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.

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, base...

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Main Authors: 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
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4011843?pdf=render
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spelling doaj-6c4a725c0eca40d991d5246661602d2c2020-11-25T02:27:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0195e9637410.1371/journal.pone.0096374A 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-CohenLaura MurphyBhismadev ChakrabartiIan CraigUma MallyaSilvia LakatošováKarola RehnstromLeena PeltonenSally WheelwrightCarrie AllisonSimon E FisherVarun WarrierMathematical 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.http://europepmc.org/articles/PMC4011843?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author 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
spellingShingle 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
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.
PLoS ONE
author_facet 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
author_sort Simon Baron-Cohen
title 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.
title_short 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.
title_full 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.
title_fullStr 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.
title_full_unstemmed 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.
title_sort genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description 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.
url http://europepmc.org/articles/PMC4011843?pdf=render
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