FMR1 gene

Known as: FRAXA, fragile X mental retardation 1, FRAGILE X MENTAL RETARDATION PROTEIN 
This gene may be involved in the regulation of mRNA trafficking.
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism in males and premature… (More)
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Highly Cited
2011
Highly Cited
2011
Fragile X syndrome (FXS) is an X-linked condition associated with intellectual disability and behavioral problems. It is caused… (More)
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Highly Cited
2011
Highly Cited
2011
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In addition to cognitive deficits, FXS… (More)
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Highly Cited
2007
Highly Cited
2007
Expansion of the polymorphic CGG repeats within the 5'-UTR of the FMR1 gene is associated with variable transcriptional… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Women who carry the FMR1 premutation allele have a significantly increased risk for ovarian dysfunction. We… (More)
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Highly Cited
2001
Highly Cited
2001
The 5' untranslated CGG repeat in the fragile X mental retardation-1 (FMR1) gene is expanded in families with fragile X syndrome… (More)
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Highly Cited
1999
Highly Cited
1999
Most fragile X syndrome patients have expansion of a (CGG)(n)sequence with >200 repeats (full mutation) in the FMR1 gene… (More)
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Highly Cited
1999
Highly Cited
1999
Mutation of FMR1 results in fragile X mental retardation. The most common FMR1 mutation is expansion of a CGG repeat tract at the… (More)
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Highly Cited
1993
Highly Cited
1993
Fragile X syndrome is the result of transcriptional suppression of the gene FMR1 as a result of a trinucleotide repeat expansion… (More)
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Highly Cited
1993
Highly Cited
1993
Fragile X syndrome is one of the most common human genetic diseases and the most common cause of hereditary mental retardation… (More)
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