Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
|
19198611 |
2009 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
We found 1 SNP that was associated with severe CAD: LPA I4399M (rs3798220).
|
17569884 |
2007 |
Coronary Artery Disease
|
0.500 |
AlteredExpression
|
disease |
LHGDN |
Circulating transforming growth factor-beta1, lipoprotein(a) and cellular adhesion molecules in angiographically assessed coronary artery disease.
|
12940514 |
2003 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
Association between lipoprotein(a) levels, apo(a) isoforms and family history of premature CAD in young Asian Indians.
|
18280807 |
2008 |
Coronary Artery Disease
|
0.500 |
AlteredExpression
|
disease |
LHGDN |
Plasma lipoprotein (a) levels are significantly elevated in patients with coronary artery disease as compared to controls.
|
11999088 |
2002 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association study on lipoprotein (a) levels and coronary artery disease severity in a Chinese population.
|
31186284 |
2019 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
|
30104761 |
2018 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.
|
30003307 |
2018 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
|
28714975 |
2017 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.
|
28714974 |
2017 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
CTD_human |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
21378990 |
2011 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
CTD_human |
A variant in LPA was consistent with a family history of coronary artery disease.
|
20435227 |
2010 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Elevated lipoprotein(a) [Lp(a)] is an independent risk factor for coronary artery disease (CAD).
|
30234895 |
2019 |
Coronary Artery Disease
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
However, clinical impacts of lipoprotein(a) levels on adverse vascular events in patients with established coronary artery disease who are undergoing statin treatment have not been fully elucidated.
|
31577620 |
2019 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Pro-inflammatory interleukin-1 genotypes potentiate the risk of coronary artery disease and cardiovascular events mediated by oxidized phospholipids and lipoprotein(a).
|
24530664 |
2014 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Elevated levels of lipoprotein(a) [Lp(a)] and the presence of small isoforms of apolipoprotein(a) [apo(a)] have been associated with coronary artery disease (CAD) in whites but not in African Americans.
|
11116062 |
2000 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Lipoprotein (a) (Lp(a)), a well-established risk factor for coronary artery diseases (CAD), would also be anticipated to be associated in a similar manner with risk of type 2 diabetes mellitus (T2DM) based on the common soil hypothesis of etiology of T2DM and CAD.
|
28132096 |
2017 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Proprotein subtilisin kexin type 9 (PCSK9) and lipoprotein (a) [Lp(a)] levels are causative risk factors for coronary heart disease.
|
29103916 |
2019 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
We examined the effects of family history of coronary artery disease (CAD), apolipoprotein E (apo E) phenotype, and lipoprotein(a) [Lp(a)] on the response of plasma lipids to change in dietary lipid intake after 3 mo of nutrition education in 125 children aged 4-10 y.
|
9356540 |
1997 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Lipoprotein(a) and Cardiovascular Outcomes in Patients With Coronary Artery Disease and Prediabetes or Diabetes.
|
31076417 |
2019 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Serum lipoprotein (a) concentrations (Lp(a)) are largely under genetic control, and are strong predictors of coronary heart disease.
|
8800499 |
1996 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We for the first time explored the association of the four SNPs in the SLC22A3-LPAL2-LPA gene cluster with CAD in a large Chinese Han sample.
|
23036009 |
2012 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The variant allele of rs3798220 in the apolipoprotein(a) gene (LPA) is used to assess the risk for coronary artery disease (CAD) in Europeans, where it is associated with short alleles of the Kringle IV-2 (KIV-2) copy number variation (CNV) and high lipoprotein(a) (Lp(a)) concentrations.
|
26302166 |
2015 |