| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle. | Nature | 2012 | 3.08 |
| 2 | Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance. | Proc Natl Acad Sci U S A | 2011 | 1.36 |
| 3 | Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. | Hum Mol Genet | 2014 | 1.25 |
| 4 | Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis. | Laryngoscope | 2012 | 1.02 |
| 5 | Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model. | Mol Ther | 2013 | 0.89 |