| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10). | Am J Hum Genet | 2002 | 2.98 |
| 2 | Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. | Am J Hum Genet | 2006 | 2.00 |
| 3 | A genome-wide linkage analysis of dementia in the Amish. | Am J Med Genet B Neuropsychiatr Genet | 2006 | 1.00 |
| 4 | A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12. | Neurogenetics | 2006 | 0.97 |
| 5 | Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432. | Neurogenetics | 2002 | 0.77 |