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

The role of gene DCDC2 in German dyslexics.

Annals of dyslexia - 1 Jun 2009

Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P

Abstract excerpt

Dyslexia is a complex reading and writing disorder with a strong genetic component. In a German case-control cohort, we studied the influence of the suspected dyslexia-associated gene DCDC2. For the first time in a German cohort, we describe association of a 2445 basepair deletion, first identifi...

Read the complete abstract on PubMed

Topics

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

Share to Germany
Share to Case-Control Studies
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dyslexia

Share to Microtubule-Associated Proteins

Share to Odds Ratio

Share to Polymerase Chain Reaction

Share to Severity of Illness Index

Source

Identifiers

PMID: 19238550
DOI: 10.1007/s11881-008-0020-7

Genes

DCDC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19238550-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of gene DCDC2 in German dyslexics.PMID 19238550Read ↗

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Semantic proximity Read ↗

Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia.Semantic proximity Read ↗

Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort.Semantic proximity Read ↗

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.Semantic proximity Read ↗

DCDC2 genetic variants and susceptibility to developmental dyslexia.Semantic proximity Read ↗

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

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

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

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

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

Association of polymorphisms in the DCDC2 gene with developmental dyslexia in the Han Chinese.Semantic proximity Read ↗

Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population.Semantic proximity Read ↗

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