| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Functional impact of global rare copy number variation in autism spectrum disorders. | Nature | 2010 | 14.66 |
| 2 | Microduplications of 16p11.2 are associated with schizophrenia. | Nat Genet | 2009 | 6.13 |
| 3 | A unified genetic theory for sporadic and inherited autism. | Proc Natl Acad Sci U S A | 2007 | 3.47 |
| 4 | A genome-wide scan for common alleles affecting risk for autism. | Hum Mol Genet | 2010 | 3.42 |
| 5 | Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. | PLoS Genet | 2009 | 3.42 |
| 6 | Individual common variants exert weak effects on the risk for autism spectrum disorderspi. | Hum Mol Genet | 2012 | 2.46 |
| 7 | Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. | Am J Hum Genet | 2002 | 1.39 |