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Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.
Ishizuka K, Fujita Y, Kawabata T, Kimura H, Iwayama Y, Inada T, Okahisa Y, Egawa J, Usami M, Kushima I, Uno Y, Okada T, Ikeda M, Aleksic B, Mori D, Someya T, Yoshikawa T, Iwata N, Nakamura H, Yamashita T, Ozaki N. Ishizuka K, et al. Among authors: egawa j. Transl Psychiatry. 2017 Aug 1;7(8):e1184. doi: 10.1038/tp.2017.173. Transl Psychiatry. 2017. PMID: 28763059 Free PMC article.
A two-stage case-control association study between the tryptophan hydroxylase 2 (TPH2) gene and schizophrenia in a Japanese population.
Watanabe Y, Egawa J, Iijima Y, Nunokawa A, Kaneko N, Shibuya M, Arinami T, Ujike H, Inada T, Iwata N, Tochigi M, Kunugi H, Itokawa M, Ozaki N, Hashimoto R, Someya T. Watanabe Y, et al. Among authors: egawa j. Schizophr Res. 2012 May;137(1-3):264-6. doi: 10.1016/j.schres.2012.01.034. Epub 2012 Feb 17. Schizophr Res. 2012. PMID: 22342331 No abstract available.
Replication in a Japanese population that a MIR30E gene variation is associated with schizophrenia.
Watanabe Y, Iijima Y, Egawa J, Nunokawa A, Kaneko N, Arinami T, Ujike H, Inada T, Iwata N, Kunugi H, Itokawa M, Sasaki T, Ozaki N, Hashimoto R, Shibuya M, Igeta H, Someya T. Watanabe Y, et al. Among authors: egawa j. Schizophr Res. 2013 Nov;150(2-3):596-7. doi: 10.1016/j.schres.2013.08.028. Epub 2013 Sep 8. Schizophr Res. 2013. PMID: 24025694 No abstract available.
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.
Egawa J, Watanabe Y, Wang C, Inoue E, Sugimoto A, Sugiyama T, Igeta H, Nunokawa A, Shibuya M, Kushima I, Orime N, Hayashi T, Okada T, Uno Y, Ozaki N, Someya T. Egawa J, et al. PLoS One. 2015 Mar 25;10(3):e0119413. doi: 10.1371/journal.pone.0119413. eCollection 2015. PLoS One. 2015. PMID: 25806950 Free PMC article.
137 results