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Cognitive and behavioural genetics
Original research
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

Authors

  • Lottie D Morison Speech and Language, Murdoch Children's Research Institute, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Elisabeth Meffert SRH University of Applied Health Sciences, Gera, Germany PubMed articlesGoogle scholar articles
  • Miriam Stampfer Medical Genetics Center, Munich, Germany PubMed articlesGoogle scholar articles
  • Irene Steiner-Wilke Centre for Cleft Palate & Craniofacial Malformations, Tuebingen University Hospital, Tubingen, Germany Department of Paediatric Neurology and Developmental Medicine, University Children’s Hospital Tuebingen, Tuebingen, Germany PubMed articlesGoogle scholar articles
  • Brigitte Vollmer Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK Paediatric Neurology, Southampton Children’s Hospital, University Hospital Southampton NHS Foundation Trust, Southampton, UK PubMed articlesGoogle scholar articles
  • Katrin Schulze Department of Psychology, Heidelberg University, Heidelberg, Germany PubMed articlesGoogle scholar articles
  • Tracy Briggs Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Health, School of Biological Sciences, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester University NHS Foundation Trust, Manchester, UK PubMed articlesGoogle scholar articles
  • Ruth Braden Speech and Language, Murdoch Children's Research Institute, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Adam Vogel Centre for Neuroscience of Speech, University of Melbourne, Melbourne, Victoria, Australia Redenlab Pty Ltd, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Daisy Thompson-Lake Great Ormond Street Institute of Child Health, University College London, London, UK PubMed articlesGoogle scholar articles
  • Chirag Patel Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia PubMed articlesGoogle scholar articles
  • Edward Blair Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK PubMed articlesGoogle scholar articles
  • Himanshu Goel Hunter Genetics, Waratah, New South Wales, Australia PubMed articlesGoogle scholar articles
  • Samantha Turner Speech and Language, Murdoch Children's Research Institute, Melbourne, Victoria, Australia School of Allied Health, Human Services and Sport, La Trobe University, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Ute Moog Institute of Human Genetics, Heidelberg University, Heidelberg, Germany PubMed articlesGoogle scholar articles
  • Angelika Riess Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articlesGoogle scholar articles
  • Frederique Liegeois Great Ormond Street Institute of Child Health, University College London, London, UK PubMed articlesGoogle scholar articles
  • David A Koolen Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center (Radboudumc), Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • David J Amor Speech and Language, Murdoch Children's Research Institute, Melbourne, Victoria, Australia Department of Pediatrics, Royal Children's Hospital, Parkville, Victoria, Australia Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Tjitske Kleefstra Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center (Radboudumc), Nijmegen, The Netherlands Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands PubMed articlesGoogle scholar articles
  • Simon E Fisher Language and Genetics, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands Donders Centre for Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Christiane Zweier Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany Department of Human Genetics, Inselspital Bern, University of Bern, Bern, Switzerland PubMed articlesGoogle scholar articles
  • Angela T Morgan Speech and Language, Murdoch Children's Research Institute, Melbourne, Victoria, Australia Department of Audiology and Speech Pathology, University of Melbourne, Melbourne, Victoria, Australia Department of Speech Pathology, Royal Children's Hospital, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Angela T Morgan, Speech and Language, Murdoch Children’s Research Institute, Melbourne, Victoria, Australia; angela.morgan{at}mcri.edu.au
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Citation

Morison LD, Meffert E, Stampfer M, et al
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2
Journal of Medical Genetics 2023;60:597-607.

Publication history

  • Received May 29, 2022
  • Accepted October 9, 2022
  • First published November 3, 2022.
Online issue publication 
May 22, 2023

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© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.