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Open Access
Peer-reviewed
Research Article
Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
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Marina Konyukh,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France
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Richard Delorme,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France, Service de Psychopathologie de l'Enfant et de l'Adolescent, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France, INSERM, U 995, IMRB, Department of Medical Genomic, Psychiatry Genetic team, Creteil, France
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Pauline Chaste,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France, Service de Psychopathologie de l'Enfant et de l'Adolescent, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France, INSERM, U 995, IMRB, Department of Medical Genomic, Psychiatry Genetic team, Creteil, France
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Claire Leblond,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France
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Nathalie Lemière,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France
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Gudrun Nygren,
Affiliation Department of Child and Adolescent Psychiatry, Göteborg University, Göteborg, Sweden
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Henrik Anckarsäter,
Affiliations Department of Child and Adolescent Psychiatry, Göteborg University, Göteborg, Sweden, Institute of Clinical Sciences, Lund University, Malmö, Sweden
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Maria Rastam,
Affiliation Department of Clinical Sciences in Lund, Lund University, Lund, Sweden
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Ola Ståhlberg,
Affiliation Department of Child and Adolescent Psychiatry, Göteborg University, Göteborg, Sweden
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Frederique Amsellem,
Affiliations Service de Psychopathologie de l'Enfant et de l'Adolescent, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France, INSERM, U 995, IMRB, Department of Medical Genomic, Psychiatry Genetic team, Creteil, France
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I. Carina Gillberg,
Affiliation Department of Child and Adolescent Psychiatry, Göteborg University, Göteborg, Sweden
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Marie Christine Mouren-Simeoni,
Affiliation Service de Psychopathologie de l'Enfant et de l'Adolescent, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France
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Evelyn Herbrecht,
Affiliations University Paris Est-Créteil, Faculty of Medicine, IFR10, Creteil, France, AP-HP, Henri Mondor-Albert Chenevier Hospitals, Department of Psychiatry, Creteil, France, Fondation FondaMental, French National Science Foundation, Créteil, France
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Fabien Fauchereau,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France, University Denis Diderot Paris 7, Paris, France
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Roberto Toro,
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France
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Christopher Gillberg,
Affiliations INSERM, U 995, IMRB, Department of Medical Genomic, Psychiatry Genetic team, Creteil, France, Saint George's Hospital Medical School, London, United Kingdom
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Marion Leboyer,
Affiliations University Paris Est-Créteil, Faculty of Medicine, IFR10, Creteil, France, AP-HP, Henri Mondor-Albert Chenevier Hospitals, Department of Psychiatry, Creteil, France, Fondation FondaMental, French National Science Foundation, Créteil, France
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Thomas Bourgeron
* E-mail: thomasb@pasteur.fr
Affiliations Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France, CNRS URA 2182 “Genes, synapses and cognition”, Institut Pasteur, Paris, France, Fondation FondaMental, French National Science Foundation, Créteil, France, University Denis Diderot Paris 7, Paris, France
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Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
- Marina Konyukh,
- Richard Delorme,
- Pauline Chaste,
- Claire Leblond,
- Nathalie Lemière,
- Gudrun Nygren,
- Henrik Anckarsäter,
- Maria Rastam,
- Ola Ståhlberg,
- Frederique Amsellem
- Published: March 4, 2011
- https://doi.org/10.1371/journal.pone.0017289