16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.

• Reinthaler EM Department of Neurology.
• Lal D Cologne Center for Genomics, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany, Department of Neuropediatrics, University Medical Faculty Giessen and Marburg, Giessen, Germany.
• Lebon S Unit of Pediatric Neurology and Neurorehabilitation, Department of Pediatrics.
• Hildebrand MS Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia.
• Dahl HH Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia.
• Regan BM Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia.
• Feucht M Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
• Steinböck H Private Practice for Pediatrics, Vienna, Austria.
• Neophytou B Department of Neuropediatrics, St. Anna Children's Hospital, Vienna, Austria.
• Ronen GM Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
• Roche L Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
• Gruber-Sedlmayr U Department of Pediatrics, Medical University of Graz, Graz, Austria.
• Geldner J Department of Pediatrics, Hospital SMZ Süd Kaiser-Franz-Josef Spital, Vienna, Austria.
• Haberlandt E Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Austria.
• Hoffmann P Institute of Human Genetics, University of Bonn, Bonn, Germany, Division of Medical Genetics, University Hospital and Department of Biomedicine, University of Basel, Basel, Switzerland.
• Herms S Institute of Human Genetics, University of Bonn, Bonn, Germany, Division of Medical Genetics, University Hospital and Department of Biomedicine, University of Basel, Basel, Switzerland.
• Gieger C Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Institute of Genetic Epidemiology, Neuherberg, Germany.
• Waldenberger M Research Unit of Molecular Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
• Franke A Institute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, Kiel, Germany.
• Wittig M Institute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, Kiel, Germany.
• Schoch S Department of Neuropathology, University of Bonn Medical Center, Bonn, Germany.
• Becker AJ Department of Neuropathology, University of Bonn Medical Center, Bonn, Germany.
• Hahn A Department of Neuropediatrics, University Medical Faculty Giessen and Marburg, Giessen, Germany.
• Männik K Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
• Toliat MR Cologne Center for Genomics.
• Winterer G Experimental and Clinical Research Center (ECRC) Charité, University Medicine Berlin, Berlin, Germany.
• Lerche H Cologne Center for Genomics, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.
• Nürnberg P Division of Genetic Medicine, University of Washington, Seattle, Washington, USA.
• Mefford H Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia, Florey Institute and Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, Australia.
• Scheffer IE Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia.
• Berkovic SF Service of Medical Genetics, Lausanne University Hospital, Lausanne, Switzerland, Swiss Institute of Bioinformatics, Lausanne, Switzerland and.
• Beckmann JS Cologne Center for Genomics.
• Sander T Department of Neurology, friedrich.zimprich@meduniwien.ac.at.
• Jacquemont S Department of Neuropediatrics, University Medical Faculty Giessen and Marburg, Giessen, Germany.
• Reymond A
• Zimprich F
• Neubauer BA

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Child

Child, Preschool

Chromosome Duplication

Chromosomes, Human, Pair 1

Chromosomes, Human, Pair 15

Chromosomes, Human, Pair 16

Chromosomes, Human, Pair 22

DNA Copy Number Variations

Epilepsy, Rolandic

Female

Humans

Infant

Male

Polymorphism, Single Nucleotide