| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. | JAMA | 2005 | 3.89 |
| 2 | Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation. | Hum Mol Genet | 2006 | 3.15 |
| 3 | Familial atrial fibrillation is a genetically heterogeneous disorder. | J Am Coll Cardiol | 2003 | 3.09 |
| 4 | ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. | Nat Genet | 2004 | 2.85 |
| 5 | Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. | N Engl J Med | 2008 | 2.14 |