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KIF6, LPA, TAS2R50, and VAMP8 genetic variation, low density lipoprotein cholesterol lowering response to pravastatin, and heart disease risk reduction in the elderlyGenetic studies of body mass index yield new insights for obesity biologyGenome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a)Novel genetic loci underlying human intracranial volume identified through genome-wide associationA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseDrug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE ConsortiumGene-gene Interaction Analyses for Atrial FibrillationMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsWhite Matter Lesion Progression: Genome-Wide Search for Genetic InfluencesDirectional dominance on stature and cognition in diverse human populationsGenome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsAssociation between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataGenome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseGenome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapyC-reactive protein and genetic variants and cognitive decline in old age: the PROSPER studyRare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart diseaseRare and low-frequency coding variants alter human adult heightKLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Non-homologous end-joining pathway associated with occurrence of myocardial infarction: gene set analysis of genome-wide association study data.Pathway analysis using genome-wide association study data for coronary restenosis--a potential role for the PARVB gene.Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adultsThyroid function within the normal range and risk of coronary heart disease: an individual participant data analysis of 14 cohortsSystematic testing of literature reported genetic variation associated with coronary restenosis: results of the GENDER Study.Subclinical thyroid dysfunction and cognitive decline in old ageNatriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysis.Assessment of causality between serum gamma-glutamyltransferase and type 2 diabetes mellitus using publicly available data: a Mendelian randomization study.Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.Association of metabolic syndrome and electrocardiographic markers of subclinical cardiovascular disease.Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers.Discovery of novel heart rate-associated loci using the Exome Chip.Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles.52 Genetic Loci Influencing Myocardial Mass.Genetic variation at the PCSK9 locus moderately lowers low-density lipoprotein cholesterol levels, but does not significantly lower vascular disease risk in an elderly populationFine mapping the CETP region reveals a common intronic insertion associated to HDL-C
P50
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P50
description
hulumtuese
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հետազոտող
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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Stella Trompet
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