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Hamostaseologie|February 15, 2021
Functional Roles of the von Willebrand Factor PropeptideOrla Rawley, David LillicrapBritish Journal of Haematology|April 26, 2012
Elevated factor VIII levels and risk of venous thrombosisP Vince Jenkins, Orla Rawley, Owen P Smith, et al.Blood|February 22, 2013
Elucidating the role of carbohydrate determinants in regulating hemostasis: insights and opportunitiesRoger J S Preston, Orla Rawley, Eimear M Gleeson, et al.Journal of Thrombosis and Haemostasis : JTH|June 21, 2021
Stabilin-2 deficiency increases thrombotic burden and alters the composition of venous thrombi in a mouse modelAlison Michels, Laura L Swystun, Courtney N Dwyer, et al.Research and Practice in Thrombosis and Haemostasis|September 2, 2025
Factor XIII deficiency due to compound heterozygosity for 2 F13A1 variantsJodie Odame, Caroline Malcolmson, Cindy Wakefield, et al.Blood Advances|December 3, 2021
Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWDHamideh Yadegari, Muhammad Ahmer Jamil, Jens Müller, et al.Journal of Thrombosis and Haemostasis : JTH|February 19, 2025
Identification of multiple novel procoagulant plasma ligands for stabilin-2Mary Underwood, Felipe Da Veiga Leprevost, Venkatesha Basrur, et al.Blood Advances|January 12, 2022
Novel cysteine substitution p.(Cys1084Tyr) causes variable expressivity of qualitative and quantitative VWF defectsOrla Rawley, Laura L Swystun, Christine Brown, et al.Blood|October 10, 2013
Altered glycosylation of platelet-derived von Willebrand factor confers resistance to ADAMTS13 proteolysisRachel T McGrath, Maartje van den Biggelaar, Barry Byrne, et al.Journal of Thrombosis and Haemostasis : JTH|December 1, 2023
The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence changePamela A Christopherson, Nathalie Tijet, Sandra L Haberichter, et al.Pageof 2