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19p13.1

A chromosome band present on 19p
National Institutes of Health

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9 relations
BRD4 wt AlleleChromosome 19 Short ArmChromosomesELL wt Allele
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Papers overview

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2016
2016
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus
A locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. Here we analyse 438 SNPs in this region in… Expand
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Review
2013
Review
2013
Genetic susceptibility to triple-negative breast cancer.
Triple-negative breast cancers (TNBC), defined by the absence of estrogen receptor, progesterone receptor, and HER-2 expression… Expand
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Highly Cited
2012
Highly Cited
2012
19p13.1 is a triple-negative-specific breast cancer susceptibility locus.
The 19p13.1 breast cancer susceptibility locus is a modifier of breast cancer risk in BRCA1 mutation carriers and is also… Expand
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2012
2012
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
BACKGROUND Genome-wide association studies (GWAS) identified variants at 19p13.1 and ZNF365 (10q21.2) as risk factors for breast… Expand
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Highly Cited
2011
Highly Cited
2011
Common breast cancer susceptibility loci are associated with triple-negative breast cancer.
Triple-negative breast cancers are an aggressive subtype of breast cancer with poor survival, but there remains little known… Expand
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Review
2010
Review
2010
Demystified molecular pathology of NUT midline carcinomas.
NUT midline carcinoma (NMC) is a rare, highly lethal cancer that occurs in children and adults of all ages. NMCs uniformly… Expand
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Highly Cited
2003
Highly Cited
2003
A major non-HLA locus in celiac disease maps to chromosome 19.
BACKGROUND AND AIMS The pathogenesis of celiac disease is still unknown despite its well-known association with human leukocyte… Expand
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2000
2000
Human EMR2, a novel EGF-TM7 molecule on chromosome 19p13.1, is closely related to CD97.
The epidermal growth factor (EGF)-TM7 proteins [EMR1, (EGF-like molecule containing mucin-like hormone receptor 1) F4/80, and… Expand
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Highly Cited
1997
Highly Cited
1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in…
Autosomal dominant cerebellar ataxia is a group of clinically and genetically heterogeneous disorders. We carried out genomewide… Expand
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Highly Cited
1995
Highly Cited
1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene
Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED) are dominantly inherited chondrodysplasias characterized by… Expand
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