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Results by year

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

Year Number of Results
1977 1
1978 1
1979 2
1980 2
1981 2
1982 6
1983 5
1984 1
1985 4
1986 4
1987 7
1988 4
1989 4
1990 4
1991 3
1992 3
1993 6
1994 5
1995 5
1996 12
1997 6
1998 7
1999 12
2000 7
2001 4
2002 7
2003 4
2004 8
2005 10
2006 17
2007 15
2008 4
2009 11
2010 11
2011 9
2012 7
2013 5
2014 11
2015 9
2016 11
2017 14
2018 12
2019 10
2020 14
2021 17
2022 18
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Publication date

Search Results

317 results
Results by year
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Page 1
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.
Cuvertino S, Stuart HM, Chandler KE, Roberts NA, Armstrong R, Bernardini L, Bhaskar S, Callewaert B, Clayton-Smith J, Davalillo CH, Deshpande C, Devriendt K, Digilio MC, Dixit A, Edwards M, Friedman JM, Gonzalez-Meneses A, Joss S, Kerr B, Lampe AK, Langlois S, Lennon R, Loget P, Ma DYT, McGowan R, Des Medt M, O'Sullivan J, Odent S, Parker MJ, Pebrel-Richard C, Petit F, Stark Z, Stockler-Ipsiroglu S, Tinschert S, Vasudevan P, Villa O, White SM, Zahir FR; DDD Study, Woolf AS, Banka S. Cuvertino S, et al. Among authors: langlois s. Am J Hum Genet. 2017 Dec 7;101(6):1021-1033. doi: 10.1016/j.ajhg.2017.11.006. Am J Hum Genet. 2017. PMID: 29220674 Free PMC article.
Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001.
Tran TH, Langlois S, Meloche C, Caron M, Saint-Onge P, Rouette A, Bataille AR, Jimenez-Cortes C, Sontag T, Bittencourt H, Laverdière C, Lavallée VP, Leclerc JM, Cole PD, Gennarini LM, Kahn JM, Kelly KM, Michon B, Santiago R, Stevenson KE, Welch JJG, Schroeder KM, Koch V, Cellot S, Silverman LB, Sinnett D. Tran TH, et al. Among authors: langlois s. Blood Adv. 2022 Feb 22;6(4):1329-1341. doi: 10.1182/bloodadvances.2021005634. Blood Adv. 2022. PMID: 34933343 Free PMC article. Clinical Trial.
Pre-conception Folic Acid and Multivitamin Supplementation for the Primary and Secondary Prevention of Neural Tube Defects and Other Folic Acid-Sensitive Congenital Anomalies.
Wilson RD; Genetics Committee, Wilson RD, Audibert F, Brock JA, Carroll J, Cartier L, Gagnon A, Johnson JA, Langlois S, Murphy-Kaulbeck L, Okun N, Pastuck M; Special Contributors, Deb-Rinker P, Dodds L, Leon JA, Lowel HL, Luo W, MacFarlane A, McMillan R, Moore A, Mundle W, O'Connor D, Ray J, Van den Hof M. Wilson RD, et al. Among authors: langlois s. J Obstet Gynaecol Can. 2015 Jun;37(6):534-52. doi: 10.1016/s1701-2163(15)30230-9. J Obstet Gynaecol Can. 2015. PMID: 26334606 English, French.
Preimplantation genetic testing.
Audibert F, Wilson RD, Allen V, Blight C, Brock JA, Désilets VA, Gagnon A, Johnson JA, Langlois S, Wyatt P; Genetics Committee. Audibert F, et al. Among authors: langlois s. J Obstet Gynaecol Can. 2009 Aug;31(8):761-75. doi: 10.1016/s1701-2163(16)34284-0. J Obstet Gynaecol Can. 2009. PMID: 19772712 Review. English, French.
317 results