| 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 | 399 | 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 | 190 | 2015 |
| DNA methylation signature of human fetal alcohol spectrum disorder E Portales-Casamar, AA Lussier, MJ Jones, JL MacIsaac, RD Edgar, ... Epigenetics & chromatin 9, 1-20, 2016 | 165 | 2016 |
| 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 | 165 | 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 | 149 | 2014 |
| Methylomic changes during conversion to psychosis O Kebir, B Chaumette, F Rivollier, F Miozzo, LP Lemieux Perreault, ... Molecular psychiatry 22 (4), 512-518, 2017 | 81 | 2017 |
| 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 | 51 | 2016 |
| Active 3D monitoring system for traffic detection Y Mimeault, L Perreault, M Dubois US Patent 8,842,182, 2014 | 44 | 2014 |
| 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 | 42 | 2014 |
| 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 | 24 | 2017 |
| 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 | 24 | 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 | 20 | 2013 |
| Optical level measurement device and method Y Mimeault, L Perreault US Patent 8,159,660, 2012 | 19 | 2012 |
| Comparison of sequencing based CNV discovery methods using monozygotic twin quartets MA Legault, S Girard, LP Lemieux Perreault, GA Rouleau, MP Dube PLoS One 10 (3), e0122287, 2015 | 17 | 2015 |
| 3D optical detection system and method for a mobile storage system Y Mimeault, L Perreault US Patent 8,823,951, 2014 | 15 | 2014 |
| The genomics of heart failure: design and rationale of the HERMES consortium RT Lumbers, S Shah, H Lin, T Czuba, A Henry, DI Swerdlow, A Mälarstig, ... ESC Heart Failure 8 (6), 5531-5541, 2021 | 12 | 2021 |
| Comparison of genotype clustering tools with rare variants LPL Perreault, MA Legault, A Barhdadi, S Provost, V Normand, JC Tardif, ... BMC bioinformatics 15, 1-12, 2014 | 12 | 2014 |
| 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 | 11 | 2021 |
| Genetics of symptom remission in outpatients with COVID-19 MP Dubé, A Lemaçon, A Barhdadi, LP Lemieux Perreault, E Oussaïd, ... Scientific Reports 11 (1), 10847, 2021 | 10 | 2021 |
| 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 | 9 | 2018 |
Marie-Pierre DubéProfessor of Medicine, Université de MontréalGeverifieerd e-mailadres voor umontreal.ca
