Articlehybrid2008

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

Kerstin U. Ludwig · Darina Roeske · Johannes Schumacher · Gerd Schulte‐Körne · Inke Regina König · Andreas Warnke +6 more

41 citations0/0 files storedJournal of Neural Transmission

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Reading and Literacy Development Language Development and Disorders Genetic Associations and Epidemiology

Abstract

The dyslexia susceptibility locus DYX2 (chr. 6p21-p22) harbours two candidate genes, DCDC2 and KIAA0319. In 2006, Harold et al. reported evidence for interaction between both genes. Having previously identified a risk haplotype for dyslexia in DCDC2, but not KIAA0319, in German families, we also tested for interaction between this risk haplotype and KIAA0319. We found a nominally significant association for the quantitative dimension "word reading", the core phenotype in the study of Harold et al., which may be considered as supportive evidence.

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References

2003Foundation literacy acquisition in European orthographies 2003Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults 1999Persistence of Dyslexia: The Connecticut Longitudinal Study at Adolescence 2005DCDC2 is associated with reading disability and modulates neuronal development in the brain 2005Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia 2006The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration 2005Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia 2004A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States

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2013Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population 2014Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

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