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Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
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. Ikeda M, et al. Among authors: hoya s. Schizophr Bull. 2019 Jun 18;45(4):824-834. doi: 10.1093/schbul/sby140. Schizophr Bull. 2019. PMID: 30285260 Free PMC article.
Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.
Egawa J, Hoya S, Watanabe Y, Nunokawa A, Shibuya M, Ikeda M, Inoue E, Okuda S, Kondo K, Saito T, Kaneko N, Muratake T, Igeta H, Iwata N, Someya T. Egawa J, et al. Among authors: hoya s. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):797-805. doi: 10.1002/ajmg.b.32444. Epub 2016 Mar 14. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26990377
Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.
Watanabe Y, Nunokawa A, Shibuya M, Ikeda M, Hishimoto A, Kondo K, Egawa J, Kaneko N, Muratake T, Saito T, Okazaki S, Shimasaki A, Igeta H, Inoue E, Hoya S, Sugai T, Sora I, Iwata N, Someya T. Watanabe Y, et al. Among authors: hoya s. Psychiatry Res. 2016 Jan 30;235:13-8. doi: 10.1016/j.psychres.2015.12.011. Epub 2015 Dec 11. Psychiatry Res. 2016. PMID: 26706132
Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.
Hoya S, Watanabe Y, Hishimoto A, Nunokawa A, Kaneko N, Muratake T, Shinmyo N, Otsuka I, Okuda S, Inoue E, Igeta H, Shibuya M, Egawa J, Orime N, Sora I, Someya T. Hoya S, et al. Psychiatry Clin Neurosci. 2017 Nov;71(11):780-788. doi: 10.1111/pcn.12549. Epub 2017 Jul 31. Psychiatry Clin Neurosci. 2017. PMID: 28657695 Free 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.
Igeta H, Watanabe Y, Morikawa R, Ikeda M, Otsuka I, Hoya S, Koizumi M, Egawa J, Hishimoto A, Iwata N, Someya T. Igeta H, et al. Among authors: hoya s. Neuropsychiatr Dis Treat. 2019 Aug 19;15:2353-2363. doi: 10.2147/NDT.S218773. eCollection 2019. Neuropsychiatr Dis Treat. 2019. PMID: 31695380 Free PMC article.
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