OR22-01 NF-κB Pathway Is Implicated in Thyroid Embryogenesis

por Vanier, Stéphanie Larrivée, Magne, Fabien, Jean-Louis, Martineau, Samuels, Mark E, Van Vliet, Guy, Deladoey, Johnny Yvan
Publicado 2020

The genetics-BIDS extension: Easing the search for genetic data associated with human brain imaging

por Moreau, Clara A, Jean-Louis, Martineau, Blair, Ross, Markiewicz, Christopher J, Turner, Jessica A, Calhoun, Vince D, Nichols, Thomas E, Pernet, Cyril R
Publicado 2020

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis

por Larrivée-Vanier, Stéphanie, Jean-Louis, Martineau, Magne, Fabien, Bui, Helen, Rouleau, Guy A., Spiegelman, Dan, Samuels, Mark E., Kibar, Zoha, Van Vliet, Guy, Deladoëy, Johnny
Publicado 2022

Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances

por Tesfaye, Rackeb, Huguet, Guillaume, Schmilovich, Zoe, Renne, Thomas, Loum, Mor Absa, Douard, Elise, Saci, Zohra, Jean-Louis, Martineau, Martineau, Jean Luc, Whelan, Rob, Desrivieres, Sylvane, Heinz, Andreas, Schumann, Gunter, Hayward, Caroline, Elsabbagh, Mayada, Jacquemont, Sebastien
Publicado 2022

Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

por Kopal, Jakub, Kumar, Kuldeep, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Tamer, Petra, Douard, Elise, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurélie, Richetin, Sonia, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Jacquemont, Sébastien, Bzdok, Danilo
Publicado 2023

Effects of eight neuropsychiatric copy number variants on human brain structure

por Modenato, Claudia, Kumar, Kuldeep, Moreau, Clara, Martin-Brevet, Sandra, Huguet, Guillaume, Schramm, Catherine, Jean-Louis, Martineau, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Douard, Elise, Thébault-Dagher, Fanny, Côté, Valérie, Charlebois, Audrey-Rose, Deguire, Florence, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, Melie-Garcia, Lester, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Chakravarty, Mallar, Bzdok, Danilo, Bearden, Carrie E., Draganski, Bogdan, Jacquemont, Sébastien
Publicado 2021

Subcortical brain alterations in carriers of genomic copy number variants

por Kumar, Kuldeep, Modenato, Claudia, Moreau, Clara, Ching, Christopher R. K., Harvey, Annabelle, Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Douard, Elise, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurélie, Richetin, Sonia, Kushan, Leila, Isaev, Dmitry, Alpert, Kathryn, Ragothaman, Anjani, Turner, Jessica A., Wang, Lei, Ho, Tiffany C., Schmaal, Lianne, Silva, Ana I., van den Bree, Marianne B.M., Linden, David E.J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Dumas, Guillaume, Draganski, Bogdan, Gutman, Boris A., Sønderby, Ida E., Andreassen, Ole A., Schultz, Laura, Almasy, Laura, Glahn, David C., Bearden, Carrie E., Thompson, Paul M., Jacquemont, Sébastien
Publicado 2023

Rare copy number variation in posttraumatic stress disorder

por Maihofer, Adam X., Engchuan, Worrawat, Huguet, Guillaume, Klein, Marieke, MacDonald, Jeffrey R., Shanta, Omar, Thiruvahindrapuram, Bhooma, Jean-louis, Martineau, Saci, Zohra, Jacquemont, Sebastien, Scherer, Stephen W., Ketema, Elizabeth, Aiello, Allison E., Amstadter, Ananda B., Avdibegović, Esmina, Babic, Dragan, Baker, Dewleen G., Bisson, Jonathan I., Boks, Marco P., Bolger, Elizabeth A., Bryant, Richard A., Bustamante, Angela C., Caldas-de-Almeida, Jose Miguel, Cardoso, Graça, Deckert, Jurgen, Delahanty, Douglas L., Domschke, Katharina, Dunlop, Boadie W., Dzubur-Kulenovic, Alma, Evans, Alexandra, Feeny, Norah C., Franz, Carol E., Gautam, Aarti, Geuze, Elbert, Goci, Aferdita, Hammamieh, Rasha, Jakovljevic, Miro, Jett, Marti, Jones, Ian, Kaufman, Milissa L., Kessler, Ronald C., King, Anthony P., Kremen, William S., Lawford, Bruce R., Lebois, Lauren A. M., Lewis, Catrin, Liberzon, Israel, Linnstaedt, Sarah D., Lugonja, Bozo, Luykx, Jurjen J., Lyons, Michael J., Mavissakalian, Matig R., McLaughlin, Katie A., McLean, Samuel A., Mehta, Divya, Mellor, Rebecca, Morris, Charles Phillip, Muhie, Seid, Orcutt, Holly K., Peverill, Matthew, Ratanatharathorn, Andrew, Risbrough, Victoria B., Rizzo, Albert, Roberts, Andrea L., Rothbaum, Alex O., Rothbaum, Barbara O., Roy-Byrne, Peter, Ruggiero, Kenneth J., Rutten, Bart P. F., Schijven, Dick, Seng, Julia S., Sheerin, Christina M., Sorenson, Michael A., Teicher, Martin H., Uddin, Monica, Ursano, Robert J., Vinkers, Christiaan H., Voisey, Joanne, Weber, Heike, Winternitz, Sherry, Xavier, Miguel, Yang, Ruoting, McD Young, Ross, Zoellner, Lori A., Salem, Rany M., Shaffer, Richard A., Wu, Tianying, Ressler, Kerry J., Stein, Murray B., Koenen, Karestan C., Sebat, Jonathan, Nievergelt, Caroline M.
Publicado 2022