Article Information
History
- March 13, 2019.
Article Versions
- Version 1 (January 31, 2019 - 09:48).
- You are viewing Version 2, the most recent version of this article.
Copyright
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
Author Information
- Samuel J.R.A. Chawner PhDa,
- Michael Owen FRCPsycha,
- Peter Holmans PhDa,
- Lucy Raymond FRCPb,
- David Skuse MRCPsychc,
- Jeremy Hall MRCPsycha1 and
- Marianne van den Bree PhDa1
- aMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom
- bDepartment of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK
- cInstitute of Child Health, University College London, London, UK
- Corresponding author: Marianne van den Bree Email: vandenbreemb{at}cardiff.ac.uk Phone: +44 (0)29 2068 8433 Fax: +44(0)29 2068 7068 Address: Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, 2nd Floor Hadyn Ellis Building, Cardiff University, Maindy Road, Cathays, Cardiff, United Kingdom, CF24 4HQ.
↵1 these authors contributed equally
Posted March 13, 2019.
Genotype-phenotype relationships in children with Copy Number Variants associated with high neuropsychiatric risk: Findings from the case-control IMAGINE-ID cohort in the United Kingdom
