Characterization of the replication timing program of 6 human model cell lines

door Hadjadj, Djihad, Denecker, Thomas, Maric, Chrystelle, Fauchereau, Fabien, Baldacci, Giuseppe, Cadoret, Jean-Charles
Gepubliceerd in Genom Data (2016)

Efficient, quick and easy-to-use DNA replication timing analysis with START-R suite

door Hadjadj, Djihad, Denecker, Thomas, Guérin, Eva, Kim, Su-Jung, Fauchereau, Fabien, Baldacci, Giuseppe, Maric, Chrystelle, Cadoret, Jean-Charles
Gepubliceerd in NAR Genom Bioinform (2020)

A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomas

door Hadjadj, Djihad, Kim, Su-Jung, Denecker, Thomas, Driss, Laura Ben, Cadoret, Jean-Charles, Maric, Chrystelle, Baldacci, Giuseppe, Fauchereau, Fabien
Gepubliceerd in Aging (Albany NY) (2017)

Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions

door Pinel, Philippe, Fauchereau, Fabien, Moreno, Antonio, Barbot, Alexis, Lathrop, Mark, Zelenika, Diana, Le Bihan, Denis, Poline, Jean-Baptiste, Bourgeron, Thomas, Dehaene, Stanislas
Gepubliceerd in J Neurosci (2012)

Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

door Pagan, Cécile, Goubran-Botros, Hany, Delorme, Richard, Benabou, Marion, Lemière, Nathalie, Murray, Kerren, Amsellem, Frédérique, Callebert, Jacques, Chaste, Pauline, Jamain, Stéphane, Fauchereau, Fabien, Huguet, Guillaume, Maronde, Erik, Leboyer, Marion, Launay, Jean-Marie, Bourgeron, Thomas
Gepubliceerd in Sci Rep (2017)

An investigation of ribosomal protein L10 gene in autism spectrum disorders

door Gong, Xiaohong, Delorme, Richard, Fauchereau, Fabien, Durand, Christelle M, Chaste, Pauline, Betancur, Catalina, Goubran-Botros, Hany, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Gillberg, I Carina, Kopp, Svenny, Mouren-Simeoni, Marie-Christine, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas
Gepubliceerd in 2009

Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations

door Konyukh, Marina, Delorme, Richard, Chaste, Pauline, Leblond, Claire, Lemière, Nathalie, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Ståhlberg, Ola, Amsellem, Frederique, Gillberg, I. Carina, Mouren-Simeoni, Marie Christine, Herbrecht, Evelyn, Fauchereau, Fabien, Toro, Roberto, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas
Gepubliceerd in 2011

Abnormal melatonin synthesis in autism spectrum disorders

door Melke, Jonas, Goubran-Botros, Hany, Chaste, Pauline, Betancur, Catalina, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Ståhlberg, Ola, Gillberg, I. Carina, Delorme, Richard, Chabane, Nadia, Mouren-Simeoni, Marie-Christine, Fauchereau, Fabien, Durand, Christelle M., Chevalier, Fabien, Drouot, Xavier, Collet, Corinne, Launay, Jean-Marie, Leboyer, Marion, Gillberg, Christopher, Bourgeron, Thomas
Gepubliceerd in 2008

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

door Durand, Christelle M., Betancur, Catalina, Boeckers, Tobias M., Bockmann, Juergen, Chaste, Pauline, Fauchereau, Fabien, Nygren, Gudrun, Rastam, Maria, Gillberg, I Carina, Anckarsäter, Henrik, Sponheim, Eili, Goubran-Botros, Hany, Delorme, Richard, Chabane, Nadia, Mouren-Simeoni, Marie-Christine, de Mas, Philippe, Bieth, Eric, Rogé, Bernadette, Héron, Delphine, Burglen, Lydie, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas
Gepubliceerd in 2007

Analysis of X chromosome inactivation in autism spectrum disorders

door Gong, Xiaohong, Bacchelli, Elena, Blasi, Francesca, Toma, Claudio, Betancur, Catalina, Chaste, Pauline, Delorme, Richard, Durand, Christelle, Fauchereau, Fabien, Botros, Hany Goubran, Leboyer, Marion, Mouren-Simeoni, Marie-Christine, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Gillberg, I Carina, Gillberg, Christopher, Moreno-De-Luca, Daniel, Carone, Simona, Nummela, Ilona, Rossi, Mari, Battaglia, Agatino, Jarvela, Irma, Maestrini, Elena, Bourgeron, Thomas
Gepubliceerd in Am J Med Genet B Neuropsychiatr Genet (2008)

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

door Becker, Jessica, Czamara, Darina, Scerri, Tom S, Ramus, Franck, Csépe, Valéria, Talcott, Joel B, Stein, John, Morris, Andrew, Ludwig, Kerstin U, Hoffmann, Per, Honbolygó, Ferenc, Tóth, Dénes, Fauchereau, Fabien, Bogliotti, Caroline, Iannuzzi, Stéphanie, Chaix, Yves, Valdois, Sylviane, Billard, Catherine, George, Florence, Soares-Boucaud, Isabelle, Gérard, Christophe-Loïc, van der Mark, Sanne, Schulz, Enrico, Vaessen, Anniek, Maurer, Urs, Lohvansuu, Kaisa, Lyytinen, Heikki, Zucchelli, Marco, Brandeis, Daniel, Blomert, Leo, Leppänen, Paavo HT, Bruder, Jennifer, Monaco, Anthony P, Müller-Myhsok, Bertram, Kere, Juha, Landerl, Karin, Nöthen, Markus M, Schulte-Körne, Gerd, Paracchini, Silvia, Peyrard-Janvid, Myriam, Schumacher, Johannes
Gepubliceerd in 2014

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

door Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Gepubliceerd in Transl Psychiatry (2019)

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

door Leblond, Claire S., Heinrich, Jutta, Delorme, Richard, Proepper, Christian, Betancur, Catalina, Huguet, Guillaume, Konyukh, Marina, Chaste, Pauline, Ey, Elodie, Rastam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Gillberg, I. Carina, Melke, Jonas, Toro, Roberto, Regnault, Beatrice, Fauchereau, Fabien, Mercati, Oriane, Lemière, Nathalie, Skuse, David, Poot, Martin, Holt, Richard, Monaco, Anthony P., Järvelä, Irma, Kantojärvi, Katri, Vanhala, Raija, Curran, Sarah, Collier, David A., Bolton, Patrick, Chiocchetti, Andreas, Klauck, Sabine M., Poustka, Fritz, Freitag, Christine M., Waltes, Regina, Kopp, Marnie, Duketis, Eftichia, Bacchelli, Elena, Minopoli, Fiorella, Ruta, Liliana, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Sequeira, Ana F., Oliveira, Barbara, Vicente, Astrid, Oliveira, Guiomar, Pinto, Dalila, Scherer, Stephen W., Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Bonneau, Dominique, Guinchat, Vincent, Devillard, Françoise, Assouline, Brigitte, Mouren, Marie-Christine, Leboyer, Marion, Gillberg, Christopher, Boeckers, Tobias M., Bourgeron, Thomas
Gepubliceerd in 2012