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Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons
Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Leonard Herault, Stéphane Gaillard, Mélanie Cahuc, Emilie Pallesi-Pocachard, Aurélie Montheil, Andreas Bosio, Jill A Rosenfeld, Eva Hudson, Kristin Lindstrom, Saadet Mercimek-Andrews, Lauren Jeffries, Arie van Haeringen, Olivier Vanakker, Bruno Pichon, Audrey Van Hecke, Dina Amrom, Sebastien Küry, Candace Gamble, Bernard Jacq, Laurent Fasano, Gabriel Santpere, Belen Lorente-Galdos, Nenad Sestan, Antoinette Gelot, Sylvie Giacuzzo, Alfonso Represa, Carlos Cardoso, Harold Cremer, View ORCID ProfileAntoine de Chevigny
doi: https://doi.org/10.1101/296889
Karen Runge
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Rémi Mathieu
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Stéphane Bugeon
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Sahra Lafi
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Corinne Beurrier
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Surajit Sahu
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Fabienne Schaller
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Arthur Loubat
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Leonard Herault
3TAGC INSERM U1090, Aix-Marseille University, Marseille, France
Stéphane Gaillard
4Phenotype Expertise, 5 Boulevard du Maréchal Koenig, 13009 Marseille, France
Mélanie Cahuc
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Emilie Pallesi-Pocachard
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Aurélie Montheil
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Andreas Bosio
5Miltenyi Biotec, Bergisch-Gladbach 51429, Germany
Jill A Rosenfeld
6Baylor College of Medicine, Houston, Texas, USA
Eva Hudson
7Cook Children’s Clinical Genetics, Fort Worth, Texas, USA
Kristin Lindstrom
8Division of genetics and Metabolism, Phoenix Children’s Hospital, Phoenix, Arizona, USA
Saadet Mercimek-Andrews
9Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, Ontario, Canada, Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada, Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada
Lauren Jeffries
10Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA
Arie van Haeringen
11Department of Clinical Genetics, Leiden University Medical Center, 2300 RC, Leiden, Netherlands
Olivier Vanakker
12Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium
Bruno Pichon
13Erasme Hospital, Route de Lennik 808, 1070 Brussels, Belgium
Audrey Van Hecke
14Department of Neurology, Queen Fabiola Children’s University Hospital, 15 JJ Crocq Avenue, 1200 Brussels, Belgium, Université Libre de Bruxelles (ULB), Brussels, Belgium, Neuropediatric Unit, Kannerklinik, Centre Hospitalier de Luxembourg, Luxembourg, Grand-Duchy of Luxembourg
Dina Amrom
14Department of Neurology, Queen Fabiola Children’s University Hospital, 15 JJ Crocq Avenue, 1200 Brussels, Belgium, Université Libre de Bruxelles (ULB), Brussels, Belgium, Neuropediatric Unit, Kannerklinik, Centre Hospitalier de Luxembourg, Luxembourg, Grand-Duchy of Luxembourg
Sebastien Küry
15Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093 Nantes, France, INSERM, CNRS, UNIV Nantes, l’institut du thorax, 44007 Nantes, France
Candace Gamble
7Cook Children’s Clinical Genetics, Fort Worth, Texas, USA
Bernard Jacq
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Laurent Fasano
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Gabriel Santpere
16Department of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA
Belen Lorente-Galdos
16Department of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA
Nenad Sestan
16Department of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA
Antoinette Gelot
17Trousseau Hospital, Paris, France
Sylvie Giacuzzo
16Department of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA
Alfonso Represa
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Carlos Cardoso
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Harold Cremer
2IBDM, Aix-Marseille University, CNRS, UMR 7288, Marseille, France
Antoine de Chevigny
1INMED INSERM U1249, Aix-Marseille University, Marseille, France
Posted February 14, 2020.
Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons
Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Leonard Herault, Stéphane Gaillard, Mélanie Cahuc, Emilie Pallesi-Pocachard, Aurélie Montheil, Andreas Bosio, Jill A Rosenfeld, Eva Hudson, Kristin Lindstrom, Saadet Mercimek-Andrews, Lauren Jeffries, Arie van Haeringen, Olivier Vanakker, Bruno Pichon, Audrey Van Hecke, Dina Amrom, Sebastien Küry, Candace Gamble, Bernard Jacq, Laurent Fasano, Gabriel Santpere, Belen Lorente-Galdos, Nenad Sestan, Antoinette Gelot, Sylvie Giacuzzo, Alfonso Represa, Carlos Cardoso, Harold Cremer, Antoine de Chevigny
bioRxiv 296889; doi: https://doi.org/10.1101/296889
Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons
Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Leonard Herault, Stéphane Gaillard, Mélanie Cahuc, Emilie Pallesi-Pocachard, Aurélie Montheil, Andreas Bosio, Jill A Rosenfeld, Eva Hudson, Kristin Lindstrom, Saadet Mercimek-Andrews, Lauren Jeffries, Arie van Haeringen, Olivier Vanakker, Bruno Pichon, Audrey Van Hecke, Dina Amrom, Sebastien Küry, Candace Gamble, Bernard Jacq, Laurent Fasano, Gabriel Santpere, Belen Lorente-Galdos, Nenad Sestan, Antoinette Gelot, Sylvie Giacuzzo, Alfonso Represa, Carlos Cardoso, Harold Cremer, Antoine de Chevigny
bioRxiv 296889; doi: https://doi.org/10.1101/296889
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