| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death. | Genome Med | 2016 | 0.76 |
| 2 | Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy. | Hum Genet | 2016 | 0.75 |
| 3 | Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics. | Genome Med | 2016 | 0.75 |