FOXP2 gene

Known as: Forkhead Box P2 Gene, TRINUCLEOTIDE REPEAT-CONTAINING GENE 10, TNRC10 
This gene is involved in brain development.
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome characterized by impaired speech development and… (More)
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Highly Cited
2009
Highly Cited
2009
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been positively selected during… (More)
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Highly Cited
2007
Highly Cited
2007
The gene encoding the forkhead box transcription factor, FOXP2, is essential for developing the full articulatory power of human… (More)
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Highly Cited
2005
Highly Cited
2005
Neurobiology of speech and language has previously been studied in the KE family, in which half of the members have severe… (More)
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Review
2005
Review
2005
That speech and language are innate capacities of the human brain has long been widely accepted, but only recently has an entry… (More)
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Highly Cited
2004
Highly Cited
2004
Most vertebrates communicate acoustically, but few, among them humans, dolphins and whales, bats, and three orders of birds… (More)
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Highly Cited
2003
Highly Cited
2003
Foxp2 and Foxp1 are recently identified members of the Fox family of winged-helix/forkhead transcription factor genes. A recent… (More)
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Highly Cited
2003
Highly Cited
2003
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe developmental disorder of verbal… (More)
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Highly Cited
2002
Highly Cited
2002
Language is a uniquely human trait likely to have been a prerequisite for the development of human culture. The ability to… (More)
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Highly Cited
2001
Highly Cited
2001
Individuals affected with developmental disorders of speech and language have substantial difficulty acquiring expressive and/or… (More)
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