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Scientific Reports|January 20, 2026
Updated global prevalence and ethnic diversity of von Willebrand disease based on population genetics analysisOmid Seidizadeh, Andrea Cairo, Camilla Oriani, et al.
Seminars in Thrombosis and Hemostasis|December 26, 2025
Von Willebrand disease type 2A: an updateOmid Seidizadeh, Luciano Baronciani, Pier Mannuccio Mannucci, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|July 19, 2021
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disordersSamin Mohsenian, Omid Seidizadeh, Mojgan Mirakhorli, et al.
NPJ Genomic Medicine|October 16, 2023
Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databasesOmid Seidizadeh, Andrea Cairo, Luciano Baronciani, et al.
Research and Practice in Thrombosis and Haemostasis|February 24, 2026
Beyond a century of discovery: the global and persistent burden of underdiagnosis in von Willebrand diseaseOmid Seidizadeh, Rezan Abdul-Kadir, Pier Mannuccio Mannucci, et al.
Blood Transfusion = Trasfusione Del Sangue|June 1, 2021
Von Willebrand disease combined with coagulation defects in IranOmid Seidizadeh, Minoo Ahmadinejad, Sanaz Homayoun, et al.
Blood Advances|June 27, 2024
Global prevalence of hereditary thrombotic thrombocytopenic purpura determined by genetic analysisOmid Seidizadeh, Andrea Cairo, Ilaria Mancini, et al.
Journal of Thrombosis and Haemostasis : JTH|June 12, 2025
The genetic spectrum of rare bleeding disordersSamin Mohsenian, Omid Seidizadeh, Andrea Cairo, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|January 12, 2023
Prevalence of hemorrhagic ovarian cysts in patients with rare inherited bleeding disordersOmid Seidizadeh, Ghasem Miri Aliabad, Ilia Mirzaei, et al.
The Lancet. Haematology|November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implicationsOmid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.
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