Rett Syndrome

Known as: disorder retts, Rett Syndrome [Disease/Finding], Rett's Disorder 
An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The… (More)

Topic mentions per year

Topic mentions per year

1960-2017
010020019602017

Papers overview

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Highly Cited
2010
Highly Cited
2010
Autism spectrum disorders (ASD) are complex neurodevelopmental diseases in which different combinations of genetic mutations may… (More)
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Highly Cited
2010
Highly Cited
2010
Mutations in the X-linked MECP2 gene, which encodes the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), cause… (More)
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Highly Cited
2010
Highly Cited
2010
OBJECTIVE Rett syndrome (RTT) is a severe neurodevelopmental disease that affects approximately 1 in 10,000 live female births… (More)
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Highly Cited
2007
Highly Cited
2007
Rett syndrome is an autism spectrum disorder caused by mosaic expression of mutant copies of the X-linked MECP2 gene in neurons… (More)
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Highly Cited
2005
Highly Cited
2005
Mutations in MECP2 are associated with Rett syndrome, an X-linked neurodevelopmental disorder. To identify genes targeted by… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in the methyl-CpG binding protein 2 (MECP2) gene cause Rett syndrome (RTT), a neurodevelopmental disorder characterized… (More)
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Highly Cited
2001
Highly Cited
2001
Rett syndrome (RTT) is an inherited neurodevelopmental disorder of females that occurs once in 10,000–15,000 births. Affected… (More)
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Highly Cited
2001
Highly Cited
2001
Mecp2 is an X-linked gene encoding a nuclear protein that binds specifically to methylated DNA (ref. 1) and functions as a… (More)
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Highly Cited
1999
Highly Cited
1999
Rett syndrome (RTT, MIM 312750) is a progressive neurodevelopmental disorder and one of the most common causes of mental… (More)
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Highly Cited
1995
Highly Cited
1995
Rett syndrome, the commonest condition associated with severe mental retardation in girls, is diagnosed only by its clinical… (More)
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