Genetic determinants of activity and antigen levels of contact system factors von Rohmann, J. L., Haan, H. G., Algra, A., Vossen, C. Y., Rosendaal, F. R., Siegerink, B.

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Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT) von VOSSEN, C. Y., CONARD, J., FONTCUBERTA, J., MAKRIS, M., VAN DER MEER, F. J. M., PABINGER, I., PALARETI, G., PRESTON, F. E., SCHARRER, I., SOUTO, J. C., SVENSSON, P., WALKER, I. D., ROSENDAAL, F. R.

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Thrombin generation profiles in deep venous thrombosis von BRUMMEL‐ZIEDINS, K. E., VOSSEN, C. Y., BUTENAS, S., MANN, K. G., ROSENDAAL, F. R.

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Hereditary thrombophilia and fetal loss: a prospective follow‐up study von Vossen, C. Y., Preston, F. E., Conard, J., Fontcuberta, J., Makris, M., Van Der Meer, F. J. M., Pabinger, I., Palareti, G., Scharrer, I., Souto, J. C., Svensson, P., Walker, I. D., Rosendaal, F. R.

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Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C‐deficient family von Vossen, C. Y., Hasstedt, S. J., Rosendaal, F. R., Callas, P. W., Bauer, K. A., Broze, G. J., Hoogendoorn, H., Long, G. L., Scott, B. T., Bovill, E. G.

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Validated Smoking Cessation and Prognosis in Patients with Stable Coronary Heart Disease von Breitling, L.P, Rothenbacher, D, Vossen, C.Y, Hahmann, H, Wüsten, B, Brenner, H

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Risk of venous thrombosis in patients with major illnesses: results from the MEGA study von OCAK, G., VOSSEN, C. Y., VERDUIJN, M., DEKKER, F. W., ROSENDAAL, F. R., CANNEGIETER, S. C., LIJFERING, W. M.

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PMU82 VARYING WILLINGNESS-TO-PAY BASED ON DISEASE BURDEN: IMPACT ON HEALTH TECHNOLOGY ASSESSMENT OUTCOMES OF SPECIALIST DRUGS IN THE NETHERLANDS von Schurer, M., Vossen, C.Y., van Keep, M., Horscroft, J., Moorhouse, J.A., Chapman, A.M., Akehurst, R.L.

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Risk of venous thrombosis in patients with chronic kidney disease: identification of high‐risk groups von Ocak, G., Lijfering, W. M., Verduijn, M., Dekker, F. W., Rosendaal, F. R., Cannegieter, S. C., Vossen, C. Y.

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Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency von EMMERICH, J., VOSSEN, C. Y., CALLAS, P. W., DEMERS, C., NAUD, S., LONG, G. L., COUTURE, P., ROSENDAAL, F. R., BOVILL, E. G.

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Chronic kidney disease stages 1–3 increase the risk of venous thrombosis von OCAK, G., VERDUIJN, M., VOSSEN, C. Y., LIJFERING, W. M., DEKKER, F. W., ROSENDAAL, F. R., GANSEVOORT, R. T., MAHMOODI, B. K.

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Mortality and inherited thrombophilia: results from the European Prospective Cohort on Thrombophilia von PABINGER, I., VOSSEN, C. Y., LANG, J., CONARD, J., GARCÍA‐DABRIO, M. C., MIESBACH, W., LEGNANI, C., SVENSSON, P., KAIDER, A., ROSENDAAL, F. R.

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The plasma hemostatic proteome: thrombin generation in healthy individuals von BRUMMEL‐ZIEDINS, K., VOSSEN, C. Y., ROSENDAAL, F. R., UMEZAKI, K., MANN, K. G.

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Familial thrombophilia and lifetime risk of venous thrombosis von Vossen, C. Y., Conard, J., Fontcuberta, J., Makris, M., Van Der Meer, F. J. M., Pabinger, I., Palareti, G., Preston, F. E., Scharrer, I., Souto, J. C., Svensson, P., Walker, I. D., Rosendaal, F. R.

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Genetic variants associated with protein C levels von Vossen, C. Y., Koeleman, B. P., Hasstedt, S. J., Nijman, I. J., Renkens, I. J., Callas, P. W., Rosendaal, F. R., Bovill, E. G.

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Risk of arterial thrombosis in carriers of familial thrombophilia von VOSSEN, C. Y., ROSENDAAL, F. R.

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The protective effect of the factor XIII Val34Leu mutation on the risk of deep venous thrombosis is dependent on the fibrinogen level von VOSSEN, C. Y., ROSENDAAL, F. R.

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Genome scan of clot lysis time and its association with thrombosis in a protein C‐deficient kindred von MELTZER, M. E., HASSTEDT, S. J., VOSSEN, C. Y., CALLAS, P. W., DE GROOT, PH. G., ROSENDAAL, F. R., LISMAN, T., BOVILL, E. G.

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Computational candidate gene prioritization for venous thrombosis von VOSSEN, C. Y., ELBERS, C. C., KOELEMAN, B. P. C., ROSENDAAL, F. R., BOVILL, E. G.

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Attitudes toward genetic testing for thrombophilia in asymptomatic members of a large family with heritable protein C deficiency von KORLAAR, I. M., VOSSEN, C. Y., ROSENDAAL, F. R., BOVILL, E. G., NAUD, S., CAMERON, L. D., KAPTEIN, A. A.

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