Distinct effects of social motivation on face evaluations in adolescents with and without autism

od Safra, Lou, Ioannou, Christina, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie
Izdano u Sci Rep (2018)

Author Correction: Distinct effects of social motivation on face evaluations in adolescents with and without autism

od Safra, Lou, Ioannou, Christina, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie
Izdano u Sci Rep (2018)

Individuals with Autism Spectrum Disorders Do Not Use Social Stereotypes in Irony Comprehension

od Zalla, Tiziana, Amsellem, Frederique, Chaste, Pauline, Ervas, Francesca, Leboyer, Marion, Champagne-Lavau, Maud
Izdano 2014

Shared mechanism for emotion processing in adolescents with and without autism

od Ioannou, Christina, Zein, Marwa El, Wyart, Valentin, Scheid, Isabelle, Amsellem, Frédérique, Delorme, Richard, Chevallier, Coralie, Grèzes, Julie
Izdano u Sci Rep (2017)

Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity

od Lefebvre, Aline, Delorme, Richard, Delanoë, Catherine, Amsellem, Frederique, Beggiato, Anita, Germanaud, David, Bourgeron, Thomas, Toro, Roberto, Dumas, Guillaume
Izdano u Front Neurosci (2018)

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother

od Tabet, Anne-Claude, Pilorge, Marion, Delorme, Richard, Amsellem, Frédérique, Pinard, Jean-Marc, Leboyer, Marion, Verloes, Alain, Benzacken, Brigitte, Betancur, Catalina
Izdano 2012

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother

od Tabet, Anne-Claude, Pilorge, Marion, Delorme, Richard, Amsellem, Frédérique, Pinard, Jean-Marc, Leboyer, Marion, Verloes, Alain, Benzacken, Brigitte, Betancur, Catalina
Izdano 2012

Interactive Psychometrics for Autism With the Human Dynamic Clamp: Interpersonal Synchrony From Sensorimotor to Sociocognitive Domains

od 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
Izdano u Front Psychiatry (2020)

Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume

od 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
Izdano u Front Psychiatry (2019)

Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome

od 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
Izdano u EBioMedicine (2016)

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

od 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
Izdano u Sci Rep (2017)

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

od 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
Izdano 2011

Heterozygous FA2H mutations in autism spectrum disorders

od 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
Izdano u BMC Med Genet (2013)

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

od 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
Izdano 2014

A framework to identify contributing genes in patients with Phelan-McDermid syndrome

od 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
Izdano u NPJ Genom Med (2017)

Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome

od 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
Izdano u NPJ Genom Med (2019)