| 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 | Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. | Am J Hum Genet | 2013 | 2.47 |
| 4 | Individual common variants exert weak effects on the risk for autism spectrum disorderspi. | Hum Mol Genet | 2012 | 2.46 |
| 5 | Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. | Sci Transl Med | 2011 | 2.29 |
| 6 | Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. | Hum Mol Genet | 2013 | 1.26 |
| 7 | Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes. | Hum Genet | 2014 | 0.75 |