Works by Igeta, Hirofumi

Results: 12

Cardiovascular pharmacodynamics of donepezil hydrochloride on the PR and QT intervals in patients with dementia.

Published in:

Human Psychopharmacology: Clinical & Experimental, 2014, v. 29, n. 3, p. 292, doi. 10.1002/hup.2398

By:

Igeta, Hirofumi;
Suzuki, Yutaro;
Tajiri, Misuzu;
Someya, Toshiyuki

Publication type:

Article

Interleukin 1 beta gene and risk of schizophrenia: detailed case-control and family-based studies and an updated meta-analysis.

Published in:

Human Psychopharmacology: Clinical & Experimental, 2014, v. 29, n. 1, p. 31, doi. 10.1002/hup.2365

By:

Shibuya, Masako;
Watanabe, Yuichiro;
Nunokawa, Ayako;
Egawa, Jun;
Kaneko, Naoshi;
Igeta, Hirofumi;
Someya, Toshiyuki

Publication type:

Article

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 797, doi. 10.1002/ajmg.b.32444

By:

Egawa, Jun;
Hoya, Satoshi;
Watanabe, Yuichiro;
Nunokawa, Ayako;
Shibuya, Masako;
Ikeda, Masashi;
Inoue, Emiko;
Okuda, Shujiro;
Kondo, Kenji;
Saito, Takeo;
Kaneko, Naoshi;
Muratake, Tatsuyuki;
Igeta, Hirofumi;
Iwata, Nakao;
Someya, Toshiyuki

Publication type:

Article

Rare nonsynonymous germline and mosaic de novo variants in Japanese patients with schizophrenia.

Published in:

Psychiatry & Clinical Neurosciences, 2025, v. 79, n. 1, p. 37, doi. 10.1111/pcn.13758

By:

Watanabe, Yuichiro;
Nishioka, Masaki;
Morikawa, Ryo;
Takano‐Isozaki, Satoko;
Igeta, Hirofumi;
Mori, Kanako;
Kato, Tadafumi;
Someya, Toshiyuki

Publication type:

Article

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.

Published in:

Psychiatry & Clinical Neurosciences, 2017, v. 71, n. 11, p. 780, doi. 10.1111/pcn.12549

By:

Hoya, Satoshi;
Watanabe, Yuichiro;
Hishimoto, Akitoyo;
Nunokawa, Ayako;
Kaneko, Naoshi;
Muratake, Tatsuyuki;
Shinmyo, Naofumi;
Otsuka, Ikuo;
Okuda, Shujiro;
Inoue, Emiko;
Igeta, Hirofumi;
Shibuya, Masako;
Egawa, Jun;
Orime, Naoki;
Sora, Ichiro;
Someya, Toshiyuki

Publication type:

Article

Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.

Published in:

Psychiatry & Clinical Neurosciences, 2017, v. 71, n. 8, p. 562, doi. 10.1111/pcn.12526

By:

Hoya, Satoshi;
Watanabe, Yuichiro;
Hishimoto, Akitoyo;
Nunokawa, Ayako;
Inoue, Emiko;
Igeta, Hirofumi;
Otsuka, Ikuo;
Shibuya, Masako;
Egawa, Jun;
Sora, Ichiro;
Someya, Toshiyuki

Publication type:

Article

Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole-exome sequencing of a multiplex family and follow-up study in a Japanese population.

Published in:

Psychiatry & Clinical Neurosciences, 2015, v. 69, n. 8, p. 472, doi. 10.1111/pcn.12274

By:

Inoue, Emiko;
Watanabe, Yuichiro;
Egawa, Jun;
Sugimoto, Atsunori;
Nunokawa, Ayako;
Shibuya, Masako;
Igeta, Hirofumi;
Someya, Toshiyuki

Publication type:

Article

Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.

Published in:

Psychiatry & Clinical Neurosciences, 2015, v. 69, n. 3, p. 131, doi. 10.1111/pcn.12205

By:

Egawa, Jun;
Watanabe, Yuichiro;
Shibuya, Masako;
Endo, Taro;
Sugimoto, Atsunori;
Igeta, Hirofumi;
Nunokawa, Ayako;
Inoue, Emiko;
Someya, Toshiyuki

Publication type:

Article

Resequencing and association analysis of MIR137 with schizophrenia in a Japanese population.

Published in:

Psychiatry & Clinical Neurosciences, 2013, v. 67, n. 4, p. 277, doi. 10.1111/pcn.12047

By:

Egawa, Jun;
Nunokawa, Ayako;
Shibuya, Masako;
Watanabe, Yuichiro;
Kaneko, Naoshi;
Igeta, Hirofumi;
Someya, Toshiyuki

Publication type:

Article

Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population.

Published in:

PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0144624

By:

Inoue, Emiko;
Watanabe, Yuichiro;
Xing, Jingrui;
Kushima, Itaru;
Egawa, Jun;
Okuda, Shujiro;
Hoya, Satoshi;
Okada, Takashi;
Uno, Yota;
Ishizuka, Kanako;
Sugimoto, Atsunori;
Igeta, Hirofumi;
Nunokawa, Ayako;
Sugiyama, Toshiro;
Ozaki, Norio;
Someya, Toshiyuki

Publication type:

Article

Novel Rare Missense Variations and Risk of Autism Spectrum Disorder: Whole-Exome Sequencing in Two Families with Affected Siblings and a Two-Stage Follow-Up Study in a Japanese Population.

Published in:

PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119413

By:

Egawa, Jun;
Watanabe, Yuichiro;
Wang, Chenyao;
Inoue, Emiko;
Sugimoto, Atsunori;
Sugiyama, Toshiro;
Igeta, Hirofumi;
Nunokawa, Ayako;
Shibuya, Masako;
Kushima, Itaru;
Orime, Naoki;
Hayashi, Taketsugu;
Okada, Takashi;
Uno, Yota;
Ozaki, Norio;
Someya, Toshiyuki

Publication type:

Article

Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study.

Published in:

Neuropsychiatric Disease & Treatment, 2019, v. 15, p. 2353, doi. 10.2147/NDT.S218773

By:

Igeta, Hirofumi;
Watanabe, Yuichiro;
Morikawa, Ryo;
Ikeda, Masashi;
Otsuka, Ikuo;
Hoya, Satoshi;
Koizumi, Masataka;
Egawa, Jun;
Hishimoto, Akitoyo;
Iwata, Nakao;
Someya, Toshiyuki

Publication type:

Article