Diagnosis and treatment of diabetic ketoacidosis and the hyperglycemic hyperosmolar state

Autor Chiasson, Jean-Louis, Aris-Jilwan, Nahla, Bélanger, Raphaël, Bertrand, Sylvie, Beauregard, Hugues, Ékoé, Jean-Marie, Fournier, Hélène, Havrankova, Jana
Vydáno 2003

Meta-Analysis for Genome-Wide Association Study Identifies Multiple Variants at the BIN1 Locus Associated with Late-Onset Alzheimer's Disease

Autor Hu, Xiaolan, Pickering, Eve, Liu, Yingxue Cathy, Hall, Stephanie, Fournier, Helene, Katz, Elyse, Dechairo, Bryan, John, Sally, Van Eerdewegh, Paul, Soares, Holly
Vydáno 2011

Hotspots of Large Rare Deletions in the Human Genome

Autor Bradley, W. Edward C., Raelson, John V., Dubois, Daniel Y., Godin, Éric, Fournier, Hélène, Privé, Charles, Allard, René, Pinchuk, Vadym, Lapalme, Micheline, Paulussen, René J. A., Belouchi, Abdelmajid
Vydáno 2010

LINGO1 Variants in the French-Canadian Population

Autor Bourassa, Cynthia V., Rivière, Jean-Baptiste, Dion, Patrick A., Bernard, Geneviève, Diab, Sabrina, Panisset, Michel, Chouinard, Sylvain, Dupré, Nicolas, Fournier, Hélène, Raelson, John, Belouchi, Majid, Rouleau, Guy A.
Vydáno 2011

Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene

Autor Franke, Andre, Hampe, Jochen, Rosenstiel, Philip, Becker, Christian, Wagner, Florian, Häsler, Robert, Little, Randall D., Huse, Klaus, Ruether, Andreas, Balschun, Tobias, Wittig, Michael, ElSharawy, Abdou, Mayr, Gabriele, Albrecht, Mario, Prescott, Natalie J., Onnie, Clive M., Fournier, Hélène, Keith, Tim, Radelof, Uwe, Platzer, Matthias, Mathew, Christopher G., Stoll, Monika, Krawczak, Michael, Nürnberg, Peter, Schreiber, Stefan
Vydáno 2007

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

Autor Merner, Nancy D., Girard, Simon L., Catoire, Hélène, Bourassa, Cynthia V., Belzil, Véronique V., Rivière, Jean-Baptiste, Hince, Pascale, Levert, Annie, Dionne-Laporte, Alexandre, Spiegelman, Dan, Noreau, Anne, Diab, Sabrina, Szuto, Anna, Fournier, Hélène, Raelson, John, Belouchi, Majid, Panisset, Michel, Cossette, Patrick, Dupré, Nicolas, Bernard, Geneviève, Chouinard, Sylvain, Dion, Patrick A., Rouleau, Guy A.
Vydáno 2012

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

Autor Raelson, John V., Little, Randall D., Ruether, Andreas, Fournier, Hélène, Paquin, Bruno, Van Eerdewegh, Paul, Bradley, W. E. C., Croteau, Pascal, Nguyen-Huu, Quynh, Segal, Jonathan, Debrus, Sophie, Allard, René, Rosenstiel, Philip, Franke, Andre, Jacobs, Gunnar, Nikolaus, Susanna, Vidal, Jean-Michel, Szego, Peter, Laplante, Nathalie, Clark, Hilary F., Paulussen, René J., Hooper, John W., Keith, Tim P., Belouchi, Abdelmajid, Schreiber, Stefan
Vydáno 2007

Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2

Autor Ellinghaus, Eva, Ellinghaus, David, Stuart, Philip E., Nair, Rajan P., Debrus, Sophie, Raelson, John V., Belouchi, Majid, Fournier, Hélène, Reinhard, Claudia, Ding, Jun, Li, Yun, Tejasvi, Trilokraj, Gudjonsson, Johann, Stoll, Stefan W., Voorhees, John J., Lambert, Sylviane, Weidinger, Stephan, Eberlein, Bernadette, Kunz, Manfred, Rahman, Proton, Gladman, Dafna D., Gieger, Christian, Wichmann, H. Erich, Karlsen, Tom H., Mayr, Gabriele, Albrecht, Mario, Kabelitz, Dieter, Mrowietz, Ulrich, Abecasis, Gonçalo R., Elder, James T., Schreiber, Stefan, Weichenthal, Michael, Franke, Andre
Vydáno 2010