Amparo Vayá

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)

Katrin Hoffmann, Christine Karin Dreger, Ada L. Olins et al. · Nature Genetics · 2002 · 346 citations

Lamin B Receptor, Granulocyte, Cell Signaling +7

PAI-1 promoter 4G/5G genotype as an additional risk factor for venous thrombosis in subjects with genetic thrombophilic defects

Rafael Giner Seguí, Amparo Estellés, Yolanda Mira et al. · British Journal of Haematology · 2000 · 100 citations

Genetic Thrombophilic Defects, Healthy Subjects, Impaired Fibrinolysis +23

Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic risk

Pilar Medina, Silvia Navarro, Amparo Estellés et al. · Thrombosis and Haemostasis · 2004 · 100 citations

Hyperlipidaemia and venous thromboembolism in patients lacking thrombophilic risk factors

Amparo Vayá, Yolanda Mira, Fernando Ferrando et al. · British Journal of Haematology · 2002 · 93 citations · Full text

Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.

José A. Aznar, Amparo Vayá, A. Estellés et al. · PubMed · 2000 · 85 citations