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19p13.1

A chromosome band present on 19p
National Institutes of Health

Related topics

Related topics

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

Semantic Scholar uses AI to extract papers important to this topic.
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
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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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
2008
Review
2008
Demystified molecular pathology of NUT midline carcinomas
  • C. French
  • Journal of Clinical Pathology
  • 2008
    • Corpus ID: 2200842
NUT midline carcinoma (NMC) is a rare, highly lethal cancer that occurs in children and adults of all ages. NMCs uniformly… Expand
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
Highly Cited
2000
Highly Cited
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
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
1997
Highly Cited
1997
A new locus for hemiplegic migraine maps to chromosome 1q31
A single familial hemiplegic migraine locus has been previously mapped to 19p13.1 and associated with mutations in a calcium… 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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