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Paper Details

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Nature
191
2018
abnormalities of other organ systems, autism, child, children, common, common-variant scores, developmental delay, genetic defect, genome, global, human, monogenic, monogenic disorders, neurodevelopmental disorders, patients, protein-coding diagnostic variant, protein-coding genetic variants1, schizophrenia
Author NameAffiliation
Hilary C MartinWellcome Sanger Institute
Hilary C MartinWellcome Sanger Institute
Scott D GordonQIMR Berghofer Medical Research Institute
Nicholas G MartinQIMR Berghofer Medical Research Institute
Caroline F WrightUniversity of Exeter Medical School, Institute of Biomedical and Clinical Science, Royal Devon & Exeter Hospital
David R FitzPatrickUniversity of Edinburgh, Western General Hospital
Helen V FirthWellcome Sanger Institute
Helen V FirthCambridge University Hospitals NHS Foundation Trust
Matthew E HurlesWellcome Sanger Institute
Matthew E HurlesWellcome Sanger Institute
Jeffrey C BarrettWellcome Sanger Institute
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