| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. | Nat Genet | 2010 | 6.62 |
| 2 | Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats. | Hum Mutat | 2011 | 1.01 |