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Results by year

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

Year Number of Results
1961 4
1962 2
1963 2
1964 3
1965 5
1966 5
1967 2
1968 7
1969 3
1970 4
1971 2
1972 1
1974 2
1975 2
1976 5
1978 1
1979 1
1980 1
1982 3
1986 1
1988 1
1990 2
1991 3
1992 5
1993 1
1994 1
1995 1
1996 3
1997 5
1998 4
1999 4
2000 8
2001 6
2002 4
2003 5
2004 4
2005 9
2006 6
2007 10
2008 5
2009 3
2010 13
2011 8
2012 8
2013 6
2014 8
2015 3
2016 4
2017 5
2018 3
2019 7
2020 1
2021 7
2022 2
2023 6
2024 2

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Publication date

Search Results

213 results

Results by year

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Page 1
Optical continuous-variable qubit.
Neergaard-Nielsen JS, Takeuchi M, Wakui K, Takahashi H, Hayasaka K, Takeoka M, Sasaki M. Neergaard-Nielsen JS, et al. Among authors: wakui k. Phys Rev Lett. 2010 Jul 30;105(5):053602. doi: 10.1103/PhysRevLett.105.053602. Epub 2010 Jul 30. Phys Rev Lett. 2010. PMID: 20867917
[Clinical cytogenetics].
Wakui K. Wakui K. Nihon Rinsho. 2010 Aug;68 Suppl 8:13-9. Nihon Rinsho. 2010. PMID: 20979264 Review. Japanese. No abstract available.
Clinical correlations of mutations affecting six components of the SWI/SNF complex: detailed description of 21 patients and a review of the literature.
Kosho T, Okamoto N, Ohashi H, Tsurusaki Y, Imai Y, Hibi-Ko Y, Kawame H, Homma T, Tanabe S, Kato M, Hiraki Y, Yamagata T, Yano S, Sakazume S, Ishii T, Nagai T, Ohta T, Niikawa N, Mizuno S, Kaname T, Naritomi K, Narumi Y, Wakui K, Fukushima Y, Miyatake S, Mizuguchi T, Saitsu H, Miyake N, Matsumoto N. Kosho T, et al. Among authors: wakui k. Am J Med Genet A. 2013 Jun;161A(6):1221-37. doi: 10.1002/ajmg.a.35933. Epub 2013 May 1. Am J Med Genet A. 2013. PMID: 23637025 Review.
CTCF deletion syndrome: clinical features and epigenetic delineation.
Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S. Hori I, et al. Among authors: wakui k. J Med Genet. 2017 Dec;54(12):836-842. doi: 10.1136/jmedgenet-2017-104854. Epub 2017 Aug 28. J Med Genet. 2017. PMID: 28848059
Comprehensive genetic screening for vascular Ehlers-Danlos syndrome through an amplification-based next-generation sequencing system.
Yamaguchi T, Hayashi S, Hayashi D, Matsuyama T, Koitabashi N, Ogiwara K, Noda M, Nakada C, Fujiki S, Furutachi A, Tanabe Y, Yamanaka M, Ishikawa A, Mizukami M, Mizuguchi A, Sugiura K, Sumi M, Yamazawa H, Izawa A, Wada Y, Fujikawa T, Takiguchi Y, Wakui K, Takano K, Nishio SY, Kosho T. Yamaguchi T, et al. Among authors: wakui k. Am J Med Genet A. 2023 Jan;191(1):37-51. doi: 10.1002/ajmg.a.62982. Epub 2022 Oct 3. Am J Med Genet A. 2023. PMID: 36189931 Free PMC article.
213 results