| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Targeted capture and massively parallel sequencing of 12 human exomes. | Nature | 2009 | 33.96 |
| 2 | Actionable, pathogenic incidental findings in 1,000 participants' exomes. | Am J Hum Genet | 2013 | 4.06 |
| 3 | Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era. | Circ Cardiovasc Genet | 2012 | 1.78 |
| 4 | Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. | Circ Cardiovasc Genet | 2013 | 1.30 |
| 5 | IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23. | Am J Hum Genet | 2009 | 1.21 |
| 6 | Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families. | Anesthesiology | 2013 | 1.06 |
| 7 | Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL. | J Lipid Res | 2012 | 0.83 |