SATAKE Wataru

J-GLOBAL         Last updated: Oct 8, 2019 at 15:12
 
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Name
SATAKE Wataru
Nickname
satake
E-mail
satakem.u-tokyo.ac.jp
Affiliation
The University of Tokyo
Section
Graduate School of Medicine Faculty of Medical Sciences
Job title
Assistant Professor

Research Areas

 
 

Awards & Honors

 
May 2018
孤発性パーキンソン病の遺伝学的研究, 学会賞, 日本神経学会
Winner: Satake Wataru
 
Nov 2011
孤発性パーキンソン病遺伝子の同定, 奨励賞, 日本人類遺伝学会
Winner: Satake Wataru
 
Oct 2010
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease, 優秀学術論文賞, 神戸大学
Winner: Satake Wataru
 

Published Papers

 
Altered regulation of serum lysosomal acid hydrolase activities in Parkinson's disease: A potential peripheral biomarker?
Niimi Y, Ito S, Mizutani Y, Murate K, Shima S, Ueda A, Satake W, Hattori N, Toda T, Mutoh T.
Parkinsonism Relat Disord   61(-) 132-137   Apr 2019   [Refereed]
Wide distribution of alpha-synuclein oligomers in multiple system atrophy brain detected by proximity ligation
Sekiya H, Kowa H, Koga H, Takata M, Satake W, Futamura N, Funakawa I, Jinnai K, Takahashi M, Kondo T, Ueno Y, Kanagawa M, Kobayashi K, Toda T
Acta Neuropathol   137(3) 455-466   Mar 2019   [Refereed]
Using global team science to identify genetic parkinson's disease worldwide
Vollstedt EJ, Kasten M, Klein C; MJFF Global Genetic Parkinson's Disease Study Group
Ann Neurol   in press    2019   [Refereed]
Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia
Taniguchi-Ikeda M, Morisada N, Inagaki H, Ouchi Y, Takami Y, Tachikawa M, Satake W, Kobayashi K, Tsuneishi S, Takada S, Yamaguchi H, Nagase H, Nozu K, Okamoto N, Nishio H, Toda T, Morioka I, Wada H, Kurahashi H, Iijima K
Clin Genet   93(4) 931-3   Apr 2018   [Refereed]
Treatment of a case of severe insulin resistance due to a PIK3R1 mutation with a sodium-glucose cotransporter-2 inhibitor
HamaguchiT, Hirota Yushi, TakeuchiT, NakagawaY, MatsuokaA, MatsumotoM, AwanoH, IijimaK, Cha Pei Cheng, Satake Wataru, Toda Tatsushi, OgawaW
J Diabetes Investig   9(5) 1224-7   Feb 2018   [Refereed]
In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease.
Uenaka T, Satake W, Cha PC, Hayakawa H, Baba K, Jiang S, Kobayashi K, Kanagawa M, Okada Y, Mochizuki H, Toda T.
Hum Mol Genet   27(22) 3974-3985   Nov 2018   [Refereed]
Endo H, Uenaka T, Satake Wataru, Suzuki Y, Tachibana H, Chihara Norio, Ueda Takehiro, Sekiguchi K, Mariko T, Kowa H, Kanda F, Toda T
Neurol Clin Neurosci.   5(4) 131-133   Jul 2017   [Refereed]
Wang L, Heckman MG, Aasly JO, Annesi G, Bozi M, Chung SJ, Clarke C, Crosiers D, Eckstein G, Garraux G, Hadjigeorgiou GM, Hattori N, Jeon B, Kim YJ, Kubo M, Lesage S, Lin JJ, Lynch T, Lichtner P, Mellick GD, Mok V, Morrison KE, Quattrone A, Satake W, Silburn PA, Stefanis L, Stockton JD, Tan EK, Toda T, Brice A, Van Broeckhoven C, Uitti RJ, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM, Gasser T, Krüger R, Farrer MJ, Ross OA, Sharma M
Neurobiol Aging   49 217   Jan 2017   [Refereed]
NakagawaT, Taniguchi-IkedaM, MurakamiY, NakamuraS, MotookaD, EmotoT, Satake Wataru, Nishiyama Masahiro, ToyoshimaD, Morisada Naoya, TakadaS, TairakuS, OkamotoN, Morioka Ichiro, KurahashiH, Toda Tatsushi, KinoshitaT, Iijima Kazumoto
Am J Med Genet A   170(1) 183-8   Jan 2016   [Refereed]
HiranoM, Satake Wataru(co-first), IharaK, TsugeI, KondoS, SaidaK, BetsuiH, OkuboK, SakamotoH, UenoS, IkunoY, IshiharaR, IwahashiH, OhishiM, ManoT, YamashitaT, SuzukiY, NakamuraY, KusunokiS, Toda Tatsushi
PLoS One   10(9) e0136317   Sep 2015   [Refereed]
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy
Oda T, Xiong H, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Cha PC, Hayashi YK, Nishino I, Suzuki Y, Sugano S, Wu X, Toda T
Hum Genome Var   16(2) 15022   Jul 2015   [Refereed]
ShigemizuD, AibaT, NakagawaH, OzakiK, MiyaF, Satake Wataru, Toda Tatsushi, MiyamotoY, FujimotoA, SuzukiY, KuboM, TsunodaT, ShimizuW, TanakaT
PLoS One   10(7) e0130329   Jul 2015   [Refereed]
Variants associated with Gaucher disease in multiple system atrophy
Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, Tsuji S
Ann Clin Transl Neurol   2(4) 417-26   Apr 2015   [Refereed]
ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout
Matsuo H, Tomiyama H, Satake Wataru, Chiba T, Onoue H, Kawamura Y, Nakayama A, Shimizu S, Sakiyama M, Funayama M, Nishioka K, Shimizu T, Kaida K, Kamakura K, Toda Tatsushi, Hattori N, Shinomiya N
Ann Clin Transl Neurol   2(3) 302-6   Mar 2015   [Refereed]
Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake Wataru, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda Tatsushi, Mizuno Y, Uchiyama Y, Ohno K, Hattori N
Lancet Neurol   14(3) 274-82   Mar 2015   [Refereed]
Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake Wataru, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL Jr
Circ Cardiovasc Genet   7(4) 466-74   Aug 2014   [Refereed]
Saida K, Inaba Y, Hirano M, Satake Wataru, Toda Tatsushi, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K
Brain Dev      Nov 2013   [Refereed]
Mizuta I, Takafuji K, Ando Y, Satake Wataru, Kanagawa Motoi, Kobayashi Kazuhiro, Nagamori S, Shinohara T, Ito C, Yamamoto M, Hattori N, Murata M, Kanai Y, Murayama S, Nakagawa M, Toda Tatsushi
J Hum Genet   58(11) 711-9   Nov 2013   [Refereed]
Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Iwata A, Goto J, Yamamoto Y, Komata M, Shirahige K, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Takashima H, Kuwano R, Watanabe H, Ito M, Sobue G, Soma H, Yabe I, Sasaki H, Aoki M, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake Wataru, Toda T, Dürr A, Brice A, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Shults CW, Tanner CM, Kukull WA, Lee VM, Masliah E, Low PA, Sandroni P, Trojanowski JQ, Ozelius L, Foroud T, Tsuji S
N Engl J Med   369(3) 233-44   Jul 2013   [Refereed]
Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon BS, Jamrozik Z, Krygowska-Wajs A, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Libioulle C, Murata M, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Meitnger T, Zimprich A, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake Wataru, Silburn PA, Strom TM, Theuns J, Tan EK, Toda Tatsushi, Tomiyama H, Uitti RJ, Van Broeckhoven C, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yomono HS, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R
J Med Genet   49(11) 721-6   Nov 2012   [Refereed]
Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake Wataru, Toda Tatsushi, Shang HF
Neurol Res   34(7) 725-9   Sep 2012   [Refereed]
Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon B, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake W, Silburn PA, Theuns J, Tan EK, Toda T, Tomiyama H, Uitti RJ, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R
Neurology   79(7) 659-67   Aug 2012   [Refereed]
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, Biernacka JM, Brice A, DeStefano AL, Do CB, Eriksson N, Factor SA, Farrer MJ, Foroud T, Gasser T, Hamza T, Hardy JA, Heutink P, Hill-Burns EM, Klein C, Latourelle JC, Maraganore DM, Martin ER, Martinez M, Myers RH, Nalls MA, Pankratz N, Payami H, Satake Wataru, Scott WK, Sharma M, Singleton AB, Stefansson K, Toda Tatsushi, Tung JY, Vance J, Wood NW, Zabetian CP, Young P, Tanzi RE, Khoury MJ, Zipp F, Lehrach H, Ioannidis JP, Bertram L
PLoS Genet   8(3) e1002548   2012   [Refereed]
Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée 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, De Nigris F, 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, Krüger R
Neurobiology of aging   32(11) 2108.e1-5   Nov 2011
Sun H, Satake Wataru, Zhang C, Nagai Y, Tian Y, Fu S, Yu J, Qian Y, Qian Y, Chu J, Toda Tatsushi
J Hum Genet   56(4) 330-4   Apr 2011   [Refereed]
Krüger 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, Genetic Epidemiology of Parkinson's disease consortium
Neurobiology of aging   32(3) 548.e9-18   Mar 2011   [Refereed]
Tan EK, Kwok HH, Tan LC, Zhao WT, Prakash KM, Au WL, Pavanni R, Ng YY, Satake W, Zhao Y, Toda T, Liu JJ
Neurology   75(6) 508-12   Aug 2010   [Refereed]
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
Nature genetics   41(12) 1303-1307   Dec 2009   [Refereed]
Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T
Human genetics   124(1) 89-94   Jun 2008   [Refereed]
Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T
Neuroreport   18(8) 937-40   Jun 2007   [Refereed]
Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T
Human molecular genetics   15(7) 1151-8   Apr 2006   [Refereed]
Okuzaki D (co-first), Satake W (co-first), Hirata A, Nojima H
Journal of cell science   116(13) 2721-35   Jul 2003   [Refereed]

Misc

 
【パーキンソン病と類縁疾患 良くなる、良くするパーキンソン病】 セミナー 日常診療に必要な具体的知識とその活用 パーキンソン病と遺伝
Satake Wataru
Medical Practice   35(3) 397-402   Mar 2018   [Invited]
【パーキンソン病の新展開-発症の分子機構と新規治療】 分子機構解明の新しい展開 ゲノムワイド関連解析(GWAS)からの新展開
戸田達史, Satake Wataru
医学のあゆみ   262(6号) 617-621   Aug 2017   [Invited]
【最新遺伝医学研究と遺伝カウンセリング シリーズ2 最新精神・神経遺伝医学研究と遺伝カウンセリング】 (第1章)総論 孤発性疾患のリスク遺伝子の発見 ゲノムワイド関連解析の現状、進化と今後
Satake Wataru, Toda Tatsushi
遺伝子医学MOOK   (別冊最新精神・神経遺伝医学研究と遺伝カウンセリング) 39-44   Apr 2017   [Invited]
【パーキンソン病の基礎と臨床の最先端】 (No.4)遺伝性パーキンソン病 遺伝性パーキンソン病Up to Date(2)
Satake Wataru
脳21   19(4号) 423-431   Oct 2016   [Invited]
【パーキンソン病の治療-変貌する概念と治療戦略-】 Key words 孤発性パーキンソン病の疾患遺伝子探索と意義
Satake Wataru
カレントテラピー   33(10号) 1032   Oct 2015   [Invited]
孤発性パーキンソン病の疾患遺伝子とその探索
Satake Wataru, Toda Tatsushi
BIO Clinica   30(8号) 806-813   Aug 2015   [Invited]
【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、Tau
Satake Wataru, Toda Tatsushi
医学のあゆみ   247(10号) 1075-1082   Dec 2013   [Invited]
【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
Satake Wataru, Toda Tatsushi
日本医師会雑誌   142(特別2) S38-S39   Oct 2013   [Invited]
【神経内科検査のみかた-脳のイメージングを中心に】 どんなイメージがあるの? 遺伝性疾患の遺伝子検査
Satake Wataru
Modern Physician   33(5号) 625-628   May 2013   [Invited]
【ゲノム多様性と疾患】 ゲノム多様性と神経変性疾患
Satake Wataru, Toda Tatsushi
細胞   45(3号) 120-123   Mar 2013   [Invited]
孤発性パーキンソン病の遺伝について
Toda Tatsushi, Satake Wataru
運動障害   22(2号) 31-37   Jan 2013   [Invited]
【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
Satake Wataru, Toda Tatsushi
Dementia Japan   26(2号) 155-162   Apr 2012   [Invited]
【パーキンソン病発症のメカニズム】 パーキンソン病の分子遺伝学 ゲノム関連解析研究
Toda Tatsushi, Satake Wataru
BIO Clinica   26巻, 8号, pp. 701-705    Aug 2011   [Invited]
パーキンソン病診療Q&A パーキンソン病の遺伝的リスクについて
Satake Wataru, Toda Tatsushi
Frontiers in Parkinson Disease   4巻, 1号, pp. 48-52    Jan 2011
各種疾患 変性疾患 パーキンソン病の発症関連遺伝子多型
Toda Tatsushi, Satake Wataru
Annual Review神経   2011巻, , pp. 260-267    Jan 2011   [Invited]
神経内科学 ゲノムワイド関連解析によるパーキンソン病リスク遺伝子の同定
戸田達史, 佐竹 渉
233(8) 640-2   May 2010   [Invited]
【パーキンソン病 最近の進歩】 病因・病態の解明 孤発性パーキンソン病のリスク遺伝子
SATAKE Wataru
65(4) 806-13   Apr 2010   [Invited]

Conference Activities & Talks

 
In silico drug screening identified a novel disease-modifying drug for Parkinson’s disease
Uenaka Takeshi, Satake Wataru, Pei-Chieng Cha, Kobayashi Kazuhiro, Kanagawa Motoi, Hideki Hayakawa, Kousuke Baba, Yukinori Okada, Hideki Mochizuki, Toda Tatsushi
2017年度生命科学系学会合同年次大会   Dec 2017   
パーキンソン病のゲノム解析とその応用 [Invited]
Satake Wataru
大阪大学 遺伝統計学・神経内科学 共催セミナー   Dec 2017   
Genome-wide association study of zonisamide responsiveness in Parkinson’s disease patients with “wearing-off”
Pei-Chieng Cha, Satake Wataru, Yuko Ando-Kanagawa, Ken Yamamoto, Miho Murata, Toda Tatsushi
The 62nd Annual Meeting of the Japan Society of Human Genetics   Nov 2017   The Japan Society of Human Genetics
In silico drug screening identified a novel disease-modifying drug for Pakinson's disease
Uenaka Takeshi, Satake Wataru, Pei-Chieng Cha, Kobayashi Kazuhiro, Kanagawa Motoi, Hideki Hayakawa, Kousuke Baba, Yukinori Okada, Hideki Mochizuki, Toda Tatsushi
The 62nd Annual Meeting of the Japan Society of Human Genetics   Nov 2017   The Japan Society of Human Genetics
Gut Microbiota in Early-Stage Pakinson's Disease
関谷博顕, Satake Wataru, 須田亙, 服部正平, Toda Tatsushi
The 62nd Annual Meeting of the Japan Society of Human Genetics   Nov 2017   The Japan Society of Human Genetics
In silico drug screening identified a novel disease-modifying drug for Parkinson’s disease
Uenaka Takeshi, Satake Wataru, Pei-Chieng Cha, Kobayashi Kazuhiro, Kanagawa Motoi, Hideki Hayakawa, Kousuke Baba, Yukinori Okada, Hideki Mochizuki, Toda Tatsushi
The 23rd World Congress of Neurology/ The 58th Annual Meeting of the Japanese Society of Neurology   Sep 2017   World Federation of Neurology/ Japanese Society of Neurology
ASSOCIATION STUDY OF PARKINSON’S DISEASE BY SNP AND EXOME SEQUENCING
Toda Tatsushi, Satake Wataru
13th International Conference on Alzheimer’s and Parkinson’s Diseases   Apr 2017   
Pharmacogenetics and Pharmacogenomics study of AD-810N (Zonisamide/Trelief) [Invited]
Pei-Chieng Cha, Satake Wataru, Toda Tatsushi
「トレリーフのファーマコゲノミクス研究」に関する検討会   Jan 2017   大日本住友製薬株式会社
パーキンソン病の遺伝背景解明とその応用 [Invited]
Satake Wataru, Toda Tatsushi
兵庫医科大学インテンシブコースセミナー   Dec 2016   
Parkinson’s disease Genomics and its Application [Invited]
Satake Wataru, Toda Tatsushi
第4回これからのパーキンソン病治療を考える会   Nov 2016   
Genetics-based approach for understanding Parkinson's disease [Invited]
Satake Wataru, Toda Tatsushi
第57回日本神経学会学術大会   May 2016   
多系統萎縮症におけるドパミントランスポーターシンチグラフィの検討
Ueda Takehiro, 徳岡 秀紀, 辻 佑木生, Satake Wataru, Sekiguchi Kenji, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
第57回日本神経学会学術大会   May 2016   
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy
Kobayashi Kazuhiro, Tetsuya Oda, Hui Xiong, Satake Wataru, Toda Tatsushi
The 13th International Congress of Human Genetics   Apr 2016   
Exome Association study and 2nd SNP-GWAS of Parkinson’s disease in Japan
Satake Wataru, Yutaka Suzuki, Daichi Shigemizu, Atsushi Takahashi, Ken Yamamoto, Miho Murata, Nobutaka Hattori, Tatsuhiko Tsunoda, Shoji Tsuji, Michiaki Kubo, Sumio Sugano, Naomichi Matsumoto, Toda Tatsushi
The 13th International Congress of human Genetics   Apr 2016   
Genome-wide association study (GWAS) identifies genetic determinants of response to Zonisamide treatment in Parkinson’s disease patients with “wearing-off”
Pei-Chieng Cha, Satake Wataru, Yuko Ando, Ken Yamamoto, Miho Murata, Toda Tatsushi
The 13th International Congress of Human Genetics Meeting   Apr 2016   East-Asian Union of Human Genetic Societies (EAUHGS), Japan Society of Human Genetics (JSHG)
Genomic study and subsequent in silico drug discovery for Parkinson’s disease
Satake Wataru, Uenaka T, Cha Pei Cheng, Okada Y, Kashihara K, Murayama S, Hasegawa K, Mochizuki H, Takeda A, Yamamoto M, Murata M, Hattori N, Toda Tatsushi
5th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress   Mar 2016   
ゲノムワイド関連解析(GWAS)データを活用したin silico解析による新規抗パーキンソン病薬の探索 [Invited]
Toda Tatsushi, 上中 健, Satake Wataru, CHA Pei-Chieng, 岡田 随象, 望月 秀樹
次世代シークエンサーを用いた弧発性の神経難病の発症機構の解明と治療法開発に関する研究   Mar 2016   
パーキンソン病のゲノム解析研究 [Invited]
Satake Wataru
神戸ニューロサイエンスネットワーク   Mar 2016   
Next step of GWAS and Exome study for Parkinson’s disease
Satake Wataru, Takeda A, Mochizuki H, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda Tatsushi
10th Annual Meeting Genetic Epidemiology of Parkinson's disease   Oct 2015   
ゲノムワイド関連解析(GWAS)データを活用したin silico解析による新規抗パーキンソン病薬の探索
上中 健, Satake Wataru, CHA Pei-Chieng, 岡田 随象, Toda Tatsushi
日本人類遺伝学会 第60回大会   Oct 2015   Movement Disorder Society of Japan
Genome-wide association study (GWAS) in neurodegenerative disorders
Satake Wataru
International Parkinson and Movement Disorder Society Basic Summer School   Aug 2015   
Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson's disease
Satake Wataru, Ando Yukihiro, Suzuki Makoto, 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, Toda Tatsushi
19th International congress of parkinson's disease and movement disorders   Jun 2015   
In silico drug discovery for Parkinsonʼs disease by using genome-wide association study (GWAS) data
Takeshi Uenaka, Satake Wataru, CHA Pei-Chieng, Yukinori Okada, Toda Tatsushi
19th International Congress of Parkinson's Disease and Movement Disorders   Jun 2015   
Exome Association Study and 2nd SNP-GWAS of Parkinson's disease [Invited]
Satake Wataru, Ando Yukihiro, Suzuki Makoto, 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 Tatsushi
第56回日本神経学会学術大会   May 2015   
Exome Association study and SNP-GWAS of Parkinson’s disease [Invited]
Satake Wataru, Suzuki Y, Shigemizu D, Cha Pei Cheng, Tsuji S, Tsunoda T, Kubo M, Sugano S, Matsumoto N, Toda Tatsushi
The 11th International workshop on Advanced Genomics   May 2015   
in silico drug discovery for Parkinson’s disease by using genome-wide association study data
Takeshi Uenaka, Satake Wataru, CHA Pei-Chieng, Yukinori Okada, Toda Tatsushi
第56回日本神経学会学術大会   May 2015   
EXOME SEQUENCING AND 2ND SNP-GWAS OF PD.
Toda Tatsushi, Satake Wataru, Nobutaka Hattori, Miho Murata
The 12th International Conference on Alzheimer's and Parkinson's Diseases and Related Neurological Disorders   Mar 2015   ADPD
Exome sequencing and 2nd SNP-GWAS of Japanese Parkinson’s disease. [Invited]
Toda Tatsushi, Satake Wataru, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Sumio Sugano.
4th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress.   Nov 2014   MDS
Risk genes and genome research of sporadic Parkinson’s disease
Satake Wataru, Toda Tatsushi
The 20th International Congress of Personalized medicine   Nov 2014   
横隔膜超音波検査と神経伝導検査の有用性
野田 佳克, Sekiguchi Kenji, 藤堂 紘行, 森本 耕平, 古東 秀介, 関谷 博顕, 本岡 里英子, 安井 直子, Ueda Takehiro, Washida Kazuo, Satake Wataru, Kuga Atsushi, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
第44回日本臨床神経生理学会学術大会   Nov 2014   臨床神経生理学会
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
Satake Wataru, 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, Toda Tatsushi
日本人類伝学会第59回大会   Nov 2014   
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy
Toda Tatsushi, Hui Xiong, Tetsuya Oda, Kobayashi Kazuhiro, Shuo Wang, Satake Wataru, Hui Jiao, Yanling Yang, Yutaka Suzuki, Sumio Sugano, Xiru Wu
19th international congress of the world muscle society   Oct 2014   world muscle society
Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease.
Satake Wataru, Daichi Shigemizu, Yutaka Suzuki, Ken Yamamoto, Hiroyuki Tomiyama, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Tatsuhiko Tsunoda, Michiaki Kubo, Shoji Tsuji, Yusuke Nakamura, Sumio Sugano, Toda Tatsushi
American Society of Human Genetics Annual meeting 2014   Oct 2014   American Society of Human Genetics
Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease. [Invited]
Satake Wataru, Kazuko Hasegawa, Miho Murata, Nobutaka Hattori, Toda Tatsushi
Genetic Epidemiology of Parkinson's disease Annual meeting 2014   Sep 2014   Genetic Epidemiology of Parkinson's disease
新規抗パーキンソン病薬の探索 [Invited]
上中 健, Satake Wataru, CHA Pei-Chieng, 岡田 随象, Aoi Takashi, Toda Tatsushi
パーキンソン病患者由来iPS細胞を中心とする多面的疾患モデルに立脚した革新的医薬品の開発 班会議   Aug 2014   
Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk.
Satake Wataru, Yuko Ando, Hiroyuki Tomiyama, Kenichi Kashihara, Hideki Mochizuki, Shigeo Murayama, Atsushi Takeda, Kazuko Hasegawa, Shoji Tsuji, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Toda Tatsushi
The MDS 18th International Congress of Parkinson's Disease and Movement Disorders   Jun 2014   Movement disorder society
Genetic analysis of a family with autosomal dominant myopathy
小田 哲也, Kobayashi Kazuhiro, 熊 暉, Satake Wataru, 鈴木 穣, 菅野 純夫, Toda Tatsushi
55th Annual Meeting of the Japanese Society of Neurology   May 2014   The Japanese Society of Neurology
Clinical features in spinocerebellar ataxia type 6 (SCA6) and type 31 (SCA31).
関谷 博顕, Ueda Takehiro, 安井 直子, 本岡 里英子, 遠藤 浩信, 野田 佳克, 大崎 理史, 徳岡 秀紀, Washida Kazuo, Satake Wataru, Kuga Atsushi, Sekiguchi Kenji, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
55th Annual Meeting of the Japanese Society of Neurology   May 2014   The Japanese Society of Neurology
遺伝性脊髄小脳変性症SCA6,SCA31における起立性低血圧の検討
Ueda Takehiro, 関谷 博顕, 安井 直子, 本岡 里英子, 遠藤 浩信, 野田 佳克, 大崎 理史, 徳岡 秀紀, Washida Kazuo, Satake Wataru, Kuga Atsushi, Sekiguchi Kenji, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
第55回日本神経学会学術大会   May 2014   日本神経学会
新規遺伝子変異を認めた同一家系内副腎白質ジストロフィー2症例の臨床的検討
本岡 里英子, 関谷 博顕, Ueda Takehiro, Washida Kazuo, Satake Wataru, Kuga Atsushi, Sekiguchi Kenji, Kowa Hisatomo, 松川 敬志, 辻 省次, Kanda Fumio, Toda Tatsushi
55th Annual Meeting of the Japanese Society of Neurology   May 2014   The Japanese Society of Neurology
Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk. [Invited]
Satake Wataru, Yuko Ando, Hiroyuki Tomiyama, Mari Suzuki, Yoshitaka Nagai, Yutaka Suzuki, Hideki Mochizuki, Shigeo Murayama, Atsushi Takeda, Kazuko Hasegawa, Keishi Wada, Shyoji Tsuji, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Toda Tatsushi
New Frontier of Molecular Neuropathology 2014   Mar 2014   Nobuyuki Nukina, Hitoshi Okazawa, Takeshi Iwatsubo
Parkinson's disease (PD) is a complex disorder caused by multiple genetic risks. We reported a genomewide association study (GWAS) which identified four PD-risk genes (Satake et al, Nature Genet 2009). In order to search for further PD-risks in ex...
Genetic analysis of a family with autosomal dominant myopathy
Oda Tetsuya, Kobayashi Kazuhiro, 熊 暉, Satake Wataru, 鈴木 穣, 菅野 純夫, Toda Tatsushi
The 58th Annual Meeting of the Japan Society of Human Genetics   Nov 2013   The Japan Society of Human Genetics
Genetic analysis of a family with autosomal dominant myopathy
Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk
Satake Wataru, Yutaka Suzuki, Yuko Ando, Hiroyuki Tomiyama, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Shoji Tsuji, Sumio Sugano, Toda Tatsushi
American Society of Human Genetics Annual meeting 2013   Oct 2013   American Society of Human Genetics
Parkinson's disease (PD) is one of the most common neurodegenerative diseases worldwide, mainly manifesting motor impairment due to degeneration of dopamigenic neurons. Common form of PD appears following a multi-factorial inheritance pattern; tha...
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 [Invited]
Satake Wataru, 安藤祐子, 鈴木マリ, 永井義隆, 鈴木穣, 山本健, 望月秀樹, 武田篤, 川上秀史, 和田圭司, 山本光利, 村田美穂, 服部信孝, Toda Tatsushi
2013年度 包括脳ネットワーク夏のワークショップ   Sep 2013   包括型脳科学研究推進支援ネットワーク
Search for rare-variant risks of Parkinson's disease by sequencing of candidate genes and exome sequencing
Satake Wataru, Yuko Ando, Hiroyuki Tomiyama, Atsushi Takeda, Kazuko Hasegawa, Mitsutoshi Yamamoto, Miho Murata, Nobutaka Hattori, Toda Tatsushi
The MDS 17th International Congress of Parkinson's Disease and Movement Disorders   Jun 2013   Movement disorder society
PD is a complex disorder caused by multiple genetic risks. Heterozygous mutations in the GBA gene, whose homozygous mutations cause one of lysosomal disorders Gaucher's disease, have been reported as strong risk factors for PD. In addition, some p...
パーキンソニズムを呈した22q11.2欠失症候群の1例
赤谷 律, 本岡里英子, 千原典夫, Satake Wataru, Sekiguchi Kenji, 濱口浩敏, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi, Fukuoka Hidenori
日本神経学会 第98回近畿地方会   Jun 2013   日本神経学会
剖検脳を用いた孤発性パーキンソン病感受性遺伝子の解析
Ueda Takehiro, Seki Tsuneyoshi, Satake Wataru, Kowa Hisatomo, Kanda Fumio, 陣内研二, Toda Tatsushi
第54回日本神経学会学術大会   May 2013   日本神経学会
Japanese 2nd GWAS Identifies Strong Association at a Novel Risk Locus and MCCC1 for Parkinson's Disease.
Toda Tatsushi, Satake Wataru, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata
The 11th international conference on alzheimer's and parkinson's diseases.   Mar 2013   the 11th International Conference on AD and PD
Japanese 2nd GWAS Identifies Strong Association at a Novel Risk Locus and MCCC1 for Parkinson's Disease.
Parkinsonismを呈した22q11.2欠失症候群の31歳男性例
赤谷 律, 本岡 里英子, 千原 典夫, Satake Wataru, Sekiguchi Kenji, 濱口 浩敏, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
第3回兵庫・岡山パーキンソン病研究会   Jan 2013   グラクソ・スミスクライン株式会社
Japanese 2nd genome-wide association study identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease.
Satake Wataru, Ando Yukihiro, Ueda Takehiro, Kowa Hisatomo, H. Tomiyama, A. Takeda, H. Kawakami, K. Hasegawa, F. Obata, M. Watanabe, A. Tamaoka, K. Nakashima, M. Yamamoto, Murata Maho, N. Hattori, Toda Tatsushi
The 17th Takeda Science Foundation symtosium on Bioscience. Therapeutic Approach for Neurogenerative Diseases: Focusing on Alzheimer & Parkinson Diseases   Dec 2012   Takeda Science Foundation
Parkinson's disease (PD) is one of the most common neurodegenerative diseases worldwide. We reported a genome-wide association study (GWAS) in a total of 2,011 cases and 18,381 controls from the Japanese (Satake W et al, Nature Genet 2009). I...
A case of facial nerve palsy with brainstem tumefactive demyelinating lesion.
本岡 里英子, 千原 典夫, 赤谷 律, Satake Wataru, Sekiguchi Kenji, 濱口 浩敏, Kowa Hisatomo, Kanda Fumio, Toda Tatsushi
第97回日本神経学会近畿地方会   Dec 2012   The Japapnese society of Neurology
Search for rare-variant risks of Parkinson's disease by sequencing of candidate genes and exome sequencing
Satake Wataru, Y. Suzuki, Ando Yukihiro, T. Nishioka, K. Syoji, H. Tomiyama, M. Yamamoto, Murata Maho, N. Hattori, S. Sugano, Toda Tatsushi
62nd Annual Meeting, The American Society of Human Genetics   Nov 2012   The American Society of Human Genetics
Parkinson's disease is one of the most common neurodegenerative diseases worldwide, mainly manifesting motor impairment due to degeneration of dopamigenic neurons. Heterozygous mutations in the GBA gene, whose homozygous mutations cause one o...
Search for rare-variant risks of Parkinson's disease -Sanger sequencing of candidate genes and Exome sequencing- [Invited]
Satake Wataru, Yamamoto M, Murata Maho, Hattori N, Toda Tatsushi
2012 Annual meeting, Genetic epidemiology of Parkinson's disease   Oct 2012   Genetic epidemiology of Parkinson's disease
Parkinson's disease is one of the most common neurodegenerative diseases worldwide, mainly manifesting motor impairment due to degeneration of dopamigenic neurons. Heterozygous mutations in the GBA gene, whose homozygous mutations cause one o...
候補遺伝子とエクソームシークエンスによるパーキンソン病の Rare Variant リスクの探索
Satake Wataru, 鈴木穣, 安藤祐子, 西岡竜也, 小路紘平, 富山弘幸, 山本光利, 村田美穂, 服部信孝, 菅野純夫, Toda Tatsushi
日本人類遺伝学会第57回大会   Oct 2012   日本人類遺伝学会
パーキンソン病 (PD) は、中脳ドパミン細胞の変性により運動障害等をきたす主要な神経難病である。この疾患の強いリスク遺伝子として、脂質代謝異常症の1つであるゴーシェ病の遺伝子GBAのヘテロ変異が報告されている。また、ゴーシェ病患者はPD症状を部分症状としてもつことが報告されている。そこで、他の脂質代謝異常症やPD症状を部分症状として示す疾患の原因遺伝子がPDのリスクとなっているかを検討した。PD患者のゲノムDNA 541検体 (孤発性500例, 家族性41例) について、脂質代謝異常症 ...
パーキンソン病および認知機能関連分子とパーソナルゲノム解析-常染色体優性遺伝形式をとる神経筋疾患家系における遺伝学的解析
Oda Tetsuya, Kobayashi Kazuhiro, Satake Wataru, Toda Tatsushi
新学術領域研究「脳疾患ゲノム情報」平成24年度第1回班会議   Sep 2012   新学術領域研究「脳疾患ゲノム情報」
常染色体優性遺伝形式をとる筋疾患家系でSNPデータを用いた連鎖解析を行い、候補領域を検出した。次世代シークエンサーを用いたエクソーム解析を行い、遺伝子Aの新規ミスセンス変異が疑われる。
Japanese 2nd GWAS identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease
Satake Wataru, Ken Yamamoto, Yuko Ando, Atsushi Takeda, Hiroyuki Tomiyama, Hideshi Kawakami, Kazuko Hasegawa, Fumiya Obata, Masahiko Watanabe, Akira Tamaoka, Kenji Nakashima, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Toda Tatsushi
16th International Congress of Parkinson's Disease and Movement Disorders   Jun 2012   The Movement Disorder Society
ObjectiveTo identify further risk genes for Parkinson's disease (PD).Background: PD is a complex disorder caused by multiple genetic risk factors. We reported a genomewide association study (GWAS) in a total of 2,011 cases and 18,381 controls...
常染色体優性遺伝形式をとる筋疾患の中国人大家系における遺伝学的解析
Oda Tetsuya, Kobayashi Kazuhiro, Satake Wataru, 熊 暉, Toda Tatsushi
第53回日本神経学会学術大会   May 2012   日本神経学会
常染色体優性遺伝形式をとる筋疾患の中国人大家系において連鎖解析を施行し、候補領域Chr 1q23.3-24.1を同定した。
パーキンソン病のゲノム解析 SNPからエクソームGWASへ [Invited]
Satake Wataru, 西岡 竜也, 安藤 祐子, 山本 光利, 服部 信孝, 村田 美穂, Toda Tatsushi
平成23年度 厚生労働科学研究費補助金 難治性疾患克服研究事業孤発性パーキンソン病遺伝子同定と創薬・テーラーメード研究 会議   Feb 2012   厚生労働科学研究費補助金 難治性疾患克服研究事業孤発性パーキンソン病遺伝子同定と創薬・テーラーメード研究
候補遺伝子リシークエンスによるパーキンソン病のRare Variantリスクの探索
西岡 竜也, Satake Wataru, 安藤 祐子, 山本 光利, 服部 信孝, 村田 美穂, Toda Tatsushi
平成23年度 厚生労働科学研究費補助金 難治性疾患克服研究事業孤発性パーキンソン病遺伝子同定と創薬・テーラーメード研究 会議   Feb 2012   厚生労働科学研究費補助金 難治性疾患克服研究事業孤発性パーキンソン病遺伝子同定と創薬・テーラーメード研究
パーキンソン病の遺伝子リスクや薬剤反応性と遺伝子多型について [Invited]
Satake Wataru, Cha PC, Ueda Takehiro, Kowa Hisatomo, 中村 祐輔, 服部 信孝, 山本 光利, 村田 美穂, Toda Tatsushi
第2回兵庫岡山パーキンソン病研究会   Jan 2012   グラクソスミスクライン株式会社
Japanese 2nd GWAS identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease
Satake W at al
16th International Congress of Parkinson's Disease and Movement Disorders, Dublin, Ireland   2012   
Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing
Satake W et al
American Society of Human Genetics 62nd Annual Meeting, California, USA   2012   
Search for rare-variant risks of Parkinson’s disease -Sanger sequencing of
Satake W
Genetic Epidemiology of Parkinson's Disease 7th Annual Meeting, Seoul, Korea   2012   
孤発性・家族性パーキンソン病のゲノム解析 [Invited]
Satake Wataru, 安藤 祐子, 西岡 竜也, Ueda Takehiro, Kowa Hisatomo, 富山 弘幸, 渡邊 雅彦, 玉岡 晃, 武田 篤, 中島 健二, 長谷川 一子, 小幡 文弥, 川上 秀史, 佐古田 三郎, 山本 光利, 服部 信孝, 村田 美穂, Toda Tatsushi
厚生労働科学研究費補助金難治疾患克服研究事業 神経変性疾患に関する調査研究班 平成23年度 班会議   Dec 2011   厚生労働科学研究費補助金難治疾患克服研究事業 神経変性疾患に関する調査研究班
Search for rare variant risks of Parkinson's disease (PD) by resequencing of candidate genes
西岡 竜也, Satake Wataru, 安藤 祐子, 小路 紘平, 山本 光利, 村田 美穂, 服部 信孝, Toda Tatsushi
第34回日本分子生物学会年会   Dec 2011   日本分子生物学会
孤発性パーキンソン病遺伝子の同定 [Invited]
Satake Wataru
日本人類遺伝学会第56回大会   Nov 2011   日本人類遺伝学会
薬剤感受性と遺伝子多型についてーゾニサミドとワーファリンを中心にー [Invited]
Satake Wataru, Cha PC, 中村 祐輔, 村田 美穂, Toda Tatsushi
トレリーフ発売2周年記念講演会   Nov 2011   大日本住友製薬
Japanese subsequent GWAS identifies strong association at a novel risk locus and MCCC1 for Parkinson's disease [Invited]
Satake Wataru, Ken Yamamoto, Yuko Nakabayashi, Michiaki Kubo, Takashi Morizono, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Hiroyuki Tomiyama, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Toda Tatsushi
The American society of Human Genetics 61st Annual Meeting   Oct 2011   The American society of Human Genetics
Japanese 2nd GWAS identifies a novel risk locus and detects a strong association at MCCC1 for Parkinson's disease [Invited]
Satake Wataru, Toda Tatsushi
Genetic Epidemiology of Parkinson's Disease Consortium 6th annual meeting   Sep 2011   Genetic Epidemiology of Parkinson's Disease Consortium
パーキンソン病のゲノム解析 [Invited]
Satake Wataru, Toda Tatsushi
文部科学省科学研究補助金新学術領域研究 パーソナルゲノム情報に基づく脳疾患メカニズム 第3回班会議   Sep 2011   文部科学省科学研究補助金新学術領域研究 パーソナルゲノム情報に基づく脳疾患メカニズム
An a-synuclein 3'-flanking region SNP interacts with Parkinson's disease susceptibility via allele-specific binding of a transcription factor. [Invited]
I Mizuta, Satake Wataru, K Takafuji, Kanagawa Motoi, Kobayashi Kazuyuki, S Nagamori, Y Kanai, Yamamoto Masashi, N Hattori, Murata Maho, Toda Tatsushi
第15回国際パーキンソン病と運動障害会議   Jun 2011   国際運動障害学会
PD GWAS in Asoan Cohort [Invited]
Satake Wataru, Toda Tatsushi
Genetics of Neurodegenerative Disease Neurochip and Beyond   Apr 2011   NIH
PD GWAS in Asian Cohort [Invited]
Satake W
The Genetics of Neurodegenerative Disease – NeuroChip and beyond. NIH/NINDS. Washington DC, USA   2011   
Genome-wide association study identifies variants at four loci as genetic risk factors for Parkinson’s disease
Satake Wataru, Yuko Nakabayashi, Ikuko Mizuta, Michiaki Kubo, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Masahiko Watanabe, Atsushi Takeda, Hiroyuki Tomiyama, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Toda Tatsushi
60th Annual Meeting of The American Society of Human Genetics   Nov 2010   The American Society of Human Genetics
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’ s disease [Invited]
Satake Wataru, 中林 祐子, 水田 依久子, 渡邊 雅彦, 武田 篤, 富山 弘幸, 中島 健二, 長谷川 一子, 小幡 文弥, 川上 秀史, 佐古田 三郎, 山本 光利, 服部 信孝, 村田 美穂, 中村 祐輔, Toda Tatsushi
近畿パーキンソン病フォーラム   Nov 2010   近畿パーキンソン病フォーラム
PDの危険因子としての遺伝子異常. [Invited]
Toda Tatsushi, Satake Wataru
第4回パーキンソン病・運動障害疾患コングレス   Oct 2010   MDSJ
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’ s disease [Invited]
Satake Wataru, 中林 祐子, 水田 依久子, 渡邊 雅彦, 武田 篤, 富山 弘幸, 中島 健二, 長谷川 一子, 小幡 文弥, 川上 秀史, 佐古田 三郎, 山本 光利, 服部 信孝, 村田 美穂, 中村 祐輔, Toda Tatsushi
日本人類遺伝学会第55回大会   Oct 2010   日本人類遺伝学会
Genome-wide association study identifies variants at four loci as genetic risk factors for Parkinson’s disease
Satake Wataru, Yuko Nakabayashi, Ikuko Mizuta, Michiaki Kubo, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Masahiko Watanabe, Atsushi Takeda, Hiroyuki Tomiyama, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Toda Tatsushi
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(Neuro2010)   Sep 2010   日本神経科学、日本神経化学会、日本神経回路学会
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Satake Wataru, Yuko Nakabayashi, Ikuko Mizuta, Masahiko Watanabe, Atsushi Takeda, Hiroyuki Tomiyama, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Toda Tatsushi
14th International Congress of Parkinson's Disease and Movement Disorders   Jun 2010   The Movement Disorder Society
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’ s disease
Satake Wataru, 水田 依久子, 渡邊 雅彦, 武田 篤, 富山 弘幸, 中島 健二, 長谷川 一子, 小幡 文弥, 川上 秀史, 佐古田 三郎, 山本 光利, 服部 信孝, 村田 美穂, 中村 祐輔, Toda Tatsushi
第51回日本神経学会総会   May 2010   日本神経学会
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’ s disease [Invited]
Satake Wataru, 水田 依久子, 渡邊 雅彦, 武田 篤, 富山 弘幸, 中島 健二, 長谷川 一子, 小幡 文弥, 川上 秀史, 佐古田 三郎, 山本 光利, 服部 信孝, 村田 美穂, 中村 祐輔, Toda Tatsushi
第18回カテコールアミンと神経疾患研究会   Apr 2010   カテコールアミンと神経疾患研究会
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
Toda Tatsushi, Satake Wataru, 久保充明, 角田達彦, 山本光利, 服部信孝, 村田美穂, 中村裕輔
The 9th East Asia Union of Human Genetics Society   Nov 2009   East Asia Union of Human Genetics Society
Genome-wide association study identifies common variants on two novel loci, α-synuclein, and upstream LRRK2 as genetic risks for Parkinson’s disease
Satake Wataru, Yuko Nakabayashi, Ikuko Mizuta, Chiyomi Ito, Michiaki Kubo, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Masahiko Watanabe, Atsushi Takeda, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Takeo Yoshikawa, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho. Murata, Yusuke Nakamura, Toda Tatsushi
The American society of human genetics, 59th annual meeting   Oct 2009   米国人類遺伝学会
Genome-wide association study for sporadic Parkinson's disease.
Toda Tatsushi, Satake Wataru, 中林祐子, 水田依久子, 久保 充明, 吉川 武男, 山本光利, 服部信孝, 村田美穂, 中村裕輔
Movement Disorder Society   Jun 2009