V. Marion

Full Title: Fibrinogen AαThr312Ala polymorphism is associated with Chronic Thromboembolic Pulmonary Hypertension Short title: Fibrinogen AαThr312Ala in CTEPH Authors

F. Dudbridge, J. Eikenboom, C. Treacy, 2007 .

Genetics In Familial Thrombosis study: sample collection and description of study population

J. Eikenboom, V. Marion, R. Minkelen, 2009 .

Genome‐wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis study

J. Houwing-Duistermaat, P. Slagboom, M. Heijer, 2013, Journal of thrombosis and haemostasis : JTH.

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

J. Goudemand, S. Lethagen, J. Eikenboom, 2006, Journal of thrombosis and haemostasis : JTH.

Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension

F. Dudbridge, J. Eikenboom, C. Treacy, 2008, European Respiratory Journal.