Conference Activities & Talks -

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

21. 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

22. 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

23. 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

24. 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

25. 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

26. 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

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

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

29. 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

30. 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

31. 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

32. 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

33. 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

34. 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

35. 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

36. 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

37. 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

38. 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

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

40. 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

41. Tanaka T.. Genetic backgrounds of myocardial infarction. . The 2008 EAUHGS Symposium and the 8th EAUHGS Annual Meeting 2008.07

42. Yamagata K, Horie M, Ogawa S, Aizawa Y, 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 LQT1 form of congenital long QT syndrome by location and coding type from Japanese multicenter registry. . 第72回日本循環器学会総会・学術集会 2008.03

43. Tanaka T.. Single-Nucleotide Polymorphisms Confer Risk of Myocardial infarction. . AHA 2007 2007.11

44. Ozaki K, Sato H, Iida A, Mizuno H, Takahashi A, Nakamura T, Lwin H, Ikegawa S, Hri M, Nakamura Y, Tanaka T. . 52,608 gene-based SNPs association study to identify genes related to myocardial infarction. . ASHG 2007 2007.10

45. Tanaka T.. Biobank Japan.. International Society for Biological and Environmental Repositories 2007.05

46. Ozaki K, Sato H, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . A functional SNP in the proteasome subunit alpha type 6 gene confers risk of myocardial infarction in Japanese population. . 第71回日本循環器学会総会・学術集会 2007.03

47. Ozaki K, Ishii N, Sato H, Mizuno H, Hori M, Saito S, Nakamura Y, and Tanaka T.. Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial Infarction. . 第71回日本循環器学会総会・学術集会 2007.03

48. Tanaka T.. Identification of genes associated with common diseases by large-scale genetic association study-Studies on myocardial infarction. . The 2nd annual international symposium of genomic medicine and pharmacogenomics 2007.03

49. Tanaka T.. Identification of genes associated with common diseases by large-scale genetic association study-Studies on myocardial infarction. . Medical Science Seminar Series 2007.03

50. Ozaki K, Sato H, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . Association study in search for genetic backgrounds of myocardial infarction, focused on SNPs in genes encoding molecules that belong to lymphotoxin-a signaling cascade. . ASHG 2006 2006.10

51. Ozaki K, Inoue K, Odashiro M, Nobuyoshi M, Nakamura Y, Tanaka T. . Identification of proteins that bind galectin-2, encoded by a gene associated with myocardial infarction using tandem affinity purification method. . ASHG 2005 2005.11

52. Tanaka T.. BioBank Japan: Toward Personalized Medicine. . NCI Symposium: International Harmonization of Biorepository Practices 2005.11

53. Tanaka T.. From SNPs to Disease Risk –Towards predictive and personalized medicine.. 3rd World Congress of Nephrology 2005.06

54. Tanaka T.. Towards Personalized Medicine.. HUGO's 10th Human Genome Meeting (HGM2005) 2005.04

55. Tanaka T.. Recent Advance in Genomics for Diagnosis and Treatment of Cardiovascular Diseases.. The 69th Annual Science Meeting of the Japanese Circulation Society 2005.03

56. Tanaka T.. Functional variations in two genes encoding functionally associated proteins, lymphotoxin-α and galectin-2, confer risk of myocardial infarction.. The 13th Takeda Science Foundation Symposium on Bioscience 2004.12

57. Tanaka T.. The Japanese Biobank.. ESHG 2004 2004.06

58. Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Functional SNPs in the lymphotoxin- gene that are associated with susceptibility to myocardial infarction. . ASHG 2003 2003.11

59. Tanaka T.. Genome-wide association study identifies functional SNPs in the lymphotoxin- gene as associated with susceptibility to myocardial infarction.. Mendel Symposium 2003.08

60. Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Functional SNPs in the lymphotoxin- gene that are associated with susceptibility to myocardial infarction. . 3rd World Congress on Heart Disease 2003.07

61. Tanaka T, Tsukada S, Iwai M, Nishiu J, Itoh M, Tomoike H, Horiuchi M, Nakamura Y. . Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor. . 3rd World Congress on Heart Disease 2003.07

62. Tanaka T.. SNP projects in Japan. . The 5th International Workshop on Advanced Genomics 2003.06

63. Ohnishi Y, Tanaka T, Ozaki K, Sekine A, Nakamura Y. . A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction. . ASHG 2002 2002.10

64. Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sekine A, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Genome-wide association study to identify genes related to myocardial infarction. . ASHG 2002 2002.10

65. Tanaka T.. SNP projects in Japan. . Osong International Symposium 2002.09

66. Tanaka T.. SNP projects in Japan. . Medical Genomics in Asia 2002.01

67. Inoue K, Tanaka T, Itoh M, Tomoike H, Yonekura K, Aoyagi T, Nagai R, Hori M, Nakamura Y.. Male-specific sudden cardiac death in mice with deficiency of a novel gene (OSR) related to ozidative stress resistance. . 第65回日本循環器学会・学術集会 2001.03

68. Yamada R, Tanaka T, Ohnishi Y, Yamamoto K, Nakamura Y. . An efficient SNP discovery procedure used in our association studies of rheumatoid arthritis. . ASHG 2000 2000.10

69. Ohnishi Y, Tanaka T, Yamada R, Hori M, Nakamura Y. . Systematic survey of SNPs (single nucleotide polymorphisms) in the candidate responsible genes for myocardial infarction in the Japanese population.. ASHG 2000 2000.10

70. Tanaka T, Ohnishi Y, Yamada R, Nakamura Y. . Large-scale SNP (single nucleotide polymorphism) discovery project in Japan. . ASHG 2000 2000.10

71. Tanaka T.. Microarray Analysis of Human Cancer; Toward Personalized Medicine.. Topic from Human Genome Project 2000.01

72. Ono K, Tanaka T, Kitahara O, Shiraishi N, Kihara C, Seki T, Yanagawa R, Ogasawara H, Okamoto T, Ohnishi Y, Kuzuya K, Tsunoda T, Takagi T, Nakamura Y.. Gene expression profiles of ovarian cancer using T7 based RNA amplification and cDNA microarray technology. . ASHG 1999 1999.10

73. Kihara C, Tanaka T, Furukawa Y, Ono K, Kitahara O, Shiraishi N, Yanagawa R, Ogasawara H, Seki T, Yamana H, Tsunoda T, Hirata K, Takagi T, Nakamura Y. . Gene expression profiles of esophageal cancer patients using cDNA microarray technology.. ASHG 1999 1999.10

74. Tanaka T, Ito T, Nagai R, Yazaki Y, Nakamura Y. . Mutational analysis of familiar long QT syndrome in Japan. . The 15th Annual Meeting of the Japanese Section 1998.12

75. Tanaka T, Itoh T, Nagai R, Yazaki Y, Nakamura Y. . Genomic organization of KVLQT1 and mutational analysis of familial long QT syndrome in Japan: further evidence for genotype/phenotype relationship. . ASHG 1998 1998.10

76. Tanaka T, Itoh T, Nagai R, Yazaki Y, Nakamura Y. . Mutational analysis of familial long QT syndrome; implication of correlation between mutated gene and response to beta-adrenergic blocking agent.. ASHG 1997 1997.10

77. Tanaka T, Nakamura Y. . Genetic analysis of long QT syndrome in Japan. . International Symposium on potassium ion channels; their molecular structure, function and diseases 1997.09

78. Tanaka T.. Genetic analysis of long QT syndrome in Japan. . International Symposium on potassium ion channels; their molecular structure, function and diseases. 1997.09

79. Tanaka T, Itoh M, Tsukada S, Orita T, Nishiu J, Tomoike H, Nakamura Y. . Isolation and characterization of novel genes related to endothelial proliferation by differential display method. . HUGO's Human Genome Meeting 1997.03

80. Tanaka T, Itoh M, Tsukada S, Orita T, Tomoike H, Nakamura Y. . Isolation of novel genes related to endothelial proliferation by differential mRNA display method.. ASHG 1996 1996.10

81. Tanaka T, Ogiwara A, Uchiyama I, Takagi T, Nakamura Y. . Construction of a normalized directionally-cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. . HGM 1996 1996.03

82. Tanaka T, Nakamura Y.. A large scale cDNA sequencing of a normalized directionally-cloned cDNA library from adult heart. . ASHG 1995 1995.10