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Article

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

American journal of human genetics - 1 Apr 2005

Cope Natalie, Harold Denise, Hill Gary, Moskvina Valentina, Stevenson Jim, Holmans Peter, Owen Michael J, O'Donovan Michael C, Williams Julie

Abstract excerpt

Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of independent samples. Recent attempts to identify the gene responsible for the linkage have produced inconsistent evidence for association of DD with a number of genes in a 575-kb region of chromosome...

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Share to Adolescent
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Share to Chromosomes, Human, Pair 6

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 15717286
DOI: 10.1086/429131
PMCID: PMC1199296

Genes

DCDC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-15717286-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.PMID 15717286Read ↗

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

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.Semantic proximity Read ↗

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.Semantic proximity Read ↗

Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Semantic proximity Read ↗

Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia.Semantic proximity Read ↗

Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.Semantic proximity Read ↗

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability.Semantic proximity Read ↗

Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.Semantic proximity Read ↗

KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Semantic proximity Read ↗

The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities.Semantic proximity Read ↗

Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohortsSemantic proximity Read ↗

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Semantic proximity Read ↗

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