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  • Genetic ablation of NMDA receptor subunit NR3B in mouse reveals motoneuronal and nonmotoneuronal phenotypes

    Niemann, S., Kanki, H., Fukui, Y., Takao, K., Fukaya, M., Hynynen, M. N., Churchill, M. J., Shefner, J. M., Bronson, R. T., Brown, R. H., Watanabe, M., Miyakawa, T., Itohara, S. & Hayashi, Y., 09-2007, In: European Journal of Neuroscience. 26, 6, p. 1407-1420 14 p.

    研究成果: Article › 査読

    35 被引用数 (Scopus)

  • Genetic ablation of Tnfα demonstrates no detectable suppressive effect on inflammation-related mouse colon tumorigenesis

    Sakai, H., Yamada, Y., Shimizu, M., Saito, K., Moriwaki, H. & Hara, A., 03-2010, In: Chemico-Biological Interactions. 184, 3, p. 423-430 8 p.

    研究成果: Article › 査読

    16 被引用数 (Scopus)

  • Genetic abnormalities effect on LDL metabolism

    Matsuyama, A. & Yamashita, S., 02-2001, In: Nippon rinsho. Japanese journal of clinical medicine. 59 Suppl 2, p. 534-538 5 p.

    研究成果: Review article › 査読

  • Genetically modified mice harboring mitochondrial DNA defects show aberrant cyclic change in wheel-running activity, which is improved by lithium

    Kasahara, T., Kubota, M., Miyauchi, T., Noda, Y., Mouri, A., Nabeshima, T. & Kato, T., 06-2006, In: Molecular Psychiatry. 11, 6, p. 523 1 p.

    研究成果: Article › 査読

    3 被引用数 (Scopus)

  • Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype

    Kano, H., Kurahashi, H. & Toda, T., 27-11-2007, In: Proceedings of the National Academy of Sciences of the United States of America. 104, 48, p. 19034-19039 6 p.

    研究成果: Article › 査読

    29 被引用数 (Scopus)

  • Genetically rescued tetrahydrobiopterin-depleted mice survive with hyperphenylalaninemia and region-specific monoaminergic abnormalities

    Sumi-Ichinose, C., Urano, F., Shimomura, A., Sato, T., Ikemoto, K., Shiraishi, H., Senda, T., Ichinose, H. & Nomura, T., 2005, In: Journal of neurochemistry. 95, 3, p. 703-714 12 p.

    研究成果: Article › 査読

    19 被引用数 (Scopus)

  • Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence

    Sakamoto, M., Ono, J., Okada, S., Nakamura, Y. & Kurahashi, H., 2000, In: Journal of Human Genetics. 45, 3, p. 167-170 4 p.

    研究成果: Article › 査読

    Open Access
    4 被引用数 (Scopus)

  • Genetic alteration of the β-catenin gene (CTNNB1) in human lung cancer and malignant mesothelioma and identification of a new 3p21.3 homozygous deletion

    Shigemitsu, K., Sekido, Y., Usami, N., Mori, S., Sato, M., Horio, Y., Hasegawa, Y., Bader, S. A., Gazdar, A. F., Minna, J. D., Hida, T., Yoshioka, H., Imaizumi, M., Ueda, Y., Takahashi, M. & Shimokata, K., 12-07-2001, In: Oncogene. 20, 31, p. 4249-4257 9 p.

    研究成果: Article › 査読

    Open Access
    87 被引用数 (Scopus)

  • Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome

    Onouchi, Y., Kurahashi, H., Tajiri, H., Ida, S., Okada, S. & Nakamura, Y., 1999, In: Journal of Human Genetics. 44, 4, p. 235-239 5 p.

    研究成果: Article › 査読

    13 被引用数 (Scopus)

  • Genetic analysis of digeorge syndrome and related disorders

    Kurahashi, H., Nakamura, T., Inazawa, J., Ntikawa, N., Okada, S. & Nishtsho, T., 1996, In: Japanese Journal of Human Genetics. 41, 1, p. 111 1 p.

    研究成果: Article › 査読

  • Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases

    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., 01-03-2018, In: Nature Genetics. 50, 3, p. 390-400 11 p.

    研究成果: Article › 査読

    119 被引用数 (Scopus)

  • Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder

    Yoshimi, A., Takahashi, N., Saito, S., Ito, Y., Aleksic, B., Usui, H., Kawamura, Y., Waki, Y., Yoshikawa, T., Kato, T., Iwata, N., Inada, T., Noda, Y. & Ozaki, N., 01-03-2008, In: Schizophrenia Research. 100, 1-3, p. 334-341 8 p.

    研究成果: Article › 査読

    14 被引用数 (Scopus)

  • Genetic analysis of type E botulinum toxin-producing Clostridium butyricum strains

    Wang, X., Maegawa, T., Karasawa, T., Kozaki, S., Tsukamoto, K., Gyobu, Y., Yamakawa, K., Oguma, K., Sakaguchi, Y. & Nakamura, S., 2000, In: Applied and Environmental Microbiology. 66, 11, p. 4992-4997 6 p.

    研究成果: Article › 査読

    Open Access
    52 被引用数 (Scopus)

  • Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia

    Sobue, A., Kushima, I., Nagai, T., Shan, W., Kohno, T., Aleksic, B., Aoyama, Y., Mori, D., Arioka, Y., Kawano, N., Yamamoto, M., Hattori, M., Nabeshima, T., Yamada, K. & Ozaki, N., 01-12-2018, In: Scientific reports. 8, 1, 13046.

    研究成果: Article › 査読

    11 被引用数 (Scopus)

  • Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: First report after establishment of HBOC registration system in Japan

    Arai, M., Yokoyama, S., Watanabe, C., Yoshida, R., Kita, M., Okawa, M., Sakurai, A., Sekine, M., Yotsumoto, J., Nomura, H., Akama, Y., Inuzuka, M., Nomizu, T., Enomoto, T. & Nakamura, S., 01-04-2018, In: Journal of Human Genetics. 63, 4, p. 447-457 11 p.

    研究成果: Article › 査読

    Open Access
    17 被引用数 (Scopus)

  • Genetic and epigenetic alterations in myelodysplastic syndrome

    Mihara, K., Takihara, Y. & Kimura, A., 01-11-2007, In: Cytogenetic and Genome Research. 118, 2-4, p. 297-303 7 p.

    研究成果: Review article › 査読

    12 被引用数 (Scopus)

  • Genetic and epigenetic events in human hepatocarcinogenesis.

    Kondoh, N., Wakatsuki, T., Hada, A., Shuda, M., Tanaka, K., Arai, M. & Yamamoto, M., 06-2001, In: International journal of oncology. 18, 6, p. 1271-1278 8 p.

    研究成果: Review article › 査読

    60 被引用数 (Scopus)

  • Genetic and Epigenetic Modulation of CD20 Expression in B-Cell Malignancies: Molecular Mechanisms and Significance to Rituximab Resistance

    Tomita, A., 2016, In: Journal of clinical and experimental hematopathology : JCEH. 56, 2, p. 89-99 11 p.

    研究成果: Article › 査読

    17 被引用数 (Scopus)

  • Genetic and functional analysis of KIF5A variants in Japanese patients with sporadic amyotrophic lateral sclerosis

    Japanese Consortium for Amyotrophic Lateral Sclerosis Research (JaCALS), 01-2021, In: Neurobiology of Aging. 97, p. 147.e11-147.e17

    研究成果: Article › 査読

  • Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population

    Hirata, J., Hosomichi, K., Sakaue, S., Kanai, M., Nakaoka, H., Ishigaki, K., Suzuki, K., Akiyama, M., Kishikawa, T., Ogawa, K., Masuda, T., Yamamoto, K., Hirata, M., Matsuda, K., Momozawa, Y., Inoue, I., Kubo, M., Kamatani, Y. & Okada, Y., 01-03-2019, In: Nature Genetics. 51, 3, p. 470-480 11 p.

    研究成果: Article › 査読

    20 被引用数 (Scopus)

  • Genetic and stimulator cell requirements for generation and activation of minor histocompatibility antigen-specific memory cytotoxic T-lymphocyte precursors

    Ando, K. I., Isobe, K. I., Hasegawa, T., Iwamoto, T., Ding, R. N., Rahman, J., Muro, Y., Yoshida, T., Nagase, F., Kawashima, K., Ohashi, M. & Nakashima, I., 1988, In: Immunology. 64, 4, p. 661-667 7 p.

    研究成果: Article › 査読

    3 被引用数 (Scopus)

  • Genetic animal models of schizophrenia related with the hypothesis of abnormal neurodevelopment

    Lu, L., Mamiya, T., Koseki, T., Mouri, A. & Nabeshima, T., 09-2011, In: Biological and Pharmaceutical Bulletin. 34, 9, p. 1358-1363 6 p.

    研究成果: Review article › 査読

    17 被引用数 (Scopus)

  • Genetic association analysis of functional polymorphisms in neuronal nitric oxide synthase 1 gene (NOS1) and mood disorders and fluvoxamine response in major depressive disorder in the japanese population

    Okumura, T., Kishi, T., Okochi, T., Ikeda, M., Kitajima, T., Yamanouchi, Y., Kinoshita, Y., Kawashima, K., Tsunoka, T., Inada, T., Ozaki, N. & Iwata, N., 02-2010, In: Neuropsychobiology. 61, 2, p. 57-63 7 p.

    研究成果: Article › 査読

    24 被引用数 (Scopus)

  • Genetic association analysis of NOS1 and methamphetamine-induced psychosis among Japanese

    Okumura, T., Okochi, T., Kishi, T., Ikeda, M., Kitajima, T., Kinoshita, Y., Kawashima, K., Tsunoka, T., Fukuo, Y., Inada, T., Yamada, M., Uchimura, N., Iyo, M., Sora, I., Ozaki, N., Ujike, H. & Iwata, N., 2011, In: Current Neuropharmacology. 9, 1, p. 155-159 5 p.

    研究成果: Article › 査読

    2 被引用数 (Scopus)

  • Genetic association analysis of NOS3 and methamphetamine-induced psychosis among Japanese

    Okochi, T., Kishi, T., Ikeda, M., Kitajima, T., Kinoshita, Y., Kawashima, K., Okumura, T., Tsunoka, T., Fukuo, Y., Inada, T., Yamada, M., Uchimura, N., Iyo, M., Sora, I., Ozaki, N., Ujike, H. & Iwata, N., 2011, In: Current Neuropharmacology. 9, 1, p. 151-154 4 p.

    研究成果: Article › 査読

    4 被引用数 (Scopus)

  • Genetic association analysis of NRG1 with methamphetamine-induced psychosis in a Japanese population

    Okochi, T., Kishi, T., Ikeda, M., Kitajima, T., Kinoshita, Y., Kawashima, K., Okumura, T., Tsunoka, T., Inada, T., Yamada, M., Uchimura, N., Iyo, M., Sora, I., Ozaki, N., Ujike, H. & Iwata, N., 01-08-2009, In: Progress in Neuro-Psychopharmacology and Biological Psychiatry. 33, 5, p. 903-905 3 p.

    研究成果: Article › 査読

    8 被引用数 (Scopus)

  • Genetic association analysis of serotonin 2A receptor gene (HTR2A) with bipolar disorder and major depressive disorder in the Japanese population

    Kishi, T., Kitajima, T., Tsunoka, T., Ikeda, M., Yamanouchi, Y., Kinoshita, Y., Kawashima, K., Okochi, T., Okumura, T., Inada, T., Ozaki, N. & Iwata, N., 01-06-2009, In: Neuroscience Research. 64, 2, p. 231-234 4 p.

    研究成果: Article › 査読

    36 被引用数 (Scopus)

  • Genetic association analysis of tagging SNPs in alpha4 and beta2 subunits of neuronal nicotinic acetylcholine receptor genes (CHRNA4 and CHRNB2) with schizophrenia in the Japanese population

    Kishi, T., Ikeda, M., Kitajima, T., Yamanouchi, Y., Kinoshita, Y., Kawashima, K., Okochi, T., Inada, T., Ozaki, N. & Iwata, N., 10-2008, In: Journal of Neural Transmission. 115, 10, p. 1457-1461 5 p.

    研究成果: Article › 査読

    11 被引用数 (Scopus)

  • Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

    Pattaro, C., Teumer, A., Gorski, M., Chu, A. Y., Li, M., Mijatovic, V., Garnaas, M., Tin, A., Sorice, R., Li, Y., Taliun, D., Olden, M., Foster, M., Yang, Q., Chen, M. H., Pers, T. H., Johnson, A. D., Ko, Y. A., Fuchsberger, C., Tayo, B. & 678 others, Nalls, M., Feitosa, M. F., Isaacs, A., Dehghan, A., D'Adamo, P., Adeyemo, A., Dieffenbach, A. K., Zonderman, A. B., Nolte, I. M., Van Der Most, P. J., Wright, A. F., Shuldiner, A. R., Morrison, A. C., Hofman, A., Smith, A. V., Dreisbach, A. W., Franke, A., Uitterlinden, A. G., Metspalu, A., Tonjes, A., Lupo, A., Robino, A., Johansson, Å., Demirkan, A., Kollerits, B., Freedman, B. I., Ponte, B., Oostra, B. A., Paulweber, B., Krämer, B. K., Mitchell, B. D., Buckley, B. M., Peralta, C. A., Hayward, C., Helmer, C., Rotimi, C. N., Shaffer, C. M., Müller, C., Sala, C., Van Duijn, C. M., Saint-Pierre, A., Ackermann, D., Shriner, D., Ruggiero, D., Toniolo, D., Lu, Y., Cusi, D., Czamara, D., Ellinghaus, D., Siscovick, D. S., Ruderfer, D., Gieger, C., Grallert, H., Rochtchina, E., Atkinson, E. J., Holliday, E. G., Boerwinkle, E., Salvi, E., Bottinger, E. P., Murgia, F., Rivadeneira, F., Ernst, F., Kronenberg, F., Hu, F. B., Navis, G. J., Curhan, G. C., Ehret, G. B., Homuth, G., Coassin, S., Thun, G. A., Pistis, G., Gambaro, G., Malerba, G., Montgomery, G. W., Eiriksdottir, G., Jacobs, G., Li, G., Wichmann, H. E., Campbell, H., Schmidt, H., Wallaschofski, H., Völzke, H., Brenner, H., Kroemer, H. K., Kramer, H., Lin, H., Leach, I. M., Ford, I., Guessous, I., Rudan, I., Prokopenko, I., Borecki, I., Heid, I. M., Kolcic, I., Persico, I., Jukema, J. W., Wilson, J. F., Felix, J. F., Divers, J., Lambert, J. C., Stafford, J. M., Gaspoz, J. M., Smith, J. A., Faul, J. D., Wang, J. J., Ding, J., Hirschhorn, J. N., Attia, J., Whitfield, J. B., Chalmers, J., Viikari, J., Coresh, J., Denny, J. C., Karjalainen, J., Fernandes, J. K., Endlich, K., Butterbach, K., Keene, K. L., Lohman, K., Portas, L., Launer, L. J., Lyytikäinen, L. P., Yengo, L., Franke, L., Ferrucci, L., Rose, L. M., Kedenko, L., Rao, M., Struchalin, M., Kleber, M. E., Cavalieri, M., Haun, M., Cornelis, M. C., Ciullo, M., Pirastu, M., De Andrade, M., McEvoy, M. A., Woodward, M., Adam, M., Cocca, M., Nauck, M., Imboden, M., Waldenberger, M., Pruijm, M., Metzger, M., Stumvoll, M., Evans, M. K., Sale, M. M., Kähönen, M., Boban, M., Bochud, M., Rheinberger, M., Verweij, N., Bouatia-Naji, N., Martin, N. G., Hastie, N., Probst-Hensch, N., Soranzo, N., Devuyst, O., Raitakari, O., Gottesman, O., Franco, O. H., Polasek, O., Gasparini, P., Munroe, P. B., Ridker, P. M., Mitchell, P., Muntner, P., Meisinger, C., Smit, J. H., Abecasis, G. R., Adair, L. S., Alexander, M., Altshuler, D., Amin, N., Arking, D. E., Arora, P., Aulchenko, Y., Bakker, S. J. L., Bandinelli, S., Barroso, I., Beckmann, J. S., Beilby, J. P., Bergman, R. N., Bergmann, S., Bis, J. C., Boehnke, M., Bonnycastle, L. L., Bornstein, S. R., Bots, M. L., Bragg-Gresham, J. L., Brand, S. M., Brand, E., Braund, P. S., Brown, M. J., Burton, P. R., Casas, J. P., Caulfield, M. J., Chakravarti, A., Chambers, J. C., Chandak, G. R., Chang, Y. P. C., Charchar, F. J., Chaturvedi, N., Cho, Y. S., Clarke, R., Collins, F. S., Collins, R., Connell, J. M., Cooper, J. A., Cooper, M. N., Cooper, R. S., Corsi, A. M., Dörr, M., Dahgam, S., Danesh, J., Smith, G. D., Day, I. N. M., Deloukas, P., Denniff, M., Dominiczak, A. F., Dong, Y., Doumatey, A., Elliott, P., Elosua, R., Erdmann, J., Eyheramendy, S., Farrall, M., Fava, C., Forrester, T., Fowkes, F. G. R., Fox, E. R., Frayling, T. M., Galan, P., Ganesh, S. K., Garcia, M., Gaunt, T. R., Glazer, N. L., Go, M. J., Goel, A., Grässler, J., Grobbee, D. E., Groop, L., Guarrera, S., Guo, X., Hadley, D., Hamsten, A., Han, B. G., Hardy, R., Hartikainen, A. L., Heath, S., Heckbert, S. R., Hedblad, B., Hercberg, S., Hernandez, D., Hicks, A. A., Hilton, G., Hingorani, A. D., Hoffman Bolton, J. A., Hopewell, J. C., Howard, P., Humphries, S. E., Hunt, S. C., Hveem, K., Ikram, M. A., Islam, M., Iwai, N., Jarvelin, M. R., Jackson, A. U., Jafar, T. H., Janipalli, C. S., Johnson, T., Kathiresan, S., Khaw, K. T., Kim, H. L., Kinra, S., Kita, Y., Kivimaki, M., Kooner, J. S., Kumar, M. J. K., Kuh, D., Kulkarni, S. R., Kumari, M., Kuusisto, J., Kuznetsova, T., Laakso, M., Laan, M., Laitinen, J., Lakatta, E. G., Langefeld, C. D., Larson, M. G., Lathrop, M., Lawlor, D. A., Lawrence, R. W., Lee, J. Y., Lee, N. R., Levy, D., Li, Y., Longstreth, W. T., Luan, J., Lucas, G., Ludwig, B., Mangino, M., Mani, K. R., Marmot, M. G., Mattace-Raso, F. U. S., Matullo, G., McArdle, W. L., McKenzie, C. A., Meitinger, T., Melander, O., Meneton, P., Meschia, J. F., Miki, T., Milaneschi, Y., Mohlke, K. L., Mooser, V., Morken, M. A., Morris, R. W., Mosley, T. H., Najjar, S., Narisu, N., Newton-Cheh, C., Nguyen, K. D. H., Nilsson, P., Nyberg, F., O'Donnell, C. J., Ogihara, T., Ohkubo, T., Okamura, T., Ong, R. T. H., Ongen, H., Onland-Moret, N. C., O'Reilly, P. F., Org, E., Orru, M., Palmas, W., Palmen, J., Palmer, L. J., Palmer, N. D., Parker, A. N., Peden, J. F., Peltonen, L., Perola, M., Pihur, V., Platou, C. G. P., Plump, A., Prabhakaran, D., Psaty, B. M., Raffel, L. J., Rao, D. C., Rasheed, A., Ricceri, F., Rice, K. M., Rosengren, A., Rotter, J. I., Rudock, M. E., Sõber, S., Salako, T., Saleheen, D., Salomaa, V., Samani, N. J., Schwartz, S. M., Schwarz, P. E. H., Scott, L. J., Scott, J., Scuteri, A., Sehmi, J. S., Seielstad, M., Seshadri, S., Sharma, P., Shaw-Hawkins, S., Shi, G., Shrine, N. R. G., Sijbrands, E. J. G., Sim, X., Singleton, A., Sjögren, M., Smith, N. L., Artigas, M. S., Spector, T. D., Staessen, J. A., Stancakova, A., Steinle, N. I., Strachan, D. P., Stringham, H. M., Sun, Y. V., Swift, A. J., Tabara, Y., Tai, E. S., Talmud, P. J., Taylor, A., Terzic, J., Thelle, D. S., Tobin, M. D., Tomaszewski, M., Tripathy, V., Tuomilehto, J., Tzoulaki, I., Uda, M., Ueshima, H., Uiterwaal, C. S. P. M., Umemura, S., Van Der Harst, P., Van Der Schouw, Y. T., Van Gilst, W. H., Vartiainen, E., Vasan, R. S., Veldre, G., Verwoert, G. C., Viigimaa, M., Vinay, D. G., Vineis, P., Voight, B. F., Vollenweider, P., Wagenknecht, L. E., Wain, L. V., Wang, X., Wang, T. J., Wareham, N. J., Watkins, H., Weder, A. B., Whincup, P. H., Wiggins, K. L., Witteman, J. C. M., Wong, A., Wu, Y., Yajnik, C. S., Yao, J., Young, J. H., Zelenika, D., Zhai, G., Zhang, W., Zhang, F., Zhao, J. H., Zhu, H., Zhu, X., Zitting, P., Zukowska-Szczechowska, E., Okada, Y., Wu, J. Y., Gu, D., Takeuchi, F., Takahashi, A., Maeda, S., Tsunoda, T., Chen, P., Lim, S. C., Wong, T. Y., Liu, J., Young, T. L., Aung, T., Teo, Y. Y., Kim, Y. J., Kang, D., Chen, C. H., Tsai, F. J., Chang, L. C., Fann, S. J. C., Mei, H., Hixson, J. E., Chen, S., Katsuya, T., Isono, M., Albrecht, E., Yamamoto, K., Kubo, M., Nakamura, Y., Kamatani, N., Kato, N., He, J., Chen, Y. T., Tanaka, T., Reilly, M. P., Schunkert, H., Assimes, T. L., Hall, A., Hengstenberg, C., König, I. R., Laaksonen, R., McPherson, R., Thompson, J. R., Thorsteinsdottir, U., Ziegler, A., Absher, D., Chen, L., Cupples, L. A., Halperin, E., Li, M., Musunuru, K., Preuss, M., Schillert, A., Thorleifsson, G., Wells, G. A., Holm, H., Roberts, R., Stewart, A. F. R., Fortmann, S., Go, A., Hlatky, M., Iribarren, C., Knowles, J., Myers, R., Quertermous, T., Sidney, S., Risch, N., Tang, H., Blankenberg, S., Schnabel, R., Sinning, C., Lackner, K. J., Tiret, L., Nicaud, V., Cambien, F., Bickel, C., Rupprecht, H. J., Perret, C., Proust, C., Münzel, T. F., Barbalic, M., Chen, I. Y. D., Demissie-Banjaw, S., Folsom, A., Lumley, T., Marciante, K., Taylor, K. D., Volcik, K., Gretarsdottir, S., Gulcher, J. 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  • Genetic differences between neurocytoma and dysembryoplastic neuroepithelial tumor and oligodendroglial tumors

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