業績
羽田 明| 2012 | 2011 | 2010 | 2009 | 2008 |
| 原著論文| 総説/著書| 国際会議| マスコミ掲載/その他 |
原著論文
Onouchi Y‚ Ozaki K‚ Burns JC‚ Shimizu C‚ Terai M‚ Hamada H‚ Honda T‚ Suzuki H‚ Suenaga T‚ Takeuchi T‚ Yoshikawa N‚ Suzuki Y‚ Yasukawa K‚ Ebata R‚ Higashi K‚ Saji T‚ Kemmotsu Y‚ Takatsuki S‚ Ouchi K‚ Kishi F‚ Yoshikawa T‚ Nagai T‚ Hamamoto K‚ Sato Y‚ Honda A‚ Kobayashi H‚ Sato J‚ Shibuta S‚ Miyawaki M‚ Oishi K‚ Yamaga H‚ Aoyagi N‚ Iwahashi S‚ Miyashita R‚ Murata Y‚ Sasago K‚ Takahashi A‚ Kamatani N‚ Kubo M‚ Tsunoda T‚ Hata A‚ Nakamura Y‚ Tanaka T; Japan Kawasaki Disease Genome Consortium‚ Abe J‚ Kobayashi T‚ Arakawa H‚ Ichida F‚ Nomura Y‚ Miura M‚ Ikeda K‚ Hara T‚ Fukazawa R‚ Ogawa S‚ Hamaoka K; US Kawasaki Disease Genetics Consortium‚ Newburger JW‚ Baker AL‚ Rowley AH‚ Shulman ST‚ Melish ME‚ Mason WH‚ Takahashi M‚ Tremoulet AH A genome-wide association study identifies three new risk loci for Kawasaki disease.
Nat Genet. 2012; 44 517-521
Yamaide F‚ Undarmaa S‚ Mashimo Y‚ Shimojo N‚ Arima T‚ Morita Y‚ Hirota T‚ Fujita K‚ Miyatake A‚ Doi S‚ Sato K‚ Suzuki S‚ Nishimura T‚ Watanabe H‚ Hoshioka A‚ Tomita M‚ Yamaide A‚ Watanabe M‚ Okamoto Y‚ Kohno Y‚ Tamari M‚ Hata A‚ Suzuki Y. Association study of matrix metalloproteinase-12 gene polymorphisms and asthma in a Japanese population
International Archives of Immunology and Immunology 2012; in press
Okamoto N‚ Hayashi S‚ Masui A‚ Kosaki R‚ Oguri I‚ Hasegawa T‚ Imoto I‚ Makita Y‚ Hata A‚ Moriyama K‚ Inazawa J. Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.
J Hum Genet. 2012; 57 (3): 191-196
Inoue H‚ Mashimo Y‚ Funamizu M‚ Yonekura S‚ Horiguchi S‚ Shimojo N‚ Kohno Y‚ Okamoto Y‚ Hata A‚ Suzuki Y. Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis.
J Hum Genet. 2012; 57 (3): 176-183
Narisawa A‚ Komatsuzaki S‚ Kikuchi A‚ Niihori T‚ Aoki Y‚ Fujiwara K‚ Tanemura M‚ Hata A‚ Suzuki Y‚ Relton CL‚ Grinham J‚ Leung KY‚ Partridge D‚ Robinson A‚ Stone V‚ Gustavsson P‚ Stanier P‚ Copp AJ‚ Greene ND‚ Tominaga T‚ Matsubara Y‚ Kure S. Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.
Hum Mol Genet. 2012; 21 (7): 1496-1503
Onouchi Y‚ Suzuki Y‚ Suzuki H‚ Terai M‚ Yasukawa K‚ Hamada H‚ Suenaga T‚ Honda T‚ Honda A‚ Kobayashi H‚ Takeuchi T‚ Yoshikawa N‚ Sato J‚ Shibuta S‚ Miyawaki M‚ Oishi K‚ Yamaga H‚ Aoyagi N‚ Iwahashi S‚ Miyashita R‚ Murata Y‚ Ebata R‚ Higashi K‚ Ozaki K‚ Sasago K‚ Tanaka T‚ Hata A. ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease.
Pharmacogenomics J. 2012; in press
Hayashi S‚ Okamoto N‚ Chinen Y‚ Takanashi J‚ Makita Y‚ Hata A‚ Imoto I‚ Inazawa J. Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH).
Hum Genet. 2012; 131 99-110
総説/著書
Onouchi‚ Y. Genetics of Kawasaki Disease Circulation Journal 2012; 76 1581-1586
国際会議
Onouchi‚ Y.‚ Ozaki‚ K.‚ Suzuki‚ H.‚ Terai‚ M.‚ Hata‚ A.‚ Tanaka‚ T. ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease
Human Genome Meeting 2012 2012-3-11 Sydney/Australia
Onouchi‚ Y. Genome-wide association study identified new susceptibility loci for Kawasaki disease -We have found milestones but still have far to go-
10th International Kawasaki Disease Symposium （国際川崎病シンポジウム） 2012-2-7 Kyoto/Japan
マスコミ掲載/その他
2012-6-15 川崎病後遺症予防に一手 日本経済新聞
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