| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. | Nat Genet | 2009 | 12.19 |
| 2 | Inactivating mutations in NPC1L1 and protection from coronary heart disease. | N Engl J Med | 2014 | 4.94 |
| 3 | Effect of ultrasound on thrombolysis of middle cerebral artery occlusion. | Ann Neurol | 2003 | 1.07 |
| 4 | Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations. | J Neurol Neurosurg Psychiatry | 2007 | 0.94 |
| 5 | Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis. | Circ Cardiovasc Genet | 2014 | 0.91 |
| 6 | Genetic polymorphisms of hemostasis genes and primary outcome of very low birth weight infants. | Pediatrics | 2006 | 0.86 |
| 7 | Effects of common atopy-associated amino acid substitutions in the IL-4 receptor alpha chain on IL-4 induced phenotypes. | Immunogenetics | 2005 | 0.83 |