Docherty, SJ and Davis, OSP and Kovas, Y and Meaburn, EL and Dale, PS and Petrill, SA and Schalkwyk, LC and Plomin, R (2010) A genome‐wide association study identifies multiple loci associated with mathematics ability and disability. Genes, Brain and Behavior, 9 (2). pp. 234-247. DOI https://doi.org/10.1111/j.1601-183x.2009.00553.x
Docherty, SJ and Davis, OSP and Kovas, Y and Meaburn, EL and Dale, PS and Petrill, SA and Schalkwyk, LC and Plomin, R (2010) A genome‐wide association study identifies multiple loci associated with mathematics ability and disability. Genes, Brain and Behavior, 9 (2). pp. 234-247. DOI https://doi.org/10.1111/j.1601-183x.2009.00553.x
Docherty, SJ and Davis, OSP and Kovas, Y and Meaburn, EL and Dale, PS and Petrill, SA and Schalkwyk, LC and Plomin, R (2010) A genome‐wide association study identifies multiple loci associated with mathematics ability and disability. Genes, Brain and Behavior, 9 (2). pp. 234-247. DOI https://doi.org/10.1111/j.1601-183x.2009.00553.x
Abstract
<jats:p> <jats:bold>Numeracy is as important as literacy and exhibits a similar frequency of disability. Although its etiology is relatively poorly understood, quantitative genetic research has demonstrated mathematical ability to be moderately heritable. In this first genome‐wide association study (GWAS) of mathematical ability and disability, 10 out of 43 single nucleotide polymorphism (SNP) associations nominated from two high‐ vs. low‐ability (<jats:italic>n</jats:italic> = 600 10‐year‐olds each) scans of pooled DNA were validated (<jats:italic>P</jats:italic> < 0.05) in an individually genotyped sample of </jats:bold><jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#fn2"><jats:bold><jats:sup>*</jats:sup></jats:bold></jats:ext-link><jats:bold>2356 individuals spanning the entire distribution of mathematical ability, as assessed by teacher reports and online tests. Although the effects are of the modest sizes now expected for complex traits and require further replication, interesting candidate genes are implicated such as <jats:italic>NRCAM</jats:italic> which encodes a neuronal cell adhesion molecule. When combined into a set, the 10 SNPs account for 2.9% (<jats:italic>F</jats:italic> = 56.85; df = 1 and 1881; <jats:italic>P</jats:italic> = 7.277e–14) of the phenotypic variance. The association is linear across the distribution consistent with a quantitative trait locus (QTL) hypothesis; the third of children in our sample who harbour 10 or more of the 20 risk alleles identified are nearly twice as likely (OR = 1.96; df = 1; <jats:italic>P</jats:italic> = 3.696e–07) to be in the lowest performing 15% of the distribution. Our results correspond with those of quantitative genetic research in indicating that mathematical ability and disability are influenced by many genes generating small effects across the entire spectrum of ability, implying that more highly powered studies will be needed to detect and replicate these QTL associations.</jats:bold> </jats:p>
Item Type: | Article |
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Uncontrolled Keywords: | DNA pooling; quantitative trait; allelic association; SNP microarrays; mathematical ability; cognitive traits |
Subjects: | Q Science > QH Natural history > QH426 Genetics |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 14 Nov 2014 16:55 |
Last Modified: | 04 Dec 2024 06:56 |
URI: | http://repository.essex.ac.uk/id/eprint/11019 |
Available files
Filename: j.1601-183X.2009.00553.x.pdf
Licence: Creative Commons: Attribution-Noncommercial-No Derivative Works 3.0