Autism risk factors: genes, environment, and gene-environment interactions

Por Chaste, Pauline, Leboyer, Marion
Publicado em 2012

Memory for Self-Performed Actions in Individuals with Asperger Syndrome

Por Zalla, Tiziana, Daprati, Elena, Sav, Anca-Maria, Chaste, Pauline, Nico, Daniele, Leboyer, Marion
Publicado em 2010

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

Por Zalla, Tiziana, Amsellem, Frederique, Chaste, Pauline, Ervas, Francesca, Leboyer, Marion, Champagne-Lavau, Maud
Publicado em 2014

Mutation screening of the ARX gene in patients with autism

Por Chaste, Pauline, Nygren, Gudrun, Anckarsäter, Henrik, Råstam, Maria, Coleman, Mary, Leboyer, Marion, Gillberg, Christopher, Betancur, Catalina
Publicado no Am J Med Genet B Neuropsychiatr Genet (2007)

High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters

Por Chaste, Pauline, Betancur, Catalina, Gérard-Blanluet, Marion, Bargiacchi, Anne, Kuzbari, Suzanne, Drunat, Séverine, Leboyer, Marion, Bourgeron, Thomas, Delorme, Richard
Publicado em 2012

Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele

Por Delorme, Richard, Betancur, Catalina, Chaste, Pauline, Kernéis, Solen, Stopin, Astrid, Mouren, Marie-Christine, Collet, Corinne, Bourgeron, Thomas, Leboyer, Marion, Launay, Jean-Marie
Publicado no Am J Med Genet B Neuropsychiatr Genet (2010)

Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders

Por Hofvander, Björn, Delorme, Richard, Chaste, Pauline, Nydén, Agneta, Wentz, Elisabet, Ståhlberg, Ola, Herbrecht, Evelyn, Stopin, Astrid, Anckarsäter, Henrik, Gillberg, Christopher, Råstam, Maria, Leboyer, Marion
Publicado em 2009

Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly

Por Buxbaum, Joseph D, Cai, Guiqing, Nygren, Gudrun, Chaste, Pauline, Delorme, Richard, Goldsmith, Juliet, Råstam, Maria, Silverman, Jeremy M, Hollander, Eric, Gillberg, Christopher, Leboyer, Marion, Betancur, Catalina
Publicado em 2007

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder

Por Delorme, Richard, Moreno-De-Luca, Daniel, Gennetier, Aurélie, Maier, Wolfgang, Chaste, Pauline, Mössner, Rainald, Grabe, Hans Jörgen, Ruhrmann, Stephan, Falkai, Peter, Mouren, Marie-Christine, Leboyer, Marion, Wagner, Michael, Betancur, Catalina
Publicado em 2010

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls

Por Delorme, Richard, Betancur, Catalina, Scheid, Isabelle, Anckarsäter, Henrik, Chaste, Pauline, Jamain, Stéphane, Schuroff, Franck, Nygren, Gudrun, Herbrecht, Evelyn, Dumaine, Anne, Mouren, Marie Christine, Råstam, Maria, Leboyer, Marion, Gillberg, Christopher, Bourgeron, Thomas
Publicado em 2010

Mutation Screening of the PTEN Gene in Patients With Autism Spectrum Disorders and Macrocephaly

Por Buxbaum, Joseph D., Cai, Guiqing, Chaste, Pauline, Nygren, Gudrun, Goldsmith, Juliet, Reichert, Jennifer, Anckarsäter, Henrik, Rastam, Maria, Smith, Christopher J., Silverman, Jeremy M., Hollander, Eric, Leboyer, Marion, Gillberg, Christopher, Verloes, Alain, Betancur, Catalina
Publicado em 2007

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

Por 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
Publicado no Sci Rep (2017)

An investigation of ribosomal protein L10 gene in autism spectrum disorders

Por 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
Publicado em 2009

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

Por 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
Publicado em 2011

Abnormal melatonin synthesis in autism spectrum disorders

Por 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
Publicado em 2008

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

Por 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
Publicado em 2010

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

Por 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
Publicado em 2007

Analysis of X chromosome inactivation in autism spectrum disorders

Por 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
Publicado no Am J Med Genet B Neuropsychiatr Genet (2008)

Common genetic variants, acting additively, are a major source of risk for autism

Por Klei Lambertus, Sanders Stephan J, Murtha Michael T, Hus Vanessa, Lowe Jennifer K, Willsey A, Moreno-De-Luca Daniel, Yu Timothy W, Fombonne Eric, Geschwind Daniel, Grice Dorothy E, Ledbetter David H, Lord Catherine, Mane Shrikant M, Martin Christa, Martin Donna M, Morrow Eric M, Walsh Christopher A, Melhem Nadine M, Chaste Pauline, Sutcliffe James S, State Matthew W, Cook Edwin H, Roeder Kathryn, Devlin Bernie
Publicado em 2012-10-01

Common genetic variants, acting additively, are a major source of risk for autism

Por Klei, Lambertus, Sanders, Stephan J, Murtha, Michael T, Hus, Vanessa, Lowe, Jennifer K, Willsey, A Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Lord, Catherine, Mane, Shrikant M, Martin, Christa Lese, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Melhem, Nadine M, Chaste, Pauline, Sutcliffe, James S, State, Matthew W, Cook, Edwin H, Roeder, Kathryn, Devlin, Bernie
Publicado em 2012