ABO Blood Group and von Willebrand Factor Levels Partially Explained the Incomplete Penetrance of Congenital Thrombophilia

Association of Variation at the ABO Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin

(2011) Stefan Kiechl et al.   Circulation-Cardiovascular Genetics

Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study

(2011) Marine Germain et al.   PLoS One

Clinical guidelines for testing for heritable thrombophilia

(2010) Trevor Baglin et al.   BRITISH JOURNAL OF HAEMATOLOGY

A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin

(2010) B. K. MAHMOODI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach

(2009) D.-A. Tregouet et al.   BLOOD

Expression of terminal  2-6-linked sialic acid on von Willebrand factor specifically enhances proteolysis by ADAMTS13

(2009) R. T. McGrath et al.   BLOOD

Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives

(2009) W. M. Lijfering et al.   BLOOD

Recommendations on Testing for Thrombophilia in Venous Thromboembolic Disease: a French Consensus Guideline

(2009)   JOURNAL DES MALADIES VASCULAIRES

Genetics of venous thrombosis

(2009) F. R. ROSENDAAL et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS