| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study. | Lancet Neurol | 2011 | 5.01 |
| 2 | Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia. | Neurobiol Aging | 2013 | 1.30 |
| 3 | Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk. | Mol Neurodegener | 2012 | 1.08 |
| 4 | C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment. | Neurobiol Aging | 2013 | 1.00 |
| 5 | Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes. | Neurobiol Aging | 2013 | 0.78 |