16q24.1

Part of the chromosome bands present on the long (q) arm of chromosome 16.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2017
0519932017

Papers overview

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2014
2014
Point mutations or genomic deletions of FOXF1 result in a lethal developmental lung disease Alveolar Capillary Dysplasia with… (More)
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Highly Cited
2012
Highly Cited
2012
Barrett's esophagus is an increasingly common disease that is strongly associated with reflux of stomach acid and usually a… (More)
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Highly Cited
2010
Highly Cited
2010
To identify new risk variants for chronic lymphocytic leukemia (CLL), we conducted a genome-wide association study of 299,983… (More)
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2010
2010
Disseminated superficial actinic porokeratosis (DSAP) is an uncommon autosomal dominant keratinization disorder with genetic… (More)
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2009
Highly Cited
2009
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, neonatally lethal developmental disorder… (More)
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Highly Cited
2007
Highly Cited
2007
We present a genome-wide association study of ileal Crohn disease and two independent replication studies that identify several… (More)
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2005
2005
OBJECTIVE To investigate the largely unknown genetic component of the common lipid disorder, familial combined hyperlipidemia… (More)
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2002
2002
We performed a genomewide scan for genes that predispose to low serum HDL cholesterol (HDL-C) in 25 well-defined Finnish families… (More)
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2000
2000
To identify the location of one or more putative tumor suppressor genes that may be involved in hepatocellular carcinoma (HCC… (More)
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1997
1997
Giant axonal neuropathy (GAN) is a rare autosomal recessive disorder described as a symmetrical distal neuropathy, with… (More)
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