SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function
FASSIO, Anna, PATRY, Lysanne, CORRADI, Anna, BALDELLI, Pietro, LAPOINTE, Line, ST-ONGE, Judith, MELOCHE, Caroline, MOTTRON, Laurent, VALTORTA, Flavia, KHOA NGUYEN, Dang, ROULEAU, Guy A, BENFENATI, Fabio, CONGIA, Sonia, COSSETTE, Patrick, ONOFRI, Franco, PITON, Amelie, GAUTHIER, Julie, POZZI, Davide, MESSA, Mirko, DEFRANCHI, Enrico, FADDA, Manuela
Published in Human molecular genetics (15.06.2011)
Published in Human molecular genetics (15.06.2011)
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Global characterization of copy number variants in epilepsy patients from whole genome sequencing
Monlong, Jean, Girard, Simon L, Meloche, Caroline, Cadieux-Dion, Maxime, Andrade, Danielle M, Lafreniere, Ron G, Gravel, Micheline, Spiegelman, Dan, Dionne-Laporte, Alexandre, Boelman, Cyrus, Hamdan, Fadi F, Michaud, Jacques L, Rouleau, Guy, Minassian, Berge A, Bourque, Guillaume, Cossette, Patrick
Published in PLoS genetics (12.04.2018)
Published in PLoS genetics (12.04.2018)
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Early Nutritional Intervention to Promote Healthy Eating Habits in Pediatric Oncology: A Feasibility Study
Bélanger, Véronique, Delorme, Josianne, Napartuk, Mélanie, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Published in Nutrients (28.02.2022)
Published in Nutrients (28.02.2022)
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Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
Bélanger, Véronique, Morel, Sophia, Napartuk, Mélanie, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Published in Lipids in health and disease (10.06.2023)
Published in Lipids in health and disease (10.06.2023)
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Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001
Tran, Thai Hoa, Langlois, Sylvie, Meloche, Caroline, Caron, Maxime, Saint-Onge, Pascal, Rouette, Alexandre, Bataille, Alain R., Jimenez-Cortes, Camille, Sontag, Thomas, Bittencourt, Henrique, Laverdière, Caroline, Lavallée, Vincent-Philippe, Leclerc, Jean-Marie, Cole, Peter D., Gennarini, Lisa M., Kahn, Justine M., Kelly, Kara M., Michon, Bruno, Santiago, Raoul, Stevenson, Kristen E., Welch, Jennifer J.G., Schroeder, Kaitlin M., Koch, Victoria, Cellot, Sonia, Silverman, Lewis B., Sinnett, Daniel
Published in Blood advances (22.02.2022)
Published in Blood advances (22.02.2022)
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Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord
Montpetit, Alexandre, Côté, Stéphanie, Brustein, Edna, Drouin, Christian A, Lapointe, Line, Boudreau, Michèle, Meloche, Caroline, Drouin, Régen, Hudson, Thomas J, Drapeau, Pierre, Cossette, Patrick
Published in PLoS genetics (01.12.2008)
Published in PLoS genetics (01.12.2008)
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Improvement of Diet after an Early Nutritional Intervention in Pediatric Oncology
Napartuk, Mélanie, Bélanger, Véronique, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Published in Children (Basel) (31.03.2023)
Published in Children (Basel) (31.03.2023)
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Needs, Barriers and Facilitators of Adolescents Participating in a Lifestyle Promotion Program in Oncology: Stakeholders, Adolescents and Parents’ Perspective
Kerba, Johanne, Demers, Catherine, Bélanger, Véronique, Napartuk, Mélanie, Bouchard, Isabelle, Meloche, Caroline, Morel, Sophia, Prud’homme, Nicolas, Gélinas, Isabelle, Higgins, Johanne, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Published in Children (Basel) (01.09.2022)
Published in Children (Basel) (01.09.2022)
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Journal Article
Human copy number variants are enriched in regions of low mappability
Monlong, Jean, Cossette, Patrick, Meloche, Caroline, Rouleau, Guy, Girard, Simon L, Bourque, Guillaume
Published in Nucleic acids research (21.08.2018)
Published in Nucleic acids research (21.08.2018)
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Journal Article
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzeniecka, Sylvia, Meloche, Caroline, Retterer, Kyle, Cho, Megan T., Rosenfeld, Jill A., Bi, Weimin, Massicotte, Christine, Miguet, Marguerite, Brunga, Ledia, Regan, Brigid M., Mo, Kelly, Tam, Cory, Hollingsworth, Georgie, FitzPatrick, David R., Canham, Natalie, Blair, Edward, Kerr, Bronwyn, Fry, Andrew E., Thomas, Rhys H., Shelagh, Joss, Hurst, Jane A., Brittain, Helen, Blyth, Moira, Lebel, Robert Roger, Gerkes, Erica H., Davis-Keppen, Laura, Stein, Quinn, Dorison, Sara J., Benke, Paul J., Fassi, Emily, Corsten-Janssen, Nicole, Kamsteeg, Erik-Jan, Mau-Them, Frederic T., Bruel, Ange-Line, Verloes, Alain, Õunap, Katrin, Wojcik, Monica H., Albert, Dara V.F., Venkateswaran, Sunita, Ware, Tyson, Liu, Yu-Chi, Mohammad, Shekeeb S., Bizargity, Peyman, Bacino, Carlos A., Leuzzi, Vincenzo, Martinelli, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Blumkin, Lubov, Wierenga, Klaas J., Purcarin, Gabriela, O’Byrne, James J., Stockler, Sylvia, Lehman, Anna, Keren, Boris, Nougues, Marie-Christine, Mignot, Cyril, Auvin, Stéphane, Nava, Caroline, Hiatt, Susan M., Bebin, Martina, Shao, Yunru, Scaglia, Fernando, Frye, Richard E., Jarjour, Imad T., Jacques, Stéphanie, Boucher, Renee-Myriam, Riou, Emilie, Srour, Myriam, Carmant, Lionel, Lortie, Anne, Major, Philippe, Diadori, Paola, Dubeau, François, D’Anjou, Guy, Bourque, Guillaume, Berkovic, Samuel F., Sadleir, Lynette G., Campeau, Philippe M., Kibar, Zoha, Lafrenière, Ronald G., Girard, Simon L., Mercimek-Mahmutoglu, Saadet, Boelman, Cyrus, Rouleau, Guy A., Scheffer, Ingrid E., Mefford, Heather C., Andrade, Danielle M., Rossignol, Elsa, Minassian, Berge A., Michaud, Jacques L.
Published in American journal of human genetics (02.11.2017)
Published in American journal of human genetics (02.11.2017)
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Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia
Cadieux-Dion, Maxime, Turcotte-Gauthier, Maude, Noreau, Anne, Martin, Caroline, Meloche, Caroline, Gravel, Micheline, Drouin, Christian Allen, Rouleau, Guy A, Nguyen, Dang Khoa, Cossette, Patrick
Published in JAMA neurology (01.04.2014)
Published in JAMA neurology (01.04.2014)
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Abstract B59: Cardiometabolic complications after pediatric cancer: Associations with chemotherapeutic agents and body-mass-index fluctuations
Belanger, Veronique, Warin, Alexandre, Tonova, Elitsa, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdiere, Caroline, Sinnett, Daniel, Marcil, Valerie
Published in Cancer research (Chicago, Ill.) (15.07.2020)
Published in Cancer research (Chicago, Ill.) (15.07.2020)
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Cardiometabolic Health After Pediatric Cancer Treatment: Adolescents Are More Affected than Children
Bélanger, Véronique, Napartuk, Mélanie, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Published in Nutrition and cancer (2022)
Published in Nutrition and cancer (2022)
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Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy
Lachance-Touchette, Pamela, Brown, Patricia, Meloche, Caroline, Kinirons, Peter, Lapointe, Line, Lacasse, Hélène, Lortie, Anne, Carmant, Lionel, Bedford, Fiona, Bowie, Derek, Cossette, Patrick
Published in The European journal of neuroscience (01.07.2011)
Published in The European journal of neuroscience (01.07.2011)
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Journal Article
Novel α1 and γ2 GABA A receptor subunit mutations in families with idiopathic generalized epilepsy
Lachance‐Touchette, Pamela, Brown, Patricia, Meloche, Caroline, Kinirons, Peter, Lapointe, Line, Lacasse, Hélène, Lortie, Anne, Carmant, Lionel, Bedford, Fiona, Bowie, Derek, Cossette, Patrick
Published in The European journal of neuroscience (01.07.2011)
Published in The European journal of neuroscience (01.07.2011)
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Abstract A57: Feasibility of physical activity in children with cancer: A multidisciplinary program in the context of the VIE study
Caru, Maxime, Duhamel, Gabrielle, Marcil, Valérie, Sultan, Serge, Meloche, Caroline, Bouchard, Isabelle, Drouin, Simon, Bertout, Laurence, Laverdière, Caroline, Sinnett, Daniel, Curnier, Daniel
Published in Cancer research (Chicago, Ill.) (15.07.2020)
Published in Cancer research (Chicago, Ill.) (15.07.2020)
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The VIE study: feasibility of a physical activity intervention in a multidisciplinary program in children with cancer
Caru, Maxime, Duhamel, Gabrielle, Marcil, Valérie, Sultan, Serge, Meloche, Caroline, Bouchard, Isabelle, Drouin, Simon, Bertout, Laurence, Laverdiere, Caroline, Sinnett, Daniel, Curnier, Daniel
Published in Supportive care in cancer (01.06.2020)
Published in Supportive care in cancer (01.06.2020)
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Novel alpha 1 and gamma 2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy
Lachance-Touchette, Pamela, Brown, Patricia, Meloche, Caroline, Kinirons, Peter, Lapointe, Line, Lacasse, Helene, Lortie, Anne, Carmant, Lionel, Bedford, Fiona, Bowie, Derek, Cossette, Patrick
Published in The European journal of neuroscience (01.07.2011)
Published in The European journal of neuroscience (01.07.2011)
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Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord: e1000296
Montpetit, Alexandre, Côté, Stéphanie, Brustein, Edna, Drouin, Christian A, Lapointe, Line, Boudreau, Michèle, Meloche, Caroline, Drouin, Régen, Hudson, Thomas J, Drapeau, Pierre, Cossette, Patrick
Published in PLoS genetics (01.12.2008)
Published in PLoS genetics (01.12.2008)
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