| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. | Lancet Neurol | 2008 | 5.33 |
| 2 | Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. | Lancet Neurol | 2007 | 2.72 |
| 3 | The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. | Arch Neurol | 2010 | 2.19 |
| 4 | Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2. | Brain | 2010 | 1.45 |
| 5 | Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype. | Arch Neurol | 2006 | 1.42 |
| 6 | Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia. | Hum Mol Genet | 2006 | 1.13 |