Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences
Autor: | Ian J. Deary, Christopher J. McNeil, John M. Starr, Antony Payton, Sarah E. Medland, Margaret J. Wright, Nicholas G. Martin, Michael A. Horan, Lawrence J. Whalley, N K Hansel, Gary Davies, Grant W. Montgomery, William Ollier, D C Liewald, Neil Pendleton, WD Hill, Timothy C. Bates |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Genetics education.field_of_study Population Single-nucleotide polymorphism Genome-wide association study Experimental and Cognitive Psychology Quantitative trait locus medicine.disease Genome Article Intellectual disabilities 03 medical and health sciences Gene set analysis 030104 developmental biology Arts and Humanities (miscellaneous) Polygene Intellectual disability Developmental and Educational Psychology medicine GWAS education Psychology Gene |
Zdroj: | Hill, W D, Davies, G, Liewald, D C, Payton, A, McNeil, C J, Whalley, L J, Horan, M, Ollier, W, Starr, J M, Pendleton, N, Hansel, N K, Montgomery, G W, Medland, S E, Martin, N G, Wright, M J, Bates, T C & Deary, I J 2016, ' Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences ', Intelligence, vol. 54, pp. 80-89 . https://doi.org/10.1016/j.intell.2015.11.005 Hill, W D, Davies, G, Liewald, D, Payton, A, Mcneil, C J, Whalley, L J, Horan, M, Ollier, W, Starr, J, Pendleton, N, Hansel, N K, Montgomery, G W, Medland, S E, Martin, N G, Wright, M J, Bates, T C & Deary, I J 2016, ' Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences ', Intelligence, vol. 54, pp. 80-89 . https://doi.org/10.1016/j.intell.2015.11.005 Intelligence |
ISSN: | 0160-2896 |
DOI: | 10.1016/j.intell.2015.11.005 |
Popis: | Two themes are emerging regarding the molecular genetic aetiology of intelligence. The first is that intelligence is influenced by many variants and those that are tagged by common single nucleotide polymorphisms account for around 30% of the phenotypic variation. The second, in line with other polygenic traits such as height and schizophrenia, is that these variants are not randomly distributed across the genome but cluster in genes that work together. Less clear is whether the very low range of cognitive ability (intellectual disability) is simply one end of the normal distribution describing individual differences in cognitive ability across a population. Here, we examined 40 genes with a known association with non-syndromic autosomal recessive intellectual disability (NS-ARID) to determine if they are enriched for common variants associated with the normal range of intelligence differences. The current study used the 3511 individuals of the Cognitive Ageing Genetics in England and Scotland (CAGES) consortium. In addition, a text mining analysis was used to identify gene sets biologically related to the NS-ARID set. Gene-based tests indicated that genes implicated in NS-ARID were not significantly enriched for quantitative trait loci (QTL) associated with intelligence. These findings suggest that genes in which mutations can have a large and deleterious effect on intelligence are not associated with variation across the range of intelligence differences. Highlights • Only three loci have been associated with intelligence. • In traits such as height common variants are found in the same genes as rare variants. • We hypothesise that intelligence may also follow this trend. • We examine genes where rare variants can produce large deleterious effects on IQ. • No enrichment was found for the non-syndromic intellectual disability gene set. |
Databáze: | OpenAIRE |
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