2p21

A chromosome band present on 2p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2017
05101519872017

Papers overview

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Highly Cited
2011
Highly Cited
2011
Polycystic ovary syndrome (PCOS) is a common metabolic disorder in women. To identify causative genes, we conducted a genome-wide… (More)
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Highly Cited
2011
Highly Cited
2011
We conducted a two-stage genome-wide association study of renal cell carcinoma (RCC) in 3,772 affected individuals (cases) and 8… (More)
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Highly Cited
2009
Highly Cited
2009
Bone mineral density (BMD) is a heritable complex trait used in the clinical diagnosis of osteoporosis and the assessment of… (More)
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Highly Cited
2001
Highly Cited
2001
The molecular mechanisms regulating the amount of dietary cholesterol retained in the body, as well as the body's ability to… (More)
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Highly Cited
1998
Highly Cited
1998
We recently reported three truncating mutations of the cytochrome P4501B1 gene (CYP1B1) in five families with primary congenital… (More)
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1998
1998
Gingival fibromatosis is characterized by a slowly progressive benign enlargement of the oral gingival tissues. The condition… (More)
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Highly Cited
1998
Highly Cited
1998
1. Cholesterol management in high-risk patients without heart disease. When is lipid-lowering medication warranted for primary… (More)
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Highly Cited
1997
Highly Cited
1997
Primary congenital glaucoma (Buphthalmos) is an autosomal recessive eye disorder, postulated to result from developmental defects… (More)
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Highly Cited
1995
Highly Cited
1995
Primary congenital glaucoma (GLC3) is an inherited eye disorder that accounts for 0.01-0.04% of total blindness. Although a large… (More)
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1990
1990
Probes corresponding to human and porcine LH (luteinizing hormone) receptor cDNA were used for in situ hybridization to human… (More)
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