MAGEL2 gene

Known as: nM15, NDNL1, MAGEL2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2017
02419992017

Papers overview

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2015
2015
BACKGROUND Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of MAGEL2 is also associated with… (More)
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2014
2014
Letter to the Editor Although it has long been known that Prader-Willi syndrome (PWS) is caused by the loss of function of… (More)
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2011
2011
Hypothalamic dysfunction may underlie endocrine abnormalities in Prader-Willi syndrome (PWS), a genetic disorder that features GH… (More)
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2010
2010
The onset of feeding at birth is a vital step for the adaptation of the neonate to extra uterine life. Prader-Willi syndrome (PWS… (More)
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2009
2009
BACKGROUND MAGEL2 is one of several genes typically inactivated in the developmental obesity disorder Prader-Willi syndrome (PWS… (More)
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2009
2009
The Prader–Willi syndrome (PWS) is caused by a 5–6 Mbp de novo deletion on the paternal chromosome 15, maternal uniparental… (More)
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2009
2009
Magel2 belongs to the MAGE/necdin family of proteins, which have roles in cell cycle, differentiation, and apoptosis. The Magel2… (More)
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Highly Cited
2001
Highly Cited
2001
The imprinted domain on human chromosome 15 consists of two oppositely imprinted gene clusters, which are under the coordinated… (More)
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2000
2000
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13. Affected individuals… (More)
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Highly Cited
1999
Highly Cited
1999
Prader-Willi syndrome (PWS) is a complex neurogenetic disorder. The phenotype is likely to be a contiguous gene syndrome… (More)
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