ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease Read more about ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease
The impact of non-additive genetic associations on age-related complex diseases Read more about The impact of non-additive genetic associations on age-related complex diseases
Genetic analyses identify widespread sex-differential participation bias Read more about Genetic analyses identify widespread sex-differential participation bias
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices Read more about Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Genetically Proxied Inhibition of Coagulation Factors and Risk of Cardiovascular Disease: A Mendelian Randomization Study Read more about Genetically Proxied Inhibition of Coagulation Factors and Risk of Cardiovascular Disease: A Mendelian Randomization Study
Plasma Cortisol and Risk of Atrial Fibrillation: A Mendelian Randomization Study Read more about Plasma Cortisol and Risk of Atrial Fibrillation: A Mendelian Randomization Study
Educational attainment protects against epilepsy independent of cognitive function: A Mendelian randomization study Read more about Educational attainment protects against epilepsy independent of cognitive function: A Mendelian randomization study
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study Read more about Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study
Gallstone disease, diabetes, calcium, triglycerides, smoking and alcohol consumption and pancreatitis risk: Mendelian randomization study Read more about Gallstone disease, diabetes, calcium, triglycerides, smoking and alcohol consumption and pancreatitis risk: Mendelian randomization study
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis Read more about Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis