| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype. | Am J Med Genet A | 2015 | 1.60 |
| 2 | Prominent Mittendorf spot. | JAMA Ophthalmol | 2015 | 0.75 |
| 3 | Age-dependent ocular phenotype in hereditary hyperferritinaemia cataract syndrome (HHCS). | Acta Ophthalmol | 2011 | 0.75 |