| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Functional impact of global rare copy number variation in autism spectrum disorders. | Nature | 2010 | 14.66 |
| 2 | A genome-wide scan for common alleles affecting risk for autism. | Hum Mol Genet | 2010 | 3.42 |
| 3 | Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. | Sci Transl Med | 2011 | 2.29 |
| 4 | Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. | PLoS Genet | 2012 | 1.44 |
| 5 | A discovery resource of rare copy number variations in individuals with autism spectrum disorder. | G3 (Bethesda) | 2012 | 1.30 |