurological diseasesPrincipal Investigator

Principal Investigator

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Research Institution

Identification of Parkinson's disease genes and development of the personalized medicinePrincipal Investigator

Principal Investigator

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Research Institution

Personal genome analysis of genes for Parkinson's disease and cognitive function

Principal Investigator

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Research Institution

[Journal Article] In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson’s disease2018

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Treatment of a case of severe insulin resistance due to a PIK3R1 mutation with a sodium-glucose cotransporter-2 inhibitor.2018

Author(s)

Journal Title

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[Journal Article] Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.2017

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[Journal Article] Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report.2017

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NAID

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[Journal Article] ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.2015

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[Journal Article] The first nationwide survey and genetic analyses of Bardet-Biedl syndrome in Japan2015

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[Journal Article] A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy2015

Satake Wataru 佐竹渉

SATAKE Wataru 佐竹渉

[Journal Article] 神経・精神疾患の動向神経疾患と遺伝子2013

[Journal Article] ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013

[Journal Article] 神経・精神疾患の動向神経疾患と遺伝子2013

[Journal Article] ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて　PARK16、BST1、α-synuclein、LRRK2、Tau2013