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

Year Number of Results
1965 1
1967 1
1969 1
1970 1
1973 2
1976 1
1978 1
1979 1
1980 1
1984 1
1990 2
1992 1
1993 1
1994 3
1995 2
1997 1
1998 1
1999 1
2000 1
2001 1
2002 6
2003 5
2004 4
2005 3
2006 6
2007 6
2008 7
2009 6
2010 6
2011 7
2012 7
2013 8
2014 7
2015 12
2016 11
2017 13
2018 10
2019 12
2020 27
2021 14
2022 0
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Search Results

174 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, Wilson LC, Wollnik B, Kosho T, Wieczorek D, Eichler E, Pfundt R, de Vries BBA, Clayton-Smith J, Santen GWE. van der Sluijs PJ, et al. Among authors: wilson lc. 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.
Bone health and SATB2-associated syndrome.
Zarate YA, Steinraths M, Matthews A, Smith WE, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish JL, Powell CM, Wasserman WW, van Karnebeek CD, Wakeling EL, Ma NS. Zarate YA, et al. Among authors: wilson lc. Clin Genet. 2018 Mar;93(3):588-594. doi: 10.1111/cge.13121. Epub 2017 Dec 27. Clin Genet. 2018. PMID: 28787087 Review.
The Prevalence of Sexual Revictimization: A Meta-Analytic Review.
Walker HE, Freud JS, Ellis RA, Fraine SM, Wilson LC. Walker HE, et al. Among authors: wilson lc. Trauma Violence Abuse. 2019 Jan;20(1):67-80. doi: 10.1177/1524838017692364. Epub 2017 Feb 8. Trauma Violence Abuse. 2019. PMID: 29333937 Review.
Albright's hereditary osteodystrophy.
Wilson LC, Trembath RC. Wilson LC, et al. J Med Genet. 1994 Oct;31(10):779-84. doi: 10.1136/jmg.31.10.779. J Med Genet. 1994. PMID: 7837255 Free PMC article. Review. No abstract available.
The COVID-19 pandemic and organ donation and transplantation: ethical issues.
Ibrahim B, Dawson R, Chandler JA, Goldberg A, Hartell D, Hornby L, Simpson C, Weiss MJ, Wilson LC, Wilson TM, Fortin MC. Ibrahim B, et al. Among authors: wilson lc. BMC Med Ethics. 2021 Oct 21;22(1):142. doi: 10.1186/s12910-021-00711-6. BMC Med Ethics. 2021. PMID: 34674700 Free PMC article. Review.
Albright's hereditary osteodystrophy.
Wilson LC. Wilson LC. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:671-3. doi: 10.1515/jpem.2006.19.s2.671. J Pediatr Endocrinol Metab. 2006. PMID: 16789633 No abstract available.
174 results