Justine Rousseau - Dissemin

Papers authored by Justine Rousseau

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2019 Benjamin Cogné, Sophie Ehresmann, Justine Rousseau

, Thomas Garcia, Slavé Petrovski, Kirsty McWalter, Stephan J. Sanders, Kévin Uguen, Jacqueline Harris, Eliane Beauregard-Lacroix, Anna Lehman, Thomas Besnard, Mindy H. Li, Usha Kini, Shelagh Joss and 100 other authors

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability

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Mathilde Soulez, Marc K. Saba-El-Leil, Benjamin Turgeon, Simon Mathien, Philippe Coulombe, Sonia Klinger, Justine Rousseau

, Kim Lévesque, Sylvain Meloche

Reevaluation of the Role of Extracellular Signal-Regulated Kinase 3 in Perinatal Survival and Postnatal Growth Using New Genetically Engineered Mouse Models

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Keren Machol

, Justine Rousseau

, Jennifer A. Sullivan, Sophie Ehresmann, Thomas Garcia, Marcia Willing, Elise Fiala, Rolph Pfundt, Thi Tuyet Mai Nguyen, Tjitske Kleefstra, Megan T. Cho, Rebecca C. Spillmann, Heather McLaughlin, Monica Rosello Piera, Anne Turner and 191 other authors

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

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2018 Patricia Wheeler, Marcia Willing, Hannah E. Warren, Ton van Essen, Ingrid M. Wentzensen, Christiane Zweier, Koen L. I. van Gassen, Ellen van Binsbergen, Saskia B. Wortmann, Dylan de Vries, Parthiban Vijayarangakannan, Julie Vogt, Emma Wakeling, Sarah Wallwark, Jonathon Waters and 369 other authors

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

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Thi Tuyet Mai Nguyen, Yoshiko Murakami, Kristen M. Wigby, Nissan V. Baratang, Justine Rousseau

, Anik St-Denis, Jill A. Rosenfeld, Stephanie C. Laniewski, Julie Jones, Alejandro D. Iglesias, Marilyn C. Jones, Diane Masser-Frye, Angela E. Scheuerle, Denise L. Perry, Ryan J. Taft and 4 other authors

Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy

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2017 Chae Syng Lee, He Fu, Nissan Baratang, Justine Rousseau

, Heena Kumra

, V. Reid Sutton, Marcello Niceta, Andrea Ciolfi, Guilherme Yamamoto, Débora Bertola, Carlo L. Marcelis, Dorien Lugtenberg, Andrea Bartuli, Choel Kim, Julie Hoover-Fong and 18 other authors

Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with “Corner Fractures”

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Thi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, Sophie Ehresmann, Justine Rousseau

, Anik St-Denis, Guoliang Chai, Norbert F. Ajeawung, Laura Fairbrother, Tyler Reimschisel, Alexandra Bateman, Elizabeth Berry-Kravis, Fan Xia, Jessica Tardif, David A. Parry and 17 other authors

Mutations in GPAA1 , Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia

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Ronit Marom, Mahim Jain, Lindsay C. Burrage, I.-Wen Song, Brett H. Graham, Chester W. Brown, Servi J. C. Stevens, Alexander P. A. Stegmann

, Andrew T. Gunter, Julie D. Kaplan, Ralitza H. Gavrilova, Marwan Shinawi, Jill A. Rosenfeld, Yangjin Bae, Alyssa A. Tran and 9 other authors

Heterozygous variants inACTL6A, encoding a component of the BAF complex, are associated with intellectual disability

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Kezhi Yan, Justine Rousseau

, Rebecca Okashah Littlejohn, Courtney Kiss, Anna Lehman, Jill A. Rosenfeld, Constance T. R. Stumpel, Alexander P. A. Stegmann

, Laurie Robak, Fernando Scaglia, Thi Tuyet Mai Nguyen, He Fu, Norbert F. Ajeawung, Maria Vittoria Camurri, Lin Li and 19 other authors

Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation

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2014 Miriam Marquis, Jean-François Daudelin, Salix Boulet, Julien Sirois, Karinn Crain, Simon Mathien, Benjamin Turgeon, Justine Rousseau

, Sylvain Meloche, Nathalie Labrecque

The Catalytic Activity of the Mitogen-Activated Protein Kinase Extracellular Signal-Regulated Kinase 3 Is Required To Sustain CD4+ CD8+ Thymocyte Survival

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Miriam Marquis, Pamé la Thébault, Salix Boulet, Simon Mathien, Justine Rousseau

, Paméla Thébault, Jean-François Daudelin, Julie Rooney, Benjamin Turgeon, Claudine Beauchamp, Sylvain Meloche, Nathalie Labrecque

The Non-Classical MAP Kinase ERK3 Controls T Cell Activation

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2012 Mathieu Lavallée-Adam, Justine Rousseau

, Céline Domecq, Annie Bouchard, Diane Forget, Denis Faubert, Mathieu Blanchette, Benoit Coulombe

Discovery of Cell Compartment Specific Protein–Protein Interactions using Affinity Purification Combined with Tandem Mass Spectrometry

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2010 Justine Rousseau

, Sonia Klinger, Adeline Rachalski, Benjamin Turgeon, Paul Déléris, Erika Vigneault, Jean-François Poirier-Héon, Maria Antonietta Davoli, Naguib Mechawar, Salah El Mestikawy, Nicolas Cermakian, Sylvain Meloche

Targeted Inactivation of Mapk4 in Mice Reveals Specific Nonredundant Functions of Erk3/Erk4 Subfamily Mitogen-Activated Protein Kinases

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2008 Paul Déléris, Justine Rousseau

, Philippe Coulombe, Geneviève Rodier, Pierre-Luc Tanguay, Sylvain Meloche

Activation loop phosphorylation of the atypical MAP kinases ERK3 and ERK4 is required for binding, activation and cytoplasmic relocalization of MK5

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Papers authored by Justine Rousseau