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Genetic and epigenetic analyses of panic disorder in the post-GWAS era.
Morimoto Y, Ono S, Kurotaki N, Imamura A, Ozawa H. Morimoto Y, et al. Among authors: ono s. J Neural Transm (Vienna). 2020 Nov;127(11):1517-1526. doi: 10.1007/s00702-020-02205-y. Epub 2020 May 9. J Neural Transm (Vienna). 2020. PMID: 32388794 Free PMC article. Review.
A unique missense variant in the E1A-binding protein P400 gene is implicated in schizophrenia by whole-exome sequencing and mutant mouse models.
Morimoto Y, Ono S, Yoshida S, Mishima H, Kinoshita A, Tanaka T, Komohara Y, Kurotaki N, Kishino T, Okazaki Y, Ozawa H, Yoshiura KI, Imamura A. Morimoto Y, et al. Among authors: ono s. Transl Psychiatry. 2021 Feb 18;11(1):132. doi: 10.1038/s41398-021-01258-1. Transl Psychiatry. 2021. PMID: 33602898 Free PMC article.
HLA class I distribution in Japanese patients with schizophrenia.
Matsumoto S, Sasaki T, Imamura A, Matsuo K, Kayashima T, Hashida A, Ono S, Tsujita T, Matsumoto S, Nakane Y, Tokunaga K, Okazaki Y. Matsumoto S, et al. Among authors: ono s. Am J Med Genet. 2002 Jan 8;114(1):42-5. doi: 10.1002/ajmg.1629. Am J Med Genet. 2002. PMID: 11840504
DNA methylation signatures of peripheral leukocytes in schizophrenia.
Kinoshita M, Numata S, Tajima A, Shimodera S, Ono S, Imamura A, Iga J, Watanabe S, Kikuchi K, Kubo H, Nakataki M, Sumitani S, Imoto I, Okazaki Y, Ohmori T. Kinoshita M, et al. Among authors: ono s. Neuromolecular Med. 2013 Mar;15(1):95-101. doi: 10.1007/s12017-012-8198-6. Epub 2012 Sep 9. Neuromolecular Med. 2013. PMID: 22961555
Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorder.
Morimoto Y, Shimada-Sugimoto M, Otowa T, Yoshida S, Kinoshita A, Mishima H, Yamaguchi N, Mori T, Imamura A, Ozawa H, Kurotaki N, Ziegler C, Domschke K, Deckert J, Umekage T, Tochigi M, Kaiya H, Okazaki Y, Tokunaga K, Sasaki T, Yoshiura KI, Ono S. Morimoto Y, et al. Among authors: ono s. Transl Psychiatry. 2018 Feb 2;8(1):41. doi: 10.1038/s41398-017-0088-0. Transl Psychiatry. 2018. PMID: 29391400 Free PMC article.
Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities.
Morimoto Y, Yoshida S, Kinoshita A, Satoh C, Mishima H, Yamaguchi N, Matsuda K, Sakaguchi M, Tanaka T, Komohara Y, Imamura A, Ozawa H, Nakashima M, Kurotaki N, Kishino T, Yoshiura KI, Ono S. Morimoto Y, et al. Among authors: ono s. Neurology. 2019 May 14;92(20):e2364-e2374. doi: 10.1212/WNL.0000000000007505. Epub 2019 Apr 19. Neurology. 2019. PMID: 31004071 Free PMC article.
3,235 results