A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease - Test2 - elhamkhani - TriplyDB

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

http://www.wikidata.org/entity/Q28267020

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Multivariate Methods for Genetic Variants Selection and Risk Prediction in Cardiovascular Diseases The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease Polygenic Epidemiology Genetics of the acute coronary syndrome Systems Medicine as an Emerging Tool for Cardiovascular Genetics Genetic Research and Women's Heart Disease: a Primer Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study Rare and low-frequency coding variants alter human adult height Leveraging human genetics to guide drug target discovery.Epidemiology of cardiovascular disease: recent novel outlooks on risk factors and clinical approaches.Functional Characterization of the GUCY1A3 Coronary Artery Disease Risk Locus.Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.Genetic analysis of a mouse cross implicates an anti-inflammatory gene in control of atherosclerosis susceptibility.Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis The Coronary Artery Disease-associated Coding Variant in Zinc Finger C3HC-type Containing 1 (ZC3HC1) Affects Cell Cycle Regulation Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease.Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Effect of handgrip on coronary artery disease and myocardial infarction: a Mendelian randomization study.The biomarker and causal roles of homoarginine in the development of cardiometabolic diseases: an observational and Mendelian randomization analysis.Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.Applications of the 1000 Genomes Project resources TCF21 and the environmental sensor aryl-hydrocarbon receptor cooperate to activate a pro-inflammatory gene expression program in coronary artery smooth muscle cells Identification of 15 novel risk loci for coronary artery disease and genetic risk of recurrent events, atrial fibrillation and heart failure.Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles.Identification of STXBP2 as a novel susceptibility locus for myocardial infarction in Japanese individuals by an exome-wide association study Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.Genetic and environmental risk factors for atherosclerosis regulate transcription of phosphatase and actin regulating gene PHACTR1.Case-control association mapping by proxy using family history of disease.Genetics of coronary artery disease: discovery, biology and clinical translation.Human Brain Reacts to Transcranial Extraocular Light.Integrative Tissue-Specific Functional Annotations in the Human Genome Provide Novel Insights on Many Complex Traits and Improve Signal Prioritization in Genome Wide Association Studies.Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction.

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A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

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