X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
Hao Hu(Max Planck Institute for Molecular Genetics), Stefan A. Haas(Max Planck Institute for Molecular Genetics), Jamel Chelly(Délégation Paris 5), Hilde Van Esch, Martine Raynaud(Université de Tours), Arjan P.M. de Brouwer(Radboud University Nijmegen), Stefanie Weinert(Max Delbrück Center), Guy Froyen(VIB-KU Leuven Center for Cancer Biology), Suzanna G.M. Frints(Maastricht University), Frédéric Laumonnier(Université de Tours), Tomasz Żemojtel(Max Planck Institute for Molecular Genetics), Michael I. Love(Max Planck Institute for Molecular Genetics), Hugues Richard(Max Planck Institute for Molecular Genetics), A-K Emde(Max Planck Institute for Molecular Genetics), Melanie Bienek(Max Planck Institute for Molecular Genetics), Corinna Jensen(Max Planck Institute for Molecular Genetics), M Hambrock(Max Planck Institute for Molecular Genetics), Utz Fischer(Max Planck Institute for Molecular Genetics), Claudia Langnick(Max Delbrück Center), Mirjam Feldkamp(Max Delbrück Center), W.M. Wissink-Lindhout(Radboud University Nijmegen), Nicolas Lebrun(Délégation Paris 5), L. Castelnau(Délégation Paris 5), J. Rucci(Délégation Paris 5), Rodrick Montjean(Délégation Paris 5), Olivier Dorseuil(Délégation Paris 5), Pierre Billuart(Délégation Paris 5), Till Stuhlmann(Max Delbrück Center), M Shaw(The University of Adelaide), Mark Corbett(The University of Adelaide), Alison Gardner(The University of Adelaide), Saffron A.G. Willis‐Owen(Imperial College London), Chuan Tan(The University of Adelaide), Kathryn Friend(South Australia Pathology), Stefanie Belet(VIB-KU Leuven Center for Cancer Biology), Kees E. P. van Roozendaal(Maastricht University), M Jimenez-Pocquet(Centre Hospitalier Universitaire de Tours), M.‐P. Moizard(Université de Tours), Nathalie Ronce(Université de Tours), Ren Sun(Max Planck Institute for Molecular Genetics), Sean O’Keeffe(Max Planck Institute for Molecular Genetics), R Chenna(Max Planck Institute for Molecular Genetics), Alena van Bömmel(Max Planck Institute for Molecular Genetics), Jonathan Göke(Max Planck Institute for Molecular Genetics), Anna Hackett(Hunter Genetics), Michael Field(Hunter Genetics), Louise Christie(Hunter Genetics), Jackie Boyle(Hunter Genetics), Eric Haan(South Australia Pathology), John W. Nelson(King Edward Memorial Hospital), Gillian Turner(Hunter Genetics), Gareth Baynam(The Kids Research Institute Australia), Gabriele Gillessen‐Kaesbach(University of Lübeck), Ulrich Müller(Justus-Liebig-Universität Gießen), Daniela Steinberger(Justus-Liebig-Universität Gießen), Bartłomiej Budny(Poznan University of Medical Sciences), Magdalena Badura‐Stronka(Poznan University of Medical Sciences), Anna Latos‐Bieleńska(Poznan University of Medical Sciences), Lilian Bomme Ousager(Odense University Hospital), Peter Wieacker(Klinik und Poliklinik für Psychosomatik und Psychotherapie), Germán Rodríguez Criado(Hospital Universitario Virgen del Rocío), M.-L. Bondeson(Uppsala University), Göran Annerén(Uppsala University), Andreas Dufke, Monika Cohen(München Klinik), Lionel Van Maldergem(Université de franche-comté), C. Vincent‐Delorme(Centre Hospitalier Universitaire de Lille), Bernard Échenne(Centre Hospitalier Universitaire de Montpellier), Brigitte Simon‐Bouy(Centre Hospitalier de Versailles), Tjitske Kleefstra(Radboud University Nijmegen), Marjolein H. Willemsen(Radboud University Nijmegen), J-P. Fryns, Koenraad Devriendt, Reinhard Ullmann(Universität Ulm), Martin Vingron(Max Planck Institute for Molecular Genetics), Klaus Wrogemann(Max Planck Institute for Molecular Genetics), Thomas F. Wienker(Max Planck Institute for Molecular Genetics), Andreas Tzschach(Max Planck Institute for Molecular Genetics), Hans van Bokhoven(Radboud University Nijmegen), Jozef Gécz(The University of Adelaide), Thomas J. Jentsch(Max Delbrück Center), W. Chen(Max Delbrück Center), H‐H Ropers(Max Planck Institute for Molecular Genetics), Vera M. Kalscheuer(Max Planck Institute for Molecular Genetics)
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