業績  

羽田 明

2012 | 2011 | 2010 | 2009 | 2008 |
| 原著論文| 総説/著書 |

原著論文

Mamtani M‚ Matsubara T‚ Shimizu C‚ Furukawa S‚ Akagi T‚ Onouchi Y‚ Hata A‚ Fujino A‚ He W‚ Ahuja SK‚ Burns JC.   Association of CCR2-CCR5 haplotypes and CCL3L1 copy number with Kawasaki Disease‚ coronary artery lesions‚ and IVIG responses in Japanese children.
PloS One  2010;  5     e11458-


Akiyama K‚ Narita A‚ Nakaoka H‚ Cui T‚ Takahashi T‚ Yasuno K‚ Tajima A‚ Krischek B‚ Yamamoto K‚ Kasuya H‚ Hata A‚ Inoue I.   Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.
J Hum Genet.  2010;  55     656-661


Nakaoka H‚ Takahashi T‚ Akiyama K‚ Cui T‚ Tajima A‚ Krischek B‚ Kasuya H‚ Hata A‚ Inoue I.   Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution.
Stroke  2010;  41     1593-1598


Onouchi Y‚ Ozaki K‚ Burns JC‚ Shimizu C‚ Hamada H‚ Honda T‚ Terai M‚ Honda A‚ Takeuchi T‚ Shibuta S‚ Suenaga T‚ Suzuki H‚ Higashi K‚ Yasukawa K‚ Suzuki Y‚ Sasago K‚ Kemmotsu Y‚ Takatsuki S‚ Saji T‚ Yoshikawa T‚ Nagai T‚ Hamamoto K‚ Kishi F‚ Ouchi K‚ Sato Y‚ Newburger JW‚ Baker AL‚ Shulman ST‚ Rowley AH‚ Yashiro M‚ Nakamura Y‚ Wakui K‚ Fukushima Y‚ Fujino A‚ Tsunoda T‚ Kawasaki T‚ Hata A‚ Nakamura Y‚ Tanaka T.   Common variants in CASP3 confer susceptibility to Kawasaki disease.
Hum Mol Genet.  2010;  19     2898-2906


Fujita M‚ Ueno K‚ Hata A.   Association of gamma­glutamyl­transferase with incidence of type 2 diabetes in Japan.
Exp Biol Med.  2010;  235     335-341


Undarmaa S‚ Mashimo Y‚ Hattori S‚ Shimojo N‚ Fujita K‚ Miyatake A‚ Doi S‚ Kohno Y‚ Okamoto Y‚ Hirota T‚ Tamari M‚ Hata A‚ Suzuki Y.   Replication of genetic association studies in asthma and related phenotypes.
J Hum Genet.  2010;  55     342-349


Yasuno K‚ Bilguvar K‚ Bijlenga P‚ Low SK‚ Krischek B‚ Auburger G‚ Simon M‚ Krex D‚ Arlier Z‚ Nayak N‚ Ruigrok YM‚ Niemelä M‚ Tajima A‚ von und zu Fraunberg M‚ Dóczi T‚ Wirjatijasa F‚ Hata A‚ Blasco J‚ Oszvald A‚ Kasuya H‚ Zilani G‚ Schoch B‚ Singh P‚ Stüer C‚ Risselada R‚ Beck J‚ Sola T‚ Ricciardi F‚ Aromaa A‚ Illig T‚ Schreiber S‚ van Duijn CM‚ van den Berg LH‚ Perret C‚ Proust C‚ Roder C‚ Ozturk AK‚ Gaál E‚ Berg D‚ Geisen C‚ Friedrich CM‚ Summers P‚ Frangi AF‚ State MW‚ Wichmann HE‚ Breteler MM‚ Wijmenga C‚ Mane S‚ Peltonen L‚ Elio V‚ Sturkenboom MC‚ Lawford P‚ Byrne J‚ Macho J‚ Sandalcioglu EI‚ Meyer B‚ Raabe A‚ Steinmetz H‚ Rüfenacht D‚ Jääskeläinen JE‚ Hernesniemi J‚ Rinkel GJ‚ Zembutsu H‚ Inoue I‚ Palotie A‚ Cambien F‚ Nakamura Y‚ Lifton RP‚ Günel M.   Genome-wide association study of intracranial aneurysm identifies three new risk loci.
Nat Genet.  2010;  42     420-425


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総説/著書

羽田 明   ゲノムメディカルリサーチコーディネーター(GMRC)制度   遺伝子診療学 第2版(日本臨床)  2010;     


羽田 明   多因子疾患   遺伝子診療学 第2版 (日本臨床)  2010;     


羽田 明   遺伝要因による疾患   家庭医学大全(法硏)  2010;     


羽田 明   がん   予防医学指導士テキスト(日本予防医学会)  2010;     


羽田 明   高血圧   改訂版 分子予防環境医学 (本の泉社)  2010;     


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