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Article

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Jun 2007

Brkanac Zoran, Chapman Nicola H, Matsushita Mark M, Chun Lani, Nielsen Kathleen, Cochrane Elizabeth, Berninger Virginia W, Wijsman Ellen M, Raskind Wendy H

Abstract excerpt

Dyslexia is a common heterogeneous disorder with a significant genetic component. Multiple studies have replicated the evidence for linkage between variously defined phenotypes of dyslexia and chromosomal regions on 15q21 (DYX1) and 6p22.2 (DYX2). Based on association studies and the possibility for functional significance of several polymorphisms, candidate genes responsible for the observed linkage signal have...

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Identifiers

PMID: 17450541
DOI: 10.1002/ajmg.b.30471

Genes

DCDC2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.PMID 17450541Read ↗

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A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.Semantic proximity Read ↗

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Semantic proximity Read ↗

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.Semantic proximity Read ↗

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.Semantic proximity Read ↗

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.Semantic proximity Read ↗

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