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15q14

A chromosome band present on 15q
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
We performed a genome-wide association study of non-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias… Expand
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Highly Cited
2013
Highly Cited
2013
We have conducted a genotyping study using a custom Illumina Infinium HD genotyping array, the ImmunoChip, in a new UK sample of… Expand
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Highly Cited
2012
Highly Cited
2012
Myopia is a complex genetic disorder and a common cause of visual impairment among working age adults. Genome-wide association… Expand
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Highly Cited
2011
Highly Cited
2011
Cancer cell molecular mimicry of stem cells (SC) imbues neoplastic cells with enhanced proliferative and renewal capacities. In… Expand
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Highly Cited
2010
Highly Cited
2010
Refractive errors are the most common ocular disorders worldwide and may lead to blindness. Although this trait is highly… Expand
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Highly Cited
2009
Highly Cited
2009
NUT midline carcinoma (NMC) is a uniformly lethal malignancy that is defined by rearrangement of the nuclear protein in testis… Expand
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Review
2008
Review
2008
NUT midline carcinoma (NMC) is a rare, highly lethal cancer that occurs in children and adults of all ages. NMCs uniformly… Expand
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Highly Cited
2002
Highly Cited
2002
BACKGROUND The alpha7 neuronal nicotinic acetylcholine receptor subunit gene (CHRNA7) has been implicated as a candidate gene for… Expand
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Highly Cited
2002
Highly Cited
2002
The CHST14 gene, localized at 15q14, is a single exon gene with an open reading frame of 1131 base pairs, encoding a 43 kDa… Expand
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Highly Cited
1999
Highly Cited
1999
The K+-Cl−cotransporters (KCCs) belong to the gene family of electroneutral cation-chloride cotransporters, which also includes… Expand
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