Context: Dyslexia is a common disorder with a strong genetic component, but despite
significant research effort, the aetiology is still largely unknown. Objective: To identify loci …

Developmental dyslexia is a specific reading disability affecting children and adults who
otherwise possess normal intelligence, cognitive skills, and adequate schooling. Difficulties …

In a genome‐wide linkage scan, we aimed at mapping risk loci for dyslexia in the German
population. Our sample comprised 1,030 individuals from 246 dyslexia families which were …

Dyslexia is a common and genetically complex trait that manifests primarily as a reading
disability independent of general intelligence and educational opportunity. Strong evidence …

In this study, we attempted to confirm genetic linkage to developmental dyslexia and reading‐
related quantitative traits of loci that have been shown to be associated with dyslexia in …

Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning
to read despite adequate intelligence, education, and environment, and normal senses. The …

Dyslexia is one of the most common childhood disorders with a prevalence of around 5–
10% in school-age children. Although an important genetic component is known to have a …

While the exact neurobiological mechanisms underlying this condition remain obscure, the
most convincing current aetiopathogenetic view of dyslexia is that impaired reading stems …

METHODS As described in detail elsewhere, 3, 4 our sample consists of 96 Canadian
families (877 subjects), each containing two or more sibs diagnosed with phonological …

Developmental dyslexia is characterised by difficulties in learning to read. As reading is a
complex cognitive process, multiple genes are expected to contribute to the pathogenesis of …