Marie-Pierre Dubé
Marie-Pierre Dubé
Professor of Medicine, Université de Montréal
Adresse e-mail validée de - Page d'accueil
Citée par
Citée par
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
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
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
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
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
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
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
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
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
New England journal of Medicine, 2016
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
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
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
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 (1), 1-10, 2014
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
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
DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions
M Buscarlet, S Provost, YF Zada, A Barhdadi, V Bourgoin, G Lépine, ...
Blood, The Journal of the American Society of Hematology 130 (6), 753-762, 2017
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
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20