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  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

Baron-Cohen, S., Murphy, L., Chakrabarti, B., Craig, I., Mallya, U., Lakatosova, S., et al. (2014). 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, 9(5): e96374. doi:10.1371/journal.pone.0096374.

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Baren_Cohen_etal_PLOS_2014.pdf (Publisher version), 381KB
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2014
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2014 Baron-Cohen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Baron-Cohen, Simon1, 2, Author
Murphy, Laura1, Author
Chakrabarti, Bhismadev1, 3, Author
Craig, Ian4, Author
Mallya, Uma1, Author
Lakatosova, Silvia1, Author
Rehnstrom, Karola5, Author
Peltonen, Leena5, Author
Wheelwright, Sally1, Author
Allison, Carrie1, Author
Fisher, Simon E.6, 7, Author           
Warrier, Varun1, Author
Affiliations:
1Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridgeshire, United Kingdom, ou_persistent22              
2CLASS Clinic, Cambridgeshire and Peterborough NHS Foundation Trust (CPFT), Cambridgeshire, United Kingdom, ou_persistent22              
3School of Psychology and Clinical Language Sciences, Centre for Integrative Neuroscience and Neurodynamics, University of Reading, Reading, United Kingdom, ou_persistent22              
4MRC Centre for Social, Genetic and Developmental Psychiatry, King’s College London, Institute of Psychiatry, London, United Kingdom, ou_persistent22              
5The Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, United Kingdom, ou_persistent22              
6Donders Institute for Brain, Cognition and Behaviour, External Organizations, ou_55236              
7Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              

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 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.

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Language(s): eng - English
 Dates: 2014-05-07
 Publication Status: Published online
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 Rev. Type: Peer
 Identifiers: DOI: 10.1371/journal.pone.0096374
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Title: PLoS One
Source Genre: Journal
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Pages: - Volume / Issue: 9 (5) Sequence Number: e96374 Start / End Page: - Identifier: ISSN: 1932-6203
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000277850