Louis-Philippe Lemieux Perreault
Louis-Philippe Lemieux Perreault
Beaulieu-Saucier Pharmacogenomics Centre
Adresse e-mail validée de statgen.org
Citée par
Citée par
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib
JC Tardif, E Rhéaume, LP Lemieux Perreault, JC Grégoire, Y Feroz Zada, ...
Circulation: Cardiovascular Genetics 8 (2), 372-382, 2015
Rare copy number variants contribute to congenital left-sided heart disease
MP Hitz, LP Lemieux-Perreault, C Marshall, Y Feroz-Zada, R Davies, ...
Public Library of Science 8 (9), e1002903, 2012
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits
PL Auer, A Teumer, U Schick, A O'Shaughnessy, KS Lo, N Chami, ...
Nature genetics 46 (6), 629-634, 2014
DNA methylation signature of human fetal alcohol spectrum disorder
E Portales-Casamar, AA Lussier, MJ Jones, JL MacIsaac, RD Edgar, ...
Epigenetics & chromatin 9 (1), 1-20, 2016
Methylomic changes during conversion to psychosis
O Kebir, B Chaumette, F Rivollier, F Miozzo, LPL Perreault, A Barhdadi, ...
Molecular psychiatry 22 (4), 512-518, 2017
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis
DW Morris, RD Pearson, P Cormican, EM Kenny, CT O'Dushlaine, ...
Human molecular genetics 23 (12), 3316-3326, 2014
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals
SL Girard, CV Bourassa, LP Lemieux Perreault, MA Legault, A Barhdadi, ...
PLoS One 11 (10), e0164212, 2016
pyGenClean: efficient tool for genetic data clean up before association testing
LP Lemieux Perreault, S Provost, MA Legault, A Barhdadi, MP Dube
Bioinformatics 29 (13), 1704-1705, 2013
genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools
LP Lemieux Perreault, MA Legault, G Asselin, MP Dubé
Bioinformatics 32 (23), 3661-3663, 2016
Comparison of sequencing based CNV discovery methods using monozygotic twin quartets
MA Legault, S Girard, LP Lemieux Perreault, GA Rouleau, MP Dubé
PLoS One 10 (3), e0122287, 2015
Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol
F Rivollier, B Chaumette, N Bendjemaa, M Chayet, B Millet, N Jaafari, ...
PloS one 12 (4), e0174783, 2017
Comparison of genotype clustering tools with rare variants
LPL Perreault, MA Legault, A Barhdadi, S Provost, V Normand, JC Tardif, ...
BMC bioinformatics 15 (1), 1-12, 2014
Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort
P Shahabi, F Lamothe, S Dumas, É Rouleau-Mailloux, YF Zada, ...
The pharmacogenomics journal 19 (2), 147-156, 2019
A genetic model of ivabradine recapitulates results from randomized clinical trials
MA Legault, J Sandoval, S Provost, A Barhdadi, LP Lemieux Perreault, ...
PloS one 15 (7), e0236193, 2020
Pharmacogenetic content of commercial genome-wide genotyping arrays
LP Lemieux Perreault, N Zaïd, M Cameron, I Mongrain, MP Dubé
Pharmacogenomics 19 (15), 1159-1167, 2018
Partitioning of copy-number genotypes in pedigrees
LPL Perreault, GU Andelfinger, G Asselin, MP Dubé
BMC bioinformatics 11 (1), 1-8, 2010
Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT
MP Dubé, MA Legault, A Lemaçon, LP Lemieux Perreault, R Fouodjio, ...
Circulation: Genomic and Precision Medicine 14 (2), e003183, 2021
Deep interpretability for GWAS
D Sharma, A Durand, MA Legault, LPL Perreault, A Lemaçon, MP Dubé, ...
arXiv preprint arXiv:2007.01516, 2020
Genetics of symptom remission in outpatients with COVID-19
MP Dubé, A Lemaçon, A Barhdadi, LPL Perreault, E Oussaïd, G Asselin, ...
Scientific reports 11 (1), 1-10, 2021
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