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 distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.

Human genetics - 1 Nov 2012

Bacon Claire, Rappold Gudrun A

Abstract excerpt

Rare disruptions of FOXP2 have been strongly implicated in deficits in language development. Research over the past decade has suggested a role in the formation of underlying neural circuits required for speech. Until recently no evidence existed to suggest that the closely related FOXP1 gene played a role in neurodevelopmental processes. However, in the last few years, novel rare disruptions in FOXP1 have been...

Read the complete abstract on PubMed

Topics

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

Share to Cognition Disorders
Share to Forkhead Transcription Factors
Share to FOXP1 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to FOXP2 gene

Share to Phenotype

Share to Repressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 22736078
DOI: 10.1007/s00439-012-1193-z
PMCID: PMC3470686

Genes

FOXP1
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

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.PMID 22736078Read ↗

Unravelling neurogenetic networks implicated in developmental language disorders.Semantic proximity Read ↗

Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.Semantic proximity Read ↗

FOXP2 as a molecular window into speech and language.Semantic proximity Read ↗

FOXP1 mutations cause intellectual disability and a recognizable phenotype.Semantic proximity Read ↗

FOXP2 and the neuroanatomy of speech and language.Semantic proximity Read ↗

What can mice tell us about Foxp2 function?Semantic proximity Read ↗

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

Novel FOXP2 Variant Associated with Speech and Language Dysfunction in a Chinese Family and literature reviewSemantic proximity Read ↗

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.Semantic proximity Read ↗

Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting<i>FOXP2</i>Semantic proximity Read ↗

Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.Semantic proximity Read ↗

Insights into the genetic foundations of human communication.Semantic proximity Read ↗

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