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Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence

How well one does at school is predictive of a wide range of important cognitive, socioeconomic, and health outcomes. The last few years have shown marked advancement in our understanding of the genetic contributions to, and correlations with, academic attainment. However, there exists a gap in our...

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Autores principales: Donati, Georgina, Dumontheil, Iroise, Pain, Oliver, Asbury, Kathryn, Meaburn, Emma L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887196/
https://www.ncbi.nlm.nih.gov/pubmed/33594131
http://dx.doi.org/10.1038/s41598-021-82877-y
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author Donati, Georgina
Dumontheil, Iroise
Pain, Oliver
Asbury, Kathryn
Meaburn, Emma L.
author_facet Donati, Georgina
Dumontheil, Iroise
Pain, Oliver
Asbury, Kathryn
Meaburn, Emma L.
author_sort Donati, Georgina
collection PubMed
description How well one does at school is predictive of a wide range of important cognitive, socioeconomic, and health outcomes. The last few years have shown marked advancement in our understanding of the genetic contributions to, and correlations with, academic attainment. However, there exists a gap in our understanding of the specificity of genetic associations with performance in academic subjects during adolescence, a critical developmental period. To address this, the Avon Longitudinal Study of Parents and Children was used to conduct genome-wide association studies of standardised national English (N = 5983), maths (N = 6017) and science (N = 6089) tests. High SNP-based heritabilities (h(2)(SNP)) for all subjects were found (41–53%). Further, h(2)(SNP) for maths and science remained after removing shared variance between subjects or IQ (N = 3197–5895). One genome-wide significant single nucleotide polymorphism (rs952964, p = 4.86 × 10(–8)) and four gene-level associations with science attainment (MEF2C, BRINP1, S100A1 and S100A13) were identified. Rs952964 remained significant after removing the variance shared between academic subjects. The findings highlight the benefits of using environmentally homogeneous samples for genetic analyses and indicate that finer-grained phenotyping will help build more specific biological models of variance in learning processes and abilities.
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spelling pubmed-78871962021-02-18 Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence Donati, Georgina Dumontheil, Iroise Pain, Oliver Asbury, Kathryn Meaburn, Emma L. Sci Rep Article How well one does at school is predictive of a wide range of important cognitive, socioeconomic, and health outcomes. The last few years have shown marked advancement in our understanding of the genetic contributions to, and correlations with, academic attainment. However, there exists a gap in our understanding of the specificity of genetic associations with performance in academic subjects during adolescence, a critical developmental period. To address this, the Avon Longitudinal Study of Parents and Children was used to conduct genome-wide association studies of standardised national English (N = 5983), maths (N = 6017) and science (N = 6089) tests. High SNP-based heritabilities (h(2)(SNP)) for all subjects were found (41–53%). Further, h(2)(SNP) for maths and science remained after removing shared variance between subjects or IQ (N = 3197–5895). One genome-wide significant single nucleotide polymorphism (rs952964, p = 4.86 × 10(–8)) and four gene-level associations with science attainment (MEF2C, BRINP1, S100A1 and S100A13) were identified. Rs952964 remained significant after removing the variance shared between academic subjects. The findings highlight the benefits of using environmentally homogeneous samples for genetic analyses and indicate that finer-grained phenotyping will help build more specific biological models of variance in learning processes and abilities. Nature Publishing Group UK 2021-02-16 /pmc/articles/PMC7887196/ /pubmed/33594131 http://dx.doi.org/10.1038/s41598-021-82877-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Donati, Georgina
Dumontheil, Iroise
Pain, Oliver
Asbury, Kathryn
Meaburn, Emma L.
Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title_full Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title_fullStr Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title_full_unstemmed Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title_short Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence
title_sort evidence for specificity of polygenic contributions to attainment in english, maths and science during adolescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887196/
https://www.ncbi.nlm.nih.gov/pubmed/33594131
http://dx.doi.org/10.1038/s41598-021-82877-y
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