| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. | Nat Genet | 2006 | 4.01 |
| 2 | Cd2+, Mn2+, Ni2+ and Se2+ toxicity to Saccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2. | Biochem Biophys Res Commun | 2009 | 1.21 |
| 3 | Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism. | Hum Mutat | 2011 | 1.19 |
| 4 | eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation. | Mol Cell | 2012 | 0.92 |
| 5 | A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss. | Am J Hum Genet | 2012 | 0.91 |
| 6 | Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. | Mov Disord | 2009 | 0.90 |