Asselin G - Search Results

1

genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools.

Lemieux Perreault LP, Legault MA, Asselin G, Dubé MP. Lemieux Perreault LP, et al. Among authors: asselin g. Bioinformatics. 2016 Dec 1;32(23):3661-3663. doi: 10.1093/bioinformatics/btw487. Epub 2016 Aug 6. Bioinformatics. 2016. PMID: 27497439 Free PMC article.

2

Partitioning of copy-number genotypes in pedigrees.

Perreault LP, Andelfinger GU, Asselin G, Dubé MP. Perreault LP, et al. Among authors: asselin g. BMC Bioinformatics. 2010 May 3;11:226. doi: 10.1186/1471-2105-11-226. BMC Bioinformatics. 2010. PMID: 20438641 Free PMC article.

3

A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy.

de Denus S, Mottet F, Korol S, Feroz Zada Y, Provost S, Mongrain I, Asselin G, Oussaïd E, Busseuil D, Lettre G, Rioux J, Racine N, O'Meara E, White M, Rouleau J, Tardif JC, Dubé MP. de Denus S, et al. Among authors: asselin g. ESC Heart Fail. 2020 Sep 1;7(6):4384-9. doi: 10.1002/ehf2.12934. Online ahead of print. ESC Heart Fail. 2020. PMID: 32869539 Free PMC article.

4

Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.

Dubé MP, Legault MA, Lemaçon A, Lemieux Perreault LP, Fouodjio R, Waters DD, Kouz S, Pinto FJ, Maggioni AP, Diaz R, Berry C, Koenig W, Lopez-Sendon J, Gamra H, Kiwan GS, Asselin G, Provost S, Barhdadi A, Sun M, Cossette M, Blondeau L, Mongrain I, Dubois A, Rhainds D, Bouabdallaoui N, Samuel M, de Denus S, L'Allier PL, Guertin MC, Roubille F, Tardif JC. Dubé MP, et al. Among authors: asselin g. Circ Genom Precis Med. 2021 Feb 9. doi: 10.1161/CIRCGEN.120.003183. Online ahead of print. Circ Genom Precis Med. 2021. PMID: 33560138

5

Genetic meta-analysis of cancer diagnosis following statin use identifies new associations and implicates human leukocyte antigen (HLA) in women.

Sun M, Lemaçon A, Legault MA, Asselin G, Provost S, Aschard H, Barhdadi A, Zada YF, Valois D, Mongrain I, Tardif JC, Dubé MP. Sun M, et al. Among authors: asselin g. Pharmacogenomics J. 2021 Mar 1. doi: 10.1038/s41397-021-00221-z. Online ahead of print. Pharmacogenomics J. 2021. PMID: 33649522

6

Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort.

Shahabi P, Lamothe F, Dumas S, Rouleau-Mailloux É, Feroz Zada Y, Provost S, Asselin G, Mongrain I, Valois D, Gaulin Marion MJ, Lemieux Perreault LP, Perreault S, Dubé MP. Shahabi P, et al. Among authors: asselin g. Pharmacogenomics J. 2019 Apr;19(2):147-156. doi: 10.1038/s41397-017-0005-1. Epub 2018 Jan 3. Pharmacogenomics J. 2019. PMID: 29298995 Free PMC article.

7

CKM and LILRB5 are associated with serum levels of creatine kinase.

Dubé MP, Zetler R, Barhdadi A, Brown AM, Mongrain I, Normand V, Laplante N, Asselin G, Zada YF, Provost S, Bergeron J, Kouz S, Dufour R, Diaz A, de Denus S, Turgeon J, Rhéaume E, Phillips MS, Tardif JC. Dubé MP, et al. Among authors: asselin g. Circ Cardiovasc Genet. 2014 Dec;7(6):880-6. doi: 10.1161/CIRCGENETICS.113.000395. Epub 2014 Sep 11. Circ Cardiovasc Genet. 2014. PMID: 25214527

8

Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib.

Tardif JC, Rhéaume E, Lemieux Perreault LP, Grégoire JC, Feroz Zada Y, Asselin G, Provost S, Barhdadi A, Rhainds D, L'Allier PL, Ibrahim R, Upmanyu R, Niesor EJ, Benghozi R, Suchankova G, Laghrissi-Thode F, Guertin MC, Olsson AG, Mongrain I, Schwartz GG, Dubé MP. Tardif JC, et al. Among authors: asselin g. Circ Cardiovasc Genet. 2015 Apr;8(2):372-82. doi: 10.1161/CIRCGENETICS.114.000663. Epub 2015 Jan 11. Circ Cardiovasc Genet. 2015. PMID: 25583994 Clinical Trial.

9

Familial ventricular aneurysms and septal defects map to chromosome 10p15.

Tremblay N, Yang SW, Hitz MP, Asselin G, Ginns J, Riopel K, Gendron R, Montpetit A, Duhig E, Dubé MP, Radford D, Andelfinger G. Tremblay N, et al. Among authors: asselin g. Eur Heart J. 2011 Mar;32(5):568-73. doi: 10.1093/eurheartj/ehq447. Epub 2010 Dec 18. Eur Heart J. 2011. PMID: 21169613

10

Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent.

Villanueva A, Biswas P, Kishaba K, Suk J, Tadimeti K, Raghavendra PB, Nadeau K, Lamontagne B, Busque L, Geoffroy S, Mongrain I, Asselin G, Provost S, Dubé MP, Nudleman E, Ayyagari R. Villanueva A, et al. Among authors: asselin g. Ophthalmic Genet. 2018 Jan-Feb;39(1):73-79. doi: 10.1080/13816810.2017.1373830. Epub 2017 Sep 25. Ophthalmic Genet. 2018. PMID: 28945494 Free PMC article.

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