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Article

Imaging genetics of FOXP2 in dyslexia.

European journal of human genetics : EJHG - 1 Feb 2012

Wilcke Arndt, Ligges Carolin, Burkhardt Jana, Alexander Michael, Wolf Christiane, Quente Elfi, Ahnert Peter, Hoffmann Per, Becker Albert, Müller-Myhsok Bertram, Cichon Sven, Boltze Johannes, Kirsten Holger

Abstract excerpt

Dyslexia is a developmental disorder characterised by extensive difficulties in the acquisition of reading or spelling. Genetic influence is estimated at 50-70%. However, the link between genetic variants and phenotypic deficits is largely unknown. Our aim was to investigate a role of genetic variants of FOXP2, a prominent speech and language gene, in dyslexia using imaging genetics. This technique combines...

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Identifiers

PMID: 21897444
DOI: 10.1038/ejhg.2011.160
PMCID: PMC3260915

Genes

FOXP2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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