| Fibrin-bound thrombin determines clot structure and blood thrombogenicity in normofibrinogenemia and dysfibrinogenemia | Haematologica |  | | 2026 | 13 | 13 |
|
| Rare Bleeding Disorders and Bleeding Disorder of Unknown Cause : Current Understanding and Recent Developments | Haemophilia | | | 2026 | 2 | 5 |
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| The fibrinogen αC region promotes arterial thrombosis in the context of hypofibrinogenemia | Blood | | | 2026 | 24 | 62 |
|
| Successful Treatment of Heavy Menstrual Bleeding in a Woman With Mild Haemophilia A Using Efanesoctocog Alfa | Haemophilia |  | | 2026 | 7 | 0 |
|
| Another step toward phenotypic characterization of hereditary dysfibrinogenemia ? | Research and practice in thrombosis and haemostasis | | | 2026 | 1 | 28 |
|
| An Unusual Association Between Acquired Hemophilia A and Type 2 Autoimmune Pancreatitis | Hämostaseologie | | | 2026 | 4 | 16 |
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| Standardization of scanning electron microscopy analysis of fibrin fiber diameter measurement : communication from the ISTH SSC subcommittee on FXIII and fibrinogen | Journal of thrombosis and haemostasis | | | 2026 | 2 | 20 |
|
| A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family | Haemophilia | | | 2026 | 1 | 0 |
|
| An integrated surveillance study of SARS-CoV-2, influenza virus, and respiratory syncytial virus infections | CMI communications | | | 2026 | 12 | 32 |
|
| The Hypofibrinolysis State Associated with the Dysfibrinogenemia Dusart is Mainly Related to the Altered Fibrin Clot Structure | Hämostaseologie | | | 2026 | 9 | 182 |
|
| Management of Young and Ageing Women with Afibrinogenemia and Hypofibrinogenemia | Hämostaseologie | | | 2025 | 36 | 293 |
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| How I treat quantitative fibrinogen disorders | Blood | | | 2025 | 74 | 8 |
|
| The thrombotic paradox in congenital fibrinogen deficiencies: from pathophysiology to practice | Research and practice in thrombosis and haemostasis | | | 2025 | 25 | 33 |
|
| Women and hereditary bleeding disorders | Hämostaseologie | | | 2025 | 85 | 852 |
|
| Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database | Research and practice in thrombosis and haemostasis | | | 2025 | 30 | 139 |
|
| Enhancing hemostasis potency in hemophilia with a small interfering ribonucleic acid targeting protein S | Journal of thrombosis and haemostasis | | | 2025 | 31 | 0 |
|
| A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec | Haemophilia | | | 2024 | 81 | 0 |
|
| Perinatal stroke and hypofibrinogenemia : Is the new missense fibrinogen variant γ p.Gly310Glu the cause of the procoagulant state ? | Thrombosis research | | | 2024 | 100 | 0 |
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| Angiologie et hémostase : ce qui a changé en 2023 | Revue médicale suisse | | | 2024 | 113 | 30 |
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| Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia | Blood coagulation & fibrinolysis | | | 2024 | 102 | 266 |
|
| Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database | Blood advances | | | 2024 | 132 | 164 |
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| Santé cardiovasculaire et médecine transgenre | Revue médicale suisse | | | 2024 | 18 | 2 |
|
| Management of anticoagulation and factor XIII replacement in a patient with severe factor XIII deficiency and recurrent venous thromboembolic disease: case report and review of literature | Research and practice in thrombosis and haemostasis | | | 2024 | 127 | 173 |
|
| Management of pregnancy and delivery in congenital fibrinogen disorders: communication from the ISTH SSC Subcommittee on Factor XIII and Fibrinogen | Journal of thrombosis and haemostasis | | | 2024 | 100 | 0 |
|
| Rare bleeding disorders: Advances in management | Haemophilia | | | 2024 | 67 | 528 |
|
| Clinical, laboratory, and molecular aspects of congenital fibrinogen disorders | Seminars in thrombosis and hemostasis | | | 2024 | 97 | 0 |
|
| How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause | International journal of laboratory hematology | | | 2024 | 88 | 668 |
|
| Saignements utérins anormaux et anomalies de l’hémostase | Revue médicale suisse | | | 2024 | 35 | 22 |
|
| Highly thrombogenic phenotype and impaired wound healing in a patient with congenital dysfibrinogenemia : case report | Research and practice in thrombosis and haemostasis | | | 2024 | 126 | 116 |
|
| Challenges in the diagnosis and management of patients with rare coagulation disorders in Lebanon and consequences of a social and economic crisis | Haemophilia | | | 2024 | 55 | 0 |
|
| 2023 ACR/EULAR antiphospholipid syndrome classification criteria | Annals of the rheumatic diseases | | | 2023 | 188 | 2,277 |
|
| Physiological correction of hereditary mild hypofibrinogenemia during pregnancy | Haemophilia | | | 2023 | 221 | 661 |
|
| Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond | Bleeding, thrombosis and vascular biology | | | 2023 | 74 | 328 |
|
| Angiologie et hémostase : ce qui a changé en 2022 | Revue médicale suisse | | | 2023 | 127 | 109 |
|
| Recommendations for the use of andexanet alfa in the management of bleeding in patients on oral factor Xa inhibitors in Switzerland: Guideline from the Working Party Hemostasis of the Swiss Society of Hematology | Swiss medical weekly | | | 2023 | 97 | 579 |
|
| Pharmacodynamics Monitoring of Emicizumab in Patients with Hemophilia A | Thrombosis and haemostasis | | | 2023 | 185 | 0 |
|
| 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria | Arthritis & rheumatology | | | 2023 | 114 | 0 |
|
| High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemia | Haemophilia | | | 2023 | 70 | 0 |
|
| International council for standardisation in haematology recommendations on fibrinogen assays, thrombin clotting time and related tests in the investigation of bleeding disorders | International journal of laboratory hematology | | | 2023 | 94 | 169 |
|
| Coexpression of factor VIII and factor von Willebrand variants in a woman with heavy menstrual bleeding | Blood coagulation & fibrinolysis | | | 2023 | 80 | 0 |
|
| Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders | European journal of haematology | | | 2023 | 98 | 785 |
|
| Longitudinal profile of estrogen-related thrombotic biomarkers after cessation of combined hormonal contraceptives | Blood | | | 2023 | 122 | 308 |
|
| Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest Study | Journal of thrombosis and haemostasis | | | 2023 | 93 | 0 |
|
| Prothrombotic biomarkers during controlled ovarian stimulation for assisted reproductive technology | Fertility and sterility | | | 2023 | 145 | 0 |
|
| Effect of therapeutic anticoagulation on gas exchange in mechanically ventilated COVID-19 patients: A secondary analysis of the COVID-HEP trial | Thrombosis research | | | 2023 | 322 | 95 |
|
| Clinicians’ adherence to guidelines for the preoperative management of direct oral anticoagulants in a tertiary hospital: a retrospective study | BMC anesthesiology | | | 2023 | 100 | 247 |
|
| Fifty years of fibrinogen structure and function | Seminars in thrombosis and hemostasis | | | 2023 | 131 | 21 |
|
| Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster | Haemophilia | | | 2022 | 246 | 2 |
|
| Differential impact of tamoxifen and aromatase inhibitors on thrombin generation: the prospective HEMOBREAST cohort | Blood advances | | | 2022 | 292 | 669 |
|
| Angiologie-hémostase - Année 2021 : morceaux choisis | Revue médicale suisse | | | 2022 | 103 | 132 |
|
| One Hundred Years of Congenital Fibrinogen Disorders | Seminars in thrombosis and hemostasis | | | 2022 | 329 | 0 |
|
| Place des anticoagulants oraux directs dans le traitement des thromboses veineuses de localisation inhabituelle | Revue médicale suisse | | | 2022 | 143 | 276 |
|
| Impact of fibrinogen infusion on thrombin generation and fibrin clot structure in patients with inherited afibrinogenemia | Thrombosis and haemostasis | | | 2022 | 180 | 2 |
|
| Therapeutic anticoagulation to prevent thrombosis, coagulopathy, and mortality in severe COVID-19: The Swiss COVID-HEP randomized clinical trial | Research and practice in thrombosis and haemostasis | | | 2022 | 253 | 317 |
|
| A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family | Haematologica | | | 2022 | 350 | 325 |
|
| Saignements d’origine indéterminée : approche diagnostique et thérapeutique | Revue médicale suisse | | | 2022 | 92 | 402 |
|
| How I treat dysfibrinogenemia | Blood | | | 2021 | 352 | 5,206 |
|
| Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemia | Thrombosis Research | | | 2021 | 216 | 258 |
|
| Afibrinogenemia with two compound heterozygous mutations in FGA gene | Haemophilia | | | 2021 | 287 | 0 |
|
| Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations | Thrombosis research | | | 2021 | 589 | 5 |
|
| Whole blood thromboelastometry by ROTEM and thrombin generation by genesia according to the genotype and clinical phenotype in congenital fibrinogen disorders | International Journal of Molecular Sciences | | | 2021 | 239 | 98 |
|
| Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia | Blood | | | 2021 | 300 | 310 |
|
| Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls | Blood Coagulation and Fibrinolysis | | | 2021 | 235 | 0 |
|
| Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype | Thrombosis Research | | | 2020 | 369 | 52 |
|
| 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 |
|
| Venous thromboembolism in COVID-19: systematic review of reported risks and current guidelines | Swiss Medical Weekly | | | 2020 | 546 | 259 |
|
| Risque thrombotique veineux induit par le SARS-CoV-2 : prévalence, recommandations et perspectives | Revue médicale suisse | | | 2020 | 349 | 253 |
|
| From Routine to Research Laboratory: Strategies for the Diagnosis of Congenital Fibrinogen Disorders | Hämostaseologie | | | 2020 | 280 | 3 |
|
| Fibrin(ogen) in human disease: both friend and foe | Haematologica | | | 2020 | 484 | 464 |
|
| A Unique Case of Acquired Hemophilia A Presenting with Transient Ischemic Attack | Acta Haematologica | | | 2020 | 344 | 400 |
|
| Contraception et maladie thromboembolique veineuse | Revue médicale suisse | | | 2020 | 283 | 343 |
|
| Suggestions for thromboprophylaxis and laboratory monitoring for in-hospital patients with COVID-19 | Swiss Medical Weekly | | | 2020 | 372 | 814 |
|
| Safety of variceal band ligation in patients with cirrhosis and portal vein thrombosis treated with anticoagulant therapy: A retrospective study | European Journal of Gastroenterology and Hepatology | | | 2020 | 420 | 626 |
|
| Recommendations on the use of anticoagulants for the treatment of patients with heparin-induced thrombocytopenia in Switzerland | Swiss Medical Weekly | | | 2020 | 621 | 390 |
|
| 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 | 172 |
|
| Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion | Haemophilia |  | | 2020 | 346 | 0 |
|
| Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and management | Blood Reviews | | | 2020 | 271 | 533 |
|
| Management of bleeding events and invasive procedures in patients with haemophilia A without inhibitors treated with emicizumab | Swiss medical weekly | | | 2020 | 203 | 137 |
|
| Hepatocellular type II fibrinogen inclusions in a patient with severe COVID-19 and hepatitis | Journal of Hepatology | | | 2020 | 415 | 141 |
|
| Congenital structural and functional fibrinogen disorders: a primer for internists | Polskie Archiwum Medycyny Wewnetrznej | | | 2019 | 551 | 457 |
|
| Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and future | Haemophilia | | | 2019 | 315 | 0 |
|
| Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: a systematic literature review | Haemophilia | | | 2019 | 435 | 1 |
|
| Impaired factor XIII activation in patients with congenital afibrinogenemia | Haematologica | | | 2019 | 363 | 145 |
|
| A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIII | Seminars in Thrombosis and Hemostasis | | | 2019 | 381 | 0 |
|
| The impact of haemophilia on the social status and the health-related quality of life in adult Lebanese persons with haemophilia | Haemophilia | | | 2019 | 379 | 0 |
|
| Thrombin generation and fibrin clot structure after vitamin D supplementation | Endocrine Connections | | | 2019 | 394 | 199 |
|
| Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus Report | HemaSphere | | | 2019 | 279 | 572 |
|
| Hereditary fibrinogen disorders: toward a tailored management | | | | 2019 | 364 | 13 |
|
| Antithrombotiques dans le syndrome des anticorps antiphospholipides thrombotique | Revue médicale suisse | | | 2018 | 360 | 180 |
|
| Clinical Consequences and Molecular Bases of Low Fibrinogen Levels | International Journal of Molecular Sciences | | | 2018 | 599 | 306 |
|
| Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis | Thrombosis Research | | | 2018 | 476 | 1 |
|
| Mutational epidemiology of congenital fibrinogen disorders | Thrombosis and Haemostasis | | | 2018 | 598 | 1,004 |
|
| Traitements antithrombotiques et anomalies constitutionnelles hémorragipares de l'hémostase | Revue médicale suisse | | | 2018 | 379 | 172 |
|
| Acide tranexamique dans la prise en charge de l'hémorragie du postpartum : connaissances actuelles | Revue médicale suisse | | | 2018 | 453 | 307 |
|
| A fibrin biofilm covers blood clots and protects from microbial invasion | Journal of Clinical Investigation | | | 2018 | 516 | 351 |
|
| Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH | Journal of Thrombosis and Haemostasis | | | 2018 | 438 | 501 |
|
| Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization | Haemophilia | | | 2017 | 444 | 1 |
|
| Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation | Journal of thrombosis and haemostasis | | | 2017 | 623 | 787 |
|
| Thromboses veineuses splanchniques | Revue médicale suisse | | | 2017 | 447 | 301 |
|
| A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion | BMC Hematology | | | 2017 | 460 | 290 |
|
| Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia | Haemophilia | | | 2017 | 567 | 4 |
|
| Impact of pneumatic tube system transport for the monitoring of heparin therapy | Thrombosis Research | | | 2017 | 470 | 0 |
|
| Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders | Seminars in thrombosis and hemostasis | | | 2016 | 587 | 0 |
|
| Pregnancy | Trauma Induced Coagulopathy | | | 2016 | 440 | 2 |
|
| Diagnostic des anomalies congénitales du fibrinogène | Annales de biologie clinique | | | 2016 | 684 | 1 |
|
| Clinical Features and Management of Congenital Fibrinogen Deficiencies | Seminars in thrombosis and hemostasis | | | 2016 | 609 | 5 |
|
| Can the phenotype of inherited fibrinogen disorders be predicted? | Haemophilia | | | 2016 | 657 | 2 |
|
| Factor concentrates for rare congenital coagulation disorders: where are we now? | Expert opinion on orphan drugs | | | 2016 | 464 | 0 |
|
| Management of congenital quantitative fibrinogen disorders: a Delphi consensus | Haemophilia | | | 2016 | 539 | 0 |
|
| Risks of venous thromboembolism after cesarean sections: A meta-analysis | Chest | | | 2016 | 500 | 0 |
|
| Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management | Nonmalignant Hematology Expert Clinical Review : Questions and Answers | | | 2016 | 511 | 0 |
|
| Natural history of patients with congenital dysfibrinogenemia | Blood | | | 2015 | 743 | 4 |
|
| Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis | Haemophilia | | | 2015 | 527 | 0 |
|
| Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management | Journal of thrombosis and haemostasis | | | 2015 | 800 | 719 |
|
| Maladies héréditaires du fibrinogène: de la biologie moléculaire à la clinique | | | | 2015 | 1,236 | 23 |
|
| Fibrin clot structure in patients with congenital dysfibrinogenaemia | Thrombosis research | | | 2015 | 563 | 2 |
|
| Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature | Haemophilia | | | 2015 | 599 | 5 |
|
| Comparing Two Types of Rabbit ATG prior to Reduced Intensity Conditioning Allogeneic Hematopoietic SCT for Hematologic Malignancies | Bone marrow research | | | 2015 | 721 | 387 |
|
| Hémostase. Aspirine: une ou deux fois par jour? | Revue médicale suisse | | | 2014 | 588 | 0 |
|
| Validation of the disease risk index for outcome of patients undergoing allogeneic hematopoietic stem cell transplantation after T cell depletion | Biology of blood and marrow transplantation | | | 2014 | 626 | 1 |
|
| Fibrinogen geneva II: a new congenitally abnormal fibrinogen alpha chain (Gly17Asp) with a review of similar mutations resulting in abnormal knob A | Blood coagulation & fibrinolysis | | | 2014 | 664 | 3 |
|
| FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations | Thrombosis research | | | 2014 | 705 | 9 |
|
| Acquired factor XIII deficiency: a therapeutic challenge | Thrombosis and haemostasis | | | 2013 | 651 | 0 |
|
| Hémostase : nouveaux anticoagulants oraux : de la théorie à la pratique | Revue médicale suisse | | | 2013 | 415 | 0 |
|
| Pulmonary embolism and fatal stroke in a patient with severe factor XI deficiency after bariatric surgery | Blood coagulation & fibrinolysis | | | 2013 | 519 | 0 |
|
| Could Factor XIII be a solution for the management of surgical bleeding? | Management and Severe Bleeding | | | 2013 | 384 | 0 |
|
| Congenital fibrinogen disorders: an update | Seminars in thrombosis and hemostasis | | | 2013 | 753 | 0 |
|
| Thrombotic complications of myeloproliferative neoplasms: risk assessment and risk-guided management | Journal of thrombosis and haemostasis | | | 2013 | 694 | 0 |
|
| Thrombophilie : quel bilan en 2012? | La Revue de médecine interne | | | 2012 | 508 | 0 |
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| Recurrent Syncope due to Esophageal Squamous Cell Carcinoma | Case reports in oncology | | | 2011 | 701 | 340 |
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