FOXG1 gene

Known as: HFK1, FORKHEAD BOX G1B, HFK2 
This gene is involved in transcriptional repression and may play a role in the development of the brain and telencephalon.
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Autism spectrum disorder (ASD) is a disorder of brain development. Most cases lack a clear etiology or genetic basis, and the… (More)
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Review
2012
Review
2012
Rett syndrome is an X-linked neurodevelopmental disorder that manifests in early childhood with developmental stagnation, and… (More)
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2012
2012
Pyramidal cells of the cerebral cortex are born in the ventricular zone and migrate through the intermediate zone to enter into… (More)
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Submicroscopic deletions in 14q12 spanning FOXG1 or intragenic mutations have been reported in patients with a… (More)
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2011
2011
The transcription factor FoxG1 regulates neurogenesis in the embryonic telencephalon as well as a number of other… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND Rett syndrome is a severe neurodevelopmental disorder representing one of the most common genetic causes of mental… (More)
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2010
2010
BACKGROUND The FOXG1 gene has been recently implicated in the congenital form of Rett syndrome (RTT). It encodes the fork-head… (More)
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Highly Cited
2008
Highly Cited
2008
Vertebrate brain hosts a diverse collection of microRNAs, but little is known about their functions in vivo. Here we propose that… (More)
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2007
2007
Cajal-Retzius (CR) cells, the earliest-born neurons in the neocortex, arise from discrete sources within the telencephalon… (More)
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Highly Cited
1995
Highly Cited
1995
The Drosophila tailless gene is a member of the orphan nuclear receptor subfamily. In Drosophila, the tailless gene is required… (More)
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