Figures & data
Figure 1 The top eleven diseases explain 37.7% of the global burden of disease measured as DALYs, with coronary artery disease as the leading cause of DALYs in 2010.
![Figure 1 The top eleven diseases explain 37.7% of the global burden of disease measured as DALYs, with coronary artery disease as the leading cause of DALYs in 2010.](/cms/asset/037a3ebc-2363-4084-ad01-6131e22ea953/dtac_a_35301_f0001_b.jpg)
Figure 2 Genetic and environmental causes of development and progression of atherosclerosis act directly or through known intermediate traits.
![Figure 2 Genetic and environmental causes of development and progression of atherosclerosis act directly or through known intermediate traits.](/cms/asset/0477a7e5-093b-423e-81ca-ad7c4f98ac9f/dtac_a_35301_f0002_b.jpg)
Table 1 Main results of different studies analyzing the heritability of several phenotypes associated with arteriosclerosis
Figure 3 Number of articles published per year according to the genome-wide association studies catalog (accessed on September 27, 2013).
![Figure 3 Number of articles published per year according to the genome-wide association studies catalog (accessed on September 27, 2013).](/cms/asset/9733c44d-3e93-461c-9952-0acfda97e1c5/dtac_a_35301_f0003_b.jpg)
Table 2 Comparison between candidate gene studies and GWAS
Table 3 Summary of main findings of most recent meta-analysis of genome-wide association studies in coronary artery disease, showing the lead single nucleotide polymorphism of each locus, the closest gene, chromosomal location, risk allele and frequency, P-value, and effect size of the reported associations
Table 4 Summary of main findings of most recent meta-analyses of genome-wide association studies of cardiovascular risk factors, showing the lead single nucleotide polymorphism of each locus, the closest gene, chromosomal location, risk allele and frequency, and P-value of the reported associations
Table 5 Main characteristics and results of studies assessing improvement of predictive capacity of classical cardiovascular risk functions after inclusion of genetic information