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Comparison of genotype clustering tools with rare variants.
Perreault LP, Legault MA, Barhdadi A, Provost S, Normand V, Tardif JC, Dubé MP. Perreault LP, et al. Among authors: tardif jc. BMC Bioinformatics. 2014 Feb 21;15:52. doi: 10.1186/1471-2105-15-52. BMC Bioinformatics. 2014. PMID: 24559245 Free PMC article.
Validation of warfarin pharmacogenetic algorithms in clinical practice.
Marin-Leblanc M, Perreault S, Bahroun I, Lapointe M, Mongrain I, Provost S, Turgeon J, Talajic M, Brugada R, Phillips M, Tardif JC, Dubé MP. Marin-Leblanc M, et al. Among authors: tardif jc. Pharmacogenomics. 2012 Jan;13(1):21-9. doi: 10.2217/pgs.11.120. Pharmacogenomics. 2012. PMID: 22176621
Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans.
Arsenault BJ, Dubé MP, Brodeur MR, de Oliveira Moraes AB, Lavoie V, Kernaleguen AE, Guauque-Olarte S, Mathieu P, Pibarot P, Messika-Zeitoun D, Bossé Y, Rhainds D, Rhéaume E, Tardif JC. Arsenault BJ, et al. Among authors: tardif jc. Arterioscler Thromb Vasc Biol. 2014 Feb;34(2):457-62. doi: 10.1161/ATVBAHA.113.302730. Epub 2013 Dec 12. Arterioscler Thromb Vasc Biol. 2014. PMID: 24334872
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Auer PL, Teumer A, Schick U, O'Shaughnessy A, Lo KS, Chami N, Carlson C, de Denus S, Dubé MP, Haessler J, Jackson RD, Kooperberg C, Perreault LP, Nauck M, Peters U, Rioux JD, Schmidt F, Turcot V, Völker U, Völzke H, Greinacher A, Hsu L, Tardif JC, Diaz GA, Reiner AP, Lettre G. Auer PL, et al. Among authors: tardif jc. Nat Genet. 2014 Jun;46(6):629-34. doi: 10.1038/ng.2962. Epub 2014 Apr 28. Nat Genet. 2014. PMID: 24777453 Free PMC article.
813 results