| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. | Am J Hum Genet | 2010 | 1.86 |
| 2 | Cancer susceptibility and embryonic lethality in Mob1a/1b double-mutant mice. | J Clin Invest | 2012 | 1.16 |
| 3 | Identifying essential genes in mouse development via an ENU-based forward genetic approach. | Methods Mol Biol | 2014 | 0.77 |