A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study

Simon Baron-Cohen, Laura Murphy, Bhismadev Chakrabarti, Ian Craig, Uma Mallya, Silvia Lakatošová, Karola Rehnstrom, Leena Peltonen, Sally Wheelwright, Carrie Allison, Simon E Fisher, Varun Warrier

Research output: Contribution to journalArticlepeer-review

Abstract

Mathematical ability is heritable, but few studies have directly investigated its molecular genetic basis. Here we aimed to identify specific genetic contributions to variation in mathematical ability. We carried out a genome wide association scan using pooled DNA in two groups of U.K. samples, based on end of secondary/high school national academic exam achievement: high (n = 419) versus low (n = 183) mathematical ability while controlling for their verbal ability. Significant differences in allele frequencies between these groups were searched for in 906,600 SNPs using the Affymetrix GeneChip Human Mapping version 6.0 array. After meeting a threshold of p<1.5×10(-5), 12 SNPs from the pooled association analysis were individually genotyped in 542 of the participants and analyzed to validate the initial associations (lowest p-value 1.14 ×10(-6)). In this analysis, one of the SNPs (rs789859) showed significant association after Bonferroni correction, and four (rs10873824, rs4144887, rs12130910 rs2809115) were nominally significant (lowest p-value 3.278 × 10(-4)). Three of the SNPs of interest are located within, or near to, known genes (FAM43A, SFT2D1, C14orf64). The SNP that showed the strongest association, rs789859, is located in a region on chromosome 3q29 that has been previously linked to learning difficulties and autism. rs789859 lies 1.3 kbp downstream of LSG1, and 700 bp upstream of FAM43A, mapping within the potential promoter/regulatory region of the latter. To our knowledge, this is only the second study to investigate the association of genetic variants with mathematical ability, and it highlights a number of interesting markers for future study.

Original languageEnglish
Pages (from-to)e96374
JournalPLoS ONE
Volume9
Issue number5
DOIs
Publication statusPublished - 2014

Keywords

  • Adolescent
  • Autistic Disorder
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3
  • Female
  • Gene Frequency
  • Genome, Human
  • Genome-Wide Association Study
  • Genotype
  • Humans
  • Learning Disorders
  • Male
  • Mathematics
  • Polymorphism, Single Nucleotide
  • Quantitative Trait Loci
  • Journal Article
  • Research Support, Non-U.S. Gov't

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