Nomura J - Search Results

1

Functional significance of rare neuroligin 1 variants found in autism.

Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T. Nakanishi M, et al. Among authors: nomura j. PLoS Genet. 2017 Aug 25;13(8):e1006940. doi: 10.1371/journal.pgen.1006940. eCollection 2017 Aug. PLoS Genet. 2017. PMID: 28841651 Free PMC article.

2

Animal models of psychiatric disorders that reflect human copy number variation.

Nomura J, Takumi T. Nomura J, et al. Neural Plast. 2012;2012:589524. doi: 10.1155/2012/589524. Epub 2012 Jul 30. Neural Plast. 2012. PMID: 22900207 Free PMC article. Review.

3

Role for neonatal D-serine signaling: prevention of physiological and behavioral deficits in adult Pick1 knockout mice.

Nomura J, Jaaro-Peled H, Lewis E, Nuñez-Abades P, Huppe-Gourgues F, Cash-Padgett T, Emiliani F, Kondo MA, Furuya A, Landek-Salgado MA, Ayhan Y, Kamiya A, Takumi T, Huganir R, Pletnikov M, O'Donnell P, Sawa A. Nomura J, et al. Mol Psychiatry. 2016 Mar;21(3):386-93. doi: 10.1038/mp.2015.61. Epub 2015 May 26. Mol Psychiatry. 2016. PMID: 26008737 Free PMC article.

4

Rodent models of genetic and chromosomal variations in psychiatric disorders.

Nomura J, Kannan G, Takumi T. Nomura J, et al. Psychiatry Clin Neurosci. 2017 Aug;71(8):508-517. doi: 10.1111/pcn.12524. Epub 2017 Apr 23. Psychiatry Clin Neurosci. 2017. PMID: 28317218 Free article. Review.

5

Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication.

Kishimoto K, Nomura J, Ellegood J, Fukumoto K, Lerch JP, Moreno-De-Luca D, Bourgeron T, Tamada K, Takumi T. Kishimoto K, et al. Among authors: nomura j. Genes Cells. 2017 May;22(5):436-451. doi: 10.1111/gtc.12487. Epub 2017 Mar 29. Genes Cells. 2017. PMID: 28370817 Free article.

6

Correction: Functional significance of rare neuroligin 1 variants found in autism.

Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T. Nakanishi M, et al. Among authors: nomura j. PLoS Genet. 2017 Oct 3;13(10):e1007035. doi: 10.1371/journal.pgen.1007035. eCollection 2017 Oct. PLoS Genet. 2017. PMID: 28972980 Free PMC article.

7

Transcriptome analysis of human neural cells derived from isogenic embryonic stem cells with 16p11.2 deletion.

Nomura Y, Nomura J, Kamiguchi H, Nishikawa T, Takumi T. Nomura Y, et al. Among authors: nomura j. Neurosci Res. 2021 Oct;171:114-123. doi: 10.1016/j.neures.2021.03.005. Epub 2021 Mar 27. Neurosci Res. 2021. PMID: 33785412

8

Molecular signatures from multi-omics of autism spectrum disorders and schizophrenia.

Nomura J, Mardo M, Takumi T. Nomura J, et al. J Neurochem. 2021 Nov;159(4):647-659. doi: 10.1111/jnc.15514. Epub 2021 Sep 29. J Neurochem. 2021. PMID: 34537986 Free article. Review.

9

A common epigenetic mechanism across different cellular origins underlies systemic immune dysregulation in an idiopathic autism mouse model.

Lin CW, Septyaningtrias DE, Chao HW, Konda M, Atarashi K, Takeshita K, Tamada K, Nomura J, Sasagawa Y, Tanaka K, Nikaido I, Honda K, McHugh TJ, Takumi T. Lin CW, et al. Among authors: nomura j. Mol Psychiatry. 2022 Aug;27(8):3343-3354. doi: 10.1038/s41380-022-01566-y. Epub 2022 May 2. Mol Psychiatry. 2022. PMID: 35491410

10

Germ-cell-specific transcriptome analysis illuminates the chromatin and ubiquitin pathway in autism spectrum disorders.

Furukawa S, Nomura J, Hanafusa H, Maegawa H, Takumi T. Furukawa S, et al. Among authors: nomura j. Autism Res. 2023 Jun;16(6):1101-1110. doi: 10.1002/aur.2939. Epub 2023 May 19. Autism Res. 2023. PMID: 37204624

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