Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals
doi: 10.1002/ajmg.b.31241
pmid: 21987501
Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals
AbstractLanguage impairments are a characteristic feature of autism and related autism spectrum disorders (ASDs). Autism is also highly heritable and one of the most promising candidate genes implicated in its pathogenesis is contactin‐associated protein‐like 2 (CNTNAP2), a gene also associated with language impairment. In the current study we investigated the functional effects of variants of CNTNAP2 associated with autism and language impairment (rs7794745 and rs2710102; presumed risk alleles T and C, respectively) in healthy individuals using functional magnetic resonance imaging (fMRI) during performance of a language task (n = 66). Against a background of normal performance and lack of behavioral abnormalities, healthy individuals with the putative risk allele versus those without demonstrated significant increases in activation in the right inferior frontal gyrus (Broca's area homologue) and right lateral temporal cortex. These findings demonstrate that risk associated variation in the CNTNAP2 gene impacts on brain activation in healthy non‐autistic individuals during a language processing task providing evidence of the effect of genetic variation in CNTNAP2 on a core feature of ASDs. © 2011 Wiley Periodicals, Inc.
- University of York United Kingdom
- Royal Edinburgh Hospital United Kingdom
- University of Edinburgh United Kingdom
- NHS Lothian United Kingdom
Adult, Male, Language Disorders, Genotype, Brain, Genetic Variation, Membrane Proteins, Nerve Tissue Proteins, Middle Aged, Magnetic Resonance Imaging, Polymorphism, Single Nucleotide, Frontal Lobe, Child Development Disorders, Pervasive, Humans, Female, Genetic Predisposition to Disease, Autistic Disorder, Child
Adult, Male, Language Disorders, Genotype, Brain, Genetic Variation, Membrane Proteins, Nerve Tissue Proteins, Middle Aged, Magnetic Resonance Imaging, Polymorphism, Single Nucleotide, Frontal Lobe, Child Development Disorders, Pervasive, Humans, Female, Genetic Predisposition to Disease, Autistic Disorder, Child
39 Research products, page 1 of 4
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsAmongTopNSimilarDocuments
- 2017IsRelatedTo
- 2015IsAmongTopNSimilarDocuments
- 2017IsRelatedTo
chevron_left - 1
- 2
- 3
- 4
chevron_right
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).88 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
