Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.
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Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serumLoci influencing lipid levels and coronary heart disease risk in 16 European population cohortsAn optimized procedure for the design and evaluation of Ecotilling assays.Association of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations.Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip.Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.Combining genome-wide data from humans and animal models of dyslipidemia and atherosclerosis.The genetics of obesity and the metabolic syndrome.Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) studyGenetic causes of high and low serum HDL-cholesterol.Pleiotropic genes for metabolic syndrome and inflammationMining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterolAssociation of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian populationA multiethnic replication study of plasma lipoprotein levels-associated SNPs identified in recent GWAS.Association of endothelial lipase genetic polymorphism with lacunar infarction in a Chinese populationOn the analysis of a repeated measure design in genome-wide association analysis.Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population.Genome-wide association study of metabolic syndrome in koreans.Implications of discoveries from genome-wide association studies in current cardiovascular practice.Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American familiesEvaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk.Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.Sex-specific association of rs16996148 SNP in the NCAN/CILP2/PBX4 and serum lipid levels in the Mulao and Han populationsRelation of lipid gene scores to longitudinal trends in lipid levels and incidence of abnormal lipid levels among individuals of European ancestry: the Atherosclerosis Risk in Communities (ARIC) studyResequencing of LPL in African Blacks and associations with lipoprotein-lipid levelsNT-proBNP Predicts Cardiovascular Death in the General Population Independent of Left Ventricular Mass and Function: Insights from a Large Population-Based Study with Long-Term Follow-Up.Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study.Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levelsAssociation between Eight Functional Polymorphisms and Haplotypes in the Cholesterol Ester Transfer Protein (CETP) Gene and Dyslipidemia in National Minority Adults in the Far West Region of China.Measurement of the phospholipase activity of endothelial lipase in mouse plasma.A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C.Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans.Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels--the Framingham Heart Study.Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins.A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
P2860
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P2860
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Genome-wide association analys ...... w light on intergenic regions.
@en
type
label
Genome-wide association analys ...... w light on intergenic regions.
@en
prefLabel
Genome-wide association analys ...... w light on intergenic regions.
@en
P2093
P50
P1476
Genome-wide association analys ...... w light on intergenic regions.
@en
P2093
Andreas Luchner
Angela Döring
Barbara Kollerits
Christian Gieger
Claudia Lamina
H-Erich Wichmann
Iris M Heid
Martina Müller
Ruth Frikke-Schmidt
P356
10.1161/CIRCGENETICS.108.776708
P50
P577
2008-10-01T00:00:00Z