Marie-Pierre Dubé
Marie-Pierre Dubé
Professor of Medicine, Université de Montréal
Verified email at - Homepage
Cited by
Cited by
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
G Papanikolaou, ME Samuels, EH Ludwig, MLE MacDonald, ...
Nature genetics 36 (1), 77-82, 2004
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy
J Robitaille, MLE MacDonald, A Kaykas, LC Sheldahl, J Zeisler, MP Dubé, ...
Nature genetics 32 (2), 326-330, 2002
Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations
YP Goldberg, J MacFarlane, ML MacDonald, J Thompson, MP Dube, ...
Clinical genetics 71 (4), 311-319, 2007
Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers
SA Narod, MP Dubé, J Klijn, J Lubinski, HT Lynch, P Ghadirian, ...
Journal of the National Cancer Institute 94 (23), 1773-1779, 2002
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
J Gauthier, N Champagne, RG Lafrenière, L Xiong, D Spiegelman, ...
Proceedings of the National Academy of Sciences 107 (17), 7863-7868, 2010
Efficacy and safety of low-dose colchicine after myocardial infarction
JC Tardif, S Kouz, DD Waters, OF Bertrand, R Diaz, AP Maggioni, FJ Pinto, ...
New England journal of medicine 381 (26), 2497-2505, 2019
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura
RG Lafrenière, MZ Cader, JF Poulin, I Andres-Enguix, M Simoneau, ...
Nature medicine 16 (10), 1157-1160, 2010
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy
CJD Ross, H Katzov-Eckert, MP Dubé, B Brooks, SR Rassekh, ...
Nature genetics 41 (12), 1345-1349, 2009
Pharmacogenomic prediction of anthracycline-induced cardiotoxicity in children
H Visscher, CJD Ross, SR Rassekh, A Barhdadi, MP Dubé, H Al-Saloos, ...
Journal of Clinical Oncology 30 (13), 1422-1428, 2012
Hereditary spastic paraplegia
JK Fink
Current neurology and neuroscience reports 6 (1), 65-76, 2006
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts
P Awadalla, J Gauthier, RA Myers, F Casals, FF Hamdan, AR Griffing, ...
The American Journal of Human Genetics 87 (3), 316-324, 2010
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
CECI Infarction Genetics Myocardial
The New England journal of medicine 374 (12), 1134, 2016
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
Common genetic vulnerability to depressive symptoms and coronary artery disease: a review and development of candidate genes related to inflammation and serotonin
JM McCaffery, N Frasure-Smith, MP Dubé, P Théroux, GA Rouleau, ...
Psychosomatic medicine 68 (2), 187-200, 2006
The genetics of congenital amusia (tone deafness): a family-aggregation study
I Peretz, S Cummings, MP Dubé
The American Journal of Human Genetics 81 (3), 582-588, 2007
Hereditary spastic paraplegia: advances in genetic research
JK Fink, T Heiman-Patterson, T Bird, F Cambi, MP Dube, DA Figlewicz, ...
Neurology 46 (6), 1507-1514, 1996
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
I Postmus, S Trompet, HA Deshmukh, MR Barnes, X Li, HR Warren, ...
Nature communications 5, 5068, 2014
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
A Piton, JL Michaud, H Peng, S Aradhya, J Gauthier, L Mottron, ...
Human molecular genetics 17 (24), 3965-3974, 2008
Lipoprotein (a) levels, genotype, and incident aortic valve stenosis: a prospective mendelian randomization study and replication in a case–control cohort
BJ Arsenault, SM Boekholdt, MP Dubé, É Rhéaume, NJ Wareham, ...
Circulation: Cardiovascular Genetics 7 (3), 304-310, 2014
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
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