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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: watanabe y. 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: watanabe y. 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.
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