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Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
Wang C, Horigane SI, Wakamori M, Ueda S, Kawabata T, Fujii H, Kushima I, Kimura H, Ishizuka K, Nakamura Y, Iwayama Y, Ikeda M, Iwata N, Okada T, Aleksic B, Mori D, Yoshida T, Bito H, Yoshikawa T, Takemoto-Kimura S, Ozaki N. Wang C, et al. Among authors: iwayama y. Transl Psychiatry. 2022 Feb 26;12(1):84. doi: 10.1038/s41398-022-01851-y. Transl Psychiatry. 2022. PMID: 35220405 Free PMC article.
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: iwayama y. Transl Psychiatry. 2017 Aug 1;7(8):e1184. doi: 10.1038/tp.2017.173. Transl Psychiatry. 2017. PMID: 28763059 Free PMC article.
A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.
Kimura H, Fujita Y, Kawabata T, Ishizuka K, Wang C, Iwayama Y, Okahisa Y, Kushima I, Morikawa M, Uno Y, Okada T, Ikeda M, Inada T, Branko A, Mori D, Yoshikawa T, Iwata N, Nakamura H, Yamashita T, Ozaki N. Kimura H, et al. Among authors: iwayama y. Transl Psychiatry. 2017 Aug 22;7(8):e1214. doi: 10.1038/tp.2017.170. Transl Psychiatry. 2017. PMID: 28892071 Free PMC article.
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
Kimura H, Tsuboi D, Wang C, Kushima I, Koide T, Ikeda M, Iwayama Y, Toyota T, Yamamoto N, Kunimoto S, Nakamura Y, Yoshimi A, Banno M, Xing J, Takasaki Y, Yoshida M, Aleksic B, Uno Y, Okada T, Iidaka T, Inada T, Suzuki M, Ujike H, Kunugi H, Kato T, Yoshikawa T, Iwata N, Kaibuchi K, Ozaki N. Kimura H, et al. Among authors: iwayama y. Schizophr Bull. 2015 May;41(3):744-53. doi: 10.1093/schbul/sbu147. Epub 2014 Oct 20. Schizophr Bull. 2015. PMID: 25332407 Free PMC article.
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Takasaki Y, Koide T, Wang C, Kimura H, Xing J, Kushima I, Ishizuka K, Mori D, Sekiguchi M, Ikeda M, Aizawa M, Tsurumaru N, Iwayama Y, Yoshimi A, Arioka Y, Yoshida M, Noma H, Oya-Ito T, Nakamura Y, Kunimoto S, Aleksic B, Uno Y, Okada T, Ujike H, Egawa J, Kuwabara H, Someya T, Yoshikawa T, Iwata N, Ozaki N. Takasaki Y, et al. Among authors: iwayama y. Sci Rep. 2016 Sep 12;6:33311. doi: 10.1038/srep33311. Sci Rep. 2016. PMID: 27616045 Free PMC article.
A population-specific uncommon variant in GRIN3A associated with schizophrenia.
Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T, Toyoshima M, Ujike H, Inada T, Kunugi H, Ozaki N, Nanko S, Nakamura K, Mori N, Kanba S, Iwata N, Kato T, Yoshikawa T. Takata A, et al. Among authors: iwayama y. Biol Psychiatry. 2013 Mar 15;73(6):532-9. doi: 10.1016/j.biopsych.2012.10.024. Epub 2012 Dec 11. Biol Psychiatry. 2013. PMID: 23237318 Free article.
Lack of association of EGR2 variants with bipolar disorder in Japanese population.
Balan S, Yamada K, Iwayama Y, Toyota T, Ohnishi T, Maekawa M, Toyoshima M, Iwata Y, Suzuki K, Kikuchi M, Ujike H, Inada T, Kunugi H, Ozaki N, Iwata N, Nanko S, Kato T, Yoshikawa T. Balan S, et al. Among authors: iwayama y. Gene. 2013 Sep 10;526(2):246-50. doi: 10.1016/j.gene.2013.05.055. Epub 2013 Jun 4. Gene. 2013. PMID: 23747400
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. Among authors: iwayama y. 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: iwayama y. 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
199 results