| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. | Am J Hum Genet | 2006 | 2.44 |
| 2 | Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism. | Eur J Hum Genet | 2006 | 0.98 |
| 3 | Molecular diagnosis reveals genetic heterogeneity for the overlapping MKKS and BBS phenotypes. | Eur J Med Genet | 2010 | 0.85 |
| 4 | Targeted apc;twist double-mutant mice: a new model of spontaneous osteosarcoma that mimics the human disease. | Transl Oncol | 2010 | 0.84 |