Phosphorylation-independent desensitization of GABA(B) receptor by GRK4

av Perroy, Julie, Adam, Lynda, Qanbar, Riad, Chénier, Sébastien, Bouvier, Michel
Publicerad 2003

Subcellular distribution of GABA(B) receptor homo- and hetero-dimers

av Villemure, Josée-France, Adam, Lynda, Bevan, Nicola J., Gearing, Katy, Chénier, Sébastien, Bouvier, Michel
Publicerad 2005

Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray

av Hayeems, Robin Z, Hoang, Ny, Chenier, Sebastien, Stavropoulos, Dimitri J, Pu, Shuye, Weksberg, Rosanna, Shuman, Cheryl
I publikationen Eur J Hum Genet (2015)

Does personal genome testing drive service utilization in an adult preventive medicine clinic?

av Hoang, Ny, Hayeems, Robin, Davies, Jill, Pu, Shuye, Wasim, Syed, Velsher, Lea, Aw, James, Chénier, Sébastien, Stavropoulos, Dimitri J, Babul-Hirji, Riyana, Weksberg, Rosanna, Shuman, Cheryl
I publikationen J Community Genet (2017)

Molecular diagnosis of muscular diseases in outpatient clinics: A Canadian perspective

av Thuriot, Fanny, Gravel, Elaine, Buote, Caroline, Doyon, Marianne, Lapointe, Elvy, Marcoux, Lydia, Larue, Sandrine, Nadeau, Amélie, Chénier, Sébastien, Waters, Paula J., Jacques, Pierre-Étienne, Gravel, Serge, Lévesque, Sébastien
I publikationen Neurol Genet (2020)

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

av Tucker, Tracy, Montpetit, Alexandre, Chai, David, Chan, Susanna, Chénier, Sébastien, Coe, Bradley P, Delaney, Allen, Eydoux, Patrice, Lam, Wan L, Langlois, Sylvie, Lemyre, Emmanuelle, Marra, Marco, Qian, Hong, Rouleau, Guy A, Vincent, David, Michaud, Jacques L, Friedman, Jan M
Publicerad 2011

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

av Chénier, Sébastien, Yoon, Grace, Argiropoulos, Bob, Lauzon, Julie, Laframboise, Rachel, Ahn, Joo Wook, Ogilvie, Caroline Mackie, Lionel, Anath C, Marshall, Christian R, Vaags, Andrea K, Hashemi, Bita, Boisvert, Karine, Mathonnet, Géraldine, Tihy, Frédérique, So, Joyce, Scherer, Stephen W, Lemyre, Emmanuelle, Stavropoulos, Dimitri J
Publicerad 2014

Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing

av Lévesque, Sébastien, Auray-Blais, Christiane, Gravel, Elaine, Boutin, Michel, Dempsey-Nunez, Laura, Jacques, Pierre-Etienne, Chenier, Sébastien, Larue, Sandrine, Rioux, Marie-France, Al-Hertani, Walla, Nadeau, Amelie, Mathieu, Jean, Maranda, Bruno, Désilets, Valérie, Waters, Paula J., Keutzer, Joan, Austin, Stephanie, Kishnani, Priya
I publikationen Orphanet J Rare Dis (2016)