| Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study | Circulation | 2014 | 2.5K |
| Defining the role of common variation in the genomic and biological architecture of adult human height | Nature Genetics | 2014 | 1.3K |
| Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease | Nature Genetics | 2014 | 1.3K |
| Aortic pulse wave velocity improves cardiovascular event prediction: an individual participant meta-analysis of prospective observational data from 17,635 subjects | Journal of the American College of Cardiology | 2014 | 1.1K |
| Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | Nature Genetics | 2014 | 784 |
| The Framingham Heart Study and the epidemiology of cardiovascular disease: a historical perspective | Lancet, The | 2014 | 642 |
| Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data | BMJ, The | 2014 | 406 |
| Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche | Nature | 2014 | 401 |
| Global epidemiology of atrial fibrillation | Nature Reviews Cardiology | 2014 | 385 |
| β-Aminoisobutyric acid induces browning of white fat and hepatic β-oxidation and is inversely correlated with cardiometabolic risk factors | Cell Metabolism | 2014 | 369 |
| Neuropsychological criteria for mild cognitive impairment improves diagnostic precision, biomarker associations, and progression rates | Journal of Alzheimer's Disease | 2014 | 324 |
| Noncardiac comorbidities in heart failure with reduced versus preserved ejection fraction | Journal of the American College of Cardiology | 2014 | 313 |
| Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study | Lancet Diabetes and Endocrinology,the | 2014 | 250 |
| Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants | Stroke | 2014 | 245 |
| Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity | Diabetes | 2014 | 235 |
| Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks | American Journal of Human Genetics | 2014 | 233 |
| New strategies for heart failure with preserved ejection fraction: the importance of targeted therapies for heart failure phenotypes | European Heart Journal | 2014 | 231 |
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | Nature Genetics | 2014 | 199 |
| Clinical subtypes of chronic traumatic encephalopathy: literature review and proposed research diagnostic criteria for traumatic encephalopathy syndrome | Alzheimer's Research and Therapy | 2014 | 185 |
| GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database | Bioinformatics | 2014 | 181 |
| Common genetic variants associated with cognitive performance identified using the proxy-phenotype method | Proceedings of the National Academy of Sciences of the United States of America | 2014 | 181 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol | American Journal of Human Genetics | 2014 | 170 |
| Serum brain-derived neurotrophic factor and the risk for dementia: the Framingham Heart Study | JAMA Neurology | 2014 | 162 |
| Epigenome-wide association study of fasting blood lipids in the Genetics of Lipid-lowering Drugs and Diet Network study | Circulation | 2014 | 161 |
| Risk factors, stroke prevention treatments, and prevalence of cerebral microbleeds in the Framingham Heart Study | Stroke | 2014 | 160 |
