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

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 3
1967 1
2001 2
2002 1
2003 6
2005 3
2006 1
2008 1
2010 2
2011 4
2012 3
2013 1
2017 2
2018 1
2019 2
2020 3
2021 2
2022 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

37 results

Results by year

Filters applied: . Clear all
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.
[Marden-Walker syndrome].
Kurotaki N, Niikawa N. Kurotaki N, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):479-80. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596443 Review. Japanese. No abstract available.
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.
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: kurotaki n. Neurology. 2019 May 14;92(20):e2364-e2374. doi: 10.1212/WNL.0000000000007505. Epub 2019 Apr 19. Neurology. 2019. PMID: 31004071 Free PMC article.
Haploinsufficiency of NSD1 causes Sotos syndrome.
Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita Ha HA, Kinoshita A, Mizuguchi T, Yoshiura Ki K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N. Kurotaki N, et al. Nat Genet. 2002 Apr;30(4):365-6. doi: 10.1038/ng863. Epub 2002 Mar 18. Nat Genet. 2002. PMID: 11896389
37 results