| Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemia | Thrombosis Research |  | | 2021 | 216 | 239 |
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| Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations | Thrombosis research | | | 2021 | 589 | 5 |
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| Chemical modulators of fibrinogen production and their impact on venous thrombosis | Thrombosis and Haemostasis | | | 2021 | 274 | 295 |
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| 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 | 236 | 499 |
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| Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype | Thrombosis Research | | | 2020 | 369 | 52 |
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| Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A | Thrombosis Research |  | | 2020 | 277 | 2 |
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| Fibrin(ogen) in human disease: both friend and foe | Haematologica | | | 2020 | 484 | 436 |
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| A novel nonsense mutation in FBG (c.1421G>A;p.Trp474Ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype | Biomedicines | | | 2020 | 285 | 166 |
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| Investigating and modulating the regulation of fibrinogen production | | | | 2020 | 601 | 19 |
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| A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis | Blood Advances | | | 2020 | 220 | 284 |
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