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

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

BMC medical genetics - 22 Jul 2010

Tolosa Amparo, Sanjuán Julio, Dagnall Adam M, Moltó María D, Herrero Neus, de Frutos Rosa

Abstract excerpt

BACKGROUND: Schizophrenia is considered a language related human specific disease. Previous studies have reported evidence of positive selection for schizophrenia-associated genes specific to the human lineage. FOXP2 shows two important features as a convincing candidate gene for schizophrenia vulnerability: FOXP2 is the first gene related to a language disorder, and it has been subject to positive selection in...

Read the complete abstract on PubMed

Topics

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

Share to CpG Islands
Share to DNA Methylation
Share to Epigenesis, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forkhead Transcription Factors

Share to Hallucinations

Share to Language Disorders

Share to Psychiatric Status Rating Scales

Share to Schizophrenia

Source

Open in PubMed Open full text

Identifiers

PMID: 20649982
DOI: 10.1186/1471-2350-11-114
PMCID: PMC2918571

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.PMID 20649982Read ↗

Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.Semantic proximity Read ↗

FoxP2 and Schizophrenia: a systematic review.Semantic proximity Read ↗

FOXP2 polymorphisms in patients with schizophrenia.Semantic proximity Read ↗

FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population.Semantic proximity Read ↗

Association between FOXP2 gene and speech sound disorder in Chinese population.Semantic proximity Read ↗

FOXP2 contributes to the cognitive impairment in chronic patients with schizophreniaSemantic proximity Read ↗

Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients.Semantic proximity Read ↗

Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population.Semantic proximity Read ↗

No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population.Semantic proximity Read ↗

The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.Semantic proximity Read ↗

Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy population.Semantic proximity Read ↗

A functional genetic link between distinct developmental language disorders.Semantic proximity Read ↗

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