Sort   by:  
 Page size 
UnknownGenome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Not available
S-EPMC3723315 | biostudies-literature
UnknownA meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.
Not available
S-EPMC4715256 | biostudies-literature
UnknownThe shared allelic architecture of adiponectin levels and coronary artery disease.
Not available
S-EPMC6139652 | biostudies-literature
UnknownMultiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Not available
S-EPMC3842025 | biostudies-literature
UnknownWhole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Not available
S-EPMC3928660 | biostudies-literature
UnknownQuantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
Not available
S-EPMC3959810 | biostudies-literature
UnknownCommon and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
Not available
S-EPMC3724194 | biostudies-literature
UnknownExome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Not available
S-EPMC4319990 | biostudies-literature
UnknownRare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Not available
S-EPMC4673986 | biostudies-literature
UnknownTGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.
Not available
S-EPMC4033668 | biostudies-literature
Sort   by:  
 Page size