Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a Prospective follow-up study

by Delorme, Richard, Bille, Arnaud, Betancur, Catalina, Mathieu, Flavie, Chabane, Nadia, Mouren-Simeoni, Marie Christine, Leboyer, Marion
Published 2006

Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder

by Delorme, Richard, Goussé, Véronique, Roy, Isabelle, Trandafir, Anca, Mathieu, Flavie, Mouren-Siméoni, Marie-Christine, Betancur, Catalina, Leboyer, Marion
Published 2007

Platelet serotonergic markers as endophenotypes for obsessive-compulsive disorder

by Delorme, Richard, Betancur, Catalina, Callebert, Jacques, Chabane, Nadia, Laplanche, Jean-Louis, Mouren-Simeoni, Marie-Christine, Launay, Jean-Marie, Leboyer, Marion
Published 2005

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

by Betancur, Catalina, Corbex, Marylis, Spielewoy, Cécile, Philippe, Anne, Laplanche, Jean-Louis, Launay, Jean-Marie, Gillberg, Christopher, Mouren-Simeoni, Marie-Christine, Hamon, Michel, Giros, Bruno, Nosten-Bertrand, Marika, Leboyer, Marion
Published 2002

An investigation of ribosomal protein L10 gene in autism spectrum disorders

by 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
Published 2009

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

by 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
Published 2011

Abnormal melatonin synthesis in autism spectrum disorders

by 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
Published 2008

Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population

by Chaste, Pauline, Clement, Nathalie, Mercati, Oriane, Guillaume, Jean-Luc, Delorme, Richard, Botros, Hany Goubran, Pagan, Cécile, Périvier, Samuel, Scheid, Isabelle, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Ståhlberg, Ola, Gillberg, Carina, Serrano, Emilie, Lemière, Nathalie, Launay, Jean Marie, Mouren-Simeoni, Marie Christine, Leboyer, Marion, Gillberg, Christopher, Jockers, Ralf, Bourgeron, Thomas
Published 2010

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

by 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
Published 2007

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

by Delorme, Richard, Betancur, Catalina, Wagner, Michael, Krebs, Marie-Odile, Gorwood, Philip, Pearl, Phillip, Nygren, Gudrun, Durand, Christelle M., Buhtz, Friederike, Pickering, P., Melke, Jonas, Ruhrmann, Stephan, Anckarsäter, Henrik, Chabane, Nadia, Kipman, Amélie, Reck, Claudia, Millet, Bruno, Roy, Isabelle, Mouren-Simeoni, Marie-Christine, Maier, Wolfgang, Råstam, Maria, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas
Published 2005

Analysis of X chromosome inactivation in autism spectrum disorders

by 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
Published in Am J Med Genet B Neuropsychiatr Genet (2008)