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

Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.

Behavior genetics - 1 Jan 2011

Marino Cecilia, Mascheretti Sara, Riva Valentina, Cattaneo Francesca, Rigoletto Catia, Rusconi Marianna, Gruen Jeffrey R, Giorda Roberto, Lazazzera Claudio, Molteni Massimo

Abstract excerpt

Converging evidence indicates that developmental problems in oral language and mathematics can predate or co-occur with developmental dyslexia (DD). Substantial genetic correlations have been found between language, mathematics and reading traits, independent of the method of sampling. We tested...

Read the complete abstract on PubMed

Topics

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

Share to Dyslexia
Share to Genetic Pleiotropy
Share to Language Development Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Learning Disabilities

Share to Linkage Disequilibrium

Share to Mathematics

Share to Neuropsychological Tests

Share to Nuclear Family

Source

Open in PubMed Open full text

Identifiers

PMID: 21046216
DOI: 10.1007/s10519-010-9412-7
PMCID: PMC3939676

Genes

DCDC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21046216-2026-09-02.2. 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

Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.PMID 21046216Read ↗

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

KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.Semantic proximity Read ↗

An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.Semantic proximity Read ↗

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

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

Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population.Semantic proximity Read ↗

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Semantic proximity Read ↗

The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.Semantic proximity Read ↗

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.Semantic proximity Read ↗

Developmental dyscalculia is a familial learning disability.Semantic proximity Read ↗

Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample.Semantic proximity Read ↗

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

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