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

Year Number of Results
1961 3
1962 1
1963 4
1964 1
1965 1
1966 3
1967 3
1968 3
1969 8
1970 2
1971 6
1972 7
1973 2
1974 3
1975 3
1976 5
1977 3
1978 4
1979 5
1980 8
1981 7
1982 4
1983 6
1984 3
1985 2
1986 4
1987 6
1988 8
1989 5
1990 16
1991 14
1992 15
1993 11
1994 22
1995 17
1996 12
1997 24
1998 27
1999 19
2000 40
2001 38
2002 17
2003 21
2004 26
2005 43
2006 38
2007 37
2008 30
2009 44
2010 62
2011 79
2012 80
2013 79
2014 72
2015 81
2016 79
2017 87
2018 85
2019 75
2020 102
2021 119
2022 123
2023 119
2024 79

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1,726 results

Results by year

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Page 1
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
van der Sluijs PJ, Jansen S, Vergano SA, Adachi-Fukuda M, Alanay Y, AlKindy A, Baban A, Bayat A, Beck-Wödl S, Berry K, Bijlsma EK, Bok LA, Brouwer AFJ, van der Burgt I, Campeau PM, Canham N, Chrzanowska K, Chu YWY, Chung BHY, Dahan K, De Rademaeker M, Destree A, Dudding-Byth T, Earl R, Elcioglu N, Elias ER, Fagerberg C, Gardham A, Gener B, Gerkes EH, Grasshoff U, van Haeringen A, Heitink KR, Herkert JC, den Hollander NS, Horn D, Hunt D, Kant SG, Kato M, Kayserili H, Kersseboom R, Kilic E, Krajewska-Walasek M, Lammers K, Laulund LW, Lederer D, Lees M, López-González V, Maas S, Mancini GMS, Marcelis C, Martinez F, Maystadt I, McGuire M, McKee S, Mehta S, Metcalfe K, Milunsky J, Mizuno S, Moeschler JB, Netzer C, Ockeloen CW, Oehl-Jaschkowitz B, Okamoto N, Olminkhof SNM, Orellana C, Pasquier L, Pottinger C, Riehmer V, Robertson SP, Roifman M, Rooryck C, Ropers FG, Rosello M, Ruivenkamp CAL, Sagiroglu MS, Sallevelt SCEH, Sanchis Calvo A, Simsek-Kiper PO, Soares G, Solaeche L, Sonmez FM, Splitt M, Steenbeek D, Stegmann APA, Stumpel CTRM, Tanabe S, Uctepe E, Utine GE, Veenstra-Knol HE, Venkateswaran S, Vilain C, Vincent-Delorme C, Vulto-van Silfhout AT, Wheeler P, Wilson GN, Wilso… See abstract for full author list ➔ van der Sluijs PJ, et al. Among authors: okamoto n. Genet Med. 2019 Jun;21(6):1295-1307. doi: 10.1038/s41436-018-0330-z. Epub 2018 Nov 8. Genet Med. 2019. PMID: 30349098 Free PMC article.
Editorial.
Gojobori T, Wada T, Watabe S, Okamoto N, Bernardi G. Gojobori T, et al. Among authors: okamoto n. Gene. 2016 Feb 1;576(2 Pt 1):592. doi: 10.1016/j.gene.2015.11.017. Gene. 2016. PMID: 26690055 No abstract available.
[Norrie disease].
Okamoto N. Okamoto N. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):524-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11032012 Review. Japanese. No abstract available.
[X-linked hydrocephalus syndrome].
Okamoto N. Okamoto N. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):47-8. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057138 Review. Japanese. No abstract available.
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences.
Yamada M, Nitta Y, Uehara T, Suzuki H, Miya F, Takenouchi T, Tamura M, Ayabe S, Yoshiki A, Maeno A, Saga Y, Furuse T, Yamada I, Okamoto N, Kosaki K, Sugie A. Yamada M, et al. Among authors: okamoto n. Eur J Med Genet. 2023 Aug;66(8):104804. doi: 10.1016/j.ejmg.2023.104804. Epub 2023 Jun 25. Eur J Med Genet. 2023. PMID: 37369308
Cytotoxic T cell function in fish.
Nakanishi T, Fischer U, Dijkstra JM, Hasegawa S, Somamoto T, Okamoto N, Ototake M. Nakanishi T, et al. Among authors: okamoto n. Dev Comp Immunol. 2002 Mar;26(2):131-9. doi: 10.1016/s0145-305x(01)00055-6. Dev Comp Immunol. 2002. PMID: 11696378 Review.
Excellently balanced water-intercalation-type heat-storage oxide.
Hatakeyama T, Okamoto NL, Otake S, Sato H, Li H, Ichitsubo T. Hatakeyama T, et al. Among authors: okamoto nl. Nat Commun. 2022 Mar 17;13(1):1452. doi: 10.1038/s41467-022-28988-0. Nat Commun. 2022. PMID: 35301294 Free PMC article.
[Dysosteosclerosis].
Okamoto N. Okamoto N. Ryoikibetsu Shokogun Shirizu. 2001;(33):590-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462584 Review. Japanese. No abstract available.
1,726 results