| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Cardiac conduction defects associate with mutations in SCN5A. | Nat Genet | 1999 | 2.73 |
| 2 | Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern. | Heart Rhythm | 2008 | 1.39 |
| 3 | Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype. | Eur Heart J | 2001 | 1.37 |
| 4 | Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias. | Am J Hum Genet | 1999 | 0.87 |
| 5 | Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28. | J Am Coll Cardiol | 2000 | 0.80 |
| 6 | Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene. | Prenat Diagn | 2009 | 0.77 |
| 7 | [Genetic aspects of cardiac conduction defects]. | Arch Mal Coeur Vaiss | 2003 | 0.75 |
| 8 | [Genetics and cardiac arrhythmias]. | Arch Mal Coeur Vaiss | 2003 | 0.75 |