Dyslexia is a common learning disability exhibited as a delay in acquiring reading skills
despite adequate intelligence, and reading single real words are impaired in many …

Dyslexia is a common disorder of reading and spelling which can negatively affect the
development and attainment of school-aged children, with deficits emerging in early …

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 …

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 …

Dyslexia, a specific reading disability, is a common (up to 10% of children) and highly
heritable (~ 70%) neurodevelopmental disorder. Behavioral and molecular genetic …

As a specific reading disability with a neurobiological origin, developmental dyslexia is
distinct from reading difficulties due to sensory impairments in vision or hearing. The …

There is a compelling body of evidence that developmental dyslexia runs in families and
seems to be highly inheritable. Several investigations during the last two decades have …

Abstract Four genes, DYX1C1, ROBO1, DCDC2 and KIAA0319 have been studied both
genetically and functionally as candidate genes for developmental dyslexia, a common …

Developmental Dyslexia (DD) is a complex, cognitive disorder which is characterised by an
impairment in reading despite adequate educational, motivational and intellectual …

Analysis of genetic linkage to dyslexia was performed using 133,165 array‐based SNPs
genotyped in 718 persons from 101 dyslexia‐affected families. Results showed five linkage …