| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data. | Can J Cardiol | 2013 | 0.95 |
| 2 | Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients. | Biochem Biophys Res Commun | 2007 | 0.88 |
| 3 | A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease. | Case Rep Med | 2009 | 0.75 |
| 4 | [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]. | Ugeskr Laeger | 2010 | 0.75 |