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

DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.

The Journal of neuroscience : the official journal of the Society for Neuroscience - 22 Oct 2014

Darki Fahimeh, Peyrard-Janvid Myriam, Matsson Hans, Kere Juha, Klingberg Torkel

Abstract excerpt

Three genes, DYX1C1, DCDC2, and KIAA0319, have been previously associated with dyslexia, neuronal migration, and ciliary function. Three polymorphisms within these genes, rs3743204 (DYX1C1), rs793842 (DCDC2), and rs6935076 (KIAA0319) have also been linked to normal variability of left temporoparietal white matter volume connecting the middle temporal cortex to the angular and supramarginal gyri. Here, we assessed...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Adolescent Development
Share to Child
Share to Child Development
Share to Microtubule-Associated Proteins
Share to Parietal Lobe
Share to Temporal Lobe
Share to White Matter
Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 25339756
DOI: 10.1523/JNEUROSCI.1216-14.2014
PMCID: PMC6608392

Genes

DCDC2

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

DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.PMID 25339756Read ↗

Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.Semantic proximity Read ↗

Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.Semantic proximity Read ↗

Progress towards a cellular neurobiology of reading disability.Semantic proximity Read ↗

DCDC2 is associated with reading disability and modulates neuronal development in the brain.Semantic proximity Read ↗

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

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.Semantic proximity Read ↗

The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects.Semantic proximity Read ↗

Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.Semantic proximity Read ↗

Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population.Semantic proximity Read ↗

Genes, cognition and dyslexia: learning to read the genome.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 ↗

Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.Semantic proximity Read ↗

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