| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. | J Mol Med (Berl) | 2005 | 1.63 |
| 2 | Novel HSF4 mutation causes congenital total white cataract in a Chinese family. | Am J Ophthalmol | 2006 | 1.11 |
| 3 | Identification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav 1.5. | J Biol Chem | 2008 | 1.06 |
| 4 | A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family. | Mol Vis | 2013 | 0.82 |
| 5 | A novel RAB7 mutation in a Chinese family with Charcot-Marie-Tooth type 2B disease. | Gene | 2014 | 0.76 |
| 6 | Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype. | J Huazhong Univ Sci Technolog Med Sci | 2010 | 0.75 |