Three-dimensional Quantification of Dendritic Spines from Pyramidal Neurons Derived from Human Induced Pluripotent Stem Cells

Por Gouder, Laura, Tinevez, Jean-Yves, Goubran-Botros, Hany, Benchoua, Alexandra, Bourgeron, Thomas, Cloëz-Tayarani, Isabelle
Publicado no J Vis Exp (2015)

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)

Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders

Por Durand, Christelle, Kappeler, Caroline, Betancur, Catalina, Delorme, Richard, Quach, Hélène, Goubran-Botros, Hany, Melke, Jonas, Nygren, Gudrun, Chabane, Nadia, Bellivier, Franck, Szoke, Andrei, Schurhoff, Franck, Rastam, Maria, Anckarsäter, Henrik, Gillberg, Christopher, Leboyer, Marion, Bourgeron, Thomas
Publicado no Am J Med Genet B Neuropsychiatr Genet (2006)

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

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

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

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

Por Mosca-Boidron, Anne-Laure, Gueneau, Lucie, Huguet, Guillaume, Goldenberg, Alice, Henry, Céline, Gigot, Nadège, Pallesi-Pocachard, Emilie, Falace, Antonio, Duplomb, Laurence, Thevenon, Julien, Duffourd, Yannis, ST-Onge, Judith, Chambon, Pascal, Rivière, Jean-Baptiste, Thauvin-Robinet, Christel, Callier, Patrick, Marle, Nathalie, Payet, Muriel, Ragon, Clemence, Goubran Botros, Hany, Buratti, Julien, Calderari, Sophie, Dumas, Guillaume, Delorme, Richard, Lagarde, Nathalie, Pinoit, Jean-Michel, Rosier, Antoine, Masurel-Paulet, Alice, Cardoso, Carlos, Mugneret, Francine, Saugier-Veber, Pascale, Campion, Dominique, Faivre, Laurence, Bourgeron, Thomas
Publicado no Eur J Hum Genet (2016)