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Wataru Satake
Researcher at Kobe University
Publications - 37
Citations - 3835
Wataru Satake is an academic researcher from Kobe University. The author has contributed to research in topics: Parkinson's disease & Medicine. The author has an hindex of 18, co-authored 32 publications receiving 3461 citations.
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Journal ArticleDOI
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Wataru Satake,Yuko Nakabayashi,Yuko Nakabayashi,Ikuko Mizuta,Ikuko Mizuta,Yushi Hirota,Yushi Hirota,Chiyomi Ito,Chiyomi Ito,Michiaki Kubo,Takahisa Kawaguchi,Tatsuhiko Tsunoda,Masahiko Watanabe,Atsushi Takeda,Hiroyuki Tomiyama,Kenji Nakashima,Kazuko Hasegawa,Fumiya Obata,Takeo Yoshikawa,Hideshi Kawakami,Saburo Sakoda,Mitsutoshi Yamamoto,Nobutaka Hattori,Miho Murata,Yusuke Nakamura,Tatsushi Toda,Tatsushi Toda +26 more
TL;DR: The results identify two new PD susceptibility loci, show involvement of autosomal dominant parkinsonism loci in typical PD and suggest that population differences contribute to genetic heterogeneity in PD.
Journal ArticleDOI
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.
Christina M. Lill,Johannes T. Roehr,Johannes T. Roehr,Matthew B. McQueen,Fotini K. Kavvoura,Fotini K. Kavvoura,Fotini K. Kavvoura,Sachin Bagade,Brit-Maren M. Schjeide,Leif M. Schjeide,Esther Meissner,Ute Zauft,Nicole C. Allen,Tian-Jing Liu,Marcel Schilling,Marcel Schilling,Kari J. Anderson,Gary W. Beecham,Daniela Berg,Daniela Berg,Joanna M. Biernacka,Alexis Brice,Anita L. DeStefano,Chuong B. Do,Nicholas Eriksson,Stewart A. Factor,Matthew J. Farrer,Tatiana Foroud,Thomas Gasser,Thomas Gasser,Taye H. Hamza,John Hardy,Peter Heutink,Erin M. Hill-Burns,Christine Klein,Jeanne C. Latourelle,Demetrius M. Maraganore,Eden R. Martin,Maria Martinez,Maria Martinez,Richard H. Myers,Mike A. Nalls,Nathan Pankratz,Haydeh Payami,Wataru Satake,William K. Scott,Manu Sharma,Manu Sharma,Andrew B. Singleton,Kari Stefansson,Tatsushi Toda,Joyce Y. Tung,Jeffery M. Vance,Nicholas W. Wood,Cyrus P. Zabetian,Peter Young,Rudolph E. Tanzi,Muin J. Khoury,Frauke Zipp,Hans Lehrach,John P. A. Ioannidis,Lars Bertram,Lars Bertram +62 more
TL;DR: This study provides an exhaustive and up-to-date summary of the status of PD genetics research that can be readily scaled to include the results of future large-scale genetics projects, including next-generation sequencing studies.
Journal ArticleDOI
O1-7-4-1Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Wataru Satake,Ikuko Mizuta,Michiaki Kubo,Takahisa Kawaguchi,Tatsuhiko Tsunoda,Takeo Yoshikawa,Saburo Sakoda,Mitsutoshi Yamamoto,Nobutaka Hattori,Miho Murata,Yusuke Nakamura,Tatsushi Toda +11 more
TL;DR: Clinical and genetic information of 5 Japanese patients with Bardet-Biedl syndrome is summarized and it is found that rare liver fibrosis was detected in two patients, while only two patients had renal dysfunction, thought to be a universal symptom.
Journal ArticleDOI
Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration
Jun Mitsui,Takashi Matsukawa,Hiroyuki Ishiura,Yoko Fukuda,Yoko Fukuda,Yaeko Ichikawa,Hidetoshi Date,Budrul Ahsan,Yasuo Nakahara,Yoshio Momose,Yuji Takahashi,Atsushi Iwata,Jun Goto,Yorihiro Yamamoto,Makiko Komata,Katsuhiko Shirahige,Kenju Hara,Akiyoshi Kakita,Mitsunori Yamada,Hitoshi Takahashi,Osamu Onodera,Masatoyo Nishizawa,Hiroshi Takashima,Ryozo Kuwano,Hirohisa Watanabe,Mizuki Ito,Gen Sobue,Hiroyuki Soma,Ichiro Yabe,Hidenao Sasaki,Masashi Aoki,Kinya Ishikawa,Hidehiro Mizusawa,Kazuaki Kanai,Takamichi Hattori,Satoshi Kuwabara,Kimihito Arai,Shigeru Koyano,Yoshiyuki Kuroiwa,Kazuko Hasegawa,Tatsuhiko Yuasa,Kenichi Yasui,Kenji Nakashima,Hijiri Ito,Yuishin Izumi,Ryuji Kaji,Takeo Kato,Susumu Kusunoki,Yasushi Osaki,Masahiro Horiuchi,Tomoyoshi Kondo,Shigeo Murayama,Nobutaka Hattori,Mitsutoshi Yamamoto,Miho Murata,Wataru Satake,Tatsushi Toda,Alexandra Durr,Alexis Brice,Alessandro Filla,Thomas Klockgether,Ullrich Wallner,Garth A. Nicholson,Sid Gilman,Clifford W. Shults,Caroline M. Tanner,Walter A. Kukull,Virginia M.-Y. Lee,Eliezer Masliah,Phillip A. Low,Paola Sandroni,John Q. Trojanowski,Laurie J. Ozelius,Tatiana Foroud,Shoji Tsuji +74 more
TL;DR: Functionally impaired variants of COQ2 were associated with an increased risk of multiple-system atrophy in multiplex families and patients with sporadic disease, providing evidence of a role of impaired COQ1 activities in the pathogenesis of this disease.
Journal ArticleDOI
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
Manabu Funayama,Kenji Ohe,Kenji Ohe,Taku Amo,Norihiko Furuya,Junji Yamaguchi,Shinji Saiki,Yuanzhe Li,Kotaro Ogaki,Maya Ando,Hiroyo Yoshino,Hiroyuki Tomiyama,Kenya Nishioka,Kazuko Hasegawa,Hidemoto Saiki,Wataru Satake,Kaoru Mogushi,Ryogen Sasaki,Yasumasa Kokubo,Shigeki Kuzuhara,Tatsushi Toda,Yoshikuni Mizuno,Yasuo Uchiyama,Kinji Ohno,Nobutaka Hattori +24 more
TL;DR: CHCHD2 mutations are associated with, and might be a cause of, autosomal dominant Parkinson's disease, and further functional studies are needed to understand how mutant CHCHD 2 might play a part in the pathophysiology of Parkinson's Disease.