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19p13

A chromosome band present on 19p
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Epithelial ovarian cancer (EOC) is the leading cause of death from gynecological malignancy in the developed world, accounting… 
Highly Cited
2010
Highly Cited
2010
Germline BRCA1 mutations predispose to breast cancer. To identify genetic modifiers of this risk, we performed a genome-wide… 
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Highly Cited
2009
Highly Cited
2009
We conducted a genome-wide association study testing single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) for… 
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Highly Cited
2008
Highly Cited
2008
Blood concentrations of lipoproteins and lipids are heritable risk factors for cardiovascular disease. Using genome-wide… 
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Highly Cited
2003
Highly Cited
2003
Hypogonadotropic hypogonadism is defined as a deficiency of the pituitary secretion of follicle-stimulating hormone and… 
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Review
2003
Review
2003
Migraine — an episodic headache — affects more than 10% of the general population. Despite recent progress, drug therapy for… 
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Highly Cited
2003
Highly Cited
2003
Nat. Genet. 33, 208–213 (2003). After the authors returned corrected proofs, some changes to Figure 5 were mistakenly omitted… 
Highly Cited
2000
Highly Cited
2000
The chronic inflammatory bowel diseases (IBDs)-Crohn disease (CD) and ulcerative colitis (UC)-are idiopathic, inflammatory… 
Highly Cited
1996
Highly Cited
1996
Genes for familial hemiplegic migraine (FHM) and episodic ataxia type-2 (EA-2) have been mapped to chromosome 19p13. We… 
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Review
1995
Review
1995
The TNF receptor superfamily members are all type I membrane glycoproteins with typical homology in the extracellular domain of… 
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