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Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.
Kondo K, Ikeda M, Kajio Y, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, Iwata N. Kondo K, et al. PLoS One. 2013 Aug 13;8(8):e70964. doi: 10.1371/journal.pone.0070964. eCollection 2013. PLoS One. 2013. PMID: 23967141 Free PMC article.
Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.
Saito T, Kondo K, Iwayama Y, Shimasaki A, Aleksic B, Yamada K, Toyota T, Hattori E, Esaki K, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, Ikeda M, Iwata N. Saito T, et al. Among authors: kondo k. Am J Med Genet B Neuropsychiatr Genet. 2014 Jul;165B(5):421-7. doi: 10.1002/ajmg.b.32246. Epub 2014 May 29. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24888570
Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia.
Higashiyama R, Ohnuma T, Takebayashi Y, Hanzawa R, Shibata N, Yamamori H, Yasuda Y, Kushima I, Aleksic B, Kondo K, Ikeda M, Hashimoto R, Iwata N, Ozaki N, Arai H. Higashiyama R, et al. Among authors: kondo k. Am J Med Genet B Neuropsychiatr Genet. 2016 Apr;171B(3):447-57. doi: 10.1002/ajmg.b.32426. Epub 2016 Feb 7. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26852906
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: kondo k. Schizophr Bull. 2019 Jun 18;45(4):824-834. doi: 10.1093/schbul/sby140. Schizophr Bull. 2019. PMID: 30285260 Free PMC 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: kondo k. 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
4,367 results