Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
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Mechanisms of ectopic calcification: implications for diabetic vasculopathyCurrent Applications of Genetic Risk Scores to Cardiovascular Outcomes and Subclinical PhenotypesGenetics of coronary artery diseaseGenome-wide association studies of late-onset cardiovascular diseaseGenetic Research and Women's Heart Disease: a PrimerSortilin, encoded by the cardiovascular risk gene SORT1, and its suggested functions in cardiovascular diseaseSortilin mediates vascular calcification via its recruitment into extracellular vesiclesPopulation ancestry and genetic risk for diabetes and kidney, cardiovascular, and bone disease: modifiable environmental factors may produce the curesGenetics of coronary artery calcification among African Americans, a meta-analysis.Genome-wide association study of subclinical interstitial lung disease in MESA.Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation.Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineAssociation of COL4A1 genetic polymorphisms with coronary artery disease in Uygur population in Xinjiang, China.Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.Vascular Calcification: Current Genetics Underlying This Complex Phenomenon.Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohorts.Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study.Towards a molecular systems model of coronary artery diseaseCDKN2B Methylation and Aortic Arch Calcification in Patients with Ischemic StrokeWhole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.Integrative DNA, RNA, and protein evidence connects TREML4 to coronary artery calcificationPolymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarctionThe relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3.Cardiac symptoms before sudden cardiac death caused by coronary artery disease: a nationwide study among young Danish people.Apolipoprotein C3 genetic polymorphisms are associated with lipids and coronary artery disease in a Chinese population.Genetic and environmental risk factors for atherosclerosis regulate transcription of phosphatase and actin regulating gene PHACTR1.Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.Single nucleotide polymorphisms within LIPA (Lysosomal Acid Lipase A) gene are associated with susceptibility to premature coronary artery disease. a replication in the genetic of atherosclerotic disease (GEA) Mexican study.Genome-wide association study of gene by smoking interactions in coronary artery calcification.HDL-3 is a superior predictor of carotid artery disease in a case-control cohort of 1725 participants.A variant in the osteoprotegerin gene is associated with coronary atherosclerosis in patients with rheumatoid arthritis: results from a candidate gene studyThe 9p21 locus is associated with coronary artery disease and cardiovascular events in the presence (but not in the absence) of coronary calcificationRelationship between CYP17A1 genetic polymorphism and coronary artery disease in a Chinese Han population.Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding.Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study.The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region.
P2860
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P2860
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Genome-wide association study ...... w-up in myocardial infarction.
@ast
Genome-wide association study ...... w-up in myocardial infarction.
@en
type
label
Genome-wide association study ...... w-up in myocardial infarction.
@ast
Genome-wide association study ...... w-up in myocardial infarction.
@en
prefLabel
Genome-wide association study ...... w-up in myocardial infarction.
@ast
Genome-wide association study ...... w-up in myocardial infarction.
@en
P2093
P2860
P50
P1433
P1476
Genome-wide association study ...... w-up in myocardial infarction.
@en
P2093
Aad van der Lugt
Aldi T Kraja
Andrew D Johnson
Arne Schillert
CARDIoGRAM Consortium
Caroline S Fox
Charles C White
Christopher J O'Donnell
David M Herrington
Gabriel P Krestin
P2860
P304
P356
10.1161/CIRCULATIONAHA.110.974899
P407
P50
P577
2011-12-05T00:00:00Z