| Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemia | Thrombosis Research |  | | 2021 | 220 | 277 |
|
| Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations | Thrombosis research | | | 2021 | 593 | 10 |
|
| Chemical modulators of fibrinogen production and their impact on venous thrombosis | Thrombosis and Haemostasis | | | 2021 | 279 | 301 |
|
| Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature | Haemophilia | | | 2021 | 240 | 557 |
|
| Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype | Thrombosis Research | | | 2020 | 373 | 61 |
|
| Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A | Thrombosis Research |  | | 2020 | 281 | 2 |
|
| Fibrin(ogen) in human disease: both friend and foe | Haematologica | | | 2020 | 488 | 488 |
|
| A novel nonsense mutation in FBG (c.1421G>A;p.Trp474Ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype | Biomedicines | | | 2020 | 290 | 176 |
|
| Investigating and modulating the regulation of fibrinogen production | | | | 2020 | 612 | 19 |
|
| A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis | Blood Advances | | | 2020 | 224 | 302 |
|
