17q21

A chromosome band present on 17q
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
A sequence variant (rs7216389-T) near the ORMDL3 gene on chromosome 17q21 was recently found to be associated with childhood… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND A genomewide association study has shown an association between variants at chromosome 17q21 and an increased risk of… (More)
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Highly Cited
2007
Highly Cited
2007
Asthma is caused by a combination of poorly understood genetic and environmental factors. We have systematically mapped the… (More)
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Highly Cited
2006
Highly Cited
2006
Frontotemporal dementia (FTD) with ubiquitin-immunoreactive neuronal inclusions (both cytoplasmic and nuclear) of unknown nature… (More)
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Highly Cited
2006
Highly Cited
2006
Frontotemporal dementia (FTD) is the second most common cause of dementia in people under the age of 65 years. A large proportion… (More)
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Highly Cited
2005
Highly Cited
2005
Autism is a heritable but genetically complex disorder characterized by deficits in language and in reciprocal social… (More)
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Highly Cited
2001
Highly Cited
2001
Hereditary frontotemporal dementia (FTD) is an autosomal dominant neurodegenerative disorder that is associated with mutations in… (More)
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Highly Cited
1999
Highly Cited
1999
The beclin 1 (BECN1) gene encodes a 60-kDa coiled-coil protein that interacts with the prototypic apoptosis inhibitor Bcl-2… (More)
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Highly Cited
1994
Highly Cited
1994
Disinhibition-dementia-parkinsonism-amyotrophy complex (DDPAC) is defined by familial adult-onset behavioral disturbance… (More)
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Highly Cited
1990
Highly Cited
1990
Human breast cancer is usually caused by genetic alterations of somatic cells of the breast, but occasionally, susceptibility to… (More)
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