Works by Nawa, Yoshihiro

Results: 15
    1

    Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study.

    Published in:
    Neuropsychopharmacology Reports, 2024, v. 44, n. 1, p. 42, doi. 10.1002/npr2.12370
    By:
    • Lo, Tzuyao;
    • Kushima, Itaru;
    • Kimura, Hiroki;
    • Aleksic, Branko;
    • Okada, Takashi;
    • Kato, Hidekazu;
    • Inada, Toshiya;
    • Nawa, Yoshihiro;
    • Torii, Youta;
    • Yamamoto, Maeri;
    • Kimura, Ryo;
    • Funabiki, Yasuko;
    • Kosaka, Hirotaka;
    • Numata, Shusuke;
    • Kasai, Kiyoto;
    • Sasaki, Tsukasa;
    • Yokoyama, Shigeru;
    • Munesue, Toshio;
    • Hashimoto, Ryota;
    • Yasuda, Yuka
    Publication type:
    Article
    2

    Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.

    Published in:
    Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-01107-7
    By:
    • Kato, Hidekazu;
    • Kushima, Itaru;
    • Mori, Daisuke;
    • Yoshimi, Akira;
    • Aleksic, Branko;
    • Nawa, Yoshihiro;
    • Toyama, Miho;
    • Furuta, Sho;
    • Yu, Yanjie;
    • Ishizuka, Kanako;
    • Kimura, Hiroki;
    • Arioka, Yuko;
    • Tsujimura, Keita;
    • Morikawa, Mako;
    • Okada, Takashi;
    • Inada, Toshiya;
    • Nakatochi, Masahiro;
    • Shinjo, Keiko;
    • Kondo, Yutaka;
    • Kaibuchi, Kozo
    Publication type:
    Article
    3

    Lateralized interictal epileptiform discharges during rapid eye movement sleep correlate with epileptogenic hemisphere in children with intractable epilepsy secondary to tuberous sclerosis complex.

    Published in:
    Epilepsia (Series 4), 2011, v. 52, n. 11, p. 1986, doi. 10.1111/j.1528-1167.2011.03198.x
    By:
    • Ochi, Ayako;
    • Hung, Ryan;
    • Weiss, Shelly;
    • Widjaja, Elysa;
    • To, Tonia;
    • Nawa, Yoshihiro;
    • Shima, Taiki;
    • Go, Cristina;
    • Akiyama, Tomoyuki;
    • Donner, Elizabeth;
    • Drake, James;
    • Rutka, James T.;
    • Snead, O. Carter;
    • Otsubo, Hiroshi
    Publication type:
    Article
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    7

    Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice.

    Published in:
    Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-023-02679-w
    By:
    • Mori, Daisuke;
    • Ikeda, Ryosuke;
    • Sawahata, Masahito;
    • Yamaguchi, Sho;
    • Kodama, Akiko;
    • Hirao, Takashi;
    • Arioka, Yuko;
    • Okumura, Hiroki;
    • Inami, Chihiro;
    • Suzuki, Toshiaki;
    • Hayashi, Yu;
    • Kato, Hidekazu;
    • Nawa, Yoshihiro;
    • Miyata, Seiko;
    • Kimura, Hiroki;
    • Kushima, Itaru;
    • Aleksic, Branko;
    • Mizoguchi, Hiroyuki;
    • Nagai, Taku;
    • Nakazawa, Takanobu
    Publication type:
    Article
    8
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    10

    Whole‐genome sequencing analysis of Japanese autism spectrum disorder trios.

    Published in:
    Psychiatry & Clinical Neurosciences, 2025, v. 79, n. 3, p. 87, doi. 10.1111/pcn.13767
    By:
    • Furukawa, Sawako;
    • Kushima, Itaru;
    • Kato, Hidekazu;
    • Kimura, Hiroki;
    • Nawa, Yoshihiro;
    • Aleksic, Branko;
    • Banno, Masahiro;
    • Yamamoto, Maeri;
    • Uematsu, Mariko;
    • Nagasaki, Yukako;
    • Ogi, Tomoo;
    • Ozaki, Norio;
    • Ikeda, Masashi
    Publication type:
    Article
    11

    Copy number variations in RNF216 and postsynaptic membrane–associated genes are associated with bipolar disorder: a case‐control study in the Japanese population.

    Published in:
    Psychiatry & Clinical Neurosciences, 2025, v. 79, n. 1, p. 12, doi. 10.1111/pcn.13752
    By:
    • Nakatochi, Masahiro;
    • Kushima, Itaru;
    • Aleksic, Branko;
    • Kimura, Hiroki;
    • Kato, Hidekazu;
    • Inada, Toshiya;
    • Torii, Youta;
    • Takahashi, Nagahide;
    • Yamamoto, Maeri;
    • Iwamoto, Kunihiro;
    • Nawa, Yoshihiro;
    • Iritani, Shuji;
    • Iwata, Nakao;
    • Saito, Takeo;
    • Ninomiya, Kohei;
    • Okochi, Tomo;
    • Hashimoto, Ryota;
    • Yamamori, Hidenaga;
    • Yasuda, Yuka;
    • Fujimoto, Michiko
    Publication type:
    Article
    12
    13

    Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility.

    Published in:
    Human Genome Variation, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1038/s41439-020-00125-7
    By:
    • Nawa, Yoshihiro;
    • Kimura, Hiroki;
    • Mori, Daisuke;
    • Kato, Hidekazu;
    • Toyama, Miho;
    • Furuta, Sho;
    • Yu, Yanjie;
    • Ishizuka, Kanako;
    • Kushima, Itaru;
    • Aleksic, Branko;
    • Arioka, Yuko;
    • Morikawa, Mako;
    • Okada, Takashi;
    • Inada, Toshiya;
    • Kaibuchi, Kozo;
    • Ikeda, Masashi;
    • Iwata, Nakao;
    • Suzuki, Michio;
    • Okahisa, Yuko;
    • Egawa, Jun
    Publication type:
    Article
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