Eleven loci with prior evidence for association with reading and language phenotypes were
sequenced in 96 unrelated subjects with significant impairment in reading performance …

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

Genetic factors contribute substantially to the development of reading disability (RD). Family
linkage studies have implicated many chromosomal regions containing RD susceptibility …

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

A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or
reading disabilities (RD) in three independent samples. In the current study, we investigated …

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

DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a
previously identified peak of association with single nucleotide polymorphism markers, we …

Reading disability (RD) is a complex genetic disorder with unknown etiology. Genes on
chromosome 6p22, including DCDC2, KIAA0319, and TTRAP, have been identified as RD …

Reading disability (RD) and language impairment (LI) are common neurodevelopmental
disorders with moderately strong genetic components and lifelong implications. RD and LI …

The status of DYX1C1 (C15q21. 3) as a susceptibility gene for dyslexia is unclear. We report
the association of this gene with reading and spelling ability in a sample of adolescent twins …