New Results
A framework to identify modifier genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard, Yline Capri, Alain Verloes, 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 Beneteau, Olivier Pichon, Bertrand Isidor, Albert David, Jean-Michel Dupont, Stephan Kemeny, Laetitia 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 Gatinois, Jacques Puechberty, Jean Chiesa, James Lespinasse, Christèle Dubourg, Chloé Quelin, Mélanie Fradin, Hubert Journel, Annick Toutain, Dominique Martin, Abdelamdjid Benmansour, Roberto Toro, Frédérique Amsellem, Richard Delorme, Thomas Bourgeron
doi: https://doi.org/10.1101/117978
Anne-Claude Tabet
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Thomas Rolland
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Marie Ducloy
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Jonathan Lévy
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Julien Buratti
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Alexandre Mathieu
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Damien Haye
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Laurence Perrin
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Céline Dupont
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Sandrine Passemard
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Yline Capri
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Alain Verloes
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Séverine Drunat
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Boris Keren
5Cytogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France
Cyril Mignot
6Neurogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France
Isabelle Marey
7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France
Aurélia Jacquette
7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France
Sandra Whalen
7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France
Eva Pipiras
8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France
Brigitte Benzacken
8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France
Sandra Chantot-Bastaraud
9Cytogenetics Unit, Trousseau Hospital, APHP, Paris, France
Alexandra Afenjar
10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France
Delphine Héron
10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France
Cédric Le Caignec
11Clinical Genetics Unit, Nantes Hospital, Nantes, France
Claire Beneteau
11Clinical Genetics Unit, Nantes Hospital, Nantes, France
Olivier Pichon
11Clinical Genetics Unit, Nantes Hospital, Nantes, France
Bertrand Isidor
11Clinical Genetics Unit, Nantes Hospital, Nantes, France
Albert David
11Clinical Genetics Unit, Nantes Hospital, Nantes, France
Jean-Michel Dupont
12Cytogenetics Unit, Cochin Hospital, APHP, Paris, France
Stephan Kemeny
13Genetics Unit, CHU Estaing, Clermont-Ferrand, France
Laetitia Gouas
13Genetics Unit, CHU Estaing, Clermont-Ferrand, France
Philippe Vago
13Genetics Unit, CHU Estaing, Clermont-Ferrand, France
Anne-Laure Mosca-Boidron
14Cytogenetics Unit, Dijon Hospital, Dijon, France
Laurence Faivre
15Clinical Genetics Unit, Dijon Hospital, Dijon, France
Chantal Missirian
16Genetics Unit, La Timone Hospital, Marseille, France
Nicole Philip
16Genetics Unit, La Timone Hospital, Marseille, France
Damien Sanlaville
17Cytogenetics Unit, Lyon Civil Hospital, Lyon, France
Patrick Edery
18Clinical Genetics Unit, Lyon Civil Hospital, Lyon, France
Véronique Satre
19Cytogenetics Unit, Grenoble Hospital, Grenoble, France
Charles Coutton
19Cytogenetics Unit, Grenoble Hospital, Grenoble, France
Françoise Devillard
19Cytogenetics Unit, Grenoble Hospital, Grenoble, France
Klaus Dieterich
20Clinical Genetics Unit, Grenoble Hospital, Grenoble, France
Marie-Laure Vuillaume
21Genetics Unit, Bordeaux Hospital, Bordeaux, France
Caroline Rooryck
21Genetics Unit, Bordeaux Hospital, Bordeaux, France
Didier Lacombe
21Genetics Unit, Bordeaux Hospital, Bordeaux, France
Lucile Pinson
22Genetics Unit, Montpellier Hospital, Montpellier, France
Vincent Gatinois
22Genetics Unit, Montpellier Hospital, Montpellier, France
Jacques Puechberty
22Genetics Unit, Montpellier Hospital, Montpellier, France
Jean Chiesa
23Genetics Unit, CHRU Nimes, Nimes, France
James Lespinasse
24Cytogenetics Unit, Chambéry-Hôtel-Dieu Hospital, Chambery, France
Christèle Dubourg
25Genetics Unit, CHU Rennes, Rennes, France
Chloé Quelin
25Genetics Unit, CHU Rennes, Rennes, France
Mélanie Fradin
25Genetics Unit, CHU Rennes, Rennes, France
Hubert Journel
26Genetics Unit, Chubert Hospital, Vannes, France
Annick Toutain
27Genetics Unit, Bretonneau Hospital, Tours, France
Dominique Martin
28Genetics Unit, CH Le Mans, Le Mans, France
Abdelamdjid Benmansour
1Genetics Department, Robert Debré Hospital, APHP, Paris, France
Roberto Toro
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Frédérique Amsellem
29Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France
Richard Delorme
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
29Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France
Thomas Bourgeron
2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France
3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France
4Université Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France
Posted March 18, 2017.
A framework to identify modifier genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard, Yline Capri, Alain Verloes, 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 Beneteau, Olivier Pichon, Bertrand Isidor, Albert David, Jean-Michel Dupont, Stephan Kemeny, Laetitia 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 Gatinois, Jacques Puechberty, Jean Chiesa, James Lespinasse, Christèle Dubourg, Chloé Quelin, Mélanie Fradin, Hubert Journel, Annick Toutain, Dominique Martin, Abdelamdjid Benmansour, Roberto Toro, Frédérique Amsellem, Richard Delorme, Thomas Bourgeron
bioRxiv 117978; doi: https://doi.org/10.1101/117978
A framework to identify modifier genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard, Yline Capri, Alain Verloes, 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 Beneteau, Olivier Pichon, Bertrand Isidor, Albert David, Jean-Michel Dupont, Stephan Kemeny, Laetitia 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 Gatinois, Jacques Puechberty, Jean Chiesa, James Lespinasse, Christèle Dubourg, Chloé Quelin, Mélanie Fradin, Hubert Journel, Annick Toutain, Dominique Martin, Abdelamdjid Benmansour, Roberto Toro, Frédérique Amsellem, Richard Delorme, Thomas Bourgeron
bioRxiv 117978; doi: https://doi.org/10.1101/117978
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