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病態ゲノム医学部

スタッフ
高橋 篤

スタッフ紹介 [高橋 篤]

氏名 高橋 篤 NoPhoto
よみ たかはし あつし
所属・職務 病態ゲノム医学部・部長
内線番号
FAX番号
Eメール
棟/部屋番号 研究棟5階
専門 遺伝統計学 / インフォマティクス
主要論文・著書

<論文>

  1. Takata, R., Takahashi, A., Fujita, M., Momozawa, Y., Saunders, E.J., Yamada, H., Maejima, K., Nakano, K., Nishida, Y., Hishida, A., Matsuo, K., Wakai, K., Yamaji, T., Sawada, N., Iwasaki, M., Tsugane, S., Sasaki, M., Shimizu, A., Tanno, K., Minegishi, N., Suzuki, K., Matsuda, K., Kubo, M., Inazawa, J., Egawa, S., Haiman, C.A., Ogawa, O., Obara, W., Kamatani, Y., Akamatsu, S. & Nakagawa, H. 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population. Nat Commun 10, 4422 (2019).
  2. Ikeda, M., Takahashi, A., Kamatani, Y., Momozawa, Y., Saito, T., Kondo, K., Shimasaki, A., Kawase, K., Sakusabe, T., Iwayama, Y., Toyota, T., Wakuda, T., Kikuchi, M., Kanahara, N., Yamamori, H., Yasuda, Y., Watanabe, Y., Hoya, S., Aleksic, B., Kushima, I., Arai, H., Takaki, M., Hattori, K., Kunugi, H., Okahisa, Y., Ohnuma, T., Ozaki, N., Someya, T., Hashimoto, R., Yoshikawa, T., Kubo, M. & Iwata, N. Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. Schizophr Bull 45, 824-834 (2019).
  3. Hori, M., Ohta, N., Takahashi, A., Masuda, H., Isoda, R., Yamamoto, S., Son, C., Ogura, M., Hosoda, K., Miyamoto, Y. & Harada-Shiba, M. Impact of LDLR and PCSK9 pathogenic variants in Japanese heterozygous familial hypercholesterolemia patients. Atherosclerosis 289, 101-108 (2019).
  4. Kanai, M., Akiyama, M., Takahashi, A., Matoba, N., Momozawa, Y., Ikeda, M., Iwata, N., Ikegawa, S., Hirata, M., Matsuda, K., Kubo, M., Okada, Y. & Kamatani, Y. Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Nat Genet 50, 390-400 (2018).
  5. Ikeda, M., Takahashi, A., Kamatani, Y., Okahisa, Y., Kunugi, H., Mori, N., Sasaki, T., Ohmori, T., Okamoto, Y., Kawasaki, H., Shimodera, S., Kato, T., Yoneda, H., Yoshimura, R., Iyo, M., Matsuda, K., Akiyama, M., Ashikawa, K., Kashiwase, K., Tokunaga, K., Kondo, K., Saito, T., Shimasaki, A., Kawase, K., Kitajima, T., Matsuo, K., Itokawa, M., Someya, T., Inada, T., Hashimoto, R., Inoue, T., Akiyama, K., Tanii, H., Arai, H., Kanba, S., Ozaki, N., Kusumi, I., Yoshikawa, T., Kubo, M. & Iwata, N. A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder. Mol Psychiatry 23, 639-647 (2018).
  6. Low, S.K., Takahashi, A., Ebana, Y., Ozaki, K., Christophersen, I.E., Ellinor, P.T., Ogishima, S., Yamamoto, M., Satoh, M., Sasaki, M., Yamaji, T., Iwasaki, M., Tsugane, S., Tanaka, K., Naito, M., Wakai, K., Tanaka, H., Furukawa, T., Kubo, M., Ito, K., Kamatani, Y. & Tanaka, T. Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Nat Genet 49, 953-958 (2017).
  7. Hachiya, T., Kamatani, Y., Takahashi, A., Hata, J., Furukawa, R., Shiwa, Y., Yamaji, T., Hara, M., Tanno, K., Ohmomo, H., Ono, K., Takashima, N., Matsuda, K., Wakai, K., Sawada, N., Iwasaki, M., Yamagishi, K., Ago, T., Ninomiya, T., Fukushima, A., Hozawa, A., Minegishi, N., Satoh, M., Endo, R., Sasaki, M., Sakata, K., Kobayashi, S., Ogasawara, K., Nakamura, M., Hitomi, J., Kita, Y., Tanaka, K., Iso, H., Kitazono, T., Kubo, M., Tanaka, H., Tsugane, S., Kiyohara, Y., Yamamoto, M., Sobue, K. & Shimizu, A. Genetic Predisposition to Ischemic Stroke: A Polygenic Risk Score. Stroke 48, 253-258 (2017).
  8. Akiyama, M., Okada, Y., Kanai, M., Takahashi, A., Momozawa, Y., Ikeda, M., Iwata, N., Ikegawa, S., Hirata, M., Matsuda, K., Iwasaki, M., Yamaji, T., Sawada, N., Hachiya, T., Tanno, K., Shimizu, A., Hozawa, A., Minegishi, N., Tsugane, S., Yamamoto, M., Kubo, M. & Kamatani, Y. Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. Nat Genet 49, 1458-1467 (2017).
  9. Ohta, N., Hori, M., Takahashi, A., Ogura, M., Makino, H., Tamanaha, T., Fujiyama, H., Miyamoto, Y. & Harada-Shiba, M. Proprotein convertase subtilisin/kexin 9 V4I variant with LDLR mutations modifies the phenotype of familial hypercholesterolemia. J Clin Lipidol 10, 547-555 e5 (2016).
  10. Shiraishi, K., Okada, Y., Takahashi, A., Kamatani, Y., Momozawa, Y., Ashikawa, K., Kunitoh, H., Matsumoto, S., Takano, A., Shimizu, K., Goto, A., Tsuta, K., Watanabe, S., Ohe, Y., Watanabe, Y., Goto, Y., Nokihara, H., Furuta, K., Yoshida, A., Goto, K., Hishida, T., Tsuboi, M., Tsuchihara, K., Miyagi, Y., Nakayama, H., Yokose, T., Tanaka, K., Nagashima, T., Ohtaki, Y., Maeda, D., Imai, K., Minamiya, Y., Sakamoto, H., Saito, A., Shimada, Y., Sunami, K., Saito, M., Inazawa, J., Nakamura, Y., Yoshida, T., Yokota, J., Matsuda, F., Matsuo, K., Daigo, Y., Kubo, M. & Kohno, T. Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. Nat Commun 7, 12451 (2016).
受賞 日本人類遺伝学会奨励賞(2013年)
学位 博士(理学)
所属学会 日本人類遺伝学会、日本物理学会
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最終更新日:2021年10月01日

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