| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Transgenic rat model of Huntington's disease. | Hum Mol Genet | 2003 | 1.66 |
| 2 | Do CTG expansions at the SCA8 locus cause ataxia? | Ann Neurol | 2003 | 1.43 |
| 3 | Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). | Ann Neurol | 2003 | 1.29 |
| 4 | Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia. | Arch Neurol | 2003 | 0.86 |
| 5 | Testing the parents to confirm genotypes of CF patients is highly recommended: report of two cases. | Eur J Hum Genet | 2008 | 0.81 |
| 6 | Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype. | Ann Neurol | 2002 | 0.80 |
| 7 | Co-occurrence of multiple sclerosis and cancer in a BRCA1 positive family. | Eur J Med Genet | 2013 | 0.78 |
| 8 | Birth as sheer pleasure. | Midwifery Today Int Midwife | 2003 | 0.75 |