Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on curation of immunofluorescence data

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Automatic assignment of GO terms using logical inference, based on on inter-ontology links

Gene Ontology annotation of human sequence-specific DNA binding transcription factors (DbTFs) based on the TFClass database

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

MRI analysis of an inherited speech and language disorder: structural brain abnormalities.

Structure of the forkhead domain of FOXP2 bound to DNA.

A functional genetic link between distinct developmental language disorders.

Human-specific transcriptional regulation of CNS development genes by FOXP2.

Protein interactome reveals converging molecular pathways among autism disorders.

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.

Transcriptional regulation by FOXP1, FOXP2, and FOXP4 dimerization.

A proteome-scale map of the human interactome network.

Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes.

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Pooled-matrix protein interaction screens using Barcode Fusion Genetics.

A reference map of the human binary protein interactome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

FOXP2: novel exons, splice variants, and CAG repeat length stability.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

FoxP2 regulates neurogenesis during embryonic cortical development.

Chromatin Decondensation by FOXP2 Promotes Human Neuron Maturation and Expression of Neurodevelopmental Disease Genes.

FOXP2 exhibits projection neuron class specific expression, but is not required for multiple aspects of cortical histogenesis.

Foxp2 and Foxp1 cooperatively regulate lung and esophagus development.

Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.