| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. | Blood | 2011 | 2.29 |
| 2 | Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study. | Br J Haematol | 2013 | 2.28 |
| 3 | ANKRD26-related thrombocytopenia and myeloid malignancies. | Blood | 2013 | 1.32 |
| 4 | Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations. | Haematologica | 2010 | 1.11 |
| 5 | Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation). | Haematologica | 2011 | 1.02 |