| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | NMNAT1 mutations cause Leber congenital amaurosis. | Nat Genet | 2012 | 1.86 |
| 2 | Mitochondrial respiratory chain dysfunction variably increases oxidant stress in Caenorhabditis elegans. | Mitochondrion | 2009 | 1.41 |
| 3 | Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy. | Am J Hum Genet | 2013 | 1.18 |
| 4 | Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice. | EMBO Mol Med | 2011 | 1.16 |
| 5 | Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling network. | PLoS One | 2013 | 0.88 |
| 6 | Stable isotopic profiling of intermediary metabolic flux in developing and adult stage Caenorhabditis elegans. | J Vis Exp | 2011 | 0.78 |