| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. | Am J Hum Genet | 2008 | 2.58 |
| 2 | Regulation of cholinergic gene expression by the neuron restrictive silencer factor/repressor element-1 silencing transcription factor. | Life Sci | 2003 | 0.84 |
| 3 | Identification of nitrated tyrosine residues of protein kinase G-Iα by mass spectrometry. | Anal Bioanal Chem | 2014 | 0.75 |