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Atrial natriuretic peptide is negatively regulated by microRNA-425.
Polymorphism, Single Nucleotide
Sex- and age-interacting eQTLs in human complex diseases.
Integromic analysis of genetic variation and gene expression identifies networks for cardiovascular disease phenotypes.
Genome-wide identification of microRNA expression quantitative trait loci.
Dissecting the roles of microRNAs in coronary heart disease via integrative genomic analyses.
Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.
Dynamic Role of trans Regulation of Gene Expression in Relation to Complex Traits.
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Identification of common genetic variants controlling transcript isoform variation in human whole blood.
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
Shared genetic regulatory networks for cardiovascular disease and type 2 diabetes in multiple populations of diverse ethnicities in the United States.
Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes.
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.
Integrative network analysis reveals molecular mechanisms of blood pressure regulation.
A systematic heritability analysis of the human whole blood transcriptome.
A systems biology framework identifies molecular underpinnings of coronary heart disease.
Polymorphism Single Nucleotide