| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | The FMR1 CGG repeat test is not a candidate prescreening tool for identifying women with a high probability of being carriers of BRCA mutations. | Eur J Hum Genet | 2013 | 0.94 |
| 2 | Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation. | Am J Med Genet A | 2015 | 0.81 |
| 3 | Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients. | Genet Med | 2016 | 0.79 |