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- 2022
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Mark
Milk intake and incident stroke and coronary heart disease in populations of European descent : A Mendelian Randomization study
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- Contribution to journal › Article
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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
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- Contribution to journal › Article
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Mark
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
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- Contribution to journal › Letter
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
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Mark
The relationship between blood pressure and risk of renal cell carcinoma
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- Contribution to journal › Article
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Mark
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
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- Contribution to journal › Article
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Mark
Genetic Variation Interacts with Selenium Exposure Regarding Breast Cancer Risk: Assessing Dietary Intake, Serum Levels and Genetically Elevated Selenium Levels
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- Contribution to journal › Article
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Mark
Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
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- Contribution to journal › Article
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Mark
The effect of a randomised controlled lifestyle intervention on weight loss and plasma proneurotensin
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- Contribution to journal › Article
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Mark
ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma
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- Contribution to journal › Article
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Mark
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults
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- Contribution to journal › Article
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Mark
Bioactive adrenomedullin for assessment of venous congestion in heart failure
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- Contribution to journal › Article
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Mark
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
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- Contribution to journal › Article
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Mark
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
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- Contribution to journal › Article
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Mark
Rare genetic variants explain missing heritability in smoking
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- Contribution to journal › Article