Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Biological psychiatry - 1 Oct 2007

Luciano Michelle, Lind Penelope A, Duffy David L, Castles Anne, Wright Margaret J, Montgomery Grant W, Martin Nicholas G, Bates Timothy C

Abstract excerpt

BACKGROUND: KIAA0319 (6p22.2) has recently been implicated as a susceptibility gene for dyslexia. We aimed to find further support for this gene by examining its association with reading and spelling ability in adolescent twins and their siblings unselected for dyslexia. METHODS: Ten single nucleotide polymorphisms (SNPs) in or near the KIAA0319 gene were typed in 440 families with up to five offspring who had...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Data Interpretation, Statistical
Share to Dyslexia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nerve Tissue Proteins

Share to Neuropsychological Tests

Share to Phosphoric Diester Hydrolases

Share to Psychomotor Performance

Share to Reading

Source

Identifiers

PMID: 17597587
DOI: 10.1016/j.biopsych.2007.03.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability.PMID 17597587Read ↗

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

Assessment for familial pattern and association of polymorphisms in KIAA0319 gene with specific reading disorder in children from North India visiting a tertiary care centre: A case-control study.Semantic proximity Read ↗

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

A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children.Semantic proximity Read ↗

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.Semantic proximity Read ↗

The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.Semantic proximity Read ↗

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

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.Semantic 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 ↗

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

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

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

⌁Select a neighboring publication to make it the new centre.