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Molecular diagnosis of 405 individuals with autism spectrum disorder.
Miyake N, Tsurusaki Y, Fukai R, Kushima I, Okamoto N, Ohashi K, Nakamura K, Hashimoto R, Hiraki Y, Son S, Kato M, Sakai Y, Osaka H, Deguchi K, Matsuishi T, Takeshita S, Fattal-Valevski A, Ekhilevitch N, Tohyama J, Yap P, Keng WT, Kobayashi H, Takubo K, Okada T, Saitoh S, Yasuda Y, Murai T, Nakamura K, Ohga S, Matsumoto A, Inoue K, Saikusa T, Hershkovitz T, Kobayashi Y, Morikawa M, Ito A, Hara T, Uno Y, Seiwa C, Ishizuka K, Shirahata E, Fujita A, Koshimizu E, Miyatake S, Takata A, Mizuguchi T, Ozaki N, Matsumoto N. Miyake N, et al. Among authors: okada t. Eur J Hum Genet. 2024 Dec;32(12):1551-1558. doi: 10.1038/s41431-023-01335-7. Epub 2023 Mar 27. Eur J Hum Genet. 2024. PMID: 36973392
[Developmental disorders].
Kushima I, Okada T, Ozaki N. Kushima I, et al. Among authors: okada t. Brain Nerve. 2012 Feb;64(2):139-47. Brain Nerve. 2012. PMID: 22308259 Review. Japanese.
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients.
Koide T, Banno M, Aleksic B, Yamashita S, Kikuchi T, Kohmura K, Adachi Y, Kawano N, Kushima I, Nakamura Y, Okada T, Ikeda M, Ohi K, Yasuda Y, Hashimoto R, Inada T, Ujike H, Iidaka T, Suzuki M, Takeda M, Iwata N, Ozaki N. Koide T, et al. Among authors: okada t. PLoS One. 2012;7(5):e36836. doi: 10.1371/journal.pone.0036836. Epub 2012 May 23. PLoS One. 2012. PMID: 22649501 Free PMC article.
Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.
Wang C, Koide T, Kimura H, Kunimoto S, Yoshimi A, Nakamura Y, Kushima I, Banno M, Kawano N, Takasaki Y, Xing J, Noda Y, Mouri A, Aleksic B, Ikeda M, Okada T, Iidaka T, Inada T, Iwata N, Ozaki N. Wang C, et al. Among authors: okada t. Schizophr Res. 2014 Aug;157(1-3):149-56. doi: 10.1016/j.schres.2014.04.032. Epub 2014 May 28. Schizophr Res. 2014. PMID: 24878430
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: okada t. 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.
Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.
Xing J, Wang C, Kimura H, Takasaki Y, Kunimoto S, Yoshimi A, Nakamura Y, Koide T, Banno M, Kushima I, Uno Y, Okada T, Aleksic B, Ikeda M, Iwata N, Ozaki N. Xing J, et al. Among authors: okada t. PLoS One. 2014 Nov 13;9(11):e112531. doi: 10.1371/journal.pone.0112531. eCollection 2014. PLoS One. 2014. PMID: 25393624 Free PMC article.
What is the nature of the autism 'spectrum'?
Okada T, Ozaki N. Okada T, et al. Psychiatry Clin Neurosci. 2015 Mar;69(3):129-30. doi: 10.1111/pcn.12276. Psychiatry Clin Neurosci. 2015. PMID: 25736520 Free article. 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. Among authors: okada t. PLoS One. 2015 Mar 25;10(3):e0119413. doi: 10.1371/journal.pone.0119413. eCollection 2015. PLoS One. 2015. PMID: 25806950 Free PMC article.
4,961 results