Rezultati pretrage - Frédérique Amsellem

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Detaljiziraj rezultate
  1. 1
    Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity

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

    Izdano 2018
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  2. 2
    Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother

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

    Izdano 2012
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  3. 3
    The serotonin-N-acetylserotonin–melatonin pathway as a biomarker for autism spectrum disorders

    The serotonin-N-acetylserotonin–melatonin pathway as a biomarker for autism spectrum disorders od C. Pagan, Richard Delorme, Jacques Callebert, Hany Goubran‐Botros, Frédérique Amsellem, Xavier Drouot, Carole Boudebesse, Katia Le Dudal, N Ngo-Nguyen, H. Laouamri, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron, J.M. Launay

    Izdano 2014
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  4. 4
    Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

    Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders od Cécile Pagan, Hany Goubran‐Botros, Richard Delorme, Marion Benabou, Nathalie Lemière, Kerren Murray, Frédérique Amsellem, Jacques Callebert, Pauline Chaste, Stéphane Jamain, Fabien Fauchereau, Guillaume Huguet, Erik Maronde, Marion Leboyer, Jean‐Marie Launay, Thomas Bourgeron

    Izdano 2017
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  5. 5
    Phenotypic effects of genetic variants associated with autism

    Phenotypic effects of genetic variants associated with autism od Thomas Rolland, Freddy Cliquet, Richard Anney, Clara Moreau, Nicolas Traut, Alexandre Mathieu, Guillaume Huguet, Jinjie Duan, Varun Warrier, Swan Portalier, Louise Dry, Claire S. Leblond, Élise Douard, Frédérique Amsellem, Simon Malesys, Anna Maruani, Roberto Toro, Anders D. Børglum, Jakob Grove, Simon Baron‐Cohen, Alan Packer, Wendy K. Chung, Sébastien Jacquemont, Richard Delorme, Thomas Bourgeron

    Izdano 2023
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  6. 6
    CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

    CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders od Oriane Mercati, Guillaume Huguet, Anne Danckaert, Gwenaëlle André-Leroux, A. Maruani, Marco Bellinzoni, Thomas Rolland, Laura Gouder, Alexandre Mathieu, Julien Buratti, Frédérique Amsellem, Max E. Benabou, Julien Van‐Gils, Anita Beggiato, Marina Konyukh, JP Bourgeois, Matthew J. Gazzellone, Ryan K. C. Yuen, Susan Walker, Marc Delépine, Anne Boland, Béatrice Regnault, M. François, T. Van Den Abbeele, Anne-Laure Mosca-Boidron, Laurence Faivre, Yasushi Shimoda, Kazutada Watanabe, Dominique Bonneau, Maria Råstam, Marion Leboyer, Stephen W. Scherer, Christopher Gillberg, Richard Delorme, Isabelle Cloëz-Tayarani, Thomas Bourgeron

    Izdano 2016
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  7. 7
    Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

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

    Izdano 2014
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  8. 8
    A framework to identify contributing genes in patients with Phelan-McDermid syndrome

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

    Izdano 2017
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