Hakutulokset - Amsellem, Frédérique

Distinct effects of social motivation on face evaluations in adolescents with and without autism Tekijä Safra, Lou, Ioannou, Christina, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Author Correction: Distinct effects of social motivation on face evaluations in adolescents with and without autism Tekijä Safra, Lou, Ioannou, Christina, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Individuals with Autism Spectrum Disorders Do Not Use Social Stereotypes in Irony Comprehension Tekijä Zalla, Tiziana, Amsellem, Frederique, Chaste, Pauline, Ervas, Francesca, Leboyer, Marion, Champagne-Lavau, Maud

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Shared mechanism for emotion processing in adolescents with and without autism Tekijä Ioannou, Christina, Zein, Marwa El, Wyart, Valentin, Scheid, Isabelle, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie, Grèzes, Julie

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity Tekijä Lefebvre, Aline, Delorme, Richard, Delanoë, Catherine, Amsellem, Frederique, Beggiato, Anita, Germanaud, David, Bourgeron, Thomas, Toro, Roberto, Dumas, Guillaume

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother Tekijä Tabet, Anne-Claude, Pilorge, Marion, Delorme, Richard, Amsellem, Frédérique, Pinard, Jean-Marc, Leboyer, Marion, Verloes, Alain, Benzacken, Brigitte, Betancur, Catalina

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother Tekijä Tabet, Anne-Claude, Pilorge, Marion, Delorme, Richard, Amsellem, Frédérique, Pinard, Jean-Marc, Leboyer, Marion, Verloes, Alain, Benzacken, Brigitte, Betancur, Catalina

Hae kokoteksti Hae kokoteksti

Interactive Psychometrics for Autism With the Human Dynamic Clamp: Interpersonal Synchrony From Sensorimotor to Sociocognitive Domains Tekijä Baillin, Florence, Lefebvre, Aline, Pedoux, Amandine, Beauxis, Yann, Engemann, Denis A., Maruani, Anna, Amsellem, Frédérique, Kelso, J. A. Scott, Bourgeron, Thomas, Delorme, Richard, Dumas, Guillaume

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume Tekijä Maruani, Anna, Dumas, Guillaume, Beggiato, Anita, Traut, Nicolas, Peyre, Hugo, Cohen-Freoua, Alicia, Amsellem, Frédérique, Elmaleh, Monique, Germanaud, David, Launay, Jean-Marie, Bourgeron, Thomas, Toro, Roberto, Delorme, Richard

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome Tekijä Darville, Hélène, Poulet, Aurélie, Rodet-Amsellem, Frédérique, Chatrousse, Laure, Pernelle, Julie, Boissart, Claire, Héron, Delphine, Nava, Caroline, Perrier, Anselme, Jarrige, Margot, Cogé, Francis, Millan, Mark J., Bourgeron, Thomas, Peschanski, Marc, Delorme, Richard, Benchoua, Alexandra

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Heterozygous FA2H mutations in autism spectrum disorders Tekijä Scheid, Isabelle, Maruani, Anna, Huguet, Guillaume, Leblond, Claire S, Nygren, Gudrun, Anckarsäter, Henrik, Beggiato, Anita, Rastam, Maria, Amsellem, Fréderique, Gillberg, I Carina, Elmaleh, Monique, Leboyer, Marion, Gillberg, Christopher, Betancur, Catalina, Coleman, Mary, Hama, Hiroko, Cook, Edwin H, Bourgeron, Thomas, Delorme, Richard

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments Tekijä Leblond, Claire S., Nava, Caroline, Polge, Anne, Gauthier, Julie, Huguet, Guillaume, Lumbroso, Serge, Giuliano, Fabienne, Stordeur, Coline, Depienne, Christel, Mouzat, Kevin, Pinto, Dalila, Howe, Jennifer, Lemière, Nathalie, Durand, Christelle M., Guibert, Jessica, Ey, Elodie, Toro, Roberto, Peyre, Hugo, Mathieu, Alexandre, Amsellem, Frédérique, Rastam, Maria, Gillberg, I. Carina, Rappold, Gudrun A., Holt, Richard, Monaco, Anthony P., Maestrini, Elena, Galan, Pilar, Heron, Delphine, Jacquette, Aurélia, Afenjar, Alexandra, Rastetter, Agnès, Brice, Alexis, Devillard, Françoise, Assouline, Brigitte, Laffargue, Fanny, Lespinasse, James, Chiesa, Jean, Rivier, François, Bonneau, Dominique, Regnault, Beatrice, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Sanlaville, Damien, Schluth-Bolard, Caroline, Edery, Patrick, Perrin, Laurence, Tabet, Anne Claude, Schmeisser, Michael J., Boeckers, Tobias M., Coleman, Mary, Sato, Daisuke, Szatmari, Peter, Scherer, Stephen W., Rouleau, Guy A., Betancur, Catalina, Leboyer, Marion, Gillberg, Christopher, Delorme, Richard, Bourgeron, Thomas

Hae kokoteksti Hae kokoteksti Hae kokoteksti

A framework to identify contributing genes in patients with Phelan-McDermid syndrome Tekijä Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S., Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome Tekijä Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S., Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas

Hae kokoteksti Hae kokoteksti Hae kokoteksti