松田 文彦

最終更新日時: 2019/07/22 13:54:39

印刷する

氏名(漢字/フリガナ/アルファベット表記)
松田 文彦/マツダ フミヒコ/Matsuda, Fumihiko
所属部署・職名(部局/所属/講座等/職名)
医学研究科/医学研究科附属ゲノム医学センター/疾患ゲノム疫学/教授
学部兼担
部局 所属 講座等 職名
医学部
連絡先住所
種別 住所(日本語) 住所(英語)
職場 〒606-8507 京都市左京区聖護院川原町53 53 Shogoinkawahara-cho, Sakyo-ku, Kyoto 606-8507 Japan
取得学位
学位名(日本語) 学位名(英語) 大学(日本語) 大学(英語) 取得区分
医科学修士 大阪大学
医学博士 京都大学
出身大学院・研究科等
大学名(日本語) 大学名(英語) 研究科名(日本語) 研究科名(英語) 専攻名(日本語) 専攻名(英語) 修了区分
京都大学 大学院医学研究科博士課程生理系専攻 修了
大阪大学 大学院医学研究科医科学修士課程 修了
出身学校・専攻等
大学名(日本語) 大学名(英語) 学部名(日本語) 学部名(英語) 学科名(日本語) 学科名(英語) 卒業区分
京都大学 理学部 卒業
researchmap URL
https://researchmap.jp/read0012371
研究テーマ
(日本語)
多因子型疾患の遺伝因子の探索、大規模ゲノムコホートを用いたヒト生物学
(英語)
Human disease genomics, large scale genome cohort study
研究分野(キーワード)
キーワード(日本語) キーワード(英語)
ゲノム疫学 genomic epidemiology
ゲノムコホート genome cohort
疾患感受性遺伝子 disease susceptibility gene
ヒト生物学 human biology
オミックス解析 multiple omics analysis
論文
著者 著者(日本語) 著者(英語) タイトル タイトル(日本語) タイトル(英語) 書誌情報等 書誌情報等(日本語) 書誌情報等(英語) 出版年月 査読の有無 記述言語 掲載種別 公開
Kumagai, K., Tabara, Y., Yamashiro, K., Miyake, M., Akagi-Kurashige, Y., Oishi, M., Yoshikawa, M., Kimura, Y., Tsujikawa, A., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T., Matsuda, F. and Yoshimura, N.; on behalf of the Nagahama Study group. Kumagai, K., Tabara, Y., Yamashiro, K., Miyake, M., Akagi-Kurashige, Y., Oishi, M., Yoshikawa, M., Kimura, Y., Tsujikawa, A., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T., Matsuda, F. and Yoshimura, N.; on behalf of the Nagahama Study group. Kumagai, K., Tabara, Y., Yamashiro, K., Miyake, M., Akagi-Kurashige, Y., Oishi, M., Yoshikawa, M., Kimura, Y., Tsujikawa, A., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T., Matsuda, F. and Yoshimura, N.; on behalf of the Nagahama Study group. Central blood pressure relates more strongly to retinal arteriolar narrowing than brachial blood pressure: the Nagahama Study. Central blood pressure relates more strongly to retinal arteriolar narrowing than brachial blood pressure: the Nagahama Study. Central blood pressure relates more strongly to retinal arteriolar narrowing than brachial blood pressure: the Nagahama Study. J. Hypertens., 33, 323-329 J. Hypertens., 33, 323-329 J. Hypertens., 33, 323-329 2015 英語 研究論文(学術雑誌) 公開
Tabara, Y., Okada, Y., Ohara, M., Uetani, E., Kido, T., Ochi, N., Nagai, T., Igase, M., Miki, T., Matsuda, F. and Kohara, K. Tabara, Y., Okada, Y., Ohara, M., Uetani, E., Kido, T., Ochi, N., Nagai, T., Igase, M., Miki, T., Matsuda, F. and Kohara, K. Tabara, Y., Okada, Y., Ohara, M., Uetani, E., Kido, T., Ochi, N., Nagai, T., Igase, M., Miki, T., Matsuda, F. and Kohara, K. Association of postural instability with asymptomatic cerebrovascular damage and cognitive decline: the Japan shimanami health promoting program study. Association of postural instability with asymptomatic cerebrovascular damage and cognitive decline: the Japan shimanami health promoting program study. Association of postural instability with asymptomatic cerebrovascular damage and cognitive decline: the Japan shimanami health promoting program study. Stroke, 46, 16-22 Stroke, 46, 16-22 Stroke, 46, 16-22 2015 英語 研究論文(学術雑誌) 公開
Miyake, M., Yamashiro, K., Tabara, Y., Suda, K., Morooka, S., Nakanishi, H., Khor, C. C., Chen, P., Qiao, F., Nakata, I., Akagi-Kurashige, Y., Gotoh, N., Tsujikawa, A., Meguro, A., Kusuhara, S., Polasek, O., Hayward, C., Wright, A. F., Campbell, H., Richardson, A. J., Schache, M., Takeuchi, M., Mackey, D. A., Hewitt, A. W., Cuellar, G., Shi, Y., Huang, L., Yang, Z., Leung, K. H., Kao, P. Y., Yap, M. K., Yip, S. P., Moriyama, M., Ohno-Matsui, K., Mizuki, N., MacGregor, S., Vitart, V., Aung, T., Saw, S. M., Tai, E. S., Wong, T. Y., Cheng, C. Y., Baird, P. N., Yamada, R., Matsuda, F; Nagahama Study Group and Yoshimura, N. Miyake, M., Yamashiro, K., Tabara, Y., Suda, K., Morooka, S., Nakanishi, H., Khor, C. C., Chen, P., Qiao, F., Nakata, I., Akagi-Kurashige, Y., Gotoh, N., Tsujikawa, A., Meguro, A., Kusuhara, S., Polasek, O., Hayward, C., Wright, A. F., Campbell, H., Richardson, A. J., Schache, M., Takeuchi, M., Mackey, D. A., Hewitt, A. W., Cuellar, G., Shi, Y., Huang, L., Yang, Z., Leung, K. H., Kao, P. Y., Yap, M. K., Yip, S. P., Moriyama, M., Ohno-Matsui, K., Mizuki, N., MacGregor, S., Vitart, V., Aung, T., Saw, S. M., Tai, E. S., Wong, T. Y., Cheng, C. Y., Baird, P. N., Yamada, R., Matsuda, F; Nagahama Study Group and Yoshimura, N. Miyake, M., Yamashiro, K., Tabara, Y., Suda, K., Morooka, S., Nakanishi, H., Khor, C. C., Chen, P., Qiao, F., Nakata, I., Akagi-Kurashige, Y., Gotoh, N., Tsujikawa, A., Meguro, A., Kusuhara, S., Polasek, O., Hayward, C., Wright, A. F., Campbell, H., Richardson, A. J., Schache, M., Takeuchi, M., Mackey, D. A., Hewitt, A. W., Cuellar, G., Shi, Y., Huang, L., Yang, Z., Leung, K. H., Kao, P. Y., Yap, M. K., Yip, S. P., Moriyama, M., Ohno-Matsui, K., Mizuki, N., MacGregor, S., Vitart, V., Aung, T., Saw, S. M., Tai, E. S., Wong, T. Y., Cheng, C. Y., Baird, P. N., Yamada, R., Matsuda, F; Nagahama Study Group and Yoshimura, N. Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Nat. Commun., 6, 6689 Nat. Commun., 6, 6689 Nat. Commun., 6, 6689 2015 英語 研究論文(学術雑誌) 公開
Sonomura, K., Kudoh, S., Sato, T.A. and Matsuda, F. Sonomura, K., Kudoh, S., Sato, T.A. and Matsuda, F. Sonomura, K., Kudoh, S., Sato, T.A. and Matsuda, F. Plasma lipid analysis by hydrophilic interaction liquid chromatography coupled with electrospray ionization tandem mass spectrometry. Plasma lipid analysis by hydrophilic interaction liquid chromatography coupled with electrospray ionization tandem mass spectrometry. Plasma lipid analysis by hydrophilic interaction liquid chromatography coupled with electrospray ionization tandem mass spectrometry. J. Sep. Sci. Apr 3. doi: 10.1002/jssc.201401440. [Epub ahead of print] J. Sep. Sci. Apr 3. doi: 10.1002/jssc.201401440. [Epub ahead of print] J. Sep. Sci. Apr 3. doi: 10.1002/jssc.201401440. [Epub ahead of print] 2015 英語 研究論文(学術雑誌) 公開
Terao, C, Ohmura, K., Kochi, Y., Ikari, K., Okada, Y., Shimizu, M., Nishina, N., Suzuki, A., Myouzen, K., Kawaguchi, T., Takahashi, M., Takasugi, K., Murasawa, A., Mizuki, S., Iwahashi, M., Funahashi, K., Natsumeda, M., Furu, M., Hashimoto, M., Ito, H., Fujii, T., Ezawa, K., Matsubara, T., Takeuchi, T., Kubo, M., Yamada, R., Taniguchi, A., Yamanaka, H., Momohara, S., Yamamoto, K., Mimori, T., and Matsuda, F. Terao, C, Ohmura, K., Kochi, Y., Ikari, K., Okada, Y., Shimizu, M., Nishina, N., Suzuki, A., Myouzen, K., Kawaguchi, T., Takahashi, M., Takasugi, K., Murasawa, A., Mizuki, S., Iwahashi, M., Funahashi, K., Natsumeda, M., Furu, M., Hashimoto, M., Ito, H., Fujii, T., Ezawa, K., Matsubara, T., Takeuchi, T., Kubo, M., Yamada, R., Taniguchi, A., Yamanaka, H., Momohara, S., Yamamoto, K., Mimori, T., and Matsuda, F. Terao, C, Ohmura, K., Kochi, Y., Ikari, K., Okada, Y., Shimizu, M., Nishina, N., Suzuki, A., Myouzen, K., Kawaguchi, T., Takahashi, M., Takasugi, K., Murasawa, A., Mizuki, S., Iwahashi, M., Funahashi, K., Natsumeda, M., Furu, M., Hashimoto, M., Ito, H., Fujii, T., Ezawa, K., Matsubara, T., Takeuchi, T., Kubo, M., Yamada, R., Taniguchi, A., Yamanaka, H., Momohara, S., Yamamoto, K., Mimori, T., and Matsuda, F. Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. Arthritis. Res. Ther. 17, 104. doi: 10.1186/s13075-015-0623-4. Arthritis. Res. Ther. 17, 104. doi: 10.1186/s13075-015-0623-4. Arthritis. Res. Ther. 17, 104. doi: 10.1186/s13075-015-0623-4. 2015 英語 研究論文(学術雑誌) 公開
Tabara, Y., Takahashi, Y., Kawaguchi, T., Setoh, K., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T. and Matsuda, F.; on behalf of the Nagahama Study Group. Tabara, Y., Takahashi, Y., Kawaguchi, T., Setoh, K., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T. and Matsuda, F.; on behalf of the Nagahama Study Group. Tabara, Y., Takahashi, Y., Kawaguchi, T., Setoh, K., Terao, C., Yamada, R., Kosugi, S., Sekine, A., Nakayama, T. and Matsuda, F.; on behalf of the Nagahama Study Group. Association of Serum-Free Fatty Acid Level With Reduced Reflection Pressure Wave Magnitude and Central Blood Pressure: The Nagahama Study. Association of Serum-Free Fatty Acid Level With Reduced Reflection Pressure Wave Magnitude and Central Blood Pressure: The Nagahama Study. Association of Serum-Free Fatty Acid Level With Reduced Reflection Pressure Wave Magnitude and Central Blood Pressure: The Nagahama Study. Hypertension, 64, 1212-1218 Hypertension, 64, 1212-1218 Hypertension, 64, 1212-1218 2014 英語 研究論文(学術雑誌) 公開
Oishi, M., Oishi, A., Gotoh, N., Ogino, K., Higasa, K., Iida, K., Makiyama, Y., Morooka, S., Matsuda, F. and Yoshimura, N. Oishi, M., Oishi, A., Gotoh, N., Ogino, K., Higasa, K., Iida, K., Makiyama, Y., Morooka, S., Matsuda, F. and Yoshimura, N. Oishi, M., Oishi, A., Gotoh, N., Ogino, K., Higasa, K., Iida, K., Makiyama, Y., Morooka, S., Matsuda, F. and Yoshimura, N. Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing. Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing. Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing. Invest. Ophthalmol. Vis. Sci., 55, 7369-7375 Invest. Ophthalmol. Vis. Sci., 55, 7369-7375 Invest. Ophthalmol. Vis. Sci., 55, 7369-7375 2014 英語 研究論文(学術雑誌) 公開
Murase, K., Tabara, Y., Takahashi, Y., Muro, S., Yamada, R., Setoh, K., Kawaguchi, T., Kadotani, H., Kosugi, S., Sekine, A., Nakayama, T., Mishima, M., Chiba, T., Chin, K. and Matsuda, F. Murase, K., Tabara, Y., Takahashi, Y., Muro, S., Yamada, R., Setoh, K., Kawaguchi, T., Kadotani, H., Kosugi, S., Sekine, A., Nakayama, T., Mishima, M., Chiba, T., Chin, K. and Matsuda, F. Murase, K., Tabara, Y., Takahashi, Y., Muro, S., Yamada, R., Setoh, K., Kawaguchi, T., Kadotani, H., Kosugi, S., Sekine, A., Nakayama, T., Mishima, M., Chiba, T., Chin, K. and Matsuda, F. Gastroesophageal Reflux Disease Symptoms and Dietary Behaviors are Significant Correlates of Short Sleep Duration in the General Population: The Nagahama Study. Gastroesophageal Reflux Disease Symptoms and Dietary Behaviors are Significant Correlates of Short Sleep Duration in the General Population: The Nagahama Study. Gastroesophageal Reflux Disease Symptoms and Dietary Behaviors are Significant Correlates of Short Sleep Duration in the General Population: The Nagahama Study. Sleep, 37, 1809-1815 Sleep, 37, 1809-1815 Sleep, 37, 1809-1815 2014 英語 研究論文(学術雑誌) 公開
Tabara, Y., Muro, S., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Kosugi, S., Sekine, A., Yamada, R., Nakayama, T., Mishima, M. and Matsuda F.; Nagahama Study Group Tabara, Y., Muro, S., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Kosugi, S., Sekine, A., Yamada, R., Nakayama, T., Mishima, M. and Matsuda F.; Nagahama Study Group Tabara, Y., Muro, S., Takahashi, Y., Setoh, K., Kawaguchi, T., Terao, C., Kosugi, S., Sekine, A., Yamada, R., Nakayama, T., Mishima, M. and Matsuda F.; Nagahama Study Group Airflow limitation in smokers is associated with arterial stiffness: The Nagahama Study. Airflow limitation in smokers is associated with arterial stiffness: The Nagahama Study. Airflow limitation in smokers is associated with arterial stiffness: The Nagahama Study. Atherosclerosis, 232, 59-64 Atherosclerosis, 232, 59-64 Atherosclerosis, 232, 59-64 2014 英語 研究論文(学術雑誌) 公開
Okada, Y., Wu, D., Trynka, G., Raj, T., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Yoshida, S., Graham, R. R., Manoharan, A., Ortmann, W., Bhangale, T., Denny, J. C., Carroll, R. J., Eyler, A. E., Greenberg, J. D., Kremer, J. M., Pappas, D. A., Jiang, L., Yin, J., Ye, L., Su, D. F., Yang, J., Xie, G., Keystone, E., Westra, H. J., Esko, T., Metspalu, A., Zhou, X., Gupta, N., Mirel, D., Stahl, E. A., Diogo, D., Cui, J., Liao, K., Guo, M. H., Myouzen, K., Kawaguchi, T., Coenen, M. J. H., van Riel, P. L. C. M., van de Laar, M. A. F. J., Guchelaar, H. J., Huizinga, T. W. J., Dieude, P., Mariette, X., Bridges Jr, S. L., Zhernakova, A., Toes, R. E. M., Tak, P. P., Miceli-Richard, C., Bang, S. Y., Lee, H. S., Martin, J., Gonzalez-Gay, M. A., Rodriguez-RodriguezL., Rantapaa-Dahlqvist, S., Arlestig, L., Choi, H. K., Kamatani, Y., Galan, P., Lathrop, M., the RACI consortium, the GARNET consortium, Eyre, S., Bowes, J., Barton, A., de Vries, N., Moreland, L. W., Criswell, L. A., Karlson, E. W., Taniguchi, A., Yamada, R., Kubo, M., Liu, J. S., Bae, S. C., Worthington, J., Padyukov, L., Klareskog, L., Gregersen, P. K., Raychaudhuri, S., Stranger, B. E., De Jager, P. L., Franke, L., Visscher, P. M., Brown, M. A., Yamanaka, H., Mimori, T., Takahashi, A., Xu, H., Behrens, T. W., Siminovitch, K. A., Momohara, S., Matsuda, F., Yamamoto, K. and Plenge, R. M. Okada, Y., Wu, D., Trynka, G., Raj, T., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Yoshida, S., Graham, R. R., Manoharan, A., Ortmann, W., Bhangale, T., Denny, J. C., Carroll, R. J., Eyler, A. E., Greenberg, J. D., Kremer, J. M., Pappas, D. A., Jiang, L., Yin, J., Ye, L., Su, D. F., Yang, J., Xie, G., Keystone, E., Westra, H. J., Esko, T., Metspalu, A., Zhou, X., Gupta, N., Mirel, D., Stahl, E. A., Diogo, D., Cui, J., Liao, K., Guo, M. H., Myouzen, K., Kawaguchi, T., Coenen, M. J. H., van Riel, P. L. C. M., van de Laar, M. A. F. J., Guchelaar, H. J., Huizinga, T. W. J., Dieude, P., Mariette, X., Bridges Jr, S. L., Zhernakova, A., Toes, R. E. M., Tak, P. P., Miceli-Richard, C., Bang, S. Y., Lee, H. S., Martin, J., Gonzalez-Gay, M. A., Rodriguez-RodriguezL., Rantapaa-Dahlqvist, S., Arlestig, L., Choi, H. K., Kamatani, Y., Galan, P., Lathrop, M., the RACI consortium, the GARNET consortium, Eyre, S., Bowes, J., Barton, A., de Vries, N., Moreland, L. W., Criswell, L. A., Karlson, E. W., Taniguchi, A., Yamada, R., Kubo, M., Liu, J. S., Bae, S. C., Worthington, J., Padyukov, L., Klareskog, L., Gregersen, P. K., Raychaudhuri, S., Stranger, B. E., De Jager, P. L., Franke, L., Visscher, P. M., Brown, M. A., Yamanaka, H., Mimori, T., Takahashi, A., Xu, H., Behrens, T. W., Siminovitch, K. A., Momohara, S., Matsuda, F., Yamamoto, K. and Plenge, R. M. Okada, Y., Wu, D., Trynka, G., Raj, T., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Yoshida, S., Graham, R. R., Manoharan, A., Ortmann, W., Bhangale, T., Denny, J. C., Carroll, R. J., Eyler, A. E., Greenberg, J. D., Kremer, J. M., Pappas, D. A., Jiang, L., Yin, J., Ye, L., Su, D. F., Yang, J., Xie, G., Keystone, E., Westra, H. J., Esko, T., Metspalu, A., Zhou, X., Gupta, N., Mirel, D., Stahl, E. A., Diogo, D., Cui, J., Liao, K., Guo, M. H., Myouzen, K., Kawaguchi, T., Coenen, M. J. H., van Riel, P. L. C. M., van de Laar, M. A. F. J., Guchelaar, H. J., Huizinga, T. W. J., Dieude, P., Mariette, X., Bridges Jr, S. L., Zhernakova, A., Toes, R. E. M., Tak, P. P., Miceli-Richard, C., Bang, S. Y., Lee, H. S., Martin, J., Gonzalez-Gay, M. A., Rodriguez-RodriguezL., Rantapaa-Dahlqvist, S., Arlestig, L., Choi, H. K., Kamatani, Y., Galan, P., Lathrop, M., the RACI consortium, the GARNET consortium, Eyre, S., Bowes, J., Barton, A., de Vries, N., Moreland, L. W., Criswell, L. A., Karlson, E. W., Taniguchi, A., Yamada, R., Kubo, M., Liu, J. S., Bae, S. C., Worthington, J., Padyukov, L., Klareskog, L., Gregersen, P. K., Raychaudhuri, S., Stranger, B. E., De Jager, P. L., Franke, L., Visscher, P. M., Brown, M. A., Yamanaka, H., Mimori, T., Takahashi, A., Xu, H., Behrens, T. W., Siminovitch, K. A., Momohara, S., Matsuda, F., Yamamoto, K. and Plenge, R. M. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature, 506, 376-381 Nature, 506, 376-381 Nature, 506, 376-381 2014 英語 研究論文(学術雑誌) 公開
Segawa, K., Kurata, S., Yanagihashi, Y., Brummelkamp, T. R., Matsuda, F. and Nagata, S. Segawa, K., Kurata, S., Yanagihashi, Y., Brummelkamp, T. R., Matsuda, F. and Nagata, S. Segawa, K., Kurata, S., Yanagihashi, Y., Brummelkamp, T. R., Matsuda, F. and Nagata, S. Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure. Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure. Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure. Science, 344, 1164-1168 Science, 344, 1164-1168 Science, 344, 1164-1168 2014 英語 研究論文(学術雑誌) 公開
Terao, C., Terada, N., Matsuo, K., Kawaguchi, T., Yoshimura, K., Hayashi, N., Shimizu, M., Soga, N., Takahashi, M.; Nagahama Cohort Study Group, Kotoura, Y., Yamada, R., Ogawa, O. and Matsuda, F. Terao, C., Terada, N., Matsuo, K., Kawaguchi, T., Yoshimura, K., Hayashi, N., Shimizu, M., Soga, N., Takahashi, M.; Nagahama Cohort Study Group, Kotoura, Y., Yamada, R., Ogawa, O. and Matsuda, F. Terao, C., Terada, N., Matsuo, K., Kawaguchi, T., Yoshimura, K., Hayashi, N., Shimizu, M., Soga, N., Takahashi, M.; Nagahama Cohort Study Group, Kotoura, Y., Yamada, R., Ogawa, O. and Matsuda, F. A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population. A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population. A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population. J. Med. Genet., 51, 530-536 J. Med. Genet., 51, 530-536 J. Med. Genet., 51, 530-536 2014 英語 研究論文(学術雑誌) 公開
Narahara, M., Higasa, K., Nakamura, S., Tabara, Y., Kawaguchi, T., Ishii, M., Matsubara, K., Matsuda, F. and Yamada, R. Narahara, M., Higasa, K., Nakamura, S., Tabara, Y., Kawaguchi, T., Ishii, M., Matsubara, K., Matsuda, F. and Yamada, R. Narahara, M., Higasa, K., Nakamura, S., Tabara, Y., Kawaguchi, T., Ishii, M., Matsubara, K., Matsuda, F. and Yamada, R. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. PLoS One, 9, e100924 PLoS One, 9, e100924 PLoS One, 9, e100924 2014 英語 研究論文(学術雑誌) 公開
Hong, K. W., Lim, J. E., Kim, J. W., Tabara, Y., Ueshima, H., Miki, T., Matsuda, F., Cho, Y. S., Kim, Y. and Oh, B. Hong, K. W., Lim, J. E., Kim, J. W., Tabara, Y., Ueshima, H., Miki, T., Matsuda, F., Cho, Y. S., Kim, Y. and Oh, B. Hong, K. W., Lim, J. E., Kim, J. W., Tabara, Y., Ueshima, H., Miki, T., Matsuda, F., Cho, Y. S., Kim, Y. and Oh, B. Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. Hum. Mol. Genet., 23, 6659-6667 Hum. Mol. Genet., 23, 6659-6667 Hum. Mol. Genet., 23, 6659-6667 2014 英語 研究論文(学術雑誌) 公開
Terao, C., Ohmura, K., Yamada, R., Kawaguchi, T., Shimizu, M., Tabara, Y., Takahashi, M., Setoh, K., Nakayama, T., Kosugi, S., Sekine, A., Matsuda, F. and Mimori, T.; on behalf of the Nagahama Study Group. Terao, C., Ohmura, K., Yamada, R., Kawaguchi, T., Shimizu, M., Tabara, Y., Takahashi, M., Setoh, K., Nakayama, T., Kosugi, S., Sekine, A., Matsuda, F. and Mimori, T.; on behalf of the Nagahama Study Group. Terao, C., Ohmura, K., Yamada, R., Kawaguchi, T., Shimizu, M., Tabara, Y., Takahashi, M., Setoh, K., Nakayama, T., Kosugi, S., Sekine, A., Matsuda, F. and Mimori, T.; on behalf of the Nagahama Study Group. An association between anti-nuclear antibody and HLA class II locus and heterogeneous characteristics of staining patterns: The Nagahama Study. An association between anti-nuclear antibody and HLA class II locus and heterogeneous characteristics of staining patterns: The Nagahama Study. An association between anti-nuclear antibody and HLA class II locus and heterogeneous characteristics of staining patterns: The Nagahama Study. Arthritis. Rheumatol., 66, 3395-3403 Arthritis. Rheumatol., 66, 3395-3403 Arthritis. Rheumatol., 66, 3395-3403 2014 英語 研究論文(学術雑誌) 公開
Yoshimura, K., Nakayama, T., Sekine, A., Matsuda, F., Kosugi, S., Sugino, Y., Yoshimura, K. and Ogawa, O. Nagahama Cohort Research Group. Yoshimura, K., Nakayama, T., Sekine, A., Matsuda, F., Kosugi, S., Sugino, Y., Yoshimura, K. and Ogawa, O. Nagahama Cohort Research Group. Yoshimura, K., Nakayama, T., Sekine, A., Matsuda, F., Kosugi, S., Sugino, Y., Yoshimura, K. and Ogawa, O. Nagahama Cohort Research Group. Prevalence of postmicturition urinary incontinence in Japanese men: Comparison with other types of incontinence. Prevalence of postmicturition urinary incontinence in Japanese men: Comparison with other types of incontinence. Prevalence of postmicturition urinary incontinence in Japanese men: Comparison with other types of incontinence. Int. J. Urol., 20, 911-916 Int. J. Urol., 20, 911-916 Int. J. Urol., 20, 911-916 2013 英語 研究論文(学術雑誌) 公開
Wakai, K., Matsuo, K., Matsuda, F., Yamada, R., Takahashi, M., Kawaguchi, T., Yatabe, Y., Ito, H., Hosono, S., Tajima, K., Naito, M., Morita, E., Yin, G., Sakamoto, T., Takashima, N., Suzuki, S., Nakahata, N., Mikami, H., Ohnaka, K., Watanabe, Y., Arisawa, K., Kubo, M., Hamajima, N. and Tanaka, H. the J-MICC Study Group. Wakai, K., Matsuo, K., Matsuda, F., Yamada, R., Takahashi, M., Kawaguchi, T., Yatabe, Y., Ito, H., Hosono, S., Tajima, K., Naito, M., Morita, E., Yin, G., Sakamoto, T., Takashima, N., Suzuki, S., Nakahata, N., Mikami, H., Ohnaka, K., Watanabe, Y., Arisawa, K., Kubo, M., Hamajima, N. and Tanaka, H. the J-MICC Study Group. Wakai, K., Matsuo, K., Matsuda, F., Yamada, R., Takahashi, M., Kawaguchi, T., Yatabe, Y., Ito, H., Hosono, S., Tajima, K., Naito, M., Morita, E., Yin, G., Sakamoto, T., Takashima, N., Suzuki, S., Nakahata, N., Mikami, H., Ohnaka, K., Watanabe, Y., Arisawa, K., Kubo, M., Hamajima, N. and Tanaka, H. the J-MICC Study Group. Genome-wide association study of the genetic factors related to confectionery intake: Potential roles of the ADIPOQ gene. Genome-wide association study of the genetic factors related to confectionery intake: Potential roles of the ADIPOQ gene. Genome-wide association study of the genetic factors related to confectionery intake: Potential roles of the ADIPOQ gene. Obesity, 21, 2413-2419 Obesity, 21, 2413-2419 Obesity, 21, 2413-2419 2013 英語 研究論文(学術雑誌) 公開
Tabara, Y., Takahashi, Y., Kohara, K., Setoh, K., Kawaguchi, T., Terao, C., Igase, M., Yamada, R., Kosugi, S., Sekine, A., Miki, T., Nakayama, T. and Matsuda, F. on behalf of the Nagahama Study Group. Tabara, Y., Takahashi, Y., Kohara, K., Setoh, K., Kawaguchi, T., Terao, C., Igase, M., Yamada, R., Kosugi, S., Sekine, A., Miki, T., Nakayama, T. and Matsuda, F. on behalf of the Nagahama Study Group. Tabara, Y., Takahashi, Y., Kohara, K., Setoh, K., Kawaguchi, T., Terao, C., Igase, M., Yamada, R., Kosugi, S., Sekine, A., Miki, T., Nakayama, T. and Matsuda, F. on behalf of the Nagahama Study Group. Association of longer QT interval with arterial waveform and lower pulse pressure amplification: The Nagahama Study. Association of longer QT interval with arterial waveform and lower pulse pressure amplification: The Nagahama Study. Association of longer QT interval with arterial waveform and lower pulse pressure amplification: The Nagahama Study. Am. J. Hypertens., 26, 973-980 Am. J. Hypertens., 26, 973-980 Am. J. Hypertens., 26, 973-980 2013 英語 研究論文(学術雑誌) 公開
Plenge, R. M., Greenberg, J. D., Mangravite, L. M., Derry, J. M., Stahl, E. A., Coenen, M. J., Barton, A., Padyukov, L., Klareskog, L., Gregersen, P. K., Mariette, X., Moreland, L. W., Bridges, S. L. Jr, de Vries, N. Huizinga, T. W. Guchelaar, H. J., International Rheumatoid Arthritis Consortium (INTERACT), Friend, S. H. and Stolovitzky, G. Plenge, R. M., Greenberg, J. D., Mangravite, L. M., Derry, J. M., Stahl, E. A., Coenen, M. J., Barton, A., Padyukov, L., Klareskog, L., Gregersen, P. K., Mariette, X., Moreland, L. W., Bridges, S. L. Jr, de Vries, N. Huizinga, T. W. Guchelaar, H. J., International Rheumatoid Arthritis Consortium (INTERACT), Friend, S. H. and Stolovitzky, G. Plenge, R. M., Greenberg, J. D., Mangravite, L. M., Derry, J. M., Stahl, E. A., Coenen, M. J., Barton, A., Padyukov, L., Klareskog, L., Gregersen, P. K., Mariette, X., Moreland, L. W., Bridges, S. L. Jr, de Vries, N. Huizinga, T. W. Guchelaar, H. J., International Rheumatoid Arthritis Consortium (INTERACT), Friend, S. H. and Stolovitzky, G. Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge. Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge. Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge. Nat. Genet., 45, 468-469 Nat. Genet., 45, 468-469 Nat. Genet., 45, 468-469 2013 英語 研究論文(学術雑誌) 公開
Yamazaki, T., Yamori, M., Asai, K., Nakano-Araki, I., Yamaguchi, A., Takahashi, K., Sekine, A., Matsuda, F., Kosugi, S., Nakayama, T., Inagaki, N. and Bessho, K.; Nagahama Study Collaboration Group. Yamazaki, T., Yamori, M., Asai, K., Nakano-Araki, I., Yamaguchi, A., Takahashi, K., Sekine, A., Matsuda, F., Kosugi, S., Nakayama, T., Inagaki, N. and Bessho, K.; Nagahama Study Collaboration Group. Yamazaki, T., Yamori, M., Asai, K., Nakano-Araki, I., Yamaguchi, A., Takahashi, K., Sekine, A., Matsuda, F., Kosugi, S., Nakayama, T., Inagaki, N. and Bessho, K.; Nagahama Study Collaboration Group. Mastication and risk for diabetes in a Japanese population: a cross-sectional study. Mastication and risk for diabetes in a Japanese population: a cross-sectional study. Mastication and risk for diabetes in a Japanese population: a cross-sectional study. PLoS One, 8, e64113 PLoS One, 8, e64113 PLoS One, 8, e64113 2013 英語 研究論文(学術雑誌) 公開
Terao, C., Yoshifuji, H., Kimura, A., Matsumura, T., Ohmura, K., Takahashi, M., Shimizu, M., Kawaguchi, T., Chen, Z., Naruse, T. K., Sato-Otsubo, A., Ebana, Y., Maejima, Y., Kinoshita, H., Murakami, K., Kawabata, D., Wada, Y., Narita, I., Tazaki, J., Kawaguchi, Y., Yamanaka, H., Yurugi, K., Miura, Y., Maekawa, T., Ogawa, S., Komuro, K., Nagai, R., Yamada, R., Tabara, Y., Isobe, M., Mimori, T. and Matsuda, F. Terao, C., Yoshifuji, H., Kimura, A., Matsumura, T., Ohmura, K., Takahashi, M., Shimizu, M., Kawaguchi, T., Chen, Z., Naruse, T. K., Sato-Otsubo, A., Ebana, Y., Maejima, Y., Kinoshita, H., Murakami, K., Kawabata, D., Wada, Y., Narita, I., Tazaki, J., Kawaguchi, Y., Yamanaka, H., Yurugi, K., Miura, Y., Maekawa, T., Ogawa, S., Komuro, K., Nagai, R., Yamada, R., Tabara, Y., Isobe, M., Mimori, T. and Matsuda, F. Terao, C., Yoshifuji, H., Kimura, A., Matsumura, T., Ohmura, K., Takahashi, M., Shimizu, M., Kawaguchi, T., Chen, Z., Naruse, T. K., Sato-Otsubo, A., Ebana, Y., Maejima, Y., Kinoshita, H., Murakami, K., Kawabata, D., Wada, Y., Narita, I., Tazaki, J., Kawaguchi, Y., Yamanaka, H., Yurugi, K., Miura, Y., Maekawa, T., Ogawa, S., Komuro, K., Nagai, R., Yamada, R., Tabara, Y., Isobe, M., Mimori, T. and Matsuda, F. Two susceptibility loci to Takayasu arteritis reveal a synergistic role of the IL12B and HLA-B regions in a Japanese population. Two susceptibility loci to Takayasu arteritis reveal a synergistic role of the IL12B and HLA-B regions in a Japanese population. Two susceptibility loci to Takayasu arteritis reveal a synergistic role of the IL12B and HLA-B regions in a Japanese population. Am. J. Hum. Genet., 93, 289-297 Am. J. Hum. Genet., 93, 289-297 Am. J. Hum. Genet., 93, 289-297 2013 英語 研究論文(学術雑誌) 公開
Khor, C. C., Miyake, M., Chen, L. J., Shi, Y., Barathi, V. A., Qiao, F., Nakata, I., Yamashiro, K., Zhou, X., Tam, P. O., Cheng, C. Y., Tai, E. S., Vithana, E. N., Aung, T., Teo, Y. Y., Wong, T. Y., Moriyama, M., Ohno-Matsui, K., Mochizuki, M., Matsuda, F.; Nagahama Study Group, Yong, R. Y., Yap, E. P., Yang, Z., Pang, C. P., Saw, S. M. and Yoshimura, N. Khor, C. C., Miyake, M., Chen, L. J., Shi, Y., Barathi, V. A., Qiao, F., Nakata, I., Yamashiro, K., Zhou, X., Tam, P. O., Cheng, C. Y., Tai, E. S., Vithana, E. N., Aung, T., Teo, Y. Y., Wong, T. Y., Moriyama, M., Ohno-Matsui, K., Mochizuki, M., Matsuda, F.; Nagahama Study Group, Yong, R. Y., Yap, E. P., Yang, Z., Pang, C. P., Saw, S. M. and Yoshimura, N. Khor, C. C., Miyake, M., Chen, L. J., Shi, Y., Barathi, V. A., Qiao, F., Nakata, I., Yamashiro, K., Zhou, X., Tam, P. O., Cheng, C. Y., Tai, E. S., Vithana, E. N., Aung, T., Teo, Y. Y., Wong, T. Y., Moriyama, M., Ohno-Matsui, K., Mochizuki, M., Matsuda, F.; Nagahama Study Group, Yong, R. Y., Yap, E. P., Yang, Z., Pang, C. P., Saw, S. M. and Yoshimura, N. Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. Hum. Mol. Genet., 22, 5288-5294 Hum. Mol. Genet., 22, 5288-5294 Hum. Mol. Genet., 22, 5288-5294 2013 英語 研究論文(学術雑誌) 公開
Terao, C., Bayoumi, N., McKenzie, C. A., Zelenika, D., Muro, S., Mishima, M.; The Nagahama Cohort Research Group, Connell, J. M., Vickers, M. A., Lathrop, G. M., Farrall, M., Matsuda, F. and Keavney, B. D. Terao, C., Bayoumi, N., McKenzie, C. A., Zelenika, D., Muro, S., Mishima, M.; The Nagahama Cohort Research Group, Connell, J. M., Vickers, M. A., Lathrop, G. M., Farrall, M., Matsuda, F. and Keavney, B. D. Terao, C., Bayoumi, N., McKenzie, C. A., Zelenika, D., Muro, S., Mishima, M.; The Nagahama Cohort Research Group, Connell, J. M., Vickers, M. A., Lathrop, G. M., Farrall, M., Matsuda, F. and Keavney, B. D. Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. Ann. Hum. Genet., 77, 465-471 Ann. Hum. Genet., 77, 465-471 Ann. Hum. Genet., 77, 465-471 2013 英語 研究論文(学術雑誌) 公開
Yamamoto, H., Higasa, K., Sakaguchi, M., Shien, K., Soh, J., Ichimura, K., Furukawa, M., Hashida, S., Tsukuda, K., Takigawa, N., Matsuo, K., Kiura, K., Miyoshi, S., Matsuda, F. and Toyooka, S. Yamamoto, H., Higasa, K., Sakaguchi, M., Shien, K., Soh, J., Ichimura, K., Furukawa, M., Hashida, S., Tsukuda, K., Takigawa, N., Matsuo, K., Kiura, K., Miyoshi, S., Matsuda, F. and Toyooka, S. Yamamoto, H., Higasa, K., Sakaguchi, M., Shien, K., Soh, J., Ichimura, K., Furukawa, M., Hashida, S., Tsukuda, K., Takigawa, N., Matsuo, K., Kiura, K., Miyoshi, S., Matsuda, F. and Toyooka, S. Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. J. Natl. Cancer Inst., 106, djt338 J. Natl. Cancer Inst., 106, djt338 J. Natl. Cancer Inst., 106, djt338 2013 英語 研究論文(学術雑誌) 公開
Okada, Y., Shimane, K., Kochi, Y., Tahira, T., Suzuki, A., Higasa, K., Takahashi, A., Horita, T., Atsumi, T., Ishii, T., Okamoto, A., Fujio, K., Hirakata, M., Amano, H., Kondo, Y., Ito, S., Takada, K., Mimori, A., Saito, K., Kamachi, M., Kawaguchi, Y., Ikari, K., Mohammed, O. W., Matsuda, K., Terao, C., Ohmura, K., Myouzen, K., Hosono, N., Tsunoda, T., Nishimoto, N., Mimori, T., Matsuda, F., Tanaka, Y., Sumida, T., Yamanaka, H., Takasaki, Y., Koike, T., Horiuchi, T., Hayashi, K., Kubo, M., Kamatani, N., Yamada, R., Nakamura, Y. and Yamamoto, K. Okada, Y., Shimane, K., Kochi, Y., Tahira, T., Suzuki, A., Higasa, K., Takahashi, A., Horita, T., Atsumi, T., Ishii, T., Okamoto, A., Fujio, K., Hirakata, M., Amano, H., Kondo, Y., Ito, S., Takada, K., Mimori, A., Saito, K., Kamachi, M., Kawaguchi, Y., Ikari, K., Mohammed, O. W., Matsuda, K., Terao, C., Ohmura, K., Myouzen, K., Hosono, N., Tsunoda, T., Nishimoto, N., Mimori, T., Matsuda, F., Tanaka, Y., Sumida, T., Yamanaka, H., Takasaki, Y., Koike, T., Horiuchi, T., Hayashi, K., Kubo, M., Kamatani, N., Yamada, R., Nakamura, Y. and Yamamoto, K. Okada, Y., Shimane, K., Kochi, Y., Tahira, T., Suzuki, A., Higasa, K., Takahashi, A., Horita, T., Atsumi, T., Ishii, T., Okamoto, A., Fujio, K., Hirakata, M., Amano, H., Kondo, Y., Ito, S., Takada, K., Mimori, A., Saito, K., Kamachi, M., Kawaguchi, Y., Ikari, K., Mohammed, O. W., Matsuda, K., Terao, C., Ohmura, K., Myouzen, K., Hosono, N., Tsunoda, T., Nishimoto, N., Mimori, T., Matsuda, F., Tanaka, Y., Sumida, T., Yamanaka, H., Takasaki, Y., Koike, T., Horiuchi, T., Hayashi, K., Kubo, M., Kamatani, N., Yamada, R., Nakamura, Y. and Yamamoto, K. A Genome-Wide Association Study Identified AFF1 as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese. A Genome-Wide Association Study Identified AFF1 as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese. A Genome-Wide Association Study Identified AFF1 as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese. PLoS Genet., 8, e1002455 PLoS Genet., 8, e1002455 PLoS Genet., 8, e1002455 2012 英語 研究論文(学術雑誌) 公開
Kato, L., Beguma, N. A., Burroughs, M., Doi, T., Kawai, J., Daub, C. O., Kawaguchi, T., Matsuda, F., Hayashizaki, Y. and Honjo, T. Kato, L., Beguma, N. A., Burroughs, M., Doi, T., Kawai, J., Daub, C. O., Kawaguchi, T., Matsuda, F., Hayashizaki, Y. and Honjo, T. Kato, L., Beguma, N. A., Burroughs, M., Doi, T., Kawai, J., Daub, C. O., Kawaguchi, T., Matsuda, F., Hayashizaki, Y. and Honjo, T. Nonimmunoglobulin target loci of activation-induced cytidine deaminase (AID) share unique features with immunoglobulin genes. Nonimmunoglobulin target loci of activation-induced cytidine deaminase (AID) share unique features with immunoglobulin genes. Nonimmunoglobulin target loci of activation-induced cytidine deaminase (AID) share unique features with immunoglobulin genes. Proc. Natl., Acad. Sci. U. S. A., 109, 2479-2484 Proc. Natl., Acad. Sci. U. S. A., 109, 2479-2484 Proc. Natl., Acad. Sci. U. S. A., 109, 2479-2484 2012 英語 研究論文(学術雑誌) 公開
Okada, Y., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Kawaguchi, T., Stahl, E. A., Kurreeman, F. A., Nishida, N., Ohmiya, H., Myouzen, K., Takahashi, M., Sawada, T., Nishioka, Y., Yukioka, M., Matsubara, T., Wakitani, S., Teshima, R., Tohma, S., Takasugi, K., Shimada, K., Murasawa, A., Honjo, S., Matsuo, K., Tanaka, H., Tajima, K., Suzuki, T., Iwamoto, T., Kawamura, Y., Tanii, H., Okazaki, Y., Sasaki, T., Gregersen, P. K., Padyukov, L., Worthington, J., Siminovitch, K. A., Lathrop, M., Taniguchi, A., Takahashi, A., Tokunaga, K., Kubo, M., Nakamura, Y., Kamatani, N., Mimori, T., Plenge, R. M., Yamanaka, H., Momohara, S., Yamada, R., Matsuda, F. and Yamamoto, K. Okada, Y., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Kawaguchi, T., Stahl, E. A., Kurreeman, F. A., Nishida, N., Ohmiya, H., Myouzen, K., Takahashi, M., Sawada, T., Nishioka, Y., Yukioka, M., Matsubara, T., Wakitani, S., Teshima, R., Tohma, S., Takasugi, K., Shimada, K., Murasawa, A., Honjo, S., Matsuo, K., Tanaka, H., Tajima, K., Suzuki, T., Iwamoto, T., Kawamura, Y., Tanii, H., Okazaki, Y., Sasaki, T., Gregersen, P. K., Padyukov, L., Worthington, J., Siminovitch, K. A., Lathrop, M., Taniguchi, A., Takahashi, A., Tokunaga, K., Kubo, M., Nakamura, Y., Kamatani, N., Mimori, T., Plenge, R. M., Yamanaka, H., Momohara, S., Yamada, R., Matsuda, F. and Yamamoto, K. Okada, Y., Terao, C., Ikari, K., Kochi, Y., Ohmura, K., Suzuki, A., Kawaguchi, T., Stahl, E. A., Kurreeman, F. A., Nishida, N., Ohmiya, H., Myouzen, K., Takahashi, M., Sawada, T., Nishioka, Y., Yukioka, M., Matsubara, T., Wakitani, S., Teshima, R., Tohma, S., Takasugi, K., Shimada, K., Murasawa, A., Honjo, S., Matsuo, K., Tanaka, H., Tajima, K., Suzuki, T., Iwamoto, T., Kawamura, Y., Tanii, H., Okazaki, Y., Sasaki, T., Gregersen, P. K., Padyukov, L., Worthington, J., Siminovitch, K. A., Lathrop, M., Taniguchi, A., Takahashi, A., Tokunaga, K., Kubo, M., Nakamura, Y., Kamatani, N., Mimori, T., Plenge, R. M., Yamanaka, H., Momohara, S., Yamada, R., Matsuda, F. and Yamamoto, K. Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Nat. Genet., 44, 511-517 Nat. Genet., 44, 511-517 Nat. Genet., 44, 511-517 2012 英語 研究論文(学術雑誌) 公開
Kawaguchi, T., Yoshio Sumida, T., Umemura, A., Matsuo, M, Takahashi, M, Takamura, T., Yasui, M., Saibara, T., Hashimoto, E., Kawanaka, M., Watanabe, S., Kawata, S., Imai, Y., Kokubo, M., Shima, T., Park, H., Tanaka, H., Tajima, K., Yamada, R., Matsuda, F. and Okanoue, T. for Japan Study Group of Nonalcoholic Fatty Liver Disease (JSG-NAFLD) Kawaguchi, T., Yoshio Sumida, T., Umemura, A., Matsuo, M, Takahashi, M, Takamura, T., Yasui, M., Saibara, T., Hashimoto, E., Kawanaka, M., Watanabe, S., Kawata, S., Imai, Y., Kokubo, M., Shima, T., Park, H., Tanaka, H., Tajima, K., Yamada, R., Matsuda, F. and Okanoue, T. for Japan Study Group of Nonalcoholic Fatty Liver Disease (JSG-NAFLD) Kawaguchi, T., Yoshio Sumida, T., Umemura, A., Matsuo, M, Takahashi, M, Takamura, T., Yasui, M., Saibara, T., Hashimoto, E., Kawanaka, M., Watanabe, S., Kawata, S., Imai, Y., Kokubo, M., Shima, T., Park, H., Tanaka, H., Tajima, K., Yamada, R., Matsuda, F. and Okanoue, T. for Japan Study Group of Nonalcoholic Fatty Liver Disease (JSG-NAFLD) Genetic Polymorphisms of the Human PNPLA3 Gene are Strongly Associated with Severity of Non-Alcoholic Fatty Liver Disease in Japanese. Genetic Polymorphisms of the Human PNPLA3 Gene are Strongly Associated with Severity of Non-Alcoholic Fatty Liver Disease in Japanese. Genetic Polymorphisms of the Human PNPLA3 Gene are Strongly Associated with Severity of Non-Alcoholic Fatty Liver Disease in Japanese. PLoS One, 7, e38322 PLoS One, 7, e38322 PLoS One, 7, e38322 2012 英語 研究論文(学術雑誌) 公開
Terao, C., Ohmura, K., Ikari, K., Kochi, Y., Maruya, E., Katayama, M., Yurugi, K., Shimada, K., Murasawa, A., Honjo, S., Takasugi, K., Matsuo, K., Tajima, K., Suzuki, A., Yamamoto, K., Momohara, S., Yamanaka, H., Yamada, R., Saji, H., Matsuda, F. and Mimori, T. Terao, C., Ohmura, K., Ikari, K., Kochi, Y., Maruya, E., Katayama, M., Yurugi, K., Shimada, K., Murasawa, A., Honjo, S., Takasugi, K., Matsuo, K., Tajima, K., Suzuki, A., Yamamoto, K., Momohara, S., Yamanaka, H., Yamada, R., Saji, H., Matsuda, F. and Mimori, T. Terao, C., Ohmura, K., Ikari, K., Kochi, Y., Maruya, E., Katayama, M., Yurugi, K., Shimada, K., Murasawa, A., Honjo, S., Takasugi, K., Matsuo, K., Tajima, K., Suzuki, A., Yamamoto, K., Momohara, S., Yamanaka, H., Yamada, R., Saji, H., Matsuda, F. and Mimori, T. ACPA-negative RA consists of two genetically distinct subsets based on RF positivity in Japanese. ACPA-negative RA consists of two genetically distinct subsets based on RF positivity in Japanese. ACPA-negative RA consists of two genetically distinct subsets based on RF positivity in Japanese. PLoS One, 7, e40067 PLoS One, 7, e40067 PLoS One, 7, e40067 2012 英語 研究論文(学術雑誌) 公開
Terao, C., Ohmura, K., Katayama, M., Takahashi, M., Kokubo, M., Diop, G., Toda, T., Yamamoto, N., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Shinkura, R., Shimizu, M., Gut, I., Heath, S., Melchers, I., Manabe, T., Lathrop, M., Mimori, T., Yamada, R. and Matsuda, F. Terao, C., Ohmura, K., Katayama, M., Takahashi, M., Kokubo, M., Diop, G., Toda, T., Yamamoto, N., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Shinkura, R., Shimizu, M., Gut, I., Heath, S., Melchers, I., Manabe, T., Lathrop, M., Mimori, T., Yamada, R. and Matsuda, F. Terao, C., Ohmura, K., Katayama, M., Takahashi, M., Kokubo, M., Diop, G., Toda, T., Yamamoto, N., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Shinkura, R., Shimizu, M., Gut, I., Heath, S., Melchers, I., Manabe, T., Lathrop, M., Mimori, T., Yamada, R. and Matsuda, F. Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis - A genome-wide study combined with immunological analyses. Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis - A genome-wide study combined with immunological analyses. Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis - A genome-wide study combined with immunological analyses. PLoS One., 6, e20457 PLoS One., 6, e20457 PLoS One., 6, e20457 2011 英語 研究論文(学術雑誌) 公開
Meziani, R., Yamada, R., Takahashi, M., Ohigashi, K., Morinobu, A., Terao, C., Hiratani, H., Ohmura, K., Yamaguchi, M., Nomura, T., Vasilescu, A., Kokubo, M., Renault, V., Hirosawa, K., Ratanajaraya, C., Heath, S., Mimori, T., Sakaguchi, S., Lathrop, M., Melchers, I., Kumagai, S. and Matsuda, F. Meziani, R., Yamada, R., Takahashi, M., Ohigashi, K., Morinobu, A., Terao, C., Hiratani, H., Ohmura, K., Yamaguchi, M., Nomura, T., Vasilescu, A., Kokubo, M., Renault, V., Hirosawa, K., Ratanajaraya, C., Heath, S., Mimori, T., Sakaguchi, S., Lathrop, M., Melchers, I., Kumagai, S. and Matsuda, F. Meziani, R., Yamada, R., Takahashi, M., Ohigashi, K., Morinobu, A., Terao, C., Hiratani, H., Ohmura, K., Yamaguchi, M., Nomura, T., Vasilescu, A., Kokubo, M., Renault, V., Hirosawa, K., Ratanajaraya, C., Heath, S., Mimori, T., Sakaguchi, S., Lathrop, M., Melchers, I., Kumagai, S. and Matsuda, F. A Trans-ethnic genetic study of Rheumatoid Arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations. A Trans-ethnic genetic study of Rheumatoid Arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations. A Trans-ethnic genetic study of Rheumatoid Arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations. Mod. Rheumatol., 22, 52-58 Mod. Rheumatol., 22, 52-58 Mod. Rheumatol., 22, 52-58 2011 英語 研究論文(学術雑誌) 公開
Toyoda, H., Kumada, T., Tada, T., Kawaguchi, T., Murakami, Y. and Matsuda F. Toyoda, H., Kumada, T., Tada, T., Kawaguchi, T., Murakami, Y. and Matsuda F. Toyoda, H., Kumada, T., Tada, T., Kawaguchi, T., Murakami, Y. and Matsuda F. Impact of genetic polymorphisms near the IL28B gene and amino acid substitutions in the hepatitis C virus core region on interferon sensitivity/resistance in patients with chronic hepatitis C. Impact of genetic polymorphisms near the IL28B gene and amino acid substitutions in the hepatitis C virus core region on interferon sensitivity/resistance in patients with chronic hepatitis C. Impact of genetic polymorphisms near the IL28B gene and amino acid substitutions in the hepatitis C virus core region on interferon sensitivity/resistance in patients with chronic hepatitis C. J. Med. Virol., 83, 1203-1211 J. Med. Virol., 83, 1203-1211 J. Med. Virol., 83, 1203-1211 2011 英語 研究論文(学術雑誌) 公開
Ratanajaraya, C., Nishiyama H., Takahashi. M., Kawaguchi, T., Saito, R., Mikami, Y., Suyama, M., Lathrop, M., Yamada, R., Ogawa, O. and Matsuda, F. Ratanajaraya, C., Nishiyama H., Takahashi. M., Kawaguchi, T., Saito, R., Mikami, Y., Suyama, M., Lathrop, M., Yamada, R., Ogawa, O. and Matsuda, F. Ratanajaraya, C., Nishiyama H., Takahashi. M., Kawaguchi, T., Saito, R., Mikami, Y., Suyama, M., Lathrop, M., Yamada, R., Ogawa, O. and Matsuda, F. A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males. A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males. A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males. J. Hum. Genet., 56, 572-576 J. Hum. Genet., 56, 572-576 J. Hum. Genet., 56, 572-576 2011 英語 研究論文(学術雑誌) 公開
Matsuse, M., Takahashi, M., Mitsutake, N., Nishihara, E., Hirokawa, M., Kawaguchi, T., Rogounovitch, T., Saenko, V., Bychkov, A., Suzuki, K., Matsuo, K., Tajima, K., Miyauchi, A., Yamada, R., Matsuda, F. and Yamashita, S. Matsuse, M., Takahashi, M., Mitsutake, N., Nishihara, E., Hirokawa, M., Kawaguchi, T., Rogounovitch, T., Saenko, V., Bychkov, A., Suzuki, K., Matsuo, K., Tajima, K., Miyauchi, A., Yamada, R., Matsuda, F. and Yamashita, S. Matsuse, M., Takahashi, M., Mitsutake, N., Nishihara, E., Hirokawa, M., Kawaguchi, T., Rogounovitch, T., Saenko, V., Bychkov, A., Suzuki, K., Matsuo, K., Tajima, K., Miyauchi, A., Yamada, R., Matsuda, F. and Yamashita, S. The FOXE1 and HKX2-1 are associated with susceptibility to papillary thyroid carcinoma in the Japanese Population. The FOXE1 and HKX2-1 are associated with susceptibility to papillary thyroid carcinoma in the Japanese Population. The FOXE1 and HKX2-1 are associated with susceptibility to papillary thyroid carcinoma in the Japanese Population. J. Mol. Genet., 48, 645-648 J. Mol. Genet., 48, 645-648 J. Mol. Genet., 48, 645-648 2011 英語 研究論文(学術雑誌) 公開
Terao. C., Yamada, R., Ohmura, K., Takahashi, M., Kawaguchi, T., Kochi, Y., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Okada, Y., Nakamura, Y., Yamamoto, K., Melchers, I., Lathrop, M., Mimori, T. and Matsuda, F. Terao. C., Yamada, R., Ohmura, K., Takahashi, M., Kawaguchi, T., Kochi, Y., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Okada, Y., Nakamura, Y., Yamamoto, K., Melchers, I., Lathrop, M., Mimori, T. and Matsuda, F. Terao. C., Yamada, R., Ohmura, K., Takahashi, M., Kawaguchi, T., Kochi, Y., Human Disease Genomics Working Group, RA Clinical and Genetic Study Consortium, Okada, Y., Nakamura, Y., Yamamoto, K., Melchers, I., Lathrop, M., Mimori, T. and Matsuda, F. The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. Hum. Mol. Genet., 20, 2680-2685 Hum. Mol. Genet., 20, 2680-2685 Hum. Mol. Genet., 20, 2680-2685 2011 英語 研究論文(学術雑誌) 公開
Nakata, I., Yamashiro, K., Yamada, R., Gotoh, N., Nakanishi, H., Hayashi, H., Tsujikawa, A., Otani, A., Saito, M., Iida, T., Oishi, A., Matsuo, K., Tajima, K., Matsuda, F. and Yoshimura, N. Nakata, I., Yamashiro, K., Yamada, R., Gotoh, N., Nakanishi, H., Hayashi, H., Tsujikawa, A., Otani, A., Saito, M., Iida, T., Oishi, A., Matsuo, K., Tajima, K., Matsuda, F. and Yoshimura, N. Nakata, I., Yamashiro, K., Yamada, R., Gotoh, N., Nakanishi, H., Hayashi, H., Tsujikawa, A., Otani, A., Saito, M., Iida, T., Oishi, A., Matsuo, K., Tajima, K., Matsuda, F. and Yoshimura, N. Association between the SERPING1 Gene and Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Japanese. Association between the SERPING1 Gene and Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Japanese. Association between the SERPING1 Gene and Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Japanese. PLoS One, 6, e19108 PLoS One, 6, e19108 PLoS One, 6, e19108 2011 英語 研究論文(学術雑誌) 公開
Yamaguchi, H., Fujimoto, T., Nakamura, S., Ohmura, K., Mimori, T., Matsuda, F. and Nagata, S. Yamaguchi, H., Fujimoto, T., Nakamura, S., Ohmura, K., Mimori, T., Matsuda, F. and Nagata, S. Yamaguchi, H., Fujimoto, T., Nakamura, S., Ohmura, K., Mimori, T., Matsuda, F. and Nagata, S. Aberrant splicing of milk fat globule EGF factor 8 gene in human systemic lupus erythematosus. Aberrant splicing of milk fat globule EGF factor 8 gene in human systemic lupus erythematosus. Aberrant splicing of milk fat globule EGF factor 8 gene in human systemic lupus erythematosus. Eur. J. Immunol., 40, 1778-1785 Eur. J. Immunol., 40, 1778-1785 Eur. J. Immunol., 40, 1778-1785 2010 英語 研究論文(学術雑誌) 公開
Kanai, M., Yoshioka, A., Tanaka, S., Nagayama, S., Matsumoto, S., Nishimura, T., Niimi, M., Teramukai, S., Takahashi, R., Mori, Y., Kitano, T., Ishiguro, H., Yanagihara, K., Chiba, T., Fukushima, M. and Matsuda, F. Kanai, M., Yoshioka, A., Tanaka, S., Nagayama, S., Matsumoto, S., Nishimura, T., Niimi, M., Teramukai, S., Takahashi, R., Mori, Y., Kitano, T., Ishiguro, H., Yanagihara, K., Chiba, T., Fukushima, M. and Matsuda, F. Kanai, M., Yoshioka, A., Tanaka, S., Nagayama, S., Matsumoto, S., Nishimura, T., Niimi, M., Teramukai, S., Takahashi, R., Mori, Y., Kitano, T., Ishiguro, H., Yanagihara, K., Chiba, T., Fukushima, M. and Matsuda, F. Associations between glutathione S-transferase pi Ile(105)Val and glyoxylate aminotransferase Pro(11)Leu and Ile(340)Met polymorphisms and early-onset oxaliplatin-induced neuropathy. Associations between glutathione S-transferase pi Ile(105)Val and glyoxylate aminotransferase Pro(11)Leu and Ile(340)Met polymorphisms and early-onset oxaliplatin-induced neuropathy. Associations between glutathione S-transferase pi Ile(105)Val and glyoxylate aminotransferase Pro(11)Leu and Ile(340)Met polymorphisms and early-onset oxaliplatin-induced neuropathy. Cancer Epidemiol., 34, 189-193 Cancer Epidemiol., 34, 189-193 Cancer Epidemiol., 34, 189-193 2010 英語 研究論文(学術雑誌) 公開
Takahashi, M., Saenko, V. A., Rogounovitch T. I., Kawaguchi, T., Drozd, V. M., Takigawa-Imamura, H., Natallia M. Akulevich, N. M., Ratanajaraya, C., Mitsutake, N., Takamura, N., Danilova, L. I., Lushchik, M. L., Demidchik, Y. E., Heath, S., Yamada, R., Lathrop, M., Matsuda, F. and Yamashita, S. Takahashi, M., Saenko, V. A., Rogounovitch T. I., Kawaguchi, T., Drozd, V. M., Takigawa-Imamura, H., Natallia M. Akulevich, N. M., Ratanajaraya, C., Mitsutake, N., Takamura, N., Danilova, L. I., Lushchik, M. L., Demidchik, Y. E., Heath, S., Yamada, R., Lathrop, M., Matsuda, F. and Yamashita, S. Takahashi, M., Saenko, V. A., Rogounovitch T. I., Kawaguchi, T., Drozd, V. M., Takigawa-Imamura, H., Natallia M. Akulevich, N. M., Ratanajaraya, C., Mitsutake, N., Takamura, N., Danilova, L. I., Lushchik, M. L., Demidchik, Y. E., Heath, S., Yamada, R., Lathrop, M., Matsuda, F. and Yamashita, S. The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. Hum. Mol. Genet., 19, 2516-2523 Hum. Mol. Genet., 19, 2516-2523 Hum. Mol. Genet., 19, 2516-2523 2010 英語 研究論文(学術雑誌) 公開
Kochi, Y., Okada, Y., Suzuki, A., Ikari, K., Terao, C., Takahashi, A., Yamazaki, K., Hosono, N., Myouzen, K., Tsunoda, T., Kamatani, N., Furuichi, T., Ikegawa, S., Ohmura, K., Mimori, T., Matsuda, F., Iwamoto, T., Momohara, S., Yamanaka, H., Yamada, R., Kubo, M., Nakamura, Y. and Yamamoto, K. Kochi, Y., Okada, Y., Suzuki, A., Ikari, K., Terao, C., Takahashi, A., Yamazaki, K., Hosono, N., Myouzen, K., Tsunoda, T., Kamatani, N., Furuichi, T., Ikegawa, S., Ohmura, K., Mimori, T., Matsuda, F., Iwamoto, T., Momohara, S., Yamanaka, H., Yamada, R., Kubo, M., Nakamura, Y. and Yamamoto, K. Kochi, Y., Okada, Y., Suzuki, A., Ikari, K., Terao, C., Takahashi, A., Yamazaki, K., Hosono, N., Myouzen, K., Tsunoda, T., Kamatani, N., Furuichi, T., Ikegawa, S., Ohmura, K., Mimori, T., Matsuda, F., Iwamoto, T., Momohara, S., Yamanaka, H., Yamada, R., Kubo, M., Nakamura, Y. and Yamamoto, K. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. Nat. Genet., 42, 515-519 Nat. Genet., 42, 515-519 Nat. Genet., 42, 515-519 2010 英語 研究論文(学術雑誌) 公開
Nalpas, B., Lavialle-Meziani, R., Plancoulaine, S., Jouanguy, E., Nalpas, A., Munteanu, M., Charlotte, F., Ranque, B., Patin, E., Heath, S., Fontaine, H., Vallet-Pichard, A., Pontoire, D., Bourlière, M., Casanova, J. L., Lathrop, M., Bréchot, C., Poynard, T., Matsuda, F., Pol, S. and Abel, L. Nalpas, B., Lavialle-Meziani, R., Plancoulaine, S., Jouanguy, E., Nalpas, A., Munteanu, M., Charlotte, F., Ranque, B., Patin, E., Heath, S., Fontaine, H., Vallet-Pichard, A., Pontoire, D., Bourlière, M., Casanova, J. L., Lathrop, M., Bréchot, C., Poynard, T., Matsuda, F., Pol, S. and Abel, L. Nalpas, B., Lavialle-Meziani, R., Plancoulaine, S., Jouanguy, E., Nalpas, A., Munteanu, M., Charlotte, F., Ranque, B., Patin, E., Heath, S., Fontaine, H., Vallet-Pichard, A., Pontoire, D., Bourlière, M., Casanova, J. L., Lathrop, M., Bréchot, C., Poynard, T., Matsuda, F., Pol, S. and Abel, L. Interferon-γ receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection. Interferon-γ receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection. Interferon-γ receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection. Gut., 59, 1120-1126 Gut., 59, 1120-1126 Gut., 59, 1120-1126 2010 英語 研究論文(学術雑誌) 公開
Wahlberg, K., Jiang, J., Rooks, H., Jawaid, K., Matsuda, F., Yamaguchi, M., Lathrop, M., Thein, S.L. and Best, S. Wahlberg, K., Jiang, J., Rooks, H., Jawaid, K., Matsuda, F., Yamaguchi, M., Lathrop, M., Thein, S.L. and Best, S. Wahlberg, K., Jiang, J., Rooks, H., Jawaid, K., Matsuda, F., Yamaguchi, M., Lathrop, M., Thein, S.L. and Best, S. The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells. The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells. The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells. Blood, 6, 1254-1262 Blood, 6, 1254-1262 Blood, 6, 1254-1262 2009 英語 研究論文(学術雑誌) 公開
Nakanishi, H., Yamada, R., Gotoh, N., Hayashi, H., Yamashiro, K., Shimada, N., Ohno-Matsui, K., Mochizuki, M., Saito, M., Iida, T., Matsuo, K., Tajima, K., Yoshimura, N. and Matsuda, F. Nakanishi, H., Yamada, R., Gotoh, N., Hayashi, H., Yamashiro, K., Shimada, N., Ohno-Matsui, K., Mochizuki, M., Saito, M., Iida, T., Matsuo, K., Tajima, K., Yoshimura, N. and Matsuda, F. Nakanishi, H., Yamada, R., Gotoh, N., Hayashi, H., Yamashiro, K., Shimada, N., Ohno-Matsui, K., Mochizuki, M., Saito, M., Iida, T., Matsuo, K., Tajima, K., Yoshimura, N. and Matsuda, F. A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1. A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1. A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1. PLoS Genetics, 5, e1000660 PLoS Genetics, 5, e1000660 PLoS Genetics, 5, e1000660 2009 英語 研究論文(学術雑誌) 公開
Hung, R.J., McKay, J.D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., Chen, C., Goodman, G., Field, J.K., Liloglou, T., Xinarianos, G., Cassidy, A., McLaughlin, J., Liu, G., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Hveem, K., Vatten, L., Linseisen, J., Clavel-Chapelon, F., Vineism P., Bueno-de-Mesquita, H.B., Lund, E., Martinez, C., Bingham, S., Rasmuson, T., Hainaut, P., Riboli, E., Ahrens, W., Benhamou, S., Lagiou, P., Trichopoulos, D., Holcátová, I., Merletti, F., Kjaerheim, K., Agudo, A., Macfarlane, G., Talamini, R., Simonato, L., Lowry, R., Conway, D.I., Znaor, A., Healy, C., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. Hung, R.J., McKay, J.D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., Chen, C., Goodman, G., Field, J.K., Liloglou, T., Xinarianos, G., Cassidy, A., McLaughlin, J., Liu, G., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Hveem, K., Vatten, L., Linseisen, J., Clavel-Chapelon, F., Vineism P., Bueno-de-Mesquita, H.B., Lund, E., Martinez, C., Bingham, S., Rasmuson, T., Hainaut, P., Riboli, E., Ahrens, W., Benhamou, S., Lagiou, P., Trichopoulos, D., Holcátová, I., Merletti, F., Kjaerheim, K., Agudo, A., Macfarlane, G., Talamini, R., Simonato, L., Lowry, R., Conway, D.I., Znaor, A., Healy, C., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. Hung, R.J., McKay, J.D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., Chen, C., Goodman, G., Field, J.K., Liloglou, T., Xinarianos, G., Cassidy, A., McLaughlin, J., Liu, G., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Hveem, K., Vatten, L., Linseisen, J., Clavel-Chapelon, F., Vineism P., Bueno-de-Mesquita, H.B., Lund, E., Martinez, C., Bingham, S., Rasmuson, T., Hainaut, P., Riboli, E., Ahrens, W., Benhamou, S., Lagiou, P., Trichopoulos, D., Holcátová, I., Merletti, F., Kjaerheim, K., Agudo, A., Macfarlane, G., Talamini, R., Simonato, L., Lowry, R., Conway, D.I., Znaor, A., Healy, C., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature, 452, 633-637 Nature, 452, 633-637 Nature, 452, 633-637 2008 英語 研究論文(学術雑誌) 公開
Gotoh, N., Yamada, R., Matsuda, F., Yoshimura, N and Iida, T. Gotoh, N., Yamada, R., Matsuda, F., Yoshimura, N and Iida, T. Gotoh, N., Yamada, R., Matsuda, F., Yoshimura, N and Iida, T. Manganase superoxide dismutase gene (SOD2) polymorphism and exudative age-related macular degeneration in the Japanese population. Manganase superoxide dismutase gene (SOD2) polymorphism and exudative age-related macular degeneration in the Japanese population. Manganase superoxide dismutase gene (SOD2) polymorphism and exudative age-related macular degeneration in the Japanese population. Am. J. Ophthalmol., 146, 146-147 Am. J. Ophthalmol., 146, 146-147 Am. J. Ophthalmol., 146, 146-147 2008 英語 研究論文(学術雑誌) 公開
SEARCH Collaborative Group, Link, E., Parish, S., Armitage, J., Bowman, L., Heath, S., Matsuda, F., Gut, I., Lathrop, M. and Collins, R. SEARCH Collaborative Group, Link, E., Parish, S., Armitage, J., Bowman, L., Heath, S., Matsuda, F., Gut, I., Lathrop, M. and Collins, R. SEARCH Collaborative Group, Link, E., Parish, S., Armitage, J., Bowman, L., Heath, S., Matsuda, F., Gut, I., Lathrop, M. and Collins, R. SLCO1B1 variants and statin-induced myopathy--a genomewide study. SLCO1B1 variants and statin-induced myopathy--a genomewide study. SLCO1B1 variants and statin-induced myopathy--a genomewide study. N. Engl. J. Med., 359, 789-799 N. Engl. J. Med., 359, 789-799 N. Engl. J. Med., 359, 789-799 2008 英語 研究論文(学術雑誌) 公開
Poupon, R., Ping, C., Chrétien, Y., Corpechot, C., Chazouillères, O., Simon, T., Heath, S.C., Matsuda, F., Poupon, R.E., Housset, C. and Barbu, V. Poupon, R., Ping, C., Chrétien, Y., Corpechot, C., Chazouillères, O., Simon, T., Heath, S.C., Matsuda, F., Poupon, R.E., Housset, C. and Barbu, V. Poupon, R., Ping, C., Chrétien, Y., Corpechot, C., Chazouillères, O., Simon, T., Heath, S.C., Matsuda, F., Poupon, R.E., Housset, C. and Barbu, V. Genetic factors of susceptibility and of severity in primary biliary cirrhosis. Genetic factors of susceptibility and of severity in primary biliary cirrhosis. Genetic factors of susceptibility and of severity in primary biliary cirrhosis. J. Hepatol., 49, 1038-1045 J. Hepatol., 49, 1038-1045 J. Hepatol., 49, 1038-1045 2008 英語 研究論文(学術雑誌) 公開
McKay, J.D., Hung, R.J., Gaborieau, V., Boffetta, P., Chabrier, A., Byrnes, G., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., McLaughlin, J., Shepherd, F., Montpetit, A., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Vatten, L., Njølstad, I., Axelsson, T., Chen, C., Goodman, G., Barnett, M., Loomis, M.M., Lubiñski, J., Matyjasik, J., Lener, M., Oszutowska, D., Field, J., Liloglou, T., Xinarianos, G., Cassidy, A.; EPIC Study, Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., González, C.A., Ramón Quirós, J., Martínez, C., Navarro, C., Ardanaz, E., Larrañaga, N., Kham, K.T., Key, T., Bueno-de-Mesquita, H.B., Peeters, P.H., Trichopoulou, A., Linseisen, J., Boeing, H., Hallmans, G., Overvad, K., Tjønneland, A., Kumle, M., Riboli, E., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. McKay, J.D., Hung, R.J., Gaborieau, V., Boffetta, P., Chabrier, A., Byrnes, G., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., McLaughlin, J., Shepherd, F., Montpetit, A., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Vatten, L., Njølstad, I., Axelsson, T., Chen, C., Goodman, G., Barnett, M., Loomis, M.M., Lubiñski, J., Matyjasik, J., Lener, M., Oszutowska, D., Field, J., Liloglou, T., Xinarianos, G., Cassidy, A.; EPIC Study, Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., González, C.A., Ramón Quirós, J., Martínez, C., Navarro, C., Ardanaz, E., Larrañaga, N., Kham, K.T., Key, T., Bueno-de-Mesquita, H.B., Peeters, P.H., Trichopoulou, A., Linseisen, J., Boeing, H., Hallmans, G., Overvad, K., Tjønneland, A., Kumle, M., Riboli, E., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. McKay, J.D., Hung, R.J., Gaborieau, V., Boffetta, P., Chabrier, A., Byrnes, G., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., McLaughlin, J., Shepherd, F., Montpetit, A., Narod, S., Krokan, H.E., Skorpen, F., Elvestad, M.B., Vatten, L., Njølstad, I., Axelsson, T., Chen, C., Goodman, G., Barnett, M., Loomis, M.M., Lubiñski, J., Matyjasik, J., Lener, M., Oszutowska, D., Field, J., Liloglou, T., Xinarianos, G., Cassidy, A.; EPIC Study, Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., González, C.A., Ramón Quirós, J., Martínez, C., Navarro, C., Ardanaz, E., Larrañaga, N., Kham, K.T., Key, T., Bueno-de-Mesquita, H.B., Peeters, P.H., Trichopoulou, A., Linseisen, J., Boeing, H., Hallmans, G., Overvad, K., Tjønneland, A., Kumle, M., Riboli, E., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M. and Brennan, P. Lung cancer susceptibility locus at 5p15.33. Lung cancer susceptibility locus at 5p15.33. Lung cancer susceptibility locus at 5p15.33. Nat. Genet., 40, 1404-1406 Nat. Genet., 40, 1404-1406 Nat. Genet., 40, 1404-1406 2008 英語 研究論文(学術雑誌) 公開
Vasilescu, A., Terashima, Y., Enomoto, M., Heath, S., Poonpiriya, V., Gatanaga, H., Do, H., Diop, G., Hirtzig, T., Auewarakul, P., Lauhakirti, D., Sura, T., Charneau, P., Marullo, S., Therwath, A., Oka, S., Kanegasaki, S., Lathrop, M., Matsushima, K., Zagury, J. -F. and Matsuda, F. Vasilescu, A., Terashima, Y., Enomoto, M., Heath, S., Poonpiriya, V., Gatanaga, H., Do, H., Diop, G., Hirtzig, T., Auewarakul, P., Lauhakirti, D., Sura, T., Charneau, P., Marullo, S., Therwath, A., Oka, S., Kanegasaki, S., Lathrop, M., Matsushima, K., Zagury, J. -F. and Matsuda, F. Vasilescu, A., Terashima, Y., Enomoto, M., Heath, S., Poonpiriya, V., Gatanaga, H., Do, H., Diop, G., Hirtzig, T., Auewarakul, P., Lauhakirti, D., Sura, T., Charneau, P., Marullo, S., Therwath, A., Oka, S., Kanegasaki, S., Lathrop, M., Matsushima, K., Zagury, J. -F. and Matsuda, F. A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. Proc. Natl. Acad. Sci. U. S. A., 104, 3354-3359 Proc. Natl. Acad. Sci. U. S. A., 104, 3354-3359 Proc. Natl. Acad. Sci. U. S. A., 104, 3354-3359 2007 英語 研究論文(学術雑誌) 公開
Yamada, R. and Matsuda, F. Yamada, R. and Matsuda, F. Yamada, R. and Matsuda, F. A novel method to express SNP-based genetic heterogeneity, Psi, and its use to measure linkage disequilibrium for multiple SNPs, D(g), and to estimate absolute maximum of haplotype frequency. A novel method to express SNP-based genetic heterogeneity, Psi, and its use to measure linkage disequilibrium for multiple SNPs, D(g), and to estimate absolute maximum of haplotype frequency. A novel method to express SNP-based genetic heterogeneity, Psi, and its use to measure linkage disequilibrium for multiple SNPs, D(g), and to estimate absolute maximum of haplotype frequency. Genet. Epidemiol., 31, 709-726 Genet. Epidemiol., 31, 709-726 Genet. Epidemiol., 31, 709-726 2007 英語 研究論文(学術雑誌) 公開
Thein, S. L., Menzel, S., Peng, X., Best, S., Jiang, J., Close, J., Silver, N., Gerovasilli, A., Ping, C., Yamaguchi, M., Wahlberg, K., Ulug, P., Spector, T. D., Garner, C., Matsuda, F., Farrall, M. and Lathrop, M. Thein, S. L., Menzel, S., Peng, X., Best, S., Jiang, J., Close, J., Silver, N., Gerovasilli, A., Ping, C., Yamaguchi, M., Wahlberg, K., Ulug, P., Spector, T. D., Garner, C., Matsuda, F., Farrall, M. and Lathrop, M. Thein, S. L., Menzel, S., Peng, X., Best, S., Jiang, J., Close, J., Silver, N., Gerovasilli, A., Ping, C., Yamaguchi, M., Wahlberg, K., Ulug, P., Spector, T. D., Garner, C., Matsuda, F., Farrall, M. and Lathrop, M. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc. Natl. Acad. Sci. U. S. A., 104, 11346-11351 Proc. Natl. Acad. Sci. U. S. A., 104, 11346-11351 Proc. Natl. Acad. Sci. U. S. A., 104, 11346-11351 2007 英語 研究論文(学術雑誌) 公開
Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., Best, S., Spector, T. D., Farrall, M., Lathrop, M. and Thein, S. L. Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., Best, S., Spector, T. D., Farrall, M., Lathrop, M. and Thein, S. L. Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., Best, S., Spector, T. D., Farrall, M., Lathrop, M. and Thein, S. L. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. Nature Genet., 39, 1197-1199 Nature Genet., 39, 1197-1199 Nature Genet., 39, 1197-1199 2007 英語 研究論文(学術雑誌) 公開
Danoy, P., Sonoda, E., Lathrop, M., Takeda, S. and Matsuda, F. Danoy, P., Sonoda, E., Lathrop, M., Takeda, S. and Matsuda, F. Danoy, P., Sonoda, E., Lathrop, M., Takeda, S. and Matsuda, F. A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. Biochem. Biophys. Res. Commun., 352, 763-768 Biochem. Biophys. Res. Commun., 352, 763-768 Biochem. Biophys. Res. Commun., 352, 763-768 2007 英語 研究論文(学術雑誌) 公開
Plancoulaine, S., Gessain, A., Tortevoye, P., Boland-Auge, A., Vasilescu, A., Matsuda, F. and Abel, L. Plancoulaine, S., Gessain, A., Tortevoye, P., Boland-Auge, A., Vasilescu, A., Matsuda, F. and Abel, L. Plancoulaine, S., Gessain, A., Tortevoye, P., Boland-Auge, A., Vasilescu, A., Matsuda, F. and Abel, L. A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27. A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27. A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27. Hum. Mol. Genet., 15, 3306-3312 Hum. Mol. Genet., 15, 3306-3312 Hum. Mol. Genet., 15, 3306-3312 2006 英語 研究論文(学術雑誌) 公開
Vionnet, N., Tregouet, D., Kazeem, G., Gut, I., Groop, P. H., Tarnow, L., Parving, H. H., Hadjadj, S., Forsblom, C., Farrall, M., Gauguier, D., Cox, R., Matsuda, F., Heath, S., Thevard, A., Rousseau, R., Cambien, F., Marre, M. and Lathrop M. Vionnet, N., Tregouet, D., Kazeem, G., Gut, I., Groop, P. H., Tarnow, L., Parving, H. H., Hadjadj, S., Forsblom, C., Farrall, M., Gauguier, D., Cox, R., Matsuda, F., Heath, S., Thevard, A., Rousseau, R., Cambien, F., Marre, M. and Lathrop M. Vionnet, N., Tregouet, D., Kazeem, G., Gut, I., Groop, P. H., Tarnow, L., Parving, H. H., Hadjadj, S., Forsblom, C., Farrall, M., Gauguier, D., Cox, R., Matsuda, F., Heath, S., Thevard, A., Rousseau, R., Cambien, F., Marre, M. and Lathrop M. Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene. Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene. Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene. Diabetes, 55, 3166-3174 Diabetes, 55, 3166-3174 Diabetes, 55, 3166-3174 2006 英語 研究論文(学術雑誌) 公開
Spanagel, R., Pendyala, G., Abarca, C., Zghoul, T., Sanchis-Segura, C., Magnone, M. C., Lascorz, J., Depner, M., Holzberg, D., Soyka, M., Schreiber, S., Matsuda, F., Lathrop, M., Schumann, G. and Albrecht U. Spanagel, R., Pendyala, G., Abarca, C., Zghoul, T., Sanchis-Segura, C., Magnone, M. C., Lascorz, J., Depner, M., Holzberg, D., Soyka, M., Schreiber, S., Matsuda, F., Lathrop, M., Schumann, G. and Albrecht U. Spanagel, R., Pendyala, G., Abarca, C., Zghoul, T., Sanchis-Segura, C., Magnone, M. C., Lascorz, J., Depner, M., Holzberg, D., Soyka, M., Schreiber, S., Matsuda, F., Lathrop, M., Schumann, G. and Albrecht U. The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. Nature Med., 11, 35-42 Nature Med., 11, 35-42 Nature Med., 11, 35-42 2005 英語 研究論文(学術雑誌) 公開
Sakuntabhai, A., Turbpaiboon, C., Casademont, I., Chuansumrit, A., Lowhnoo, T., Kajaste-Rudnitski, A., Kalayanarooj, S. M., Tangnararatchakit, K., Tangthawornchaikul, N., Vasanawathana, S., Chaiyaratana, W., Yenchitsomanus, P. T., Suriyaphol, P., Avirutnan, P., Chokephaibulkit, K., Matsuda, F., Yoksan, S., Jacob, Y., Lathrop, G. M., Malasit, P., Despres, P. and Julier C. Sakuntabhai, A., Turbpaiboon, C., Casademont, I., Chuansumrit, A., Lowhnoo, T., Kajaste-Rudnitski, A., Kalayanarooj, S. M., Tangnararatchakit, K., Tangthawornchaikul, N., Vasanawathana, S., Chaiyaratana, W., Yenchitsomanus, P. T., Suriyaphol, P., Avirutnan, P., Chokephaibulkit, K., Matsuda, F., Yoksan, S., Jacob, Y., Lathrop, G. M., Malasit, P., Despres, P. and Julier C. Sakuntabhai, A., Turbpaiboon, C., Casademont, I., Chuansumrit, A., Lowhnoo, T., Kajaste-Rudnitski, A., Kalayanarooj, S. M., Tangnararatchakit, K., Tangthawornchaikul, N., Vasanawathana, S., Chaiyaratana, W., Yenchitsomanus, P. T., Suriyaphol, P., Avirutnan, P., Chokephaibulkit, K., Matsuda, F., Yoksan, S., Jacob, Y., Lathrop, G. M., Malasit, P., Despres, P. and Julier C. A variant in the CD209 promoter is associated with severity of dengue disease. A variant in the CD209 promoter is associated with severity of dengue disease. A variant in the CD209 promoter is associated with severity of dengue disease. Nature Genetics, 37, 507-513 Nature Genetics, 37, 507-513 Nature Genetics, 37, 507-513 2005 英語 研究論文(学術雑誌) 公開
de Parseval, N., Diop, G., Blaise, S., Helle, F., Vasilescu, A., Matsuda, F. and Heidmann T. de Parseval, N., Diop, G., Blaise, S., Helle, F., Vasilescu, A., Matsuda, F. and Heidmann T. de Parseval, N., Diop, G., Blaise, S., Helle, F., Vasilescu, A., Matsuda, F. and Heidmann T. Comprehensive search for intra- and inter-specific sequence polymorphisms among coding envelope genes of retroviral origin found in the human genome: genes and pseudogenes. Comprehensive search for intra- and inter-specific sequence polymorphisms among coding envelope genes of retroviral origin found in the human genome: genes and pseudogenes. Comprehensive search for intra- and inter-specific sequence polymorphisms among coding envelope genes of retroviral origin found in the human genome: genes and pseudogenes. BMC Genomics, 6, 117 BMC Genomics, 6, 117 BMC Genomics, 6, 117 2005 英語 研究論文(学術雑誌) 公開
Vasilescu, A., Heath, S. C., Diop, G., Do, H., Hirtzig, T., Hendel, H, Bertin-Maghit, S., Rappaport, J., Therwath, A., Lathrop, G. M., Matsuda, F. and Zagury J. -F. Vasilescu, A., Heath, S. C., Diop, G., Do, H., Hirtzig, T., Hendel, H, Bertin-Maghit, S., Rappaport, J., Therwath, A., Lathrop, G. M., Matsuda, F. and Zagury J. -F. Vasilescu, A., Heath, S. C., Diop, G., Do, H., Hirtzig, T., Hendel, H, Bertin-Maghit, S., Rappaport, J., Therwath, A., Lathrop, G. M., Matsuda, F. and Zagury J. -F. Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS. Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS. Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS. Immunogenetics, 56, 56-60 Immunogenetics, 56, 56-60 Immunogenetics, 56, 56-60 2004 英語 研究論文(学術雑誌) 公開
International Human Genome Sequencing Consortium International Human Genome Sequencing Consortium International Human Genome Sequencing Consortium Finishing the euchromatic sequence of the human genome. Finishing the euchromatic sequence of the human genome. Finishing the euchromatic sequence of the human genome. Nature, 431, 931-945 Nature, 431, 931-945 Nature, 431, 931-945 2004 英語 研究論文(学術雑誌) 公開
Heilig, R., Eckenberg, R., Petit, J. L., Fonknechten, N., DaSilva, C., Cattolico, L., Levy, M., Barbe, V., DeBerardinis, V., Ureta-Vidal, A., Pelletier, E., Vico, V., Anthouard, V., Rowen, L., Madan, A., Qin, Sun, S. H., Du, H., Pepin, K., Artiguenave, F., Robert, C, Cruaud, C., Brüls, T., Friedlander, L., Samson, G., Brottier, P., Cure, S., Ségurens, B., Samain, S., Abbasi, N., Aiach, N., Boscus, D., Dickhoff, R, Dors, M., Dubois, I., Friedman, C., Gouyvenoux, M., James, R., Madan, A., Mairey–Estrada, B., Mangenot, S., Martins, N., Ménard, M., Oztas, S., Ratcliffe, A., Shaffer, T., Vacherie, B., Bellemere, C., Belser, C., Besnard-Gonnet, M., Bartol–Mavel, D., Boutard, M., Briez-Silla, S., Combette, S., Dufosse-Laurent, V., Ferron, C., Lechaplais, C., Louesse, C., Muselet, D., Magelenat, G., Pateau, E., Petit, E., Sirvain-Trukniewicz, P., Trybou, A., Vega-Czarny, N., Bataille, E., Bluet, E., Bordelais, I., Dubois, M., Dumont, C., Guérin, T., Haffray, S., Hammadi, R., Muanga, J., Laure, L., Pellouin, V., Robert, D., Wunderle, E., Anière, F., Gauguet, G., Roy, A., Sainte-Marthe, L., Verdier, J., Verdier-Discalla, C., Hillier, L., Fulton, L., McPherson, J., Matsuda, F., Trask, B. J., Wilson, R., Scarpelli, C., Gyapay, G., Wincker, P., Saurin, W., Quétier, F., Waterston, R., Hood, L. and Weissenbach, J. Heilig, R., Eckenberg, R., Petit, J. L., Fonknechten, N., DaSilva, C., Cattolico, L., Levy, M., Barbe, V., DeBerardinis, V., Ureta-Vidal, A., Pelletier, E., Vico, V., Anthouard, V., Rowen, L., Madan, A., Qin, Sun, S. H., Du, H., Pepin, K., Artiguenave, F., Robert, C, Cruaud, C., Brüls, T., Friedlander, L., Samson, G., Brottier, P., Cure, S., Ségurens, B., Samain, S., Abbasi, N., Aiach, N., Boscus, D., Dickhoff, R, Dors, M., Dubois, I., Friedman, C., Gouyvenoux, M., James, R., Madan, A., Mairey–Estrada, B., Mangenot, S., Martins, N., Ménard, M., Oztas, S., Ratcliffe, A., Shaffer, T., Vacherie, B., Bellemere, C., Belser, C., Besnard-Gonnet, M., Bartol–Mavel, D., Boutard, M., Briez-Silla, S., Combette, S., Dufosse-Laurent, V., Ferron, C., Lechaplais, C., Louesse, C., Muselet, D., Magelenat, G., Pateau, E., Petit, E., Sirvain-Trukniewicz, P., Trybou, A., Vega-Czarny, N., Bataille, E., Bluet, E., Bordelais, I., Dubois, M., Dumont, C., Guérin, T., Haffray, S., Hammadi, R., Muanga, J., Laure, L., Pellouin, V., Robert, D., Wunderle, E., Anière, F., Gauguet, G., Roy, A., Sainte-Marthe, L., Verdier, J., Verdier-Discalla, C., Hillier, L., Fulton, L., McPherson, J., Matsuda, F., Trask, B. J., Wilson, R., Scarpelli, C., Gyapay, G., Wincker, P., Saurin, W., Quétier, F., Waterston, R., Hood, L. and Weissenbach, J. Heilig, R., Eckenberg, R., Petit, J. L., Fonknechten, N., DaSilva, C., Cattolico, L., Levy, M., Barbe, V., DeBerardinis, V., Ureta-Vidal, A., Pelletier, E., Vico, V., Anthouard, V., Rowen, L., Madan, A., Qin, Sun, S. H., Du, H., Pepin, K., Artiguenave, F., Robert, C, Cruaud, C., Brüls, T., Friedlander, L., Samson, G., Brottier, P., Cure, S., Ségurens, B., Samain, S., Abbasi, N., Aiach, N., Boscus, D., Dickhoff, R, Dors, M., Dubois, I., Friedman, C., Gouyvenoux, M., James, R., Madan, A., Mairey–Estrada, B., Mangenot, S., Martins, N., Ménard, M., Oztas, S., Ratcliffe, A., Shaffer, T., Vacherie, B., Bellemere, C., Belser, C., Besnard-Gonnet, M., Bartol–Mavel, D., Boutard, M., Briez-Silla, S., Combette, S., Dufosse-Laurent, V., Ferron, C., Lechaplais, C., Louesse, C., Muselet, D., Magelenat, G., Pateau, E., Petit, E., Sirvain-Trukniewicz, P., Trybou, A., Vega-Czarny, N., Bataille, E., Bluet, E., Bordelais, I., Dubois, M., Dumont, C., Guérin, T., Haffray, S., Hammadi, R., Muanga, J., Laure, L., Pellouin, V., Robert, D., Wunderle, E., Anière, F., Gauguet, G., Roy, A., Sainte-Marthe, L., Verdier, J., Verdier-Discalla, C., Hillier, L., Fulton, L., McPherson, J., Matsuda, F., Trask, B. J., Wilson, R., Scarpelli, C., Gyapay, G., Wincker, P., Saurin, W., Quétier, F., Waterston, R., Hood, L. and Weissenbach, J. Analysis of the complete sequence of human chromosome 14. Analysis of the complete sequence of human chromosome 14. Analysis of the complete sequence of human chromosome 14. Nature, 421, 601-607 Nature, 421, 601-607 Nature, 421, 601-607 2003 英語 研究論文(学術雑誌) 公開
Hoh, J., Matsuda, F., Peng, X., Markovic, D., Lathrop, M. G. and Ott, J. Hoh, J., Matsuda, F., Peng, X., Markovic, D., Lathrop, M. G. and Ott, J. Hoh, J., Matsuda, F., Peng, X., Markovic, D., Lathrop, M. G. and Ott, J. SNP haplotype tagging from DNA pools of two individuals. SNP haplotype tagging from DNA pools of two individuals. SNP haplotype tagging from DNA pools of two individuals. BMC Bioinformatics, 4, 14 BMC Bioinformatics, 4, 14 BMC Bioinformatics, 4, 14 2003 英語 研究論文(学術雑誌) 公開
Yang, Y., Zhang, J., Hoh, J., Matsuda, F., Xu, P., Lathrop, M. and Ott, J. Yang, Y., Zhang, J., Hoh, J., Matsuda, F., Xu, P., Lathrop, M. and Ott, J. Yang, Y., Zhang, J., Hoh, J., Matsuda, F., Xu, P., Lathrop, M. and Ott, J. Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Proc. Natl. Acad. Sci. U. S. A., 100, 7225-7230 Proc. Natl. Acad. Sci. U. S. A., 100, 7225-7230 Proc. Natl. Acad. Sci. U. S. A., 100, 7225-7230 2003 英語 研究論文(学術雑誌) 公開
Vasilescu, A., Heath, S. C., Ivanova, R., H. Hendel, H., Do, H., Mazoyer, A., Khadivpour, E., Goutalier, F. X., Khalili, K., Rappaport, J., Lathrop, G. M., Matsuda, F. and Zagury, J. -F. Vasilescu, A., Heath, S. C., Ivanova, R., H. Hendel, H., Do, H., Mazoyer, A., Khadivpour, E., Goutalier, F. X., Khalili, K., Rappaport, J., Lathrop, G. M., Matsuda, F. and Zagury, J. -F. Vasilescu, A., Heath, S. C., Ivanova, R., H. Hendel, H., Do, H., Mazoyer, A., Khadivpour, E., Goutalier, F. X., Khalili, K., Rappaport, J., Lathrop, G. M., Matsuda, F. and Zagury, J. -F. Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression. Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression. Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression. Genes and Immunity, 4, 441-449 Genes and Immunity, 4, 441-449 Genes and Immunity, 4, 441-449 2003 英語 研究論文(学術雑誌) 公開
Kim-Saijo, M., Akamizu, T., Ikuta, K., Iida, Y., Ohmori, K., Matsubara, K., Matsuda, Y., Suzuki, M., Matsuda, F. and Nakao, N. Kim-Saijo, M., Akamizu, T., Ikuta, K., Iida, Y., Ohmori, K., Matsubara, K., Matsuda, Y., Suzuki, M., Matsuda, F. and Nakao, N. Kim-Saijo, M., Akamizu, T., Ikuta, K., Iida, Y., Ohmori, K., Matsubara, K., Matsuda, Y., Suzuki, M., Matsuda, F. and Nakao, N. Generation of a Transgenic Animal Model of Hyperthyroid Graves’ Disease. Generation of a Transgenic Animal Model of Hyperthyroid Graves’ Disease. Generation of a Transgenic Animal Model of Hyperthyroid Graves’ Disease. Eur. J. Immunol., 33, 2531-2538 Eur. J. Immunol., 33, 2531-2538 Eur. J. Immunol., 33, 2531-2538 2003 英語 研究論文(学術雑誌) 公開
de Roux, N., Genin, E., Carel, J. C., Matsuda, F., Chaussain, J. L. and Milgrom E. de Roux, N., Genin, E., Carel, J. C., Matsuda, F., Chaussain, J. L. and Milgrom E. de Roux, N., Genin, E., Carel, J. C., Matsuda, F., Chaussain, J. L. and Milgrom E. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc. Natl. Acad. Sci. U. S. A., 100, 10972-10976 Proc. Natl. Acad. Sci. U. S. A., 100, 10972-10976 Proc. Natl. Acad. Sci. U. S. A., 100, 10972-10976 2003 英語 研究論文(学術雑誌) 公開
Matsuda, F. Matsuda, F. Matsuda, F. The human immunoglobulin heavy-chain loci in human. The human immunoglobulin heavy-chain loci in human. The human immunoglobulin heavy-chain loci in human. in ‘Molecular Biology of B cells’ (T. Honjo, F. Alt, M. Neuberger, eds) Academic press. London U. K., 1-24 in ‘Molecular Biology of B cells’ (T. Honjo, F. Alt, M. Neuberger, eds) Academic press. London U. K., 1-24 in ‘Molecular Biology of B cells’ (T. Honjo, F. Alt, M. Neuberger, eds) Academic press. London U. K., 1-24 2003 英語 研究論文(学術雑誌) 公開
Soubrier, F., Martin, S., Alonso, A., Visvikis, S., Tiret, L., Matsuda, F., Lathrop, G. M. and Farrall, M. Soubrier, F., Martin, S., Alonso, A., Visvikis, S., Tiret, L., Matsuda, F., Lathrop, G. M. and Farrall, M. Soubrier, F., Martin, S., Alonso, A., Visvikis, S., Tiret, L., Matsuda, F., Lathrop, G. M. and Farrall, M. High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. Eur. J. Hum. Genet., 10, 553-561 Eur. J. Hum. Genet., 10, 553-561 Eur. J. Hum. Genet., 10, 553-561 2002 英語 研究論文(学術雑誌) 公開
Nervi, S., Nicodeme, S., Gartioux, C., Atlan, C., Lathrop, G. M., Reviron, D., Naquet, P., Matsuda, F., Imbert, J. and Vialettes, B. Nervi, S., Nicodeme, S., Gartioux, C., Atlan, C., Lathrop, G. M., Reviron, D., Naquet, P., Matsuda, F., Imbert, J. and Vialettes, B. Nervi, S., Nicodeme, S., Gartioux, C., Atlan, C., Lathrop, G. M., Reviron, D., Naquet, P., Matsuda, F., Imbert, J. and Vialettes, B. No association between lck gene polymorphisms and protein level in type 1 diabetes. No association between lck gene polymorphisms and protein level in type 1 diabetes. No association between lck gene polymorphisms and protein level in type 1 diabetes. Diabetes, 51, 3326-3330 Diabetes, 51, 3326-3330 Diabetes, 51, 3326-3330 2002 英語 研究論文(学術雑誌) 公開
Cox, R., Bouzekri, N., Martin, S., Southam, L., Hugill, A., Golamaully, M., Cooper, R., Adeyemo, A., Soubrier, F., Ward, R., Lathrop, M., Matsuda, F. and Farrall, M. Cox, R., Bouzekri, N., Martin, S., Southam, L., Hugill, A., Golamaully, M., Cooper, R., Adeyemo, A., Soubrier, F., Ward, R., Lathrop, M., Matsuda, F. and Farrall, M. Cox, R., Bouzekri, N., Martin, S., Southam, L., Hugill, A., Golamaully, M., Cooper, R., Adeyemo, A., Soubrier, F., Ward, R., Lathrop, M., Matsuda, F. and Farrall, M. Angiotensin-1 converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Angiotensin-1 converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Angiotensin-1 converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Hum. Mol. Genet., 11, 2969-2977 Hum. Mol. Genet., 11, 2969-2977 Hum. Mol. Genet., 11, 2969-2977 2002 英語 研究論文(学術雑誌) 公開
Bruls, T., Gyapay, G., Petit, J-L., Artiguenave, F., Vico, V., Qin, S., Tin-Wollam, A. M., Da Silva, C., Muselet, D., Mavel, D., Pelletier, E., Levy, M., Fujiyama, A., Matsuda, F., Wilson, R., Rowen, L., Hood, L., Weissenbach, J., Saurin, W. and Heilig, R. Bruls, T., Gyapay, G., Petit, J-L., Artiguenave, F., Vico, V., Qin, S., Tin-Wollam, A. M., Da Silva, C., Muselet, D., Mavel, D., Pelletier, E., Levy, M., Fujiyama, A., Matsuda, F., Wilson, R., Rowen, L., Hood, L., Weissenbach, J., Saurin, W. and Heilig, R. Bruls, T., Gyapay, G., Petit, J-L., Artiguenave, F., Vico, V., Qin, S., Tin-Wollam, A. M., Da Silva, C., Muselet, D., Mavel, D., Pelletier, E., Levy, M., Fujiyama, A., Matsuda, F., Wilson, R., Rowen, L., Hood, L., Weissenbach, J., Saurin, W. and Heilig, R. A clone map of human chromosome 14. A clone map of human chromosome 14. A clone map of human chromosome 14. Nature, 409, 947-948 Nature, 409, 947-948 Nature, 409, 947-948 2001 英語 研究論文(学術雑誌) 公開
Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. The human immunoglobulin VH locus. The human immunoglobulin VH locus. The human immunoglobulin VH locus. The Immunologist, 7, 171-176 The Immunologist, 7, 171-176 The Immunologist, 7, 171-176 2000 英語 研究論文(学術雑誌) 公開
Farrall, M., Keavney, B., Mckenzie, C., Delepine, M., Matsuda, F. and Lathrop, M. Farrall, M., Keavney, B., Mckenzie, C., Delepine, M., Matsuda, F. and Lathrop, M. Farrall, M., Keavney, B., Mckenzie, C., Delepine, M., Matsuda, F. and Lathrop, M. Fine-mapping of an ancestral recombination breakpoint in DCP1. Fine-mapping of an ancestral recombination breakpoint in DCP1. Fine-mapping of an ancestral recombination breakpoint in DCP1. Nature Genetics, 23, 270-271 Nature Genetics, 23, 270-271 Nature Genetics, 23, 270-271 1999 英語 研究論文(学術雑誌) 公開
Shinkura, R., Kitada, K., Matsuda, F., Tashiro, K., Ikuta, K., Suzuki, M., Kogishi, K., Serikawa T. and Honjo T. Shinkura, R., Kitada, K., Matsuda, F., Tashiro, K., Ikuta, K., Suzuki, M., Kogishi, K., Serikawa T. and Honjo T. Shinkura, R., Kitada, K., Matsuda, F., Tashiro, K., Ikuta, K., Suzuki, M., Kogishi, K., Serikawa T. and Honjo T. Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kb-inducing kinase. Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kb-inducing kinase. Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kb-inducing kinase. Nature Genetics, 22, 74-77 Nature Genetics, 22, 74-77 Nature Genetics, 22, 74-77 1999 英語 研究論文(学術雑誌) 公開
Pallares, N., Lefebvre, S., Contet, V., Matsuda, F. and Lefranc, M-. P. Pallares, N., Lefebvre, S., Contet, V., Matsuda, F. and Lefranc, M-. P. Pallares, N., Lefebvre, S., Contet, V., Matsuda, F. and Lefranc, M-. P. The human immunoglobulin heavy variable genes. The human immunoglobulin heavy variable genes. The human immunoglobulin heavy variable genes. Exp. Clin. Immunogenet., 16, 36-60 Exp. Clin. Immunogenet., 16, 36-60 Exp. Clin. Immunogenet., 16, 36-60 1999 英語 研究論文(学術雑誌) 公開
Matsuda, F., Ishii, K., Bouvagnet, P., Kuma, K., Hayashida, H., Miyata, T. and Honjo, T. Matsuda, F., Ishii, K., Bouvagnet, P., Kuma, K., Hayashida, H., Miyata, T. and Honjo, T. Matsuda, F., Ishii, K., Bouvagnet, P., Kuma, K., Hayashida, H., Miyata, T. and Honjo, T. The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus. The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus. The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus. J. Exp. Med., 188, 2151-2162 J. Exp. Med., 188, 2151-2162 J. Exp. Med., 188, 2151-2162 1998 英語 研究論文(学術雑誌) 公開
Kim, N., Kage, K., Matsuda, F., Lefranc, M.P. and Storb U. Kim, N., Kage, K., Matsuda, F., Lefranc, M.P. and Storb U. Kim, N., Kage, K., Matsuda, F., Lefranc, M.P. and Storb U. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. J. Exp. Med., 186, 413-419 J. Exp. Med., 186, 413-419 J. Exp. Med., 186, 413-419 1997 英語 研究論文(学術雑誌) 公開
Bona, C. A., Murai, C., Casares, S., Kasturi, K., Nishimura, H., Honjo, T. and Matsuda, F. Bona, C. A., Murai, C., Casares, S., Kasturi, K., Nishimura, H., Honjo, T. and Matsuda, F. Bona, C. A., Murai, C., Casares, S., Kasturi, K., Nishimura, H., Honjo, T. and Matsuda, F. Structure of the mutant fibrillin-1 gene in the Tight Skin (TSK) mouse. Structure of the mutant fibrillin-1 gene in the Tight Skin (TSK) mouse. Structure of the mutant fibrillin-1 gene in the Tight Skin (TSK) mouse. DNA Research, 4, 267-271 DNA Research, 4, 267-271 DNA Research, 4, 267-271 1997 英語 研究論文(学術雑誌) 公開
Ueda, Y., Matsuda, F., Misawa, S. and Taniwaki, M. Ueda, Y., Matsuda, F., Misawa, S. and Taniwaki, M. Ueda, Y., Matsuda, F., Misawa, S. and Taniwaki, M. Tumor-specific rearrangements of the immunoglobulin heavy-chain gene in B-cell Non-Hodgkin's lymphoma detected by in situ hybridization. Tumor-specific rearrangements of the immunoglobulin heavy-chain gene in B-cell Non-Hodgkin's lymphoma detected by in situ hybridization. Tumor-specific rearrangements of the immunoglobulin heavy-chain gene in B-cell Non-Hodgkin's lymphoma detected by in situ hybridization. Blood, 87, 292-298 Blood, 87, 292-298 Blood, 87, 292-298 1996 英語 研究論文(学術雑誌) 公開
Shinkura, R., Matsuda, F., Sakiyama, T., Tsubata, T., Hiai, H., Paumen, M., Miyawaki, S. and Honjo, T. Shinkura, R., Matsuda, F., Sakiyama, T., Tsubata, T., Hiai, H., Paumen, M., Miyawaki, S. and Honjo, T. Shinkura, R., Matsuda, F., Sakiyama, T., Tsubata, T., Hiai, H., Paumen, M., Miyawaki, S. and Honjo, T. Defects of somatic hypermutation and class switching in alymphoplasia (aly) mutant mice. Defects of somatic hypermutation and class switching in alymphoplasia (aly) mutant mice. Defects of somatic hypermutation and class switching in alymphoplasia (aly) mutant mice. Int. Immunol., 8, 1067-1075 Int. Immunol., 8, 1067-1075 Int. Immunol., 8, 1067-1075 1996 英語 研究論文(学術雑誌) 公開
Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. Organization of the Human Immunoglobulin Heavy-Chain Locus. Organization of the Human Immunoglobulin Heavy-Chain Locus. Organization of the Human Immunoglobulin Heavy-Chain Locus. in "Advances in Immunology" (F. Dixon, ed.) Academic Press, San Diego, U. S. A., 62, 1-29 in "Advances in Immunology" (F. Dixon, ed.) Academic Press, San Diego, U. S. A., 62, 1-29 in "Advances in Immunology" (F. Dixon, ed.) Academic Press, San Diego, U. S. A., 62, 1-29 1996 英語 研究論文(学術雑誌) 公開
Akamizu, T., Matsuda, F., Okuda, J., Li, H., Kanda, H., Watanabe, T., Honjo, T. and Mori, T. Akamizu, T., Matsuda, F., Okuda, J., Li, H., Kanda, H., Watanabe, T., Honjo, T. and Mori, T. Akamizu, T., Matsuda, F., Okuda, J., Li, H., Kanda, H., Watanabe, T., Honjo, T. and Mori, T. Molecular analysis of stimulatory anti-thyrotropin receptor antibodies (TSAbs) involved in Graves' disease: Isolation and reconstitution of antibody genes, and production of monoclonal TSAbs. Molecular analysis of stimulatory anti-thyrotropin receptor antibodies (TSAbs) involved in Graves' disease: Isolation and reconstitution of antibody genes, and production of monoclonal TSAbs. Molecular analysis of stimulatory anti-thyrotropin receptor antibodies (TSAbs) involved in Graves' disease: Isolation and reconstitution of antibody genes, and production of monoclonal TSAbs. J. Immunol., 157, 3148-3152 J. Immunol., 157, 3148-3152 J. Immunol., 157, 3148-3152 1996 英語 研究論文(学術雑誌) 公開
Honjo, T. and Matsuda, F. Honjo, T. and Matsuda, F. Honjo, T. and Matsuda, F. Immunoglobulin heavy chain loci of mouse and man. Immunoglobulin heavy chain loci of mouse and man. Immunoglobulin heavy chain loci of mouse and man. in "Immunoglobulin Genes" (T. Honjo and F. W. Alt, eds.) Academic Press, London, U. K., 145-171 in "Immunoglobulin Genes" (T. Honjo and F. W. Alt, eds.) Academic Press, London, U. K., 145-171 in "Immunoglobulin Genes" (T. Honjo and F. W. Alt, eds.) Academic Press, London, U. K., 145-171 1995 英語 研究論文(学術雑誌) 公開
Nagaoka, H., Ozawa, K., Matsuda, F., Hayashida, H., Matsumura, R., Haino, M., Shin, E. K., Fukita, Y., Imai, T., Anand, R., Yokoyama, K., Eki, T., Soeda, E. and Honjo, T. Nagaoka, H., Ozawa, K., Matsuda, F., Hayashida, H., Matsumura, R., Haino, M., Shin, E. K., Fukita, Y., Imai, T., Anand, R., Yokoyama, K., Eki, T., Soeda, E. and Honjo, T. Nagaoka, H., Ozawa, K., Matsuda, F., Hayashida, H., Matsumura, R., Haino, M., Shin, E. K., Fukita, Y., Imai, T., Anand, R., Yokoyama, K., Eki, T., Soeda, E. and Honjo, T. Recent translocation of variable and diversity (D) segment of the human immunoglobulin heavy chain from chromosome 14 to chromosomes 15 and 16. Recent translocation of variable and diversity (D) segment of the human immunoglobulin heavy chain from chromosome 14 to chromosomes 15 and 16. Recent translocation of variable and diversity (D) segment of the human immunoglobulin heavy chain from chromosome 14 to chromosomes 15 and 16. Genomics, 22, 189-197 Genomics, 22, 189-197 Genomics, 22, 189-197 1994 英語 研究論文(学術雑誌) 公開
Nakamura, N., Azuma, C., Akamizu, T., Sugawa, H., Matsuda, F., Mitsuda, N., Honjo, T., Mori, T. and Yamaji, K. Nakamura, N., Azuma, C., Akamizu, T., Sugawa, H., Matsuda, F., Mitsuda, N., Honjo, T., Mori, T. and Yamaji, K. Nakamura, N., Azuma, C., Akamizu, T., Sugawa, H., Matsuda, F., Mitsuda, N., Honjo, T., Mori, T. and Yamaji, K. Heterogeneity and diversity of IgM and IgG lupus anticoagulants in an individual with systemic lupus erythematosus. Heterogeneity and diversity of IgM and IgG lupus anticoagulants in an individual with systemic lupus erythematosus. Heterogeneity and diversity of IgM and IgG lupus anticoagulants in an individual with systemic lupus erythematosus. Biochem. Biophys. Res. Commun., 203, 1789-1794 Biochem. Biophys. Res. Commun., 203, 1789-1794 Biochem. Biophys. Res. Commun., 203, 1789-1794 1994 英語 研究論文(学術雑誌) 公開
Okuda, J., Akamizu, T., Sugawa, H., Matsuda, F., Hua, L. and Mori, T. Okuda, J., Akamizu, T., Sugawa, H., Matsuda, F., Hua, L. and Mori, T. Okuda, J., Akamizu, T., Sugawa, H., Matsuda, F., Hua, L. and Mori, T. Preparation and characterization of monoclonal antithyrotropin receptor antibodies obtained from peripheral lymphocytes of hypothyroid patients with primary myxedema. Preparation and characterization of monoclonal antithyrotropin receptor antibodies obtained from peripheral lymphocytes of hypothyroid patients with primary myxedema. Preparation and characterization of monoclonal antithyrotropin receptor antibodies obtained from peripheral lymphocytes of hypothyroid patients with primary myxedema. J. Clin. Endocrinol. Metab., 79, 1600-1604 J. Clin. Endocrinol. Metab., 79, 1600-1604 J. Clin. Endocrinol. Metab., 79, 1600-1604 1994 英語 研究論文(学術雑誌) 公開
Matsumura, R., Matsuda, F., Nagaoka, H., Shin, E. K., Fukita, Y., Haino, M., Fujikura, J. and Honjo, T. Matsumura, R., Matsuda, F., Nagaoka, H., Shin, E. K., Fukita, Y., Haino, M., Fujikura, J. and Honjo, T. Matsumura, R., Matsuda, F., Nagaoka, H., Shin, E. K., Fukita, Y., Haino, M., Fujikura, J. and Honjo, T. Structural analysis of the human VH locus using non-repetitive intergenic probes and repetitive sequence probes; Evidence for recent reshuffling. Structural analysis of the human VH locus using non-repetitive intergenic probes and repetitive sequence probes; Evidence for recent reshuffling. Structural analysis of the human VH locus using non-repetitive intergenic probes and repetitive sequence probes; Evidence for recent reshuffling. J. Immunol., 152, 660-666 J. Immunol., 152, 660-666 J. Immunol., 152, 660-666 1994 英語 研究論文(学術雑誌) 公開
Haino, M., Hayashida, H., Miyata, T., Shin, E. K., Matsuda, F., Nagaoka, H., Matsumura, R., Taka-ishi, S., Fukita, Y., Fujikura, J. and Honjo, T. Haino, M., Hayashida, H., Miyata, T., Shin, E. K., Matsuda, F., Nagaoka, H., Matsumura, R., Taka-ishi, S., Fukita, Y., Fujikura, J. and Honjo, T. Haino, M., Hayashida, H., Miyata, T., Shin, E. K., Matsuda, F., Nagaoka, H., Matsumura, R., Taka-ishi, S., Fukita, Y., Fujikura, J. and Honjo, T. Comparison and evolution of human immunoglobulin VH segments located in the 3' 0.8-megabase region: evidence for unidirectional transfer of segmental gene sequences. Comparison and evolution of human immunoglobulin VH segments located in the 3' 0.8-megabase region: evidence for unidirectional transfer of segmental gene sequences. Comparison and evolution of human immunoglobulin VH segments located in the 3' 0.8-megabase region: evidence for unidirectional transfer of segmental gene sequences. J. Biol. Chem., 269, 2619-2626 J. Biol. Chem., 269, 2619-2626 J. Biol. Chem., 269, 2619-2626 1994 英語 研究論文(学術雑誌) 公開
Shin, E. K., Akamizu, T., Matsuda, F., Sugawa, H., Fujikura, J., Mori, T. and Honjo, T. Shin, E. K., Akamizu, T., Matsuda, F., Sugawa, H., Fujikura, J., Mori, T. and Honjo, T. Shin, E. K., Akamizu, T., Matsuda, F., Sugawa, H., Fujikura, J., Mori, T. and Honjo, T. Variable-regions of immunoglobulin heavy-chain genes encoding anti-thyrotropin (TSH) receptor antibodies of patients with Graves' disease. Variable-regions of immunoglobulin heavy-chain genes encoding anti-thyrotropin (TSH) receptor antibodies of patients with Graves' disease. Variable-regions of immunoglobulin heavy-chain genes encoding anti-thyrotropin (TSH) receptor antibodies of patients with Graves' disease. J. Immunol., 152, 1485-1492 J. Immunol., 152, 1485-1492 J. Immunol., 152, 1485-1492 1994 英語 研究論文(学術雑誌) 公開
Taniwaki, M., Matsuda, F., Jauch, A., Nishida, K., Takashima, T., Tagawa, S., Sugiyama, H., Misawa, S., Abe, T. and Kashima, K. Taniwaki, M., Matsuda, F., Jauch, A., Nishida, K., Takashima, T., Tagawa, S., Sugiyama, H., Misawa, S., Abe, T. and Kashima, K. Taniwaki, M., Matsuda, F., Jauch, A., Nishida, K., Takashima, T., Tagawa, S., Sugiyama, H., Misawa, S., Abe, T. and Kashima, K. Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locus. Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locus. Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locus. Blood, 83, 2962-2969 Blood, 83, 2962-2969 Blood, 83, 2962-2969 1994 英語 研究論文(学術雑誌) 公開
Matsuda, F., Shin, E. K., Nagaoka, H., Matsumura, R., Haino, M., Fukita, Y., Taka-ishi, S., Imai, T., Riley, J. H., Anand, R., Soeda, E. and Honjo, T. Matsuda, F., Shin, E. K., Nagaoka, H., Matsumura, R., Haino, M., Fukita, Y., Taka-ishi, S., Imai, T., Riley, J. H., Anand, R., Soeda, E. and Honjo, T. Matsuda, F., Shin, E. K., Nagaoka, H., Matsumura, R., Haino, M., Fukita, Y., Taka-ishi, S., Imai, T., Riley, J. H., Anand, R., Soeda, E. and Honjo, T. Structure and physical map of 64 variable segments in the 0.8-megabase region of the human immunoglobulin heavy-chain locus. Structure and physical map of 64 variable segments in the 0.8-megabase region of the human immunoglobulin heavy-chain locus. Structure and physical map of 64 variable segments in the 0.8-megabase region of the human immunoglobulin heavy-chain locus. Nature genetics, 3, 88-94 Nature genetics, 3, 88-94 Nature genetics, 3, 88-94 1993 英語 研究論文(学術雑誌) 公開
Shin, E. K., Matsuda, F., Ozaki, S., Kumagai, S., Olerup, O., Strom, H., Melchers, I. and Honjo, T. Shin, E. K., Matsuda, F., Ozaki, S., Kumagai, S., Olerup, O., Strom, H., Melchers, I. and Honjo, T. Shin, E. K., Matsuda, F., Ozaki, S., Kumagai, S., Olerup, O., Strom, H., Melchers, I. and Honjo, T. Polymorphism of the human immunoglobulin variable region segment V1-4.1. Polymorphism of the human immunoglobulin variable region segment V1-4.1. Polymorphism of the human immunoglobulin variable region segment V1-4.1. Immunogenetics, 38, 304-306 Immunogenetics, 38, 304-306 Immunogenetics, 38, 304-306 1993 英語 研究論文(学術雑誌) 公開
Haire, R. N., Buell, R. D., Litman, R. T., Ohta, Y., Fu, S. M., Honjo, T., Matsuda, F., de la Morena, M., Carro, J., Good, R. A. and Litman, G. W. Haire, R. N., Buell, R. D., Litman, R. T., Ohta, Y., Fu, S. M., Honjo, T., Matsuda, F., de la Morena, M., Carro, J., Good, R. A. and Litman, G. W. Haire, R. N., Buell, R. D., Litman, R. T., Ohta, Y., Fu, S. M., Honjo, T., Matsuda, F., de la Morena, M., Carro, J., Good, R. A. and Litman, G. W. Diversification, not utilization, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome. Diversification, not utilization, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome. Diversification, not utilization, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome. J. Exp. Med., 178, 825-834 J. Exp. Med., 178, 825-834 J. Exp. Med., 178, 825-834 1993 英語 研究論文(学術雑誌) 公開
Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. Matsuda, F. and Honjo, T. Physical mapping of variable region gene locus of human immunoglobulin heavy chain. Physical mapping of variable region gene locus of human immunoglobulin heavy chain. Physical mapping of variable region gene locus of human immunoglobulin heavy chain. in "Methods in Molecular Genetics" (K. Adolph, ed.), 2, 226-245 in "Methods in Molecular Genetics" (K. Adolph, ed.), 2, 226-245 in "Methods in Molecular Genetics" (K. Adolph, ed.), 2, 226-245 1993 英語 研究論文(学術雑誌) 公開
Shin, E. K., Matsuda, F., Fujikura, J., Akamizu, T., Sugawa, H., Mori, T. and Honjo, T. Shin, E. K., Matsuda, F., Fujikura, J., Akamizu, T., Sugawa, H., Mori, T. and Honjo, T. Shin, E. K., Matsuda, F., Fujikura, J., Akamizu, T., Sugawa, H., Mori, T. and Honjo, T. Cloning of a human immunoglobulin gene fragment containing both VH-D and D-JH rearrangements: implication for VH-D as an intermediate to VH-D-JH formation. Cloning of a human immunoglobulin gene fragment containing both VH-D and D-JH rearrangements: implication for VH-D as an intermediate to VH-D-JH formation. Cloning of a human immunoglobulin gene fragment containing both VH-D and D-JH rearrangements: implication for VH-D as an intermediate to VH-D-JH formation. Eur. J. Immunol., 23, 2365-2367 Eur. J. Immunol., 23, 2365-2367 Eur. J. Immunol., 23, 2365-2367 1993 英語 研究論文(学術雑誌) 公開
Shin, E. K., Matsuda, F., Nagaoka, H., Fukita, Y., Imai, T., Yokoyama, K., Soeda, E. and Honjo, T. Shin, E. K., Matsuda, F., Nagaoka, H., Fukita, Y., Imai, T., Yokoyama, K., Soeda, E. and Honjo, T. Shin, E. K., Matsuda, F., Nagaoka, H., Fukita, Y., Imai, T., Yokoyama, K., Soeda, E. and Honjo, T. Physical map of the 3' region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype. Physical map of the 3' region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype. Physical map of the 3' region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype. EMBO J., 10, 3641-3645 EMBO J., 10, 3641-3645 EMBO J., 10, 3641-3645 1991 英語 研究論文(学術雑誌) 公開
Matsuda, F., Shin, E. K., Hirabayashi, Y., Nagaoka, H., Yoshida, M. C., Zong, S. K. and Honjo, T. Matsuda, F., Shin, E. K., Hirabayashi, Y., Nagaoka, H., Yoshida, M. C., Zong, S. K. and Honjo, T. Matsuda, F., Shin, E. K., Hirabayashi, Y., Nagaoka, H., Yoshida, M. C., Zong, S. K. and Honjo, T. Organization of variable region segments of the human immunoglobulin heavy chain: duplication of the D5 cluster within the locus and interchromosomal translocation of variable region segments. Organization of variable region segments of the human immunoglobulin heavy chain: duplication of the D5 cluster within the locus and interchromosomal translocation of variable region segments. Organization of variable region segments of the human immunoglobulin heavy chain: duplication of the D5 cluster within the locus and interchromosomal translocation of variable region segments. EMBO J., 9, 2501-2506 EMBO J., 9, 2501-2506 EMBO J., 9, 2501-2506 1990 英語 研究論文(学術雑誌) 公開
Matsuda, F., Lee, K. H., Nakai, S., Sato, T., Kodaira, M., Zong, S. K., Ohno, H., Fukuhara, S. and Honjo, T. Matsuda, F., Lee, K. H., Nakai, S., Sato, T., Kodaira, M., Zong, S. K., Ohno, H., Fukuhara, S. and Honjo, T. Matsuda, F., Lee, K. H., Nakai, S., Sato, T., Kodaira, M., Zong, S. K., Ohno, H., Fukuhara, S. and Honjo, T. Dispersed localization of D segments in the human immunoglobulin heavy-chain locus. Dispersed localization of D segments in the human immunoglobulin heavy-chain locus. Dispersed localization of D segments in the human immunoglobulin heavy-chain locus. EMBO J., 7, 1047-1051 EMBO J., 7, 1047-1051 EMBO J., 7, 1047-1051 1988 英語 研究論文(学術雑誌) 公開
Zong, S. K., Nakai, S., Matsuda, F., Lee, K. H. and Honjo, T. Zong, S. K., Nakai, S., Matsuda, F., Lee, K. H. and Honjo, T. Zong, S. K., Nakai, S., Matsuda, F., Lee, K. H. and Honjo, T. Human immunoglobulin D segments: isolation of a new D segment and polymorphic deletion of the D1 segment. Human immunoglobulin D segments: isolation of a new D segment and polymorphic deletion of the D1 segment. Human immunoglobulin D segments: isolation of a new D segment and polymorphic deletion of the D1 segment. Immunol. Lett., 17, 329-334 Immunol. Lett., 17, 329-334 Immunol. Lett., 17, 329-334 1988 英語 研究論文(学術雑誌) 公開
Sato, T., Matsuda, F., Lee, K. H., Shin, E. K. and Honjo, T. Honjo, T. Sato, T., Matsuda, F., Lee, K. H., Shin, E. K. and Honjo, T. Honjo, T. Sato, T., Matsuda, F., Lee, K. H., Shin, E. K. and Honjo, T. Honjo, T. Physical linkage of a variable region segment and the joining region segment of the human immunoglobulin heavy chain locus. Physical linkage of a variable region segment and the joining region segment of the human immunoglobulin heavy chain locus. Physical linkage of a variable region segment and the joining region segment of the human immunoglobulin heavy chain locus. Biochem. Biophys. Res. Commun., 154, 265-271 Biochem. Biophys. Res. Commun., 154, 265-271 Biochem. Biophys. Res. Commun., 154, 265-271 1988 英語 研究論文(学術雑誌) 公開
Ueda, S., Matsuda, F. and Honjo, T. Ueda, S., Matsuda, F. and Honjo, T. Ueda, S., Matsuda, F. and Honjo, T. Multiple recombinatorial events in primate immunoglobulin Epsilon and Alpha genes suggest closer relationship of humans to chimpanzees than to gorillas. Multiple recombinatorial events in primate immunoglobulin Epsilon and Alpha genes suggest closer relationship of humans to chimpanzees than to gorillas. Multiple recombinatorial events in primate immunoglobulin Epsilon and Alpha genes suggest closer relationship of humans to chimpanzees than to gorillas. J. Mol. Evol., 27, 77-83 J. Mol. Evol., 27, 77-83 J. Mol. Evol., 27, 77-83 1988 英語 研究論文(学術雑誌) 公開
Lee, K. H., Matsuda, F., Kinashi, T., Kodaira, M. and Honjo, T. Lee, K. H., Matsuda, F., Kinashi, T., Kodaira, M. and Honjo, T. Lee, K. H., Matsuda, F., Kinashi, T., Kodaira, M. and Honjo, T. A novel family of variable region genes of the human immunoglobulin heavy chain. A novel family of variable region genes of the human immunoglobulin heavy chain. A novel family of variable region genes of the human immunoglobulin heavy chain. J. Mol. Biol., 195, 761-768 J. Mol. Biol., 195, 761-768 J. Mol. Biol., 195, 761-768 1987 英語 研究論文(学術雑誌) 公開
Noma, Y., Sideras, P., Naito, T., Bergstedt-Lindqvist, S., Azuma, C., Severinson, E., Tanabe, T., Kinashi, T., Matsuda, F., Yaoita, Y. and Honjo, T. Noma, Y., Sideras, P., Naito, T., Bergstedt-Lindqvist, S., Azuma, C., Severinson, E., Tanabe, T., Kinashi, T., Matsuda, F., Yaoita, Y. and Honjo, T. Noma, Y., Sideras, P., Naito, T., Bergstedt-Lindqvist, S., Azuma, C., Severinson, E., Tanabe, T., Kinashi, T., Matsuda, F., Yaoita, Y. and Honjo, T. Cloning of cDNA encoding the murine IgG1 induction factor by a novel strategy using SP6 promoter. Cloning of cDNA encoding the murine IgG1 induction factor by a novel strategy using SP6 promoter. Cloning of cDNA encoding the murine IgG1 induction factor by a novel strategy using SP6 promoter. Nature, 319, 640-646 Nature, 319, 640-646 Nature, 319, 640-646 1986 英語 研究論文(学術雑誌) 公開
Kodaira, M., Kinashi, T., Umemura, I., Matsuda, F., Noma, T., Ono, Y. and Honjo, T. Kodaira, M., Kinashi, T., Umemura, I., Matsuda, F., Noma, T., Ono, Y. and Honjo, T. Kodaira, M., Kinashi, T., Umemura, I., Matsuda, F., Noma, T., Ono, Y. and Honjo, T. Organization and evolution of variable region genes of the human immunoglobulin heavy chain. Organization and evolution of variable region genes of the human immunoglobulin heavy chain. Organization and evolution of variable region genes of the human immunoglobulin heavy chain. J. Mol. Biol., 190, 529-541 J. Mol. Biol., 190, 529-541 J. Mol. Biol., 190, 529-541 1986 英語 研究論文(学術雑誌) 公開
Kinashi, T., Harada, N., Severinson, E., Tanabe, T., Sideras, P., Konishi, M., Azuma, C., Tominaga, A., Bergstedt-Lindqvist, S., Takahashi, M., Matsuda, F., Yaoita, Y., Takatsu, K. and Honjo, T. Kinashi, T., Harada, N., Severinson, E., Tanabe, T., Sideras, P., Konishi, M., Azuma, C., Tominaga, A., Bergstedt-Lindqvist, S., Takahashi, M., Matsuda, F., Yaoita, Y., Takatsu, K. and Honjo, T. Kinashi, T., Harada, N., Severinson, E., Tanabe, T., Sideras, P., Konishi, M., Azuma, C., Tominaga, A., Bergstedt-Lindqvist, S., Takahashi, M., Matsuda, F., Yaoita, Y., Takatsu, K. and Honjo, T. Cloning of complementary DNA encoding T-cell replacing factor and identity with B-cell growth factor II. Cloning of complementary DNA encoding T-cell replacing factor and identity with B-cell growth factor II. Cloning of complementary DNA encoding T-cell replacing factor and identity with B-cell growth factor II. Nature, 324, 70-73 Nature, 324, 70-73 Nature, 324, 70-73 1986 英語 研究論文(学術雑誌) 公開

  • <<
  • >>
  • 表示
タイトル言語:
学術賞等
賞の名称(日本語) 賞の名称(英語) 授与組織名(日本語) 授与組織名(英語) 年月
日本生化学会奨励賞 Young Investigator Award 日本生化学会 The Japanese Biochemical Society 2000
日本免疫学会賞 Award of Japanese Society for Immunology 日本免疫学会 Japanese Society for Immunology 2000
外部資金:競争的資金・科学研究費補助金
種別 代表/分担 テーマ(日本語) テーマ(英語) 期間
H20-21年度 科学研究費補助金 特定領域研究 代表 ゲノムワイドアプローチを用いた日本人成人性T細胞白血病の感受性遺伝子・多型の探索 2008〜2009
H20-22年度 厚生労働科学研究費補助金 医療技術実用化総合研究事業  分担 「重症クローン病患者に対するタクロリムス療法」に向けての臨床試験の実現に関する研究 2008〜2010
H20-22年度 厚生労働科学研究費補助金 肝炎等克服緊急対策研究事業 分担 非アルコール性脂肪性肝疾患の病態解明と新療法、治療法の開発に関する研究 2008〜2010
H20-22年度 科学技術推進費補助金 アジア・アフリカ科学技術協力の戦略的推進 代表 デング熱の発症と病態に関連する遺伝因子の同定 2008〜2010
H21-23年度 厚生労働科学研究費補助金 難治性疾患克服研究事業 分担 IgG4関連全身硬化性疾患の診断法の確立と治療方法の開発に関する研究 2008〜2010
H21-23年度 厚生労働科学研究費補助金 第3次対がん総合戦略研究事業 分担 ヒトT細胞白血病ウイルス1型関連疾患における感受性遺伝子多型の同定と発症危機群へアプローチ 2009〜2011
H22-23年度 科学研究費補助金 特定領域研究 代表 大規模リウマチ前向きコホートのゲノム解析によるリウマチのテイラーメイド医療の試み 2009〜2010
H23-25年度 厚生労働科学研究費補助金 難病・がん等の疾患分野の医療の実用化研究事業(がん関係研究分野) 代表 網羅的統合オミックス解析を用いた難病の原因究明と新規診断・治療法の確立 2011〜2013
H23-25年度 厚生科学研究費補助金 創薬基盤推進研究事業  分担 ゲノム網羅的関連解析の大規模メタ解析を基礎としたcommon diseaseのテーラーメイド医療実現化に関する研究 2011〜2013
H24-25年度 厚生労働科学研究費補助金 難治性疾患等克服研究事業(難治性疾患克服研究事業) 代表 難病・がん等の疾患分野の医療の実用化研究事業の成果を基にした原因遺伝子変異データベースの構築 2012〜2013
H25年度 厚生労働科学研究費補助金 難治性疾患等克服研究事業(難治性疾患克服研究事業) 分担 遺伝学的検査の実施拠点の在り方に関する研究 2013〜2013
H25-26年度 科学研究費補助金 基盤研究(B) 分担 肺癌におけるEGFRチロシンキナーゼ阻害剤耐性化の解明と克服に向けた基礎的研究 2013〜
H25-26年度 科学研究費補助金 基盤研究(B) 分担 高齢者フレイルティの包括的疫学研究 2013〜
H26年度 科学研究費補助金 基盤研究(B) 分担 気道疾患の肺機能経年変化と全身病態に対する睡眠障害の影響と新治療体系の構築 2014〜
H26年度 科学研究費補助金 基盤研究(A) 分担 真に実用可能な、卵巣癌の薬剤感受性予測バイオマーカーの確立 2014〜
H29年度 厚生労働科学研究費補助金 がん対策推進総合研究事業 分担 環境要因・遺伝要因との統合解析による肺がん罹患リスクの検証と 能動・受動喫煙に関する行動変容に資するエビデンスの構築 2017/04/01〜2018/03/31
H30年度 厚生労働科学研究費補助金 がん対策推進総合研究事業 分担 環境要因・遺伝要因との統合解析による肺がん罹患リスクの検証と 能動・受動喫煙に関する行動変容に資するエビデンスの構築 2018/04/01〜2019/03/31

  • <<
  • >>
  • 表示
外部資金:競争的資金・科学研究費補助金以外
制度名 代表者名 研究課題(日本語) 研究課題(英語) 期間
科学技術振興機構 戦略的創造研究事業 (CREST)  松田文彦 日仏共同研究体制による人種間ゲノム多型の比較解析 2003〜2008
科学技術振興機構 ライフサイエンスデータベース統合推進事業 松田文彦 大規模ゲノム疫学研究の統合情報基盤の構築 2011〜2013
厚生労働省 H26年度 厚生労働科学研究委託費 難治性疾患実用化研究事業 松田文彦 集約的オミックス解析による難病の原因究明と疾患別遺伝子診断ネットワークの構築 2014〜2014
厚生労働省 H26年度 厚生労働科学研究委託費 難治性疾患実用化研究事業 三森経世 IgG4関連疾患の病態解明と新規治療法の確立に関する研究 2014〜2014
厚生労働省 H26年度 厚生労働科学研究委託費 難治性疾患実用化研究事業 山野嘉久 HAMの革新的な医療品等の開発促進に関する研究 2014〜2014
厚生労働省 H26年度 厚生労働科学研究委託費 革新的がん医療実用化研究事業 河野隆志 肺腺がんの個別化・層別化・早期発見のための高危険度群捕捉手法の確立に関する研究 2014〜2014
厚生労働省 H26年度 厚生労働科学研究委託費 長寿科学研究開発事業 松田秀一 変形性膝関節症の発症・増悪予測スコア作成により要介護を防止する治療戦略構築 2014〜2014
科学技術振興機構 センター・オブ・イノベーション(COI)プログラム 活力ある生涯のためのLast 5X イノベーション 2013〜
文部科学省 次世代がん研究シーズ戦略的育成プログラム 濱西潤三 効果的な複合免疫療法の開発(抗PD-1抗体免疫療法における有効性・非有効性の原因解明とその克服に向けた手法の開発) 2014〜
担当科目
講義名(日本語) 講義名(英語) 開講期 学部/研究科 年度
ゲノム科学と医療 後期不定 医学研究科 2011/04〜2012/03
遺伝・ゲノム医学(演習) 通年不定 医学研究科 2011/04〜2012/03
遺伝・ゲノム医学(実習) 通年不定 医学研究科 2011/04〜2012/03
ゲノム科学と医療 Genome Science and Medicine 後期不定 医学研究科 2012/04〜2013/03
遺伝・ゲノム医学(実習) Genetics and Genome Medicine (Practice) 通年 医学研究科 2012/04〜2013/03
遺伝・ゲノム医学(演習) Genetics and Genome Medicine (Seminar) 通年 医学研究科 2012/04〜2013/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2013/04〜2014/03
遺伝・ゲノム医学(演習) Genetics and Genome Medicine (Seminar) 通年不定 医学研究科 2013/04〜2014/03
遺伝・ゲノム医学(実習) Genetics and Genome Medicine (Practice) 通年不定 医学研究科 2013/04〜2014/03
オミックス統計学入門 I Introductory Omics-Statistics I 前期不定 医学研究科 2014/04〜2015/03
オミックス統計学入門 II Introductory Omics-Statistics II 後期不定 医学研究科 2014/04〜2015/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2014/04〜2015/03
遺伝・ゲノム医学(演習) Genetics and Genome Medicine (Seminar) 通年不定 医学研究科 2014/04〜2015/03
遺伝・ゲノム医学(実習) Genetics and Genome Medicine (Practice) 通年不定 医学研究科 2014/04〜2015/03
検査機器学・研究機器学:講義(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2014/04〜2015/03
検査機器学・研究機器学:実習(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2014/04〜2015/03
ゲノムコホート研究(LIMS) Genome Cohort Study 前期集中 医学研究科 2014/04〜2015/03
ゲノムコホート研究 Genomic medicine and comprehensive human bioscience 前期 工学研究科 2014/04〜2015/03
フィールドワーク Fieldwork 通年集中 医学研究科 2015/04〜2016/03
検査機器学・研究機器学:実習(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2015/04〜2016/03
検査機器学・研究機器学:講義(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2015/04〜2016/03
生物学のフロンティア Frontiers of Biology 前期 全学共通科目 2015/04〜2016/03
ゲノムコホート研究 Genomic medicine and comprehensive human bioscience 前期 工学研究科 2015/04〜2016/03
ゲノムコホート研究(LIMS) Genome Cohort Study 前期集中 医学研究科 2015/04〜2016/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2015/04〜2016/03
フィールドワーク Fieldwork 通年集中 医学研究科 2016/04〜2017/03
検査機器学・研究機器学:実習(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2016/04〜2017/03
検査機器学・研究機器学:講義(LIMS) Inspection equipment studies Science research equipment 後期集中 医学研究科 2016/04〜2017/03
生物学のフロンティア Frontiers of Biology 前期 全学共通科目 2016/04〜2017/03
ゲノムコホート研究 Genomic medicine and comprehensive human bioscience 前期 工学研究科 2016/04〜2017/03
ゲノムコホート研究(LIMS) Genome Cohort Study 前期集中 医学研究科 2016/04〜2017/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2016/04〜2017/03
検査機器学・研究機器学:実習(LIMS) Inspection equipment studies Science research equipment (LIMS) 後期集中 医学研究科 2017/04〜2018/03
検査機器学・研究機器学:講義(LIMS) Inspection equipment studies Science research equipment (LIMS) 後期集中 医学研究科 2017/04〜2018/03
ゲノムコホート研究 Genomic medicine and comprehensive human bioscience 前期 工学研究科 2017/04〜2018/03
ゲノムコホート研究(LIMS) Genome Cohort Study (LIMS) 前期集中 医学研究科 2017/04〜2018/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2017/04〜2018/03
フィールドワーク Fieldwork 通年集中 医学研究科 2018/04〜2019/03
ゲノム医学 I Genomic Medicine I 前期集中 医学研究科 2018/04〜2019/03
ゲノム医学 II Genomic Medicine II 後期集中 医学研究科 2018/04〜2019/03
検査機器学・研究機器学:実習(LIMS) Inspection equipment studies Science research equipment (LIMS) 後期集中 医学研究科 2018/04〜2019/03
検査機器学・研究機器学:講義(LIMS) Inspection equipment studies Science research equipment (LIMS) 後期集中 医学研究科 2018/04〜2019/03
次世代シークエンス技術を用いたゲノム解析とその応用 Genome Analysis Using NGS and Its Applications 後期集中 医学研究科 2018/04〜2019/03
ゲノムコホート研究 Genomic medicine and comprehensive human bioscience 前期 工学研究科 2018/04〜2019/03
ゲノムコホート研究(LIMS) Genome Cohort Study (LIMS) 前期集中 医学研究科 2018/04〜2019/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2018/04〜2019/03
フィールドワーク Fieldwork 通年集中 医学研究科 2019/04〜2020/03
ゲノム医学 I Genomic Medicine I 前期 医学研究科 2019/04〜2020/03
ゲノム医学 II Genomic Medicine II 後期 医学研究科 2019/04〜2020/03
次世代シークエンス技術を用いたゲノム解析とその応用 Genome Analysis Using NGS and Its Applications 後期集中 医学研究科 2019/04〜2020/03
ゲノムコホート研究(LIMS) Genome Cohort Study (LIMS) 前期集中 医学研究科 2019/04〜2020/03
ゲノム科学と医療 Genome Science and Medicine 後期 医学研究科 2019/04〜2020/03

  • <<
  • >>
  • 表示
全学運営(役職等)
役職名 期間
京都大学国際交流推進機構協議会 協議員 2014/10/01〜2016/09/30
京都大学国際交流推進機構協議会幹事会 協議員 2014/10/01〜2016/03/31
国際交流委員会 委員 2010/06/01〜2013/06/30
国際科学イノベーション棟運営委員 2号委員 2015/04/01〜2019/03/31
国際展開委員会 委員 2016/04/01〜2018/09/30
国際戦略本部 全学海外拠点運営専門部会 副部会長 2016/05/25〜2018/09/30
国際戦略委員会 委員 2014/10/16〜2016/09/30
国際戦略委員会 海外拠点運営専門委員会 副委員長 2014/10/16〜2016/06/03
教育制度委員会 委員 2014/10/01〜2018/09/30
教育制度委員会WG3 委員 2014/10/01〜2017/03/31
理事補 2014/10/16〜2018/09/30
ゲノム医学センター長 2012/11/09〜2018/11/08
スーパーグローバルコース実施運営協議会 委員 2015/12/01〜2018/03/31
スーパーグローバルコース企画運営幹事会 委員 2016/04/01〜2018/03/31
教育制度委員会 委員 2016/10/01〜2018/09/30
全学共用スペース有効活用専門委員会 5号委員 2014/10/01〜2018/09/30
教育制度委員会 委員 2016/10/01〜2020/09/30
スーパーグローバルコース企画運営幹事会 委員 2016/04/01〜2019/03/31
スーパーグローバルコース実施運営協議会 委員 2015/12/01〜2020/09/30
理事補 2014/10/16〜2020/09/30
ゲノム医学センター長 2012/11/09〜2020/11/08
国際戦略本部運営協議会 協議員 2018/10/01〜2020/09/30
国際戦略本部運営協議会 パートナーシップ専門部会 部会長 2018/10/01〜2020/09/30
国際科学イノベーション棟運営委員会 委員 2019/04/01〜2021/03/31
全学共用スペース有効活用専門委員会 委員 2014/10/01〜2020/09/30

  • <<
  • >>
  • 表示
部局運営(役職等)
役職名 期間
医学研究科・医学部放射性同位元素等管理委員会 委員
医学研究科学術情報システム・情報セキュリティ委員会 委員 2014/04/01〜2020/03/31
寄附講座運営委員会(免疫ゲノム医学) 委員 2013/04/01〜2015/03/31
バイオ・フロンティア・プラットフォーム運営委員会 委員 2012/01/26〜
附属ゲノム医学センター運営委員会 委員 2005/07/14〜2008/10/31
附属ゲノム医学センター運営委員会 委員長 2008/11/01〜
管理体制委員会 委員 2014/10/01〜2020/09/30
国際交流委員会 委員 2015/04/01〜2020/09/30
国際交流委員会 委員長 2010/06/01〜2013/06/30
学術情報メディアセンター協議員 2012/04/01〜2014/03/31
附属ゲノム医学センター長 2008/11/01〜2020/11/08
将来計画検討委員会 2018/04/01〜2020/03/31
放射線障害防止委員会
京都大学・マギル大学ゲノム医学国際連携専攻長 2018/04/01〜2019/03/31
医学研究科専攻長会議

  • <<
  • >>
  • 表示
その他活動:国・地方公共団体での活動
委員会名(日本語) 委員会名(英語) 役職名 公共団体の名称 期間
内閣府 疫学・コホート検討会およびゲノムコホート研究に関する検討会 委員