112 results on '"Tybjaerg-Hansen, Anne"'
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2. Variants in the GPR146 Gene Are Associated With a Favorable Cardiometabolic Risk Profile
3. Abstract 14649: Low Plasma Transthyretin is Associated With All-Cause and Cardiovascular Mortality in the General Population
4. Abstract 14613: Amyloidosis-Related Orthopedic Events, Low Plasma Transthyretin, and Risk of Cardiac Events
5. Epigenetic Regulation of F2RL3 Associates with Myocardial Infarction and Platelet Function
6. Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome
7. Naturally Occurring Variants in LRP1 (Low-Density Lipoprotein Receptor–Related Protein 1) Affect HDL (High-Density Lipoprotein) Metabolism Through ABCA1 (ATP-Binding Cassette A1) and SR-B1 (Scavenger Receptor Class B Type 1) in Humans
8. APOC3 Loss-of-Function Mutations, Remnant Cholesterol, Low-Density Lipoprotein Cholesterol, and Cardiovascular Risk: Mediation- and Meta-Analyses of 137 895 Individuals
9. Using genetics to explore whether the cholesterol-lowering drug ezetimibe may cause an increased risk of cancer
10. Abstract 20818: Liver Fat Content, NAFLD, and Ischemic Heart Disease: Mendelian Randomization and Meta-Analysis of 279,013 Individuals
11. Abstract 19762: High LDL Cholesterol Levels and Risk of Peripheral Vascular Diseases - A Mendelian Randomization Study Including 106,548 Individuals From the General Population
12. Abstract 19755: Statin Treatment, Genetic Inhibition of HMGCR, and Risk of Symptomatic Gallstone Disease
13. Abstract 15369: Low Ldl-Cholesterol by Pcsk9 Variation and Mortality in 109,800 Individuals From the General Population
14. Genetic Variation in GSTP1, Lung Function, Risk of Lung Cancer, and Mortality
15. The Sialylation Pathway and Coronary Artery Disease
16. Effect of APOE ε Genotype on Lipoprotein(a) and the Associated Risk of Myocardial Infarction and Aortic Valve Stenosis
17. Genetic variation in WRN and ischemic stroke: General population studies and meta-analyses
18. Rare and low-frequency coding variants alter human adult height
19. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment
20. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society
21. Change in Body Mass Index Associated With Lowest Mortality in Denmark, 1976-2013
22. Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
23. Using human genetics to predict the effects and side-effects of drugs
24. HEART DISEASE: Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
25. Sex Hormones and Ischemic Stroke: A Prospective Cohort Study and Meta-Analyses
26. The UK10K project identifies rare variants in health and disease
27. Supplement to: Loss-of-function mutations in APOC3 and risk of ischemic vascular disease.
28. HDL Cholesterol and Risk of Type 2 Diabetes: A Mendelian Randomization Study
29. Genetic variation in the cholesterol transporter NPC1L1, ischaemic vascular disease, and gallstone disease
30. Novel genes in LDL metabolism – a comprehensive overview
31. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
32. Subgroups at high risk for ischaemic heart disease: identification and validation in 67 000 individuals from the general population
33. Plasma levels of apolipoprotein E and risk of dementia in the general population
34. Loss-of-Function Mutations in APOC3 and Risk of Ischemic Vascular Disease
35. Assessing Risk Prediction Models Using Individual Participant Data From Multiple Studies
36. Total and Cause-Specific Mortality by Elevated Transferrin Saturation and Hemochromatosis Genotype in Individuals With Diabetes: Two General Population Studies
37. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease : Consensus Statement of the European Atherosclerosis Society
38. Elevated body mass index as a causal risk factor for symptomatic gallstone disease: A Mendelian randomization study
39. Total Mortality by Elevated Transferrin Saturation in Patients With Diabetes
40. Cascade Screening in Families with Inherited Cardiac Diseases Driven by Cardiologists: Feasibility and Nationwide Outcome in Long QT Syndrome
41. Exploring causal associations between alcohol and coronary heart disease risk factors: findings from a Mendelian randomization study in the Copenhagen General Population Study
42. Association of plasma uric acid with ischaemic heart disease and blood pressure: mendelian randomisation analysis of two large cohorts
43. Extreme Bilirubin Levels as a Causal Risk Factor for Symptomatic Gallstone Disease
44. AT1 mutations and risk of atrial fibrillation based on genotypes from 71 000 individuals from the general population
45. Genetically elevated non-fasting triglycerides and calculated remnant cholesterol as causal risk factors for myocardial infarction
46. Short Telomere Length, Cancer Survival, and Cancer Risk in 47102 Individuals
47. Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: Systematic review and meta-analysis of 14 015 stroke cases and pooled analysis of primary biomarker data from up to 60 883 individuals
48. Genetic Associations with Valvular Calcification and Aortic Stenosis
49. Elevated Fibrinogen Levels Are Associated with Risk of Pulmonary Embolism, but Not with Deep Venous Thrombosis
50. ABC Transporter Genes and Risk of Type 2 Diabetes: A study of 40,000 individuals from the general population
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