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GWAS Study

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

Donati G, Dumontheil I, Pain O et al.

33594131 PubMed ID
GWAS Study Type
5983 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DG
Donati G
DI
Dumontheil I
PO
Pain O
AK
Asbury K
ME
Meaburn EL
Chapter II

Abstract

Summary of the research findings

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 (h2SNP) for all subjects were found (41-53%). Further, h2SNP 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.

5,983 European ancestry adolescents

Chapter III

Study Statistics

Key metrics and study information

5983
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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