Published in J Am Heart Assoc on March 20, 2017
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet (2011) 13.25
External review and validation of the Swedish national inpatient register. BMC Public Health (2011) 11.28
Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet (2012) 7.59
Clinical utility of different lipid measures for prediction of coronary heart disease in men and women. JAMA (2007) 6.95
An introduction to instrumental variables for epidemiologists. Int J Epidemiol (2000) 6.17
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses. Lancet (2010) 6.07
The Malmo Diet and Cancer Study. Design and feasibility. J Intern Med (1993) 5.35
Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring. JAMA (2004) 4.63
Mendelian randomization as an instrumental variable approach to causal inference. Stat Methods Med Res (2007) 4.04
Non-high-density lipoprotein cholesterol and apolipoprotein B in the prediction of coronary heart disease in men. Circulation (2005) 3.85
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials. Lancet (2015) 3.75
A prospective study of parental history of myocardial infarction and coronary artery disease in men. Am J Cardiol (1991) 2.45
Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. Arterioscler Thromb Vasc Biol (2007) 2.36
Atrial fibrillation in the Malmö Diet and Cancer study: a study of occurrence, risk factors and diagnostic validity. Eur J Epidemiol (2010) 2.13
Direct and indirect effects in a survival context. Epidemiology (2011) 2.11
Genetics of human cardiovascular disease. Cell (2012) 1.90
Maternal and paternal history of myocardial infarction and risk of cardiovascular disease in men and women. Circulation (2001) 1.86
A prospective study of parental history of myocardial infarction and coronary heart disease in women. Am J Epidemiol (1986) 1.74
Family history of heart attack as an independent predictor of death due to cardiovascular disease. Circulation (1984) 1.73
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration. Eur Heart J (2011) 1.73
Family history as an independent risk factor for coronary artery disease. J Am Coll Cardiol (1984) 1.65
Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history. Eur Heart J (2015) 1.65
A simple unified approach for estimating natural direct and indirect effects. Am J Epidemiol (2012) 1.58
Multilocus genetic risk scores for coronary heart disease prediction. Arterioscler Thromb Vasc Biol (2013) 1.32
Parental history of premature coronary heart disease: an independent risk factor of myocardial infarction. J Clin Epidemiol (1996) 1.20
Assessing natural direct and indirect effects through multiple pathways. Am J Epidemiol (2013) 1.11
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial). Circulation (2016) 0.97
A review of instrumental variable estimators for Mendelian randomization. Stat Methods Med Res (2015) 0.96
Familial clustering of myocardial infarction in first-degree relatives: a nationwide study. Eur Heart J (2013) 0.89
Non-HDL cholesterol vs. apo B for risk of coronary heart disease in healthy individuals: the EPIC-Norfolk prospective population study. Eur J Clin Invest (2013) 0.84
Risk factor exposure in individuals free from cardiovascular disease differs according to age at first myocardial infarction. Eur Heart J (2016) 0.78
Mediation analysis of the relationship between sex, cardiovascular risk factors and mortality from coronary heart disease: Findings from the population-based VHM&PP cohort. Atherosclerosis (2015) 0.78
Paternal or maternal history of cardiovascular disease and the risk of cardiovascular disease in offspring. A systematic review and meta-analysis. Int J Cardiol (2014) 0.77
Family or SNPs: what counts for hereditary risk of coronary artery disease? Eur Heart J (2015) 0.75
Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke. Stroke (2014) 1.08
Use of low density lipoprotein particle number levels as an aid in statin treatment decisions for intermediate risk patients: a cost-effectiveness analysis. BMC Cardiovasc Disord (2016) 0.75
Fasting levels of growth hormone are associated with carotid intima media thickness but are not affected by fluvastatin treatment. BMC Cardiovasc Disord (2017) 0.75
A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death. PLoS One (2017) 0.75
Syndromes of orthostatic intolerance and syncope in young adults. Open Heart (2017) 0.75
Urinary UBC Rapid and NMP22 Test for Bladder Cancer Surveillance in Comparison to Urinary Cytology: Results from a Prospective Single-Center Study. Int J Med Sci (2017) 0.75
Prediction of Type 2 Diabetes by Hemoglobin A1c in Two Community-Based Cohorts. Diabetes Care (2017) 0.75
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium. Sci Rep (2017) 0.75
Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variants. J Hum Genet (2017) 0.75