| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation. | Genet Med | 2011 | 1.15 |
| 2 | Diagnostic approaches to apparent homozygosity. | Genet Med | 2012 | 0.93 |
| 3 | Mitochondrial myopathy due to novel missense mutation in the cytochrome c oxidase 1 gene. | J Neurol Sci | 2012 | 0.75 |