Y
Yuji Murata
Publications - 2
Citations - 300
Yuji Murata is an academic researcher. The author has contributed to research in topics: Genome-wide association study & Kawasaki disease. The author has an hindex of 2, co-authored 2 publications receiving 261 citations.
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A genome-wide association study identifies three new risk loci for Kawasaki disease
Yoshihiro Onouchi,Kouichi Ozaki,Jane C. Burns,Jane C. Burns,Chisato Shimizu,Chisato Shimizu,Masaru Terai,Hiromichi Hamada,Takafumi Honda,Hiroyuki Suzuki,Tomohiro Suenaga,Takashi Takeuchi,Norishige Yoshikawa,Yoichi Suzuki,Kumi Yasukawa,Ryota Ebata,Kouji Higashi,Tsutomu Saji,Yasushi Kemmotsu,Shinichi Takatsuki,Kazunobu Ouchi,Fumio Kishi,Tetsushi Yoshikawa,Toshiro Nagai,Kunihiro Hamamoto,Yoshitake Sato,Akihito Honda,Hironobu Kobayashi,Junichi Sato,Shoichi Shibuta,Masakazu Miyawaki,Ko Oishi,Hironobu Yamaga,Noriyuki Aoyagi,Seiji Iwahashi,Ritsuko Miyashita,Yuji Murata,Kumiko Sasago,Atsushi Takahashi,Naoyuki Kamatani,Michiaki Kubo,Tatsuhiko Tsunoda,Akira Hata,Yusuke Nakamura,Toshihiro Tanaka +44 more
TL;DR: A genome-wide association study of Kawasaki disease in Japanese subjects using data from 428 individuals with Kawasaki Disease and 3,379 controls genotyped at 473,803 SNPs provides new insights into the pathogenesis and pathophysiology of Kaw Osaka disease.
Journal ArticleDOI
Variations in ORAI1 Gene Associated with Kawasaki Disease.
Yoshihiro Onouchi,Ryuji Fukazawa,Kenichiro Yamamura,Hiroyuki Suzuki,Nobuyuki Kakimoto,Tomohiro Suenaga,Takashi Takeuchi,Hiromichi Hamada,Takafumi Honda,Kumi Yasukawa,Masaru Terai,Ryota Ebata,Kouji Higashi,Tsutomu Saji,Yasushi Kemmotsu,Shinichi Takatsuki,Kazunobu Ouchi,Fumio Kishi,Tetsushi Yoshikawa,Toshiro Nagai,Kunihiro Hamamoto,Yoshitake Sato,Akihito Honda,Hironobu Kobayashi,Junichi Sato,Shoichi Shibuta,Masakazu Miyawaki,Ko Oishi,Hironobu Yamaga,Noriyuki Aoyagi,Megumi Yoshiyama,Ritsuko Miyashita,Yuji Murata,Akihiro Fujino,Kouichi Ozaki,Tomisaku Kawasaki,Jun Abe,Mitsuru Seki,Tohru Kobayashi,Hirokazu Arakawa,Shunichi Ogawa,Toshiro Hara,Akira Hata,Toshihiro Tanaka +43 more
TL;DR: Data indicate that ORAI1 gene variations are associated with KD and may suggest the potential importance of the Ca(2+)/NFAT pathway in the pathogenesis of this disorder.