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Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.
Hoya S, Watanabe Y, Hishimoto A, Nunokawa A, Inoue E, Igeta H, Otsuka I, Shibuya M, Egawa J, Sora I, Someya T. Hoya S, et al. Among authors: inoue e. Psychiatry Clin Neurosci. 2017 Aug;71(8):562-568. doi: 10.1111/pcn.12526. Epub 2017 May 10. Psychiatry Clin Neurosci. 2017. PMID: 28317220 Free article.
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. Among authors: inoue e. 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 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: inoue e. 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 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: inoue e. 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
513 results