| human | Q5 |
| P106 | occupation | researcher | Q1650915 |
| Q57611776 | A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1 |
| Q33772964 | A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. |
| Q24615584 | A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease |
| Q24601469 | A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy |
| Q49028473 | A multiple biomarker risk score for guiding clinical decisions using a decision curve approach |
| Q36854870 | A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk |
| Q53494325 | Adrenomedullin and arterial stiffness: integrative approach combining monocyte ADM expression, plasma MR-Pro-ADM, and genome-wide association study. |
| Q40458738 | Analysis of N-terminal-pro-brain natriuretic peptide and C-reactive protein for risk stratification in stable and unstable coronary artery disease: results from the AtheroGene study. |
| Q40397164 | Asymmetric dimethylarginine and the risk of cardiovascular events and death in patients with coronary artery disease: results from the AtheroGene Study |
| Q40353088 | B-type natriuretic peptide and the risk of cardiovascular events and death in patients with stable angina: results from the AtheroGene study |
| Q33931897 | C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies |
| Q28728919 | Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis |
| Q51773327 | Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. |
| Q28659915 | Common variants associated with plasma triglycerides and risk for coronary artery disease |
| Q34430255 | Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression |
| Q38416428 | Contribution of 30 biomarkers to 10-year cardiovascular risk estimation in 2 population cohorts: the MONICA, risk, genetics, archiving, and monograph (MORGAM) biomarker project |
| Q34113939 | Copeptin improves early diagnosis of acute myocardial infarction |
| Q45908500 | Correction: Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression. |
| Q46157359 | Cystatin C and cardiovascular mortality in patients with coronary artery disease and normal or mildly reduced kidney function: results from the AtheroGene study |
| Q56893651 | Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis |
| Q28661470 | Discovery and refinement of loci associated with lipid levels |
| Q36309248 | Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy |
| Q34945566 | GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm |
| Q44207349 | Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular disease |
| Q24288778 | Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy |
| Q34660068 | Genetic regulation of serum phytosterol levels and risk of coronary artery disease |
| Q28752094 | Genetics and beyond--the transcriptome of human monocytes and disease susceptibility |
| Q28744518 | Genetics of venous thrombosis: insights from a new genome wide association study |
| Q34574923 | Genome-wide haplotype analysis of cis expression quantitative trait loci in monocytes |
| Q43617306 | Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease |
| Q40422793 | Glutathione peroxidase-1 and homocysteine for cardiovascular risk prediction: results from the AtheroGene study |
| Q34570830 | Graphical modeling of gene expression in monocytes suggests molecular mechanisms explaining increased atherosclerosis in smokers |
| Q40315651 | Haplotypes of the caspase-1 gene, plasma caspase-1 levels, and cardiovascular risk |
| Q57315333 | Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project |
| Q40265832 | Impact of C-reactive protein and fibrinogen on cardiovascular prognosis in patients with stable angina pectoris: the AtheroGene study. |
| Q34200936 | Influence of sex and genetic variability on expression of X-linked genes in human monocytes. |
| Q34092395 | Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans |
| Q43840390 | Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients |
| Q33453963 | Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project |
| Q56458636 | Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction |
| Q39689346 | Midregional proadrenomedullin for prediction of cardiovascular events in coronary artery disease: results from the AtheroGene study. |
| Q36199740 | Molecular Characterization of the NLRC4 Expression in Relation to Interleukin-18 Levels |
| Q45573743 | Multiple marker approach to risk stratification in patients with stable coronary artery disease |
| Q37225243 | New susceptibility locus for coronary artery disease on chromosome 3q22.3. |
| Q40380481 | Prognostic value of tissue inhibitor of metalloproteinase-1 for cardiovascular death among patients with cardiovascular disease: results from the AtheroGene study. |
| Q31106182 | Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data |
| Q37211205 | Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease |
| Q40310798 | Resistin, acute coronary syndrome and prognosis results from the AtheroGene study |
| Q38839872 | SASH1, a new potential link between smoking and atherosclerosis |
| Q84473723 | Sensitive troponin I assay in early diagnosis of acute myocardial infarction |
| Q57605684 | Single polymorphism nucleotide rs1333049 on chromosome 9p21 is associated with carotid plaques but not with common carotid intima-media thickness in older adults. A combined analysis of the Three-City and the EVA studies |
| Q34017796 | The choice of the filtering method in microarrays affects the inference regarding dosage compensation of the active X-chromosome |
| Q37226746 | The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts |
| Q30495275 | The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations |
| Q46736337 | The value of N-terminal fragment of brain natriuretic peptide and tissue inhibitor of metalloproteinase-1 levels as predictors of cardiovascular outcome in the LIPID study |
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