Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

37 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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: kurotaki n. 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.
Case of undiagnosed catecholaminergic polymorphic ventricular tachycardia presenting with ventricular fibrillation after administration of succinylcholine during anesthesia for modified electroconvulsive therapy.
Kubo T, Horai S, Ando Y, Ozawa H, Kurotaki N. Kubo T, et al. Among authors: kurotaki n. Psychiatry Clin Neurosci. 2011 Jun;65(4):397. doi: 10.1111/j.1440-1819.2011.02222.x. Psychiatry Clin Neurosci. 2011. PMID: 21682817 Free article. No abstract available.
Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions.
Ono S, Yoshiura K, Kinoshita A, Kikuchi T, Nakane Y, Kato N, Sadamatsu M, Konishi T, Nagamitsu S, Matsuura M, Yasuda A, Komine M, Kanai K, Inoue T, Osamura T, Saito K, Hirose S, Koide H, Tomita H, Ozawa H, Niikawa N, Kurotaki N. Ono S, et al. Among authors: kurotaki n. J Hum Genet. 2012 May;57(5):338-41. doi: 10.1038/jhg.2012.23. Epub 2012 Mar 8. J Hum Genet. 2012. PMID: 22399141
De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.
Nishi A, Numata S, Tajima A, Zhu X, Ito K, Saito A, Kato Y, Kinoshita M, Shimodera S, Ono S, Ochi S, Imamura A, Kurotaki N, Ueno SI, Iwata N, Fukui K, Imoto I, Kamiya A, Ohmori T. Nishi A, et al. Among authors: kurotaki n. Sci Rep. 2017 Jun 6;7(1):2887. doi: 10.1038/s41598-017-02792-z. Sci Rep. 2017. PMID: 28588275 Free PMC article.
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: kurotaki n. Transl Psychiatry. 2018 Feb 2;8(1):41. doi: 10.1038/s41398-017-0088-0. Transl Psychiatry. 2018. PMID: 29391400 Free PMC article.
37 results