| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. | PLoS Genet | 2012 | 2.65 |
| 2 | Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. | J Pineal Res | 2011 | 0.90 |
| 3 | Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population. | PLoS One | 2010 | 0.88 |
| 4 | Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway. | J Pineal Res | 2012 | 0.87 |
| 5 | Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations. | PLoS One | 2011 | 0.86 |