| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. | Lancet | 2005 | 3.09 |
| 2 | Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease. | Eur J Hum Genet | 2006 | 1.56 |
| 3 | Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. | Hum Mutat | 2013 | 1.10 |
| 4 | Olfactory heterogeneity in LRRK2 related Parkinsonism. | Mov Disord | 2010 | 0.87 |
| 5 | GIGYF2 mutations are not a frequent cause of familial Parkinson's disease. | Parkinsonism Relat Disord | 2009 | 0.77 |