coronary artery disease phenotype

Aliases

CAD

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Mentioned in (44)

Papers in which this entity is mentioned.

• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Epsin Nanotherapy Regulates Cholesterol Transport to Fortify Atheroma Regression. (2023)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
• Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation. (2022)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• Maternal Anxiety and Depression during Late Pregnancy and Newborn Brain White Matter Development. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• The 3D Genome Browser: a web-based browser for visualizing 3D genome organization and long-range chromatin interactions. (2018)
• Specific circulating microRNA signature of bicuspid aortic valve disease. (2017)
• Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
• Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
• Alcohol-Induced Developmental Origins of Adult-Onset Diseases. (2016)
• Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• A review of the nonpressor and nonantidiuretic actions of the hormone vasopressin. (2015)
• The CXCL12/CXCR4 chemokine ligand/receptor axis in cardiovascular disease. (2014)
• The genetics of alcohol dependence: advancing towards systems-based approaches. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
• Haemolysis during sample preparation alters microRNA content of plasma. (2011)
• Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
• Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
• The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
• Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
• Genomewide association studies and human disease. (2009)
• Discrimination and racial disparities in health: evidence and needed research. (2009)
• 3' end mRNA processing: molecular mechanisms and implications for health and disease. (2008)
• C-reactive protein: a critical update. (2003)

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