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Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders.
Published in:
Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02962-4
By:
- Hayashi, Yu;
- Okumura, Hiroki;
- Arioka, Yuko;
- Kushima, Itaru;
- Mori, Daisuke;
- Lo, Tzuyao;
- Otgonbayar, Gantsooj;
- Kato, Hidekazu;
- Nawa, Yoshihiro;
- Kimura, Hiroki;
- Aleksic, Branko;
- Ozaki, Norio
Publication type:
Article
Study of the genetic association between selected 3q29 region genes and schizophrenia and autism spectrum disorder in the Japanese population.
Published in:
Nagoya Journal of Medical Science, 2024, v. 86, n. 2, p. 216, doi. 10.18999/nagjms.86.2.216
By:
- Otgonbayar, Gantsooj;
- Tzuyao Lo;
- Yu Hayashi;
- Sho Furuta;
- Aleksic, Branko;
- Yoshihiro Nawa;
- Itaru Kushima;
- Hidekazu Kato;
- Hiroki Kimura;
- Norio Ozaki
Publication type:
Article
Clinical manifestations of schizophrenia in four patients with variants in voltage‐gated calcium channel‐encoding genes: a case series.
Published in:
Psychiatry & Clinical Neurosciences, 2023, v. 77, n. 1, p. 57, doi. 10.1111/pcn.13494
By:
- Lo, Tzuyao;
- Kushima, Itaru;
- Aleksic, Branko;
- Yoshimi, Akira;
- Someya, Toshiyuki;
- Watanabe, Yuichiro;
- Ozaki, Norio
Publication type:
Article
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization.
Published in:
Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 12, p. 667, doi. 10.1111/pcn.13474
By:
- Kushima, Itaru;
- Aleksic, Branko;
- Kimura, Hiroki;
- Nakatochi, Masahiro;
- Lo, Tzuyao;
- Ikeda, Masashi;
- Arai, Makoto;
- Hashimoto, Ryota;
- Numata, Shusuke;
- Okamura, Yasunobu;
- Obara, Taku;
- Inada, Toshiya;
- Ozaki, Norio
Publication type:
Article
Case report of a female with bipolar disorder and MBD5 deletion.
Published in:
Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 4, p. 127, doi. 10.1111/pcn.13329
By:
- Kushima, Itaru;
- Lo, Tzuyao;
- Aleksic, Branko;
- Ozaki, Norio
Publication type:
Article
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

Found: 6

Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders.

Study of the genetic association between selected 3q29 region genes and schizophrenia and autism spectrum disorder in the Japanese population.

Clinical manifestations of schizophrenia in four patients with variants in voltage‐gated calcium channel‐encoding genes: a case series.

X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization.

Case report of a female with bipolar disorder and MBD5 deletion.

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