| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Genotype, haplotype and copy-number variation in worldwide human populations. | Nature | 2008 | 12.40 |
| 2 | A genome-wide association study identifies protein quantitative trait loci (pQTLs). | PLoS Genet | 2008 | 4.75 |
| 3 | Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. | PLoS Genet | 2007 | 2.09 |
| 4 | A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. | Hum Mol Genet | 2009 | 1.93 |
| 5 | A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20. | Hum Mol Genet | 2008 | 0.87 |
| 6 | Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series. | Mov Disord | 2010 | 0.76 |