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Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia.
Yamada K, Gerber DJ, Iwayama Y, Ohnishi T, Ohba H, Toyota T, Aruga J, Minabe Y, Tonegawa S, Yoshikawa T. Yamada K, et al. Among authors: ohba h. Proc Natl Acad Sci U S A. 2007 Feb 20;104(8):2815-20. doi: 10.1073/pnas.0610765104. Epub 2007 Feb 20. Proc Natl Acad Sci U S A. 2007. PMID: 17360599 Free PMC article.
Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels.
Yamada K, Ohnishi T, Hashimoto K, Ohba H, Iwayama-Shigeno Y, Toyoshima M, Okuno A, Takao H, Toyota T, Minabe Y, Nakamura K, Shimizu E, Itokawa M, Mori N, Iyo M, Yoshikawa T. Yamada K, et al. Among authors: ohba h. Biol Psychiatry. 2005 Jun 15;57(12):1493-503. doi: 10.1016/j.biopsych.2005.03.018. Biol Psychiatry. 2005. PMID: 15953485
A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia.
Aoki-Suzuki M, Yamada K, Meerabux J, Iwayama-Shigeno Y, Ohba H, Iwamoto K, Takao H, Toyota T, Suto Y, Nakatani N, Dean B, Nishimura S, Seki K, Kato T, Itohara S, Nishikawa T, Yoshikawa T. Aoki-Suzuki M, et al. Among authors: ohba h. Biol Psychiatry. 2005 Feb 15;57(4):382-93. doi: 10.1016/j.biopsych.2004.11.022. Biol Psychiatry. 2005. PMID: 15705354
A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia.
Itokawa M, Yamada K, Yoshitsugu K, Toyota T, Suga T, Ohba H, Watanabe A, Hattori E, Shimizu H, Kumakura T, Ebihara M, Meerabux JM, Toru M, Yoshikawa T. Itokawa M, et al. Among authors: ohba h. Pharmacogenetics. 2003 May;13(5):271-8. doi: 10.1097/00008571-200305000-00006. Pharmacogenetics. 2003. PMID: 12724619
Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.
Toyota T, Yoshitsugu K, Ebihara M, Yamada K, Ohba H, Fukasawa M, Minabe Y, Nakamura K, Sekine Y, Takei N, Suzuki K, Itokawa M, Meerabux JM, Iwayama-Shigeno Y, Tomaru Y, Shimizu H, Hattori E, Mori N, Yoshikawa T. Toyota T, et al. Among authors: ohba h. Hum Mol Genet. 2004 Mar 1;13(5):551-61. doi: 10.1093/hmg/ddh047. Epub 2004 Jan 6. Hum Mol Genet. 2004. PMID: 14709596
Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression.
Yamada K, Hattori E, Iwayama Y, Ohnishi T, Ohba H, Toyota T, Takao H, Minabe Y, Nakatani N, Higuchi T, Detera-Wadleigh SD, Yoshikawa T. Yamada K, et al. Among authors: ohba h. Biol Psychiatry. 2006 Jul 15;60(2):192-201. doi: 10.1016/j.biopsych.2005.11.008. Epub 2006 Feb 17. Biol Psychiatry. 2006. PMID: 16487942
A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription.
Ohnishi T, Yamada K, Ohba H, Iwayama Y, Toyota T, Hattori E, Inada T, Kunugi H, Tatsumi M, Ozaki N, Iwata N, Sakamoto K, Iijima Y, Iwata Y, Tsuchiya KJ, Sugihara G, Nanko S, Osumi N, Detera-Wadleigh SD, Kato T, Yoshikawa T. Ohnishi T, et al. Among authors: ohba h. Neuropsychopharmacology. 2007 Aug;32(8):1727-37. doi: 10.1038/sj.npp.1301307. Epub 2007 Jan 24. Neuropsychopharmacology. 2007. PMID: 17251911
390 results