1. Freitas, Samuel da Silva, Rezende, Suely Meireles, de Oliveira, Luciana Correa, Carvalho, Maria Raquel Santos, Chaves, Daniel Gonçalves. 2019. Genetic variants of VWF gene in type 2 von Willebrand disease. In Haemophilia : the official journal of the World Federation of Hemophilia, 25, e78-e85. doi:10.1111/hae.13714. https://pubmed.ncbi.nlm.nih.gov/30817071/
2. Keightley, A M, Lam, Y M, Brady, J N, Cameron, C L, Lillicrap, D. . Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter. In Blood, 93, 4277-83. doi:. https://pubmed.ncbi.nlm.nih.gov/10361125/
3. Zhao, Yawei, He, Meihui, Cui, Lianzhi, Zhang, Hansi, Chen, Li. 2024. Systematic screening of protein-coding gene expression identified VWF as a potential key regulator in anthracycline-based chemotherapy-exacerbated metastasis of breast cancer. In BMC cancer, 24, 1243. doi:10.1186/s12885-024-12999-9. https://pubmed.ncbi.nlm.nih.gov/39379897/
4. Yadegari, Hamideh, Jamil, Muhammad Ahmer, Müller, Jens, Lillicrap, David, Oldenburg, Johannes. . Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD. In Blood advances, 6, 1038-1053. doi:10.1182/bloodadvances.2021005895. https://pubmed.ncbi.nlm.nih.gov/34861678/
5. Castaman, Giancarlo, Federici, Augusto B. 2016. Type 2B von Willebrand Disease: A Matter of Plasma Plus Platelet Abnormality. In Seminars in thrombosis and hemostasis, 42, 478-82. doi:10.1055/s-0036-1579638. https://pubmed.ncbi.nlm.nih.gov/27148840/