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19p13

A chromosome band present on 19p
National Institutes of Health

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6 relations
CD209 wt AlleleCDKN2D wt AlleleChromosome 19 Short ArmChromosomes
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Highly Cited
2013
Highly Cited
2013
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
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
Common variants at 19p13 are associated with susceptibility to ovarian cancer
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
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population
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
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
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
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
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 due to loss of function of the KiSS1-derived peptide receptor GPR54
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
Neurological diseases: Neurobiology of migraine
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
t(11;19)(q21;p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway
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
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.
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
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
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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