Abstract. Autism spectrum disorders (ASD) is a neurodevelopmental disease with complex genetics; however, the genes that are responsible for this disease still remain mostly unknown. Here, we focus on the FOXP family of transcription factors as there is emerging evidence strongly linking these genes to ASD and other genes implicated in ASD. The FOXP family of genes includes three genes expressed in the central nervous system: FOXP1, FOPX2, and FOXP4. This unique group of transcription factors has known functions in brain development as well as the evolution of language. We will also discuss the other genes including transcriptional targets of FOXP genes that have been found to be associated with language and may be important in the pathophy...
The ability to use language is a uniquely human trait involving one of the most complex and poorly u...
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with deficits in social ...
The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech a...
Autism spectrum disorders (ASD) comprise a range of neurodevelopmental syndromes characterized by ex...
Background: Comparative gene expression profiling analysis is useful in discovering differentially e...
Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to c...
The gene encoding the fork-head box p2 (FOXP2) transcription factor is commonly understood to be a p...
Autism Spectrum Disorder (ASD) is a heterogeneous disorder that is often accompanied with many co-mo...
BACKGROUND: Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and lan...
Heterozygous variants disrupting the FOXP1 transcription factor (forkhead box protein P1; OMIM 60551...
ASD is as a pervasive neurodevelopmental disorder defined by impairments in social functioning and r...
Several genomewide screens indicated that chromosome 7q was linked to autistic disorder. FOXP2, loca...
De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause o...
Intellectual disability (ID) is a neurodevelopmental disorder manifesting in children before the age...
BACKGROUND: Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and lan...
The ability to use language is a uniquely human trait involving one of the most complex and poorly u...
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with deficits in social ...
The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech a...
Autism spectrum disorders (ASD) comprise a range of neurodevelopmental syndromes characterized by ex...
Background: Comparative gene expression profiling analysis is useful in discovering differentially e...
Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to c...
The gene encoding the fork-head box p2 (FOXP2) transcription factor is commonly understood to be a p...
Autism Spectrum Disorder (ASD) is a heterogeneous disorder that is often accompanied with many co-mo...
BACKGROUND: Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and lan...
Heterozygous variants disrupting the FOXP1 transcription factor (forkhead box protein P1; OMIM 60551...
ASD is as a pervasive neurodevelopmental disorder defined by impairments in social functioning and r...
Several genomewide screens indicated that chromosome 7q was linked to autistic disorder. FOXP2, loca...
De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause o...
Intellectual disability (ID) is a neurodevelopmental disorder manifesting in children before the age...
BACKGROUND: Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and lan...
The ability to use language is a uniquely human trait involving one of the most complex and poorly u...
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with deficits in social ...
The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech a...