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Virginia Clowes

affiliation not provided to SSRN

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Scholarly Papers (1)

1.

Neuropsychiatric Risk in Children With Intellectual Disability of Genetic Origin: IMAGINE - The UK National Cohort Study

Number of pages: 24 Posted: 07 Feb 2022
University College London, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Aberdeen Royal Infirmary, Ninewells Hospital and Medical School, University of Edinburgh - Western General Hospital, affiliation not provided to SSRN, affiliation not provided to SSRN, Leeds Teaching Hospitals NHS Trust, affiliation not provided to SSRN, The University of Manchester - Manchester University NHS Foundation Trust, affiliation not provided to SSRN, affiliation not provided to SSRN, Nottingham University Hospitals NHS Trust, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Government of the United Kingdom - Royal Devon and Exeter Hospital, University of Southampton, affiliation not provided to SSRN, University of Cambridge - Department of Psychiatry, affiliation not provided to SSRN, Cardiff University, Cardiff University, Cardiff University, Cardiff University, affiliation not provided to SSRN, University College London - University College London Medical School and University of Cambridge - Department of Medical Genetics
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Abstract:

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IMAGINE consortium, neuropsychiatric risk, children, intellectual disability, genetic, genomic, UK national cohort study, CNV, SNV, IMD, social deprivation, socioeconomic, autistic spectrum disorder, attention deficit disorder, familial variants, pathogenic variant