Personnel Information

写真a

TANAKA Toshihiro


Job title

Professor

Laboratory Address

1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510 Japan

Laboratory Phone number

+81-35803-5230

Laboratory Fax number

+81-3-5803-5230

Mail Address

ttana.brc@tmd.ac.jp

Graduating School 【 display / non-display

  • The University of Tokyo, Faculty of Medicine, 1990.03, Graduated

Graduate School 【 display / non-display

  • The University of Tokyo, Graduate School, Division of Medical Sciences, Doctor's Course, 1996.03, Completed

Degree 【 display / non-display

  • MD, The University of Tokyo

Campus Career 【 display / non-display

  • 2013.04
    -
    2014.09
    Tokyo Medical and Dental University, Joint Institutes for Education and Research, Bioresource Research Center, Professor
  • 2013.04
    -
    2017.03
    Tokyo Medical and Dental University, Research and Industry-University Alliance Organization, Bioresource Research Center, Professor
  • 2013.04
    -
    Now
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Advanced Therapeutic Sciences, Human Genetics and Disease Diversity, Professor
  • 2014.10
    -
    2016.02
    Tokyo Medical and Dental University, Research and Industry-University Alliance Organization, Bioresource Research Center, Professor
  • 2017.04
     
     
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Professor
  • 2017.05
    -
    2020.05
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Professor
  • 2020.06
    -
    2020.09
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Professor
  • 2020.10
    -
    2021.03
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Professor
  • 2021.04
    -
    Now
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Professor
  • 2022.04
    -
    Now
    Tokyo Medical and Dental University, Institute of Research, Research Facility Cluster, Bioresource Research Center, Director

▼display all

Academic Society Affiliations 【 display / non-display

  • American Heart Association

  • American Society of Human Genetics

  • International Society for Heart Research

Research Areas 【 display / non-display

  • Cardiology

  • Genetics

 

Published Papers & Misc 【 display / non-display

  1. Takayuki Honda, Katsutoshi Seto, Satoshi Endo, Akira Takemoto, Kousuke Tanimoto, Masashi Kobayashi, Masatake Kitano, Rie Sakakibara, Takahiro Mitsumura, Hironori Ishibashi, Johji Inazawa, Toshihiro Tanaka, Yasunari Miyazaki, Kenichi Okubo. The possibility of mutations of RAS signaling genes and/or TP53 in combination as a negative prognostic impact on pathological stage I non-small cell lung cancer. Cancer Med. 2023.10; 12 (19): 19406-19413. ( PubMed, DOI )

  2. Tetsuo Sasano, Kensuke Ihara, Toshihiro Tanaka, Tetsushi Furukawa. Risk stratification of atrial fibrillation and stroke using single nucleotide polymorphism and circulating biomarkers. PLoS One. 2023.10; 18 (10): e0292118. ( PubMed, DOI )

  3. Mayumi Hangai, Takahisa Kawaguchi, Masatoshi Takagi, Keitaro Matsuo, Soyoung Jeon, Charleston W K Chiang, Andrew T Dewan, Adam J De Smith, Toshihiko Imamura, Yasuhiro Okamoto, Akiko M Saito, Takao Deguchi, Michiaki Kubo, Yoichi Tanaka, Yoko Ayukawa, Toshinari Hori, Kentaro Ohki, Nobutaka Kiyokawa, Takeshi Inukai, Yuki Arakawa, Makiko Mori, Daisuke Hasegawa, Daisuke Tomizawa, Hiroko Fukushima, Yuki Yuza, Yasushi Noguchi, Yuichi Taneyama, Setsuo Ota, Hiroaki Goto, Masakatsu Yanagimachi, Dai Keino, Kazutoshi Koike, Daisuke Toyama, Yozo Nakazawa, Kozue Nakamura, Koichi Moriwaki, Yujin Sekinaka, Daisuke Morita, Shinsuke Hirabayashi, Yosuke Hosoya, Yuri Yoshimoto, Hiroki Yoshihara, Miwa Ozawa, Shinobu Kobayashi, Naho Morisaki, Tshewang Gyeltshen, Osamu Takahashi, Yukinori Okada, Makiko Matsuda, Toshihiro Tanaka, Johji Inazawa, Junko Takita, Yasushi Ishida, Akira Ohara, Catherine Metayer, Joseph L Wiemels, Xiaomei Ma, Shuki Mizutani, Katsuyoshi Koh, Yukihide Momozawa, Keizo Horibe, Fumihiko Matsuda, Motohiro Kato, Atsushi Manabe, Kevin Y Urayama. Genome-wide assessment of genetic risk loci for childhood acute lymphoblastic leukemia in Japanese patients. Haematologica. 2023.10; ( PubMed, DOI )

  4. Kazunari Hara, Masanori Murakami, Yoshihiro Niitsu, Akira Takeuchi, Masato Horino, Kumiko Shiba, Kazutaka Tsujimoto, Chikara Komiya, Kenji Ikeda, Mika Tsuiki, Akiyo Tanabe, Toshihiro Tanaka, Minato Yokoyama, Yasuhisa Fujii, Mitsuhide Naruse, Tetsuya Yamada. Heterogeneous circulating miRNA profiles of PBMAH. Front Endocrinol (Lausanne). 2022.12; 13 1073328. ( PubMed, DOI )

  5. Yuki Nagata, Ryo Watanabe, Christian Eichhorn, Seiko Ohno, Takeshi Aiba, Taisuke Ishikawa, Yukiko Nakano, Yoshiyasu Aizawa, Kenshi Hayashi, Nobuyuki Murakoshi, Tadashi Nakajima, Nobue Yagihara, Hiroyuki Mishima, Takeaki Sudo, Chihiro Higuchi, Atsushi Takahashi, Akihiro Sekine, Takeru Makiyama, Yoshihiro Tanaka, Atsuyuki Watanabe, Motomi Tachibana, Hiroshi Morita, Koh-Ichiro Yoshiura, Tatsuhiko Tsunoda, Hiroshi Watanabe, Masahiko Kurabayashi, Akihiko Nogami, Yasuki Kihara, Minoru Horie, Wataru Shimizu, Naomasa Makita, Toshihiro Tanaka. Targeted deep sequencing analyses of long QT syndrome in a Japanese population. PLoS One. 2022.12; 17 (12): e0277242. ( PubMed, DOI )

  6. Yumi Inagaki, Takuya Ogawa, Makoto J Tabata, Yuki Nagata, Ryo Watanabe, Tatsuo Kawamoto, Keiji Moriyama, Toshihiro Tanaka. Correction to: Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population. J Hum Genet. 2022.04; 67 (4): 245. ( PubMed, DOI )

  7. Yuki Sagawa, Takuya Ogawa, Yusuke Matsuyama, Junka Nakagawa Kang, Miyu Yoshizawa Araki, Yuko Unnai Yasuda, Tsasan Tumurkhuu, Ganjargal Ganburged, Amarsaikhan Bazar, Toshihiro Tanaka, Takeo Fujiwara, Keiji Moriyama. Association between Smoking during Pregnancy and Short Root Anomaly in Offspring. Int J Environ Res Public Health. 2021.11; 18 (21): ( PubMed, DOI )

  8. Yumi Inagaki, Takuya Ogawa, Makoto J Tabata, Yuki Nagata, Ryo Watanabe, Tatsuo Kawamoto, Keiji Moriyama, Toshihiro Tanaka. Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population. J Hum Genet. 2021.08; 66 (8): 769-775. ( PubMed, DOI )

  9. Todd A Johnson, Yoichi Mashimo, Jer-Yuarn Wu, Dankyu Yoon, Akira Hata, Michiaki Kubo, Atsushi Takahashi, Tatsuhiko Tsunoda, Kouichi Ozaki, Toshihiro Tanaka, Kaoru Ito, Hiroyuki Suzuki, Hiromichi Hamada, Tohru Kobayashi, Toshiro Hara, Chien-Hsiun Chen, Yi-Ching Lee, Yi-Min Liu, Li-Ching Chang, Chun-Ping Chang, Young-Mi Hong, Gi-Young Jang, Sin-Weon Yun, Jeong-Jin Yu, Kyung-Yil Lee, Jae-Jung Kim, Taesung Park, , Jong-Keuk Lee, Yuan-Tsong Chen, Yoshihiro Onouchi. Association of an IGHV3-66 gene variant with Kawasaki disease. J Hum Genet. 2021.05; ( PubMed, DOI )

  10. Kazuyoshi Ishigaki, Masato Akiyama, Masahiro Kanai, Atsushi Takahashi, Eiryo Kawakami, Hiroki Sugishita, Saori Sakaue, Nana Matoba, Siew-Kee Low, Yukinori Okada, Chikashi Terao, Tiffany Amariuta, Steven Gazal, Yuta Kochi, Momoko Horikoshi, Ken Suzuki, Kaoru Ito, Satoshi Koyama, Kouichi Ozaki, Shumpei Niida, Yasushi Sakata, Yasuhiko Sakata, Takashi Kohno, Kouya Shiraishi, Yukihide Momozawa, Makoto Hirata, Koichi Matsuda, Masashi Ikeda, Nakao Iwata, Shiro Ikegawa, Ikuyo Kou, Toshihiro Tanaka, Hidewaki Nakagawa, Akari Suzuki, Tomomitsu Hirota, Mayumi Tamari, Kazuaki Chayama, Daiki Miki, Masaki Mori, Satoshi Nagayama, Yataro Daigo, Yoshio Miki, Toyomasa Katagiri, Osamu Ogawa, Wataru Obara, Hidemi Ito, Teruhiko Yoshida, Issei Imoto, Takashi Takahashi, Chizu Tanikawa, Takao Suzuki, Nobuaki Sinozaki, Shiro Minami, Hiroki Yamaguchi, Satoshi Asai, Yasuo Takahashi, Ken Yamaji, Kazuhisa Takahashi, Tomoaki Fujioka, Ryo Takata, Hideki Yanai, Akihide Masumoto, Yukihiro Koretsune, Hiromu Kutsumi, Masahiko Higashiyama, Shigeo Murayama, Naoko Minegishi, Kichiya Suzuki, Kozo Tanno, Atsushi Shimizu, Taiki Yamaji, Motoki Iwasaki, Norie Sawada, Hirokazu Uemura, Keitaro Tanaka, Mariko Naito, Makoto Sasaki, Kenji Wakai, Shoichiro Tsugane, Masayuki Yamamoto, Kazuhiko Yamamoto, Yoshinori Murakami, Yusuke Nakamura, Soumya Raychaudhuri, Johji Inazawa, Toshimasa Yamauchi, Takashi Kadowaki, Michiaki Kubo, Yoichiro Kamatani. Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Nat Genet. 2020.07; 52 (7): 669-679. ( PubMed, DOI )

  11. Yoshiki Higashijima, Yusuke Matsui, Teppei Shimamura, Ryo Nakaki, Nao Nagai, Shuichi Tsutsumi, Yohei Abe, Verena M Link, Mizuko Osaka, Masayuki Yoshida, Ryo Watanabe, Toshihiro Tanaka, Akashi Taguchi, Mai Miura, Xiaoan Ruan, Guoliang Li, Tsuyoshi Inoue, Masaomi Nangaku, Hiroshi Kimura, Tetsushi Furukawa, Hiroyuki Aburatani, Youichiro Wada, Yijun Ruan, Christopher K Glass, Yasuharu Kanki. Coordinated demethylation of H3K9 and H3K27 is required for rapid inflammatory responses of endothelial cells. EMBO J. 2020.04; 39 (7): e103949. ( PubMed, DOI )

  12. Kyaw Thiha, Yoichi Mashimo, Hiroyuki Suzuki, Hiromichi Hamada, Akira Hata, Toshiro Hara, Toshihiro Tanaka, Kaoru Ito, Yoshihiro Onouchi, . Correction to: Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease. J Hum Genet. 2019.10; 64 (10): 1049. ( PubMed, DOI )

  13. Yusuke Ebana, Yihan Sun, Xiaoxi Yang, Taiju Watanabe, Satoru Makita, Kouichi Ozaki, Toshihiro Tanaka, Hirokuni Arai, Tetsushi Furukawa. Pathway analysis with genome-wide association study (GWAS) data detected the association of atrial fibrillation with the mTOR signaling pathway. Int J Cardiol Heart Vasc. 2019.09; 24 100383. ( PubMed, DOI )

  14. Chisato Shimizu, Jihoon Kim, Hariklia Eleftherohorinou, Victoria J Wright, Long T Hoang, Adriana H Tremoulet, Alessandra Franco, Martin L Hibberd, Atsushi Takahashi, Michiaki Kubo, Kaoru Ito, Toshihiro Tanaka, Yoshihiro Onouchi, Lachlan J M Coin, Michael Levin, Jane C Burns, Hiroko Shike, . HLA-C variants associated with amino acid substitutions in the peptide binding groove influence susceptibility to Kawasaki disease. Hum. Immunol.. 2019.09; 80 (9): 731-738. ( PubMed, DOI )

  15. Yujiro Nakano, Takanobu Yoshimoto, Ryo Watanabe, Masanori Murakami, Tatsuya Fukuda, Kazutaka Saito, Yasuhisa Fujii, Takumi Akashi, Toshihiro Tanaka, Tetsuya Yamada, Mitsuhide Naruse, Yoshihiro Ogawa. miRNA299 involvement in CYP11B2 expression in aldosterone-producing adenoma. Eur. J. Endocrinol.. 2019.07; 181 (1): 69-78. ( PubMed, DOI )

  16. Kyaw Thiha, Yoichi Mashimo, Hiroyuki Suzuki, Hiromichi Hamada, Akira Hata, Toshiro Hara, Toshihiro Tanaka, Kaoru Ito, Yoshihiro Onouchi, . Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease. J. Hum. Genet.. 2019.06; 64 (6): 511-519. ( PubMed, DOI )

  17. Wataru Shimizu, Hisaki Makimoto, Kenichiro Yamagata, Tsukasa Kamakura, Mitsuru Wada, Koji Miyamoto, Yuko Inoue-Yamada, Hideo Okamura, Kohei Ishibashi, Takashi Noda, Satoshi Nagase, Aya Miyazaki, Heima Sakaguchi, Isao Shiraishi, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Hiroshi Watanabe, Kenshi Hayashi, Masakazu Yamagishi, Hiroshi Morita, Masao Yoshinaga, Yoshiyasu Aizawa, Kengo Kusano, Yoshihiro Miyamoto, Shiro Kamakura, Satoshi Yasuda, Hisao Ogawa, Toshihiro Tanaka, Naotaka Sumitomo, Nobuhisa Hagiwara, Keiichi Fukuda, Satoshi Ogawa, Yoshifusa Aizawa, Naomasa Makita, Tohru Ohe, Minoru Horie, Takeshi Aiba. Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients. JAMA Cardiol. 2019.03; 4 (3): 246-254. ( PubMed, DOI )

  18. El Rouby N, McDonough CW, Gong Y, McClure LA, Mitchell BD, Horenstein RB, Talbert RL, Crawford DC; eMERGE network, Gitzendanner MA, Takahashi A, Tanaka T, Kubo M, Pepine CJ, Cooper-DeHoff RM, Benavente OR, Shuldiner AR, Johnson JA.. Genome-wide association analysis of common genetic variants of resistant hypertension. Pharmacogenomics J. 2018.09; ( DOI )

  19. Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, Bis JC, Bloom HL, Boerwinkle E, Bottinger EB, Brody JA, Calkins H, Campbell A, Cappola TP, Carlquist J, Chasman DI, Chen LY, Chen YI, Choi EK, Choi SH, Christophersen IE, Chung MK, Cole JW, Conen D, Cook J, Crijns HJ, Cutler MJ, Damrauer SM, Daniels BR, Darbar D, Delgado G, Denny JC, Dichgans M, Dörr M, Dudink EA, Dudley SC, Esa N, Esko T, Eskola M, Fatkin D, Felix SB, Ford I, Franco OH, Geelhoed B, Grewal RP, Gudnason V, Guo X, Gupta N, Gustafsson S, Gutmann R, Hamsten A, Harris TB, Hayward C, Heckbert SR, Hernesniemi J, Hocking LJ, Hofman A, Horimoto ARVR, Huang J, Huang PL, Huffman J, Ingelsson E, Ipek EG, Ito K, Jimenez-Conde J, Johnson R, Jukema JW, Kääb S, Kähönen M, Kamatani Y, Kane JP, Kastrati A, Kathiresan S, Katschnig-Winter P, Kavousi M, Kessler T, Kietselaer BL, Kirchhof P, Kleber ME, Knight S, Krieger JE, Kubo M, Launer LJ, Laurikka J, Lehtimäki T, Leineweber K, Lemaitre RN, Li M, Lim HE, Lin HJ, Lin H, Lind L, Lindgren CM, Lokki ML, London B, Loos RJF, Low SK, Lu Y, Lyytikäinen LP, Macfarlane PW, Magnusson PK, Mahajan A, Malik R, Mansur AJ, Marcus GM, Margolin L, Margulies KB, März W, McManus DD5, Melander O, Mohanty S, Montgomery JA, Morley MP, Morris AP, Müller-Nurasyid M, Natale A, Nazarian S, Neumann B, Newton-Cheh C, Niemeijer MN, Nikus K, Nilsson P, Noordam R, Oellers H, Olesen MS, Orho-Melander M, Padmanabhan S, Pak HN, Paré G, Pedersen NL, Pera J, Pereira A, Porteous D, Psaty BM, Pulit SL, Pullinger CR, Rader DJ, Refsgaard L, Ribasés M, Ridker PM, Rienstra M, Risch L, Roden DM, Rosand J, Rosenberg MA, Rost N, Rotter JI, Saba S, Sandhu RK, Schnabel RB, Schramm K, Schunkert H, Schurman C, Scott SA, Seppälä I, Shaffer C, Shah S, Shalaby AA, Shim J, Shoemaker MB, Siland JE, Sinisalo J, Sinner MF, Slowik A, Smith AV, Smith BH, Smith JG, Smith JD, Smith NL, Soliman EZ, Sotoodehnia N, Stricker BH Sun A, Sun H, Svendsen JH, Tanaka T, Tanriverdi K, Taylor KD, Teder-Laving M, Teumer A, Thériault S, Trompet S Tucker NR, Tveit A, Uitterlinden AG, Van Der Harst P, Van Gelder IC, Van Wagoner DR, Verweij N, Vlachopoulou E, Völker U, Wang B, Weeke PE, Weijs B, Weiss R, Weiss S, Wells QS, Wiggins KL, Wong JA, Woo D, Worrall BB, Yang PS, Yao J, Yoneda ZT, Zeller T, Zeng L, Lubitz SA, Lunetta KL, Ellinor PT.. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018.09; 50 (9): 1225-1233. ( DOI )

  20. Hirata J, Hirota T, Ozeki T, Kanai M, Sudo T, Tanaka T, Hizawa N, Nakagawa H, Sato S, Mushiroda T, Saeki H, Tamari M, Okada Y.. Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese. J Invest Dermatol. 2018.03; 138 (3): 542-548. ( DOI )

  21. Urayama KY, Takagi M, Kawaguchi T, Matsuo K, Tanaka Y, Ayukawa Y, Arakawa Y, Hasegawa D, Yuza Y, Kaneko T, Noguchi Y, Taneyama Y, Ota S, Inukai T, Yanagimachi M, Keino D, Koike K, Toyama D, Nakazawa Y, Kurosawa H, Nakamura K, Moriwaki K, Goto H, Sekinaka Y, Morita D, Kato M, Takita J, Tanaka T, Inazawa J, Koh K, Ishida Y, Ohara A, Mizutani S, Matsuda F, Manabe A.. Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese. Sci Rep. 2018.01; 8 (1): 789. ( DOI )

  22. McCormack M, Gui H, Ingason A, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, Depondt C, Sills GJ, Marson AG, Auce P, Brodie MJ, Francis B, Johnson MR, Koeleman BPC, Striano P, Coppola A, Zara F, Kunz WS, Sander JW, Lerche H, Klein KM, Weckhuysen S, Krenn M, Gudmundsson LJ, Stefánsson K, Krause R, Shear N, Ross CJD, Delanty N; EPIGEN Consortium;, Pirmohamed M, Carleton BC; Canadian Pharmacogenomics Network for Drug Safety;, Cendes F, Lopes-Cendes I, Liao WP, O'Brien TJ, Sisodiya SM; EpiPGX Consortium;, Cherny S, Kwan P, Baum L; International League Against Epilepsy Consortium on Complex Epilepsies;, Cavalleri GL.. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology. . 2018.01; 90 (4): e332-e341. ( DOI )

  23. T Sudo, Y Okada, K Ozaki, K Urayama, M Kanai, H Kobayashi, M Gokyu, Y Izumi, T Tanaka. Association of NOD2 Mutations with Aggressive Periodontitis. J. Dent. Res.. 2017.06; 22034517715432. ( PubMed, DOI )

  24. Spracklen Cassandra N, Chen Peng, Kim Young Jin, Wang Xu, Cai Hui, Li Shengxu, Long Jirong, Wu Ying, Wang Ya Xing, Takeuchi Fumihiko, Wu Jer-Yuarn, Jung Keum-Ji, Hu Cheng, Akiyama Koichi, Zhang Yonghong, Moon Sanghoon, Johnson Todd A, Li Huaixing, Dorajoo Rajkumar, He Meian, Cannon Maren E, Roman Tamara S, Salfati Elias, Lin Keng-Hung, Guo Xiuqing, Sheu Wayne H H, Absher Devin, Adair Linda S, Assimes Themistocles L, Aung Tin, Cai Qiuyin, Chang Li-Ching, Chen Chien-Hsiun, Chien Li-Hsin, Chuang Lee-Ming, Chuang Shu-Chun, Du Shufa, Fan Qiao, Fann Cathy S J, Feranil Alan B, Friedlander Yechiel, Gordon-Larsen Penny, Gu Dongfeng, Gui Lixuan, Guo Zhirong, Heng Chew-Kiat, Hixson James, Hou Xuhong, Hsiung Chao Agnes, Hu Yao, Hwang Mi Yeong, Hwu Chii-Min, Isono Masato, Juang Jyh-Ming Jimmy, Khor Chiea-Chuen, Kim Yun Kyoung, Koh Woon-Puay, Kubo Michiaki, Lee I-Te, Lee Sun-Ju, Lee Wen-Jane, Liang Kae-Woei, Lim Blanche, Lim Sing-Hui, Liu Jianjun, Nabika Toru, Pan Wen-Harn, Peng Hao, Quertermous Thomas, Sabanayagam Charumathi, Sandow Kevin, Shi Jinxiu, Sun Liang, Tan Pok Chien, Tan Shu-Pei, Taylor Kent D, Teo Yik-Ying, Toh Sue-Anne, Tsunoda Tatsuhiko, van Dam Rob M, Wang Aili, Wang Feijie, Wang Jie, Wei Wen Bin, Xiang Yong-Bing, Yao Jie, Yuan Jian-Min, Zhang Rong, Zhao Wanting, Chen Yii-Der Ida, Rich Stephen S, Rotter Jerome I, Wang Tzung-Dau, Wu Tangchun, Lin Xu, Han Bok-Ghee, Tanaka Toshihiro, Cho Yoon Shin, Katsuya Tomohiro, Jia Weiping, Jee Sun-Ha, Chen Yuan-Tsong, Kato Norihiro, Jonas Jost B, Cheng Ching-Yu, Shu Xiao-Ou, He Jiang, Zheng Wei, Wong Tien-Yin, Huang Wei, Kim Bong-Jo, Tai E-Shyong, Mohlke Karen L, Sim Xueling. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Hum Mol Genet. 2017.05; 26 (9): 1770-1784. ( PubMed, DOI )

  25. Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihiro, AFGen Consortium. Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Nat Genet. 2017.04; ( PubMed, DOI )

  26. Christophersen Ingrid E, Rienstra Michiel, Roselli Carolina, Yin Xiaoyan, Geelhoed Bastiaan, Barnard John, Lin Honghuang, Arking Dan E, Smith Albert V, Albert Christine M, Chaffin Mark, Tucker Nathan R, Li Molong, Klarin Derek, Bihlmeyer Nathan A, Low Siew-Kee, Weeke Peter E, Muller-Nurasyid Martina, Smith J Gustav, Brody Jennifer A, Niemeijer Maartje N, Dorr Marcus, Trompet Stella, Huffman Jennifer, Gustafsson Stefan, Schurmann Claudia, Kleber Marcus E, Lyytikainen Leo-Pekka, Seppala Ilkka, Malik Rainer, Horimoto Andrea R V R, Perez Marco, Sinisalo Juha, Aeschbacher Stefanie, Theriault Sebastien, Yao Jie, Radmanesh Farid, Weiss Stefan, Teumer Alexander, Choi Seung Hoan, Weng Lu-Chen, Clauss Sebastian, Deo Rajat, Rader Daniel J, Shah Svati H, Sun Albert, Hopewell Jemma C, Debette Stephanie, Chauhan Ganesh, Yang Qiong, Worrall Bradford B, Pare Guillaume, Kamatani Yoichiro, Hagemeijer Yanick P, Verweij Niek, Siland Joylene E, Kubo Michiaki, Smith Jonathan D, Van Wagoner David R, Bis Joshua C, Perz Siegfried, Psaty Bruce M, Ridker Paul M, Magnani Jared W, Harris Tamara B, Launer Lenore J, Shoemaker M Benjamin, Padmanabhan Sandosh, Haessler Jeffrey, Bartz Traci M, Waldenberger Melanie, Lichtner Peter, Arendt Marina, Krieger Jose E, Kahonen Mika, Risch Lorenz, Mansur Alfredo J, Peters Annette, Smith Blair H, Lind Lars, Scott Stuart A, Lu Yingchang, Bottinger Erwin B, Hernesniemi Jussi, Lindgren Cecilia M, Wong Jorge A, Huang Jie, Eskola Markku, Morris Andrew P, Ford Ian, Reiner Alex P, Delgado Graciela, Chen Lin Y, Chen Yii-Der Ida, Sandhu Roopinder K, Li Man, Boerwinkle Eric, Eisele Lewin, Lannfelt Lars, Rost Natalia, Anderson Christopher D, Taylor Kent D, Campbell Archie, Magnusson Patrik K, Porteous David, Hocking Lynne J, Vlachopoulou Efthymia, Pedersen Nancy L, Nikus Kjell, Orho-Melander Marju, Hamsten Anders, Heeringa Jan, Denny Joshua C, Kriebel Jennifer, Darbar Dawood, Newton-Cheh Christopher, Shaffer Christian, Macfarlane Peter W, Heilmann-Heimbach Stefanie, Almgren Peter, Huang Paul L, Sotoodehnia Nona, Soliman Elsayed Z, Uitterlinden Andre G, Hofman Albert, Franco Oscar H, Volker Uwe, Jockel Karl-Heinz, Sinner Moritz F, Lin Henry J, Guo Xiuqing, Dichgans Martin, Ingelsson Erik, Kooperberg Charles, Melander Olle, Loos Ruth J F, Laurikka Jari, Conen David, Rosand Jonathan, van der Harst Pim, Lokki Marja-Liisa, Kathiresan Sekar, Pereira Alexandre, Jukema J Wouter, Hayward Caroline, Rotter Jerome I, Marz Winfried, Lehtimaki Terho, Stricker Bruno H, Chung Mina K, Felix Stephan B, Gudnason Vilmundur, Alonso Alvaro, Roden Dan M, Kaab Stefan, Chasman Daniel I, Heckbert Susan R, Benjamin Emelia J, Tanaka Toshihiro, Lunetta Kathryn L, Lubitz Steven A, Ellinor Patrick T, METASTROKE Consortium of the ISGC. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017.04; ( PubMed, DOI )

  27. Yamagata Kenichiro, Horie Minoru, Aiba Takeshi, Ogawa Satoshi, Aizawa Yoshifusa, Ohe Toru, Yamagishi Masakazu, Makita Naomasa, Sakurada Harumizu, Tanaka Toshihiro, Shimizu Akihiko, Hagiwara Nobuhisa, Kishi Ryoji, Nakano Yukiko, Takagi Masahiko, Makiyama Takeru, Ohno Seiko, Fukuda Keiichi, Watanabe Hiroshi, Morita Hiroshi, Hayashi Kenshi, Kusano Kengo, Kamakura Shiro, Yasuda Satoshi, Ogawa Hisao, Miyamoto Yoshihiro, Kapplinger Jamie D, Ackerman Michael J, Shimizu Wataru. Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands with Brugada Syndrome: A Japanese Multicenter Registry. Circulation. 2017.03; ( PubMed, DOI )

  28. Hirata Makoto, Nagai Akiko, Kamatani Yoichiro, Ninomiya Toshiharu, Tamakoshi Akiko, Yamagata Zentaro, Kubo Michiaki, Muto Kaori, Kiyohara Yutaka, Mushiroda Taisei, Murakami Yoshinori, Yuji Koichiro, Furukawa Yoichi, Zembutsu Hitoshi, Tanaka Toshihiro, Ohnishi Yozo, Nakamura Yusuke, Matsuda Koichi, BioBank Japan Cooperative Hospital Group. Overview of BioBank Japan follow-up data in 32 diseases. J Epidemiol. 2017.03; 27 (3S): S22-S28. ( PubMed, DOI )

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  145. Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T. Genetic variations in five genes involved in the excitement of cardiomyocytes. J Hum Genet. 2001; 46 (9): 549-552. ( PubMed, DOI )

  146. Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Suzuki H, Nakamura Y. A high-throughput SNP typing system for genome-wide association studies. J Hum Genet. 2001; 46 (8): 471-477. ( PubMed, DOI )

  147. Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T. Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome. J Hum Genet. 2001; 46 (1): 38-40. ( PubMed, DOI )

  148. Nakajima T, Kurabayashi M, Ohyama Y, Kaneko Y, Furukawa T, Itoh T, Taniguchi Y, Tanaka T, Nakamura Y, Hiraoka M, Nagai R. Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties. FEBS Lett. 2000.09; 481 (2): 197-203. ( PubMed )

  149. Ono K, Tanaka T, Tsunoda T, Kitahara O, Kihara C, Okamoto A, Ochiai K, Takagi T, Nakamura Y. Identification by cDNA microarray of genes involved in ovarian carcinogenesis. Cancer Res. 2000.09; 60 (18): 5007-5011. ( PubMed )

  150. Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000.04; 31 (4): 930-935. ( PubMed )

  151. Ohnishi Y, Tanaka T, Yamada R, Suematsu K, Minami M, Fujii K, Hoki N, Kodama K, Nagata S, Hayashi T, Kinoshita N, Sato H, Sato H, Kuzuya T, Takeda H, Hori M, Nakamura Y. Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population. Hum Genet. 2000.03; 106 (3): 288-292. ( PubMed )

  152. Yamada R, Tanaka T, Ohnishi Y, Suematsu K, Minami M, Seki T, Yukioka M, Maeda A, Murata N, Saiki O, Teshima R, Kudo O, Ishikawa K, Ueyosi A, Tateishi H, Inaba M, Goto H, Nishizawa Y, Tohma S, Ochi T, Yamamoto K, Nakamura Y. Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population. Hum Genet. 2000.03; 106 (3): 293-297. ( PubMed )

  153. Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T. Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population. J Hum Genet. 2000; 45 (3): 182-183. ( PubMed, DOI )

  154. Seki T, Tanaka T, Nakamura Y. Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene. J Hum Genet. 2000; 45 (5): 299-302. ( PubMed, DOI )

  155. Tsunoda T, Yamada R, Tanaka T, Ohnishi Y, Kamatani N. Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine. Genome Inform Ser Workshop Genome Inform. 2000; 11 96-105. ( PubMed )

  156. Kunishima S, Kojima T, Tanaka T, Kamiya T, Ozawa K, Nakamura Y, Saito H. Mapping of a gene for May-Hegglin anomaly to chromosome 22q. Hum Genet. 1999.11; 105 (5): 379-383. ( PubMed )

  157. Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M. Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2. Cardiovasc Res. 1999.11; 44 (2): 283-293. ( PubMed )

  158. Mikami M, Yasuda T, Terao A, Nakamura M, Ueno S, Tanabe H, Tanaka T, Onuma T, Goto Y, Kaneko S, Sano A. Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am J Hum Genet. 1999.09; 65 (3): 745-751. ( PubMed )

  159. Tsujikawa M, Kurahashi H, Tanaka T, Nishida K, Shimomura Y, Tano Y, Nakamura Y. Identification of the gene responsible for gelatinous drop-like corneal dystrophy. Nat Genet. 1999.04; 21 (4): 420-423. ( PubMed, DOI )

  160. Tsujikawa M, Kurahashi H, Tanaka T, Okada M, Yamamoto S, Maeda N, Watanabe H, Inoue Y, Kiridoshi A, Matsumoto K, Ohashi Y, Kinoshita S, Shimomura Y, Nakamura Y, Tano Y. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. Am J Hum Genet. 1998.10; 63 (4): 1073-1077. ( PubMed, DOI )

  161. Nishiu J, Tanaka T, Nakamura Y. Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3. Genomics. 1998.09; 52 (3): 378-381. ( PubMed, DOI )

  162. Itoh T, Tanaka T, Nagai R, Kikuchi K, Ogawa S, Okada S, Yamagata S, Yano K, Yazaki Y, Nakamura Y. Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome. Hum Genet. 1998.09; 103 (3): 290-294. ( PubMed )

  163. Nakajima T, Furukawa T, Tanaka T, Katayama Y, Nagai R, Nakamura Y, Hiraoka M. Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation. Circ Res. 1998.08; 83 (4): 415-422. ( PubMed )

  164. Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y. Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome. Hum Genet. 1998.04; 102 (4): 435-439. ( PubMed )

  165. Nishiu J, Tanaka T, Nakamura Y. Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method. Genomics. 1998.03; 48 (2): 254-257. ( PubMed, DOI )

  166. Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3. Hum Genet. 1998.02; 102 (2): 203-206. ( PubMed )

  167. Yamane-Tanaka Y, Kogawa K, Tanaka T, Nakamura Y, Isomura M. Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population. J Hum Genet. 1998; 43 (3): 165-168. ( PubMed, DOI )

  168. Itoh M, Tsukada S, Orita T, Nishiu J, Tomoike H, Nakamura Y, Tanaka T. Identification by differential display of eight known genes induced during in vivo intimal hyperplasia. J Hum Genet. 1998; 43 (1): 9-13. ( PubMed, DOI )

  169. Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y. Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation. 1997.02; 95 (3): 565-567. ( PubMed )

  170. Tanaka T, Ogiwara A, Uchiyama I, Takagi T, Yazaki Y, Nakamura Y. Construction of a normalized directionally cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. Genomics. 1996.07; 35 (1): 231-235. ( PubMed, DOI )

  171. Tanaka T, Inazawa J, Nakamura Y. Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1). Genomics. 1996.02; 32 (1): 128-130. ( PubMed, DOI )

  172. Tanaka T, Inazawa J, Nakamura Y. Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1. Cytogenet Cell Genet. 1996; 74 (1-2): 120-123. ( PubMed )

  173. Chatterjee A, Tanaka T, Parrish JE, Herman GE. Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mamm Genome. 1995.11; 6 (11): 802-804. ( PubMed )

  174. Tanaka T, Okui K, Nakamura Y. Assignment of the human caltractin gene (CALT) to Xq28 by fluorescence in situ hybridization. Genomics. 1994.12; 24 (3): 609-610. ( PubMed )

  175. Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M. Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families. Hum Genet. 1994.10; 94 (4): 380-384. ( PubMed )

▼display all

Books etc 【 display / non-display

  1. Ozaki K, and Tanaka T. Genes and Cardiovascular Function. 2011 Genetic Background of Myocardial Infarction

  2. Ozaki K, and Tanaka T. Methods in Molecular Medicine. 2006 Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction.

  3. Tanaka T, and Nakamura Y. Current Topics in Membranes. 1999 Mutational analysis of familial long QT syndrome in Japan

Conference Activities & Talks 【 display / non-display

  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. 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

  32. 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

  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

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  • Tanaka T. Chairs,2016.04

    Complex traits and polygenic disorders2.
    Concurrent Oral Session 20.
    ICHG2016