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Rare diseases load through the study of a regional population 通过区域人群研究来评估罕见病负担 Michel, Elisa; Moreau, Claudia; Gagnon, Laurence; Gagnon, Mylene; Leblanc, Josianne; Tardif, Jessica; Girard, Lysanne; Mathieu, Jean; Gagnon, Cynthia; Desmeules, Mathieu; Brisson, Jean-Denis; Bouchard, Luigi; Girard, Simon L. 分享 收藏
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SF3B1 mutations provide genetic vulnerability to copper ionophores in human acute myeloid leukemia Moison, Celine; Gracias, Deanne; Schmitt, Julie; Girard, Simon; Spinella, Jean-Francois; Fortier, Simon; Boivin, Isabel; Mendoza-Sanchez, Rodrigo; Thavonekham, Bounkham; Macrae, Tara; Mayotte, Nadine; Bonneil, Eric; Wittman, Mark; Carmichael, James; Ruel, Rejean; Thibault, Pierre; Hebert, Josee; Marinier, Anne; Sauvageau, Guy 分享 收藏
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The role of common genetic variation in presumed monogenic epilepsies Campbell, Ciaran; Leu, Costin; Feng, Yen-Chen Anne; Wolking, Stefan; Moreau, Claudia; Ellis, Colin; Ganesan, Shiva; Martins, Helena; Oliver, Karen; Boothman, Isabelle; Benson, Katherine; Molloy, Anne; Brody, Lawrence; Michaud, Jacques L.; Hamdan, Fadi F.; Minassian, Berge A.; Lerche, Holger; Scheffer, Ingrid E.; Sisodiya, Sanjay; Girard, Simon; Cosette, Patrick; Delanty, Norman; Lal, Dennis; Cavalleri, Gianpiero L. 分享 收藏
Assessment of burden and segregation profiles of CNVs in patients with epilepsy Moreau, Claudia; Tremblay, Frederique; Wolking, Stefan; Girard, Alexandre; Laprise, Catherine; Hamdan, Fadi F.; Michaud, Jacques L.; Minassian, Berge A.; Cossette, Patrick; Girard, Simon L. 分享 收藏
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 评估罕见遗传变异在耐药非病灶局灶性癫痫中的作用 Wolking, Stefan; Moreau, Claudia; McCormack, Mark; Krause, Roland; Krenn, Martin; Berkovic, Samuel; Cavalleri, Gianpiero L.; Delanty, Norman; Depondt, Chantal; Johnson, Michael R.; Koeleman, Bobby P. C.; Kunz, Wolfram S.; Lerche, Holger; Marson, Anthony G.; O'Brien, Terence J.; Petrovski, Slave; Sander, Josemir W.; Sills, Graeme J.; Striano, Pasquale; Zara, Federico; Zimprich, Fritz; Sisodiya, Sanjay M.; Girard, Simon L.; Cossette, Patrick 分享 收藏
Polygenic risk score for atopic dermatitis in the Canadian population Simard, Mathieu; Madore, Anne-Marie; Girard, Simon; Waserman, Susan; Duan, Qingling; Subbarao, Padmaja; Sears, Malcolm R.; Moraes, Theo J.; Becker, Allan B.; Turvey, Stuart E.; Mandhane, Piushkumar J.; Morin, Charles; Begin, Philippe; Laprise, Catherine 分享 收藏
UM171 Preserves Epigenetic Marks that Are Reduced in Ex Vivo Culture of Human HSCs via Potentiation of the CLR3-KBTBD4 Complex Chagraoui, Jalila; Girard, Simon; Spinella, Jean-Francois; Simon, Laura; Bonneil, Eric; Mayotte, Nadine; MacRae, Tara; Coulombe-Huntington, Jasmin; Bertomeu, Thierry; Moison, Celine; Tomellini, Elisa; Thibault, Pierre; Tyers, Mike; Marinier, Anne; Sauvageau, Guy 分享 收藏
Polygenic risk scores of several subtypes of epilepsies in a founder population Moreau, Claudia; Rebillard, Rose-Marie; Wolking, Stefan; Michaud, Jacques; Tremblay, Frederique; Girard, Alexandre; Bouchard, Joanie; Minassian, Berge; Laprise, Catherine; Cossette, Patrick; Girard, Simon L. 分享 收藏
Testing association of rare genetic variants with resistance to three common antiseizure medications Wolking, Stefan; Moreau, Claudia; Nies, Anne T.; Schaeffeler, Elke; McCormack, Mark; Auce, Pauls; Avbersek, Andreja; Becker, Felicitas; Krenn, Martin; Moller, Rikke S.; Nikanorova, Marina; Weber, Yvonne G.; Weckhuysen, Sarah; Cavalleri, Gianpiero L.; Delanty, Norman; Depondt, Chantal; Johnson, Michael R.; Koeleman, Bobby P. C.; Kunz, Wolfram S.; Marson, Anthony G.; Sander, Josemir W.; Sills, Graeme J.; Striano, Pasquale; Zara, Federico; Zimprich, Fritz; Schwab, Matthias; Krause, Roland; Sisodiya, Sanjay M.; Cossette, Patrick; Girard, Simon L.; Lerche, Holger 分享 收藏
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Genome-wide estimates of heritability and genetic correlations in essential tremor 特发性震颤的遗传力和遗传相关性的全基因组估计 Diez-Fairen, Monica; Bandres-Ciga, Sara; Houle, Gabrielle; Nalls, Mike A.; Girard, Simon L.; Dion, Patrick A.; Blauwendraat, Cornelis; Singleton, Andrew B.; Rouleau, Guy A.; Pastor, Pau 分享 收藏
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