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19p13

A chromosome band present on 19p
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
2010
Highly Cited
2010
Epithelial ovarian cancer (EOC) is the leading cause of death from gynecological malignancy in the developed world, accounting… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
2000
Highly Cited
2000
The chronic inflammatory bowel diseases (IBDs)-Crohn disease (CD) and ulcerative colitis (UC)-are idiopathic, inflammatory… Expand
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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… Expand
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