講演・口頭発表等 - 田中　敏博

分割表示  258 件中 1 - 20 件目  ／  全件表示 >>

  1. Yuki Nagata, Toshihiro Tanaka. Targeted deep sequencing analyses of long QT syndrome in a Japanese population.. The 67th Annual Meeting of the Japan Society of Human Genetics 2022.12.14 Yokohama, Japan

  2. Yuki Nagata, Toshihiro Tanaka. Targeted deep sequencing analyses of long QT syndrome in a Japanese population. ASHG annual meeting 2022 2022.10.25 Los Angels, USA

  3. Tanaka T. Exome Analyses of Long QT Syndrome. Symposium20 Annual Meeting of the Japanese Heart Rhythm Society 2016 2016.07.16 Sapporo Convention Center

  4. Ozaki K, Morizono T, Tsunoda T, Kubo M, Tanaka T. Up-regulation of FLT1 by a novel functional SNP increases risk of coronary artery disease through an inflammatory activation. ICHG2016 2016.04.07

  5. Kanai M, Okada Y, Muramatsu T, Suita N, Kawakami E, Iotchkova V, Soranzo N, Inazawa J, Tanaka T. Significant impact of miRNA–target gene networks on genetics of human complex traits. ICHG2016 2016.04.07

  6. Kanai M, Tanaka T, Okada Y. Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project dataset. ICHG2016 2016.04.07

  7. Fares Taie L, Gerber S, Tawara A, Ramirez-Miranda A, Douet JY, Verdin H, Zanteno JC, Kondo H, Passet B, Yamamoto K, Iwai M, Tanaka T, Nakamura Y, Kimura W, Munnich A, Baere ED, Raymond-Letron I, Kaplan J, Calvas P, Roche O, Rozet JM. Submicroscopic deletions at 13q32.1 cause congenital microcoria. ICHG2016 2016.04.05

  8. Onouchi Y, Nakagawa H, Shigemizu D, Ozaki K, Nakamura Y, Asami Y, Seki M, Kobayashi T, Kochi Y, Toda T, Satake W, Hata A, Tsunoda T, Tanaka T, Japan Kawasaki Disease Genome Consortium. Search for genetic variations responsible for giant coronary aneurysms in Kawasaki disease patients by whole exome sequencing. ICHG2016 2016.04.04

  9. Takeaki Sudo, Yukinori Okada, Hiroaki Kobayashi, Misa Gokyu, Yuichi Izumi, Toshihiro Tanaka. Whole-exome sequencing reveals a novel gene as a cause of Aggressive periodontitis in Japanese consanguineous families. The 13th International Congress of Human Genetics 2016.04.04

  10. El Rouby N, McDonough CW, Gong Y, McClure LA, Mitchell BD, Horenstein RB, Talbert RL, Takahashi A, Tanaka T, Kubo M, Pepine CJ, Cooper-DeHoff RM, Benavente OR, Shuldiner AR, Johnson JA. Novel genetic loci for resistant hypertension discovered through a genome-wide association approach (GWAS) in the INternational VErapamil SR-Trandolapril STudy (INVEST) and the Secondary Prevention of Subcortical Strokes (SPS3) Study. American Society of Human Genetics 2015.10

  11. Higuchi C, Tanaka T and Okada Y. Systematic comparison of machine learning methods for identification of miRNA species as disease biomarkers. The IWBBIO 2015 (3rd International Work-Conference on Bioinformatics and Biomedical Engineering) 2015.04 Spain Granada

  12. Aiba T, Makimoto H, Makiyama T, Watanabe H, Hayashi K, Nakano Y, Miyauchi Y, Morita H, Aonuma K, Hagiwara N, Fukuda K, Yoshinaga M, Horigome H, Sumitomo N, Tanaka T, Sekine A, Shiraishi I, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Makita N, Horie M, Shimizu W. Diverse gender difference of arrhythmic risk in patients with congenital Long QT Syndrome: from Japanese congenital LQTS multicenter registry. AHA 2014 2014.11 Chicago

  13. Ozaki K, Sakata Y, Suna S, Onouchi Y, Tsunoda T, Kubo M, Komuro I, Tanaka T. A replication study for fifteen coronary artery disease susceptible loci in a Japanese population. ASHG 2014 2014.10 San Diego

  14. Rouby N, McDonough C, Gong Y, Pepine C, Takahashi A, Tanaka T, Kubo M, Cooper-DeHoff R, Johnson J. Genome-wide association study of resistant hypertension in INVEST. ASHG 2014 2014.10 San Diego

  15. Johnson T, Boroevich K, Tanaka T, Qi L, He, Xu M, Wu T, Kubo M, Tsunoda T. Integrated analysis of known height association signals with novel signals from an East Asian GWAS decodes the genetic architecture of height through in silico functional candidate prioritization and gene network analysis. ASHG 2014 2014.10 San Diego

  16. Ozaki K, Morizono T, Onouchi Y, Takahashi A, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genome-wide association study for arteriosclerosis obliterans in a Japanese population. American Society of Human Genetics . ASHG 2013 2013.10

  17. Onouchi Y, Fukazawa R, Ozaki K, Terai M, Hamada H, Honda T, Suzuki H, Suenaga T, Takeuchi T, Yasukawa K, Ebata R, Higashi K, Saji T, Kemmotsu Y, Takatsuki S, Ouchi K, Kishi F, Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Abe J, Seki M, Kobayashi T, Takahashi A, Tsunoda T, Kubo M, Nakamura Y, Hata A, Tanaka T.. Variations in ORAI1 gene associated with Kawasaki disease. . ASHG 2013 2013.10

  18. Ozaki K, and Tanaka T. Whole genome association study for atrial fibrillation in a Japanese population. ISHR 2013 2013.07

  19. Ozaki K, Morizono T, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genetic risk factors for atrial fibrillation in the Japanese population.. ESHG2013 2013.06

  20. Onouchi Y, Ozaki K, 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, Kubo M, Tsunoda T, Hata A, Nakamura Y, Tanaka T. . A fine mapping of the genetic variation influencing the ratio of alternatively spliced CD40 transcripts and conferring susceptibility to Kawasaki disease. . ASHG 2012 2012.11

< 前のページ - 次のページ >

このページの先頭へ▲