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Longitudinal Reading Measures and Genome Imputation in the National Child Development Study: Prospects for Future Reading Research.
Bridges, Elinor C; Rayner, N William; Mountford, Hayley S; Bates, Timothy C; Luciano, Michelle.
Affiliation
  • Bridges EC; School of Philosophy, Psychology and Language Sciences, University of Edinburgh, Edinburgh, United Kingdom.
  • Rayner NW; Institute of Translational Genomics, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.
  • Mountford HS; Oxford Centre for Diabetes, Endocrinology and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Bates TC; Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Luciano M; School of Philosophy, Psychology and Language Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Twin Res Hum Genet ; 26(1): 10-20, 2023 02.
Article in En | MEDLINE | ID: mdl-36896826
Reading difficulties are prevalent worldwide, including in economically developed countries, and are associated with low academic achievement and unemployment. Longitudinal studies have identified several early childhood predictors of reading ability, but studies frequently lack genotype data that would enable testing of predictors with heritable influences. The National Child Development Study (NCDS) is a UK birth cohort study containing direct reading skill variables at every data collection wave from age 7 years through to adulthood with a subsample (final n = 6431) for whom modern genotype data are available. It is one of the longest running UK cohort studies for which genotyped data are currently available and is a rich dataset with excellent potential for future phenotypic and gene-by-environment interaction studies in reading. Here, we carry out imputation of the genotype data to the Haplotype Reference Panel, an updated reference panel that offers greater imputation quality. Guiding phenotype choice, we report a principal components analysis of nine reading variables, yielding a composite measure of reading ability in the genotyped sample. We include recommendations for use of composite scores and the most reliable variables for use during childhood when conducting longitudinal, genetically sensitive analyses of reading ability.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development / Cognition Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Humans Language: En Journal: Twin Res Hum Genet Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development / Cognition Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Humans Language: En Journal: Twin Res Hum Genet Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: United kingdom