ALG: Automated Genotype Calling of Luminex Assays

Por Bourgey, Mathieu, Lariviere, Mathieu, Richer, Chantal, Sinnett, Daniel
Publicado em 2011

Identification of functional DNA variants in the constitutive promoter region of MDM2

Por Lalonde, Marie-Eve, Ouimet, Manon, Larivière, Mathieu, Kritikou, Ekaterini A, Sinnett, Daniel
Publicado em 2012

Rare allelic forms of PRDM9 associated with childhood leukemogenesis

Por Hussin, Julie, Sinnett, Daniel, Casals, Ferran, Idaghdour, Youssef, Bruat, Vanessa, Saillour, Virginie, Healy, Jasmine, Grenier, Jean-Christophe, de Malliard, Thibault, Busche, Stephan, Spinella, Jean-François, Larivière, Mathieu, Gibson, Greg, Andersson, Anna, Holmfeldt, Linda, Ma, Jing, Wei, Lei, Zhang, Jinghui, Andelfinger, Gregor, Downing, James R., Mullighan, Charles G., Awadalla, Philip
Publicado em 2013

Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

Por Casals, Ferran, Hodgkinson, Alan, Hussin, Julie, Idaghdour, Youssef, Bruat, Vanessa, de Maillard, Thibault, Grenier, Jean-Cristophe, Gbeha, Elias, Hamdan, Fadi F., Girard, Simon, Spinella, Jean-François, Larivière, Mathieu, Saillour, Virginie, Healy, Jasmine, Fernández, Isabel, Sinnett, Daniel, Michaud, Jacques L., Rouleau, Guy A., Haddad, Elie, Le Deist, Françoise, Awadalla, Philip
Publicado em 2013

Allele-Specific Chromatin Remodeling in the ZPBP2/GSDMB/ORMDL3 Locus Associated with the Risk of Asthma and Autoimmune Disease

Por Verlaan, Dominique J., Berlivet, Soizik, Hunninghake, Gary M., Madore, Anne-Marie, Larivière, Mathieu, Moussette, Sanny, Grundberg, Elin, Kwan, Tony, Ouimet, Manon, Ge, Bing, Hoberman, Rose, Swiatek, Marcin, Dias, Joana, Lam, Kevin C.L., Koka, Vonda, Harmsen, Eef, Soto-Quiros, Manuel, Avila, Lydiana, Celedón, Juan C., Weiss, Scott T., Dewar, Ken, Sinnett, Daniel, Laprise, Catherine, Raby, Benjamin A., Pastinen, Tomi, Naumova, Anna K.
Publicado em 2009