講演・口頭発表等 - 田中　敏博

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  1. Ozaki K, Kubo M, Tsunoda T, Onouchi Y, Kamatani N, Nakamura Y, Tanaka T. . Six chromosome loci for atrial fibrillation susceptibility identified in Japanese.. AHA 2012 2012.11

  2. Ozaki K, Onouchi Y, Kamatani N, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genome-wide association study for atrial fibrillation in the Japanese population. . ASHG 2012 2012.11

  3. Ozaki K, Tanaka T. . Identification of protein that interact BRAP, encoded by a gene associated with myocardial infarction susceptibility.. World Congress of Cardiology Scientific Sessions 2012.04

  4. 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 2012.03

  5. Ozaki K, Onouchi Y, Nakamura Y, Tanaka T. . BRAP, encoded by a gene associated with myocardial infarction, binds several key inflammatory molecules.. ICHG 2011 2011.10

  6. Onouchi Y, Ozaki K, Burns J.C, Shimizu C, Terai M, Hamada H, Suzuki H, Suenaga T, Suzuki Y, Yasukawa K, Ebata R, Saji T, Kemmotsu Y, Ouchi K, Kishi F,Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Sasago K, Takahashi A, Kamatani N, Kubo M, Tsunoda T, Hata A, Nakamura Y, Tanaka T.. Genome-wide association study identified new susceptibility loci for Kawasaki disease. . ICHG 2011 2011.10

  7. Tanaka T.. Genetic Epidemiology~Understanding the human diversity towards personalized medicine~. . The 6th International Syompsium of Nagasaki University Global COE program 2011.10

  8. Tanaka T.. BioBank Japan. . KOGO satellite session 2011.09

  9. Todd J, 田中敏博, 久保充明, 中村祐輔, 角田達彦 . Analyzing contiguous homozygosity to quantify haplotype structure differences between case and control samples. 日本人類遺伝学会第55回大会 2010.10

  10. Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Makiyama T, Akao M, Hagiwara N, Kishi R, Miyamoto Y, Kamakura S, Shimizu W. . Clinical Phenotype and Prognosis of Probands with Brugada Syndrome in Relation to SCN5A Mutation. . 第74回日本循環器学会総会・学術集会 2010.03

  11. Ozaki K, Sato H, Inoue K, Tsunoda T, Sakata Y, Mizuno H, Onouchi Y, Odashiro K, Nobuyoshi M, Juo H S-H, Hori H, Nakamura Y, Tanaka T. . SNPs in Genes Encoding an Inflammatory Cascade Confer Risk of Myocardial Infarction.. 第74回日本循環器学会総会・学術集会 2010.03

  12. Makimoto H, Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Makiyama T, Akao M, Yoshinaga M, Miyamoto Y, Kamakura S, Shimizu W. . Clinical Features of Long QT Syndrome in Pre-Elementary Age.. 第74回日本循環器学会総会・学術集会 2010.03

  13. Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Yoshinaga M, Okamura H, Noda T, Miyamoto Y, Kamakura S, Shimizu W.. Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry. . 第73回日本循環器学会総会・学術集会 2009.03

  14. Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Kishi R, Okamura H, Noda T, Satomi K, Suyama K, Kurita T, Aihara N, Kamaukura S, Miyamoto Y, Shimizu W. . Clinical and Electrocardiographic Characteristics of Japanese Probands with Brugada Syndrome with an SCN5A Mutation from Japanese Multicenter Registry. . 第73回日本循環器学会総会・学術集会 2009.03

  15. Ozaki K, Sato H, Inoue K, Tsunoda T, Sakata Y, Mizuno H, Aoki A, Odashiro K, Nobuyoshi M, Juo H S-H, Hori M, Nakamura Y, Tanaka T. . A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations.. 第73回日本循環器学会総会・学術集会 2009.03

  16. Ozaki K, Sato H, Inoue K, Mizuno H, Sakata Y, Odashiro K, Nobuyoshi M, Hori M, Nakamura Y, Tanaka T. . Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction. . 第73回日本循環器学会総会・学術集会 2009.03

  17. Aoki A, Ozaki K, Sato H, Takahashi A, Kubo M, Sakata Y, Mizuno H, Kamatani N, Tsunoda T, Takano H, Yasutake M, Mizuno K, Hori M, Nakamura Y, Tanaka T.. Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study. . 第73回日本循環器学会総会・学術集会 2009.03

  18. Kato M, Miya F, Kanemura Y, Tanaka T, Nakamura Y, Tsunoda T. . Patterns of high-resolution recombination rates in human genes.. HGM 2008 2008.09

  19. Tanaka T.. Genetic background of myocardial infarction.. Mendel Symposium II Genes and the Heart 2008.09

  20. Ozaki K, Sato H, Ishii N, Ebana Y, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . Large scale SNPs association study to identify genes confer risk of myocardial infarction. . 14th World Congress on Heart Disease 2008.07

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