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19p13
A chromosome band present on 19p
National Institutes of Health
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Related topics
Related topics
6 relations
CD209 wt Allele
CDKN2D wt Allele
Chromosome 19 Short Arm
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
D. Ellinghaus
,
E. Ellinghaus
,
+27 authors
A. Franke
American Journal of Human Genetics
2012
Corpus ID: 6664557
Highly Cited
2010
Highly Cited
2010
Common variants at 19p13 are associated with susceptibility to ovarian cancer
K. Bolton
,
J. Tyrer
,
+113 authors
S. Gayther
Nature Genetics
2010
Corpus ID: 13000712
Epithelial ovarian cancer (EOC) is the leading cause of death from gynecological malignancy in the developed world, accounting…
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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
A. Antoniou
,
Xianshu Wang
,
+175 authors
F. Couch
Nature Genetics
2010
Corpus ID: 2027492
Germline BRCA1 mutations predispose to breast cancer. To identify genetic modifiers of this risk, we performed a genome-wide…
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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
S. Kathiresan
,
B. Voight
,
+123 authors
D. Siscovick
Nature Genetics
2009
Corpus ID: 11170944
We conducted a genome-wide association study testing single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) for…
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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
S. Kathiresan
,
O. Melander
,
+23 authors
M. Orho-Melander
Nature Genetics
2008
Corpus ID: 205357246
Blood concentrations of lipoproteins and lipids are heritable risk factors for cardiovascular disease. Using genome-wide…
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Highly Cited
2003
Highly Cited
2003
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
N. de Roux
,
E. Génin
,
J. Carel
,
F. Matsuda
,
J. Chaussain
,
E. Milgrom
Proceedings of the National Academy of Sciences…
2003
Corpus ID: 22904571
Hypogonadotropic hypogonadism is defined as a deficiency of the pituitary secretion of follicle-stimulating hormone and…
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Review
2003
Review
2003
Neurological diseases: Neurobiology of migraine
D. Pietrobon
,
J. Striessnig
Nature Reviews Neuroscience
2003
Corpus ID: 5698886
Migraine — an episodic headache — affects more than 10% of the general population. Despite recent progress, drug therapy for…
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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
R. Ophoff
,
G. Terwindt
,
+13 authors
R. Frants
Cell
1996
Corpus ID: 16840573
Highly Cited
1993
Highly Cited
1993
Molecular and biological characterization of a ligand for CD27 defines a new family of cytokines with homology to tumor necrosis factor
R. Goodwin
,
M. Alderson
,
+15 authors
M. Beckmann
Cell
1993
Corpus ID: 9587823
Highly Cited
1989
Highly Cited
1989
lyl-1, a novel gene altered by chromosomal translocation in T cell leukemia, codes for a protein with a helix-loop-helix DNA binding motif
J. Mellentin
,
Stephen D. Smith
,
M. Cleary
Cell
1989
Corpus ID: 24737263
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