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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Papers overview

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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… (More)
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Highly Cited
2011
Highly Cited
2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
Exome sequencing is a powerful tool for discovery of the Mendelian disease genes. Previously, we reported a novel locus for… (More)
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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… (More)
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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… (More)
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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… (More)
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2006
2006
Idiopathic scoliosis: identification of candidate regions on chromosome 19p13.
STUDY DESIGN We performed genomic screening, statistical linkage analysis, and fine mapping of 202 families with at least 2… (More)
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Highly Cited
2005
Highly Cited
2005
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.
CONTEXT Traditionally, the search for genes involved in predisposition to major psychoses has proceeded with separate studies of… (More)
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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… (More)
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Highly Cited
2000
Highly Cited
2000
DC-SIGN; a related gene, DC-SIGNR; and CD23 form a cluster on 19p13.
DC-SIGN is a C-type lectin, expressed on a dendritic cell subset. It is able to bind ICAM3 and HIV gp120 in a calcium-dependent… (More)
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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… (More)
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