Dyslexia is a common heterogeneous disorder with a significant genetic component.
Multiple studies have replicated the evidence for linkage between variously defined …

We applied a family-based association approach to investigate the role of the DYX1C1 gene
on chromosome 15q as a candidate gene for developmental dyslexia (DD) to 158 families …

Objective Dyslexia-susceptibility-1-candidate-1 (DYX1C1) was the first gene associated with
dyslexia. Since the original report of 2003, eight replication attempts have been published …

Reading disabilities (RD) have a significant genetic basis and have shown linkage to
multiple regions including chromosome 15q. Dyslexia susceptibility 1 candidate gene 1 …

Dyslexia is a common, complex disorder, which is thought to have a genetic component.
There have been numerous reports of linkage to several regions of the genome for dyslexia …

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 …

A substantial genetic contribution in the etiology of developmental dyslexia (DD) has been
well documented with independent groups reporting a susceptibility locus on chromosome …

The DYX2 locus on chromosome 6p22. 2 is the most replicated region of linkage to
developmental dyslexia (DD). Two candidate genes within this region have recently been …

Abstract DYX1C1 and KIAA0319 have been two of the most extensively studied candidate
genes for dyslexia given their important roles in the neuronal migration and neurite growth …

Developmental dyslexia, or reading disability, is a multigenic complex disease for which at
least five loci, ie DYX1–3 and DYX5–6, have been clearly identified from the human …