Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …

Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …

Candidate genes have been identified for both reading and language, but most of the
heritable variance in these traits remains unexplained. Here, we report a genome‐wide …

Reading disabilities (RD) are the most common neurocognitive disorder, affecting 5% to
17% of children in North America. These children often have comorbid neurodevelopmental …

Dyslexia is a common pediatric disorder that affects 5–17% of schoolchildren in the United
States. It is marked by unexpected difficulties in fluent reading despite adequate intelligence …

Linkage studies have identified a locus on chromosome 3 as reading disabilities (RD) and
speech and sound disorder (SSD) susceptibility region, with both RD and SSD sharing …

Cytoplasmic assembly of ciliary dyneins, a process known as preassembly, requires
numerous non-dynein proteins, but the identities and functions of these proteins are not fully …

Although a genetic component is known to have an important role in the etiology of
developmental dyslexia (DD), we are far from understanding the molecular etiopathogenetic …

Developmental dyslexia (DD) is a neurodevelopmental condition with complex genetic
mechanisms. A number of candidate genes have been identified, some of which are linked …

Recent genome‐wide association scans (GWAS) for reading and language abilities have
pin‐pointed promising new candidate loci. However, the potential contributions of these loci …