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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu, H; Haas, S A; Chelly, J; Van Esch, H; Raynaud, M; de Brouwer, A P M; Weinert, S; Froyen, G; Frints, S G M; Laumonnier, F; Zemojtel, T; Love, M I; Richard, H; Emde, A-K; Bienek, M; Jensen, C; Hambrock, M; Fischer, U; Langnick, C; Feldkamp, M; Wissink-Lindhout, W; Lebrun, N; Castelnau, L; Rucci, J; Montjean, R; Dorseuil, O; Billuart, P; Stuhlmann, T; Shaw, M; Corbett, M A; Gardner, A; Willis-Owen, S; Tan, C; Friend, K L; Belet, S; van Roozendaal, K E P; Jimenez-Pocquet, M; Moizard, M-P; Ronce, N; Sun, R; O'Keeffe, S; Chenna, R; van Bömmel, A; Göke, J; Hackett, A; Field, M; Christie, L; Boyle, J; Haan, E; Nelson, J.
Affiliation
  • Hu H; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Haas SA; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Chelly J; University Paris Descartes, Paris, France.
  • Van Esch H; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Raynaud M; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • de Brouwer AP; Inserm U930 'Imaging and Brain', Tours, France.
  • Weinert S; University François-Rabelais, Tours, France.
  • Froyen G; Centre Hospitalier Régional Universitaire, Service de Génétique, Tours, France.
  • Frints SG; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
  • Laumonnier F; Max-Delbrück-Centrum für Molekulare Medizin, Berlin, Germany.
  • Zemojtel T; Leibniz-Institut für Molekulare Pharmakologie, Berlin, Germany.
  • Love MI; Human Genome Laboratory, VIB Center for the Biology of Disease, Leuven, Belgium.
  • Richard H; Human Genome Laboratory, Department of Human Genetics, K.U. Leuven, Leuven, Belgium.
  • Emde AK; Department of Clinical Genetics, Maastricht University Medical Center, azM, Maastricht, The Netherlands.
  • Bienek M; School for Oncology and Developmental Biology, GROW, Maastricht University, Maastricht, The Netherlands.
  • Jensen C; Inserm U930 'Imaging and Brain', Tours, France.
  • Hambrock M; University François-Rabelais, Tours, France.
  • Fischer U; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Langnick C; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Feldkamp M; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Wissink-Lindhout W; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Lebrun N; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Castelnau L; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Rucci J; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Montjean R; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Dorseuil O; Max-Delbrück-Centrum für Molekulare Medizin, Berlin, Germany.
  • Billuart P; Max-Delbrück-Centrum für Molekulare Medizin, Berlin, Germany.
  • Stuhlmann T; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
  • Shaw M; University Paris Descartes, Paris, France.
  • Corbett MA; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Gardner A; University Paris Descartes, Paris, France.
  • Willis-Owen S; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Tan C; University Paris Descartes, Paris, France.
  • Friend KL; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Belet S; University Paris Descartes, Paris, France.
  • van Roozendaal KE; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Jimenez-Pocquet M; University Paris Descartes, Paris, France.
  • Moizard MP; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • Ronce N; University Paris Descartes, Paris, France.
  • Sun R; Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Institut National de la Santé et de la Recherche Médicale Unité 1016, Institut Cochin, Paris, France.
  • O'Keeffe S; Max-Delbrück-Centrum für Molekulare Medizin, Berlin, Germany.
  • Chenna R; Leibniz-Institut für Molekulare Pharmakologie, Berlin, Germany.
  • van Bömmel A; School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, SA, Australia.
  • Göke J; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
  • Hackett A; School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, SA, Australia.
  • Field M; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
  • Christie L; School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, SA, Australia.
  • Boyle J; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
  • Haan E; School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, SA, Australia.
  • Nelson J; National Heart and Lung Institute, Imperial College London, London, UK.
Mol Psychiatry ; 21(1): 133-48, 2016 Jan.
Article in En | MEDLINE | ID: mdl-25644381
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Full text: 1 Database: MEDLINE Main subject: Genetic Variation / Mental Retardation, X-Linked Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Animals / Humans / Male Language: En Journal: Mol Psychiatry Journal subject: BIOLOGIA MOLECULAR / PSIQUIATRIA Year: 2016 Type: Article Affiliation country: Germany
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Genetic Variation / Mental Retardation, X-Linked Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Animals / Humans / Male Language: En Journal: Mol Psychiatry Journal subject: BIOLOGIA MOLECULAR / PSIQUIATRIA Year: 2016 Type: Article Affiliation country: Germany