Works matching AU Dube, Marie-Pierre


Results: 92
    1
    2
    3
    4

    Study of effect modifiers of genetically predicted CETP reduction.

    Published in:
    Genetic Epidemiology, 2023, v. 47, n. 2, p. 198, doi. 10.1002/gepi.22514
    By:
    • Legault, Marc‐André;
    • Barhdadi, Amina;
    • Gamache, Isabel;
    • Lemaçon, Audrey;
    • Lemieux Perreault, Louis‐Philippe;
    • Grenier, Jean‐Christophe;
    • Sylvestre, Marie‐Pierre;
    • Hussin, Julie G.;
    • Rhainds, David;
    • Tardif, Jean‐Claude;
    • Dubé, Marie‐Pierre
    Publication type:
    Article
    5
    6

    The challenge of detecting epistasis (G×G Interactions): Genetic Analysis Workshop 16.

    Published in:
    Genetic Epidemiology, 2009, v. 33, n. S1, p. S58, doi. 10.1002/gepi.20474
    By:
    • An, Ping;
    • Mukherjee, Odity;
    • Chanda, Pritam;
    • Yao, Li;
    • Engelman, Corinne D.;
    • Huang, Chien-Hsun;
    • Zheng, Tian;
    • Kovac, Ilija P.;
    • Dubé, Marie-Pierre;
    • Liang, Xueying;
    • Li, Jia;
    • de Andrade, Mariza;
    • Culverhouse, Robert;
    • Malzahn, Doerthe;
    • Manning, Alisa K.;
    • Clarke, Geraldine M.;
    • Jung, Jeesun;
    • Province, Michael A.
    Publication type:
    Article
    7
    8

    A Study Of the effect of Sex on drug dosing, concentrations, and pharmacogenomics in the Montreal Heart Institute Hospital Cohort (SOS-PGx): methodology and research progress.

    Published in:
    European Journal of Clinical Pharmacology, 2025, v. 81, n. 2, p. 321, doi. 10.1007/s00228-024-03786-3
    By:
    • Pilon, Marc-Olivier;
    • Hindi, Jessica;
    • St-Jean, Isabelle;
    • Jutras, Martin;
    • Brouillette, Maxime Meloche;
    • Mongrain, Ian;
    • Lagacé, Caroline;
    • Vazquez, Karla;
    • Provost, Sylvie;
    • Lemieux Perreault, Louis-Philippe;
    • Oussaid, Essaid;
    • Busseuil, David;
    • Cyr, Marie-Christyne;
    • Tardif, Jean-Claude;
    • Dubé, Marie-Pierre;
    • Leclair, Grégoire;
    • de Denus, Simon
    Publication type:
    Article
    9
    10
    11
    12
    13
    14

    Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.

    Published in:
    European Journal of Human Genetics, 2000, v. 8, n. 5, p. 372, doi. 10.1038/sj.ejhg.5200471
    By:
    • Kibar, Zoha;
    • Dubé, Marie-Pierre;
    • Powell, Julie;
    • McCuaïg, Catherine;
    • Hayflick, Susan J;
    • Zonana, Jonathan;
    • Hovnanian, Alain;
    • Radhakrishna, Uppala;
    • Antonarakis, Stylianos E;
    • Benohanian, Antranik;
    • Sheeran, Amy D;
    • Stephan, Mark L;
    • Gosselin, Richard;
    • Kelsell, David P;
    • Christianson, Arnold L;
    • Fraser, F Clarke;
    • Der Kaloustian, Vazken M;
    • Rouleau, Guy A
    Publication type:
    Article
    15

    A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.

    Published in:
    Nature Medicine, 2010, v. 16, n. 10, p. 1157, doi. 10.1038/nm.2216
    By:
    • Lafrenière, Ronald G.;
    • Cader, M. Zameel;
    • Poulin, Jean-François;
    • Andres-Enguix, Isabelle;
    • Simoneau, Maryse;
    • Gupta, Namrata;
    • Boisvert, Karine;
    • Lafrenière, François;
    • McLaughlan, Shannon;
    • Dubé, Marie-Pierre;
    • Marcinkiewicz, Martin M.;
    • Ramagopalan, Sreeram;
    • Ansorge, Olaf;
    • Brais, Bernard;
    • Sequeiros, Jorge;
    • Pereira-Monteiro, Jose Maria;
    • Griffiths, Lyn R.;
    • Tucker, Stephen J.;
    • Ebers, George;
    • Rouleau, Guy A.
    Publication type:
    Article
    16

    Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

    Published in:
    Nature Genetics, 2014, v. 46, n. 6, p. 629, doi. 10.1038/ng.2962
    By:
    • Auer, Paul L;
    • Teumer, Alexander;
    • Schick, Ursula;
    • O'Shaughnessy, Andrew;
    • Lo, Ken Sin;
    • Chami, Nathalie;
    • Carlson, Chris;
    • de Denus, Simon;
    • Dubé, Marie-Pierre;
    • Haessler, Jeff;
    • Jackson, Rebecca D;
    • Kooperberg, Charles;
    • Perreault, Louis-Philippe Lemieux;
    • Nauck, Matthias;
    • Peters, Ulrike;
    • Rioux, John D;
    • Schmidt, Frank;
    • Turcot, Valérie;
    • Völker, Uwe;
    • Völzke, Henry
    Publication type:
    Article
    17
    18
    19

    Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.

    Published in:
    2004
    By:
    • Papanikolaou, George;
    • Dubé, Marie-Pierre;
    • Andres, Lisa;
    • MacFarlane, Julie;
    • Sakellaropoulos, Nikos;
    • Politou, Marianna;
    • Nemeth, Elizabeta;
    • Thompson, Jay;
    • Zaborowska, Catherine;
    • Babakaiff, Ryan;
    • Davidas, Owen;
    • Christakis, John;
    • Brissot, Pierre;
    • Lockitch, Gillian;
    • Ganz, Tomas;
    • Samuels, Mark E.;
    • Ludwig,, Erwin H.;
    • MacDonald,, Marcia L. E.;
    • Franchini, Patrick L.;
    • Risler, Jenni K.
    Publication type:
    Letter
    20

    Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.

    Published in:
    Nature Genetics, 2002, v. 32, n. 2, p. 326, doi. 10.1038/ng957
    By:
    • Robitaille, Johane;
    • MacDonald, Marcia L.E.;
    • Kaykas, Ajamete;
    • Sheldahl, Laird C.;
    • Zeisler, Jutta;
    • Dubé, Marie-Pierre;
    • Zhang, Lin-Hua;
    • Singaraja, Roshni R.;
    • Guernsey, Duane L.;
    • Zheng, Binyou;
    • Siebert, Lee F.;
    • Hoskin-Mott, Ann;
    • Trese, Michael T.;
    • Pimstone, Simon N.;
    • Shastry, Barkur S.;
    • Moon, Randall T.;
    • Hayden, Michael R.;
    • Goldberg, Y. Paul;
    • Samuels, Mark E.
    Publication type:
    Article
    21
    22
    23
    24
    25

    A sex-specific evolutionary interaction between ADCY9 and CETP.

    Published in:
    eLife, 2021, p. 1, doi. 10.7554/eLife.69198
    By:
    • Gamache, Isabel;
    • Legault, Marc-André;
    • Grenier, Jean-Christophe;
    • Sanchez, Rocio;
    • Rhéaume, Eric;
    • Asgari, Samira;
    • Barhdadi, Amina;
    • Zada, Yassamin Feroz;
    • Trochet, Holly;
    • Yang Luo;
    • Lecca, Leonid;
    • Murray, Megan;
    • Raychaudhuri, Soumya;
    • Tardif, Jean-Claude;
    • Dubé, Marie-Pierre;
    • Hussin, Julie
    Publication type:
    Article
    26
    27

    Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30875-7
    By:
    • Cadby, Gemma;
    • Giles, Corey;
    • Melton, Phillip E.;
    • Huynh, Kevin;
    • Mellett, Natalie A.;
    • Duong, Thy;
    • Nguyen, Anh;
    • Cinel, Michelle;
    • Smith, Alex;
    • Olshansky, Gavriel;
    • Wang, Tingting;
    • Brozynska, Marta;
    • Inouye, Mike;
    • McCarthy, Nina S.;
    • Ariff, Amir;
    • Hung, Joseph;
    • Hui, Jennie;
    • Beilby, John;
    • Dubé, Marie-Pierre;
    • Watts, Gerald F.
    Publication type:
    Article
    28

    DNA methylation signature of human fetal alcohol spectrum disorder.

    Published in:
    Epigenetics & Chromatin, 2016, v. 9, p. 1, doi. 10.1186/s13072-016-0074-4
    By:
    • Portales-Casamar, Elodie;
    • Lussier, Alexandre A.;
    • Jones, Meaghan J.;
    • MacIsaac, Julia L.;
    • Edgar, Rachel D.;
    • Mah, Sarah M.;
    • Barhdadi, Amina;
    • Provost, Sylvie;
    • Lemieux-Perreault, Louis-Philippe;
    • Cynader, Max S.;
    • Chudley, Albert E.;
    • Dubé, Marie-Pierre;
    • Reynolds, James N.;
    • Pavlidis, Paul;
    • Kobor, Michael S.
    Publication type:
    Article
    29

    Mutation Burden of Rare Variants in Schizophrenia Candidate Genes.

    Published in:
    PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128988
    By:
    • Girard, Simon L.;
    • Dion, Patrick A.;
    • Bourassa, Cynthia V.;
    • Geoffroy, Steve;
    • Lachance-Touchette, Pamela;
    • Barhdadi, Amina;
    • Langlois, Mathieu;
    • Joober, Ridha;
    • Krebs, Marie-Odile;
    • Dubé, Marie-Pierre;
    • Rouleau, Guy A.
    Publication type:
    Article
    30
    31
    32
    33
    34
    35
    36
    37

    Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.

    Published in:
    ESC Heart Failure, 2022, v. 9, n. 5, p. 2997, doi. 10.1002/ehf2.14026
    By:
    • Dubé, Marie‐Pierre;
    • Chazara, Olympe;
    • Lemaçon, Audrey;
    • Asselin, Géraldine;
    • Provost, Sylvie;
    • Barhdadi, Amina;
    • Lemieux Perreault, Louis‐Philippe;
    • Mongrain, Ian;
    • Wang, Quanli;
    • Carss, Keren;
    • Paul, Dirk S.;
    • Cunningham, Jonathan W.;
    • Rouleau, Jean;
    • Solomon, Scott D.;
    • McMurray, John J.V.;
    • Yusuf, Salim;
    • Granger, Chris B.;
    • Haefliger, Carolina;
    • de Denus, Simon;
    • Tardif, Jean‐Claude
    Publication type:
    Article
    38

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

    Published in:
    ESC Heart Failure, 2020, v. 7, n. 6, p. 4384, doi. 10.1002/ehf2.12934
    By:
    • Denus, Simon;
    • Mottet, Fannie;
    • Korol, Sandra;
    • Feroz Zada, Yassamin;
    • Provost, Sylvie;
    • Mongrain, Ian;
    • Asselin, Géraldine;
    • Oussaïd, Essaïd;
    • Busseuil, David;
    • Lettre, Guillaume;
    • Rioux, John;
    • Racine, Normand;
    • O'Meara, Eileen;
    • White, Michel;
    • Rouleau, Jean;
    • Tardif, Jean Claude;
    • Dubé, Marie‐Pierre
    Publication type:
    Article
    39
    40
    41

    Testing the role of predicted gene knockouts in human anthropometric trait variation.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 10, p. 2082, doi. 10.1093/hmg/ddw055
    By:
    • Lessard, Samuel;
    • Manning, Alisa K.;
    • Cécile Low-Kam;
    • Auer, Paul L.;
    • Giri, Ayush;
    • Graff, Mariaelisa;
    • Schurmann, Claudia;
    • Yaghootkar, Hanieh;
    • Luan, Jian'an;
    • Esko, Tonu;
    • Karaderi, Tugce;
    • Bottinger, Erwin P.;
    • Yingchang Lu;
    • Carlson, Chris;
    • Caulfield, Mark;
    • Dubé, Marie-Pierre;
    • Jackson, Rebecca D.;
    • Kooperberg, Charles;
    • McKnight, Barbara;
    • Mongrain, Ian
    Publication type:
    Article
    42
    43

    Oral Contraceptives and the Risk of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2002, v. 94, n. 23, p. 1773, doi. 10.1093/jnci/94.23.1773
    By:
    • Narod, Steven A.;
    • Dube, Marie-Pierre;
    • Klijn, Jan;
    • Lubinski, Jan;
    • Lynch, Henry T.;
    • Ghadirian, Parviz;
    • Provencher, Diane;
    • Heimdal, Ketil;
    • Moller, Pal;
    • Robson, Mark;
    • Offit, Kenneth;
    • Isaacs, Claudine;
    • Weber, Barbara;
    • Friedman, Eitan;
    • Gershoni-Baruch, Ruth;
    • Rennert, Gad;
    • Pasini, Barbara;
    • Wagner, Theresa;
    • Daly, Mary
    Publication type:
    Article
    44

    CORRESPONDENCE.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2001, v. 93, n. 2, p. 151
    By:
    • Narod, Steven A.;
    • Dube, Marie-Pierre
    Publication type:
    Article
    45
    46
    47
    48
    49

    Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome: the dal-GenE trial.

    Published in:
    European Heart Journal, 2022, v. 43, n. 39, p. 3947, doi. 10.1093/eurheartj/ehac374
    By:
    • Tardif, Jean Claude;
    • Pfeffer, Marc A;
    • Kouz, Simon;
    • Koenig, Wolfgang;
    • Maggioni, Aldo P;
    • McMurray, John J V;
    • Mooser, Vincent;
    • Waters, David D;
    • Grégoire, Jean C;
    • L'Allier, Philippe L;
    • Jukema, J Wouter;
    • White, Harvey D.;
    • Heinonen, Therese;
    • Black, Donald M;
    • Laghrissi-Thode, Fouzia;
    • Levesque, Sylvie;
    • Guertin, Marie Claude;
    • Dubé, Marie Pierre;
    • Investigators, for the dal-GenE
    Publication type:
    Article
    50

    Time-to-treatment initiation of colchicine and cardiovascular outcomes after myocardial infarction in the Colchicine Cardiovascular Outcomes Trial (COLCOT).

    Published in:
    European Heart Journal, 2020, v. 41, n. 42, p. 4092, doi. 10.1093/eurheartj/ehaa659
    By:
    • Bouabdallaoui, Nadia;
    • Tardif, Jean-Claude;
    • Waters, David D;
    • Pinto, Fausto J;
    • Maggioni, Aldo P;
    • Diaz, Rafael;
    • Berry, Colin;
    • Koenig, Wolfgang;
    • Lopez-Sendon, Jose;
    • Gamra, Habib;
    • Kiwan, Ghassan S;
    • Blondeau, Lucie;
    • Orfanos, Andreas;
    • Ibrahim, Reda;
    • Grégoire, Jean C;
    • Dubé, Marie-Pierre;
    • Samuel, Michelle;
    • Morel, Olivier;
    • Lim, Pascal;
    • Bertrand, Olivier F
    Publication type:
    Article