Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency von Pintao, Maria C, Garcia, A. A, Borgel, D, Alhenc-Gelas, M, Spek, C. A, de Visser, M. C. H, Gandrille, S, Reitsma, Pieter H

Volltext

Genome‐wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis study von Visser, M.C.H., Minkelen, R., Marion, V., Heijer, M., Eikenboom, J., Vos, H.L., Slagboom, P.E., Houwing‐Duistermaat, J.J., Rosendaal, F.R., Bertina, R.M.

Volltext

Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis von Uitte De Willige, S., Van Marion, V., Rosendaal, F. R., Vos, H. L., De Visser, M. C. H., Bertina, R. M.

Volltext

ABO blood group genotypes and the risk of venous thrombosis: effect of factor V Leiden von MORELLI, V. M., DE VISSER, M. C. H., VOS, H. L., BERTINA, R. M., ROSENDAAL, F. R.

Volltext

High levels of protein C are determined by PROCR haplotype 3 von PINTAO, M. C., ROSHANI, S., DE VISSER, M. C. H., TIEKEN, C., TANCK, M. W. T., WICHERS, I. M., MEIJERS, J. C. M., ROSENDAAL, F. R., MIDDELDORP, S., REITSMA, P. H.

Volltext

Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes von Haan, H. G., Hylckama Vlieg, A., Lotta, L. A., Gorski, M. M., Bucciarelli, P., Martinelli, I., Baglin, T. P., Peyvandi, F., Rosendaal, F. R., Amouyel, P., Andrade, M., Basu, S., Berr, C., Brody, J. A., Chasman, D. I, Dartigues, J.‐F., Folsom, A. R., Germain, M., Heit, J., Houwing‐Duitermaat, J., Kabrhel, C., Kraft, P., Le Gal, G., Lindström, S., Monajemi, R., Morange, P.‐E., Psaty, B. M., Reitsma, P. H., Ridker, P. M., Rose, L. M., Saut, N., Slagboom, E., Smadja, D., Smith, N. L., Suchon, P., Tang, W., Taylor, K. D., Trégouët, D.‐A., Tzourio, C., Visser, M. C. H., Weng, L.‐C., Wiggins, K. L.

Volltext

Sequence variants and haplotypes of the factor IX gene and the risk of venous thrombosis von VAN MINKELEN, R., DE VISSER, M. C. H., VAN HYLCKAMA VLIEG, A., VOS, H. L., BERTINA, R. M.

Volltext

The −589C>T polymorphism in the interleukin‐4 gene (IL‐4) is associated with a reduced risk of myocardial infarction in young individuals von PAFFEN, E., MEDINA, P., DE VISSER, M. C. H., VAN WIJNGAARDEN, A., ZORIO, E., ESTELLÉS, A., ROSENDAAL, F. R., ESPAÑA, F., BERTINA, R. M., DOGGEN, C. J. M.

Volltext

Selectin haplotypes and the risk of venous thrombosis: influence of linkage disequilibrium with the factor V Leiden mutation von UITTE DE WILLIGE, S., DE VISSER, M. C. H., VOS, H. L., HOUWING‐DUISTERMAAT, J. J., ROSENDAAL, F. R., BERTINA, R. M.

Volltext

Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci von De Visser, M. C. H., Sandkuijl, L. A., Lensen, R. P. M., Vos, H. L., Rosendaal, F. R., Bertina, R. M.

Volltext

Determinants of the APTT‐ and ETP‐based APC sensitivity tests von VISSER, M. C. H., HYLCKAMA VLIEG, A., TANS, G., ROSING, J., DAHM, A. E. A., SANDSET, P. M., ROSENDAAL, F. R., BERTINA, R. M.

Volltext

Estimation of genetic effects in multiple cases family studies using penalized maximum likelihood methodology von Tsonaka, Roula, De Visser, Marieke C H, Houwing-Duistermaat, Jeanine

Volltext

Haplotypes of VKORC1, NQO1 and GGCX, their effect on activity levels of vitamin K-dependent coagulation factors, and the risk of venous thrombosis von Visser, Marieke C. H. de, Roshani, Sara, Rutten, Julie W., Vlieg, Astrid van Hylckama, Vos, Hans L., Rosendaal, Frits R., Reitsma, Pieter H.

Volltext

Haplotypes of the fibrinogen gamma gene do not affect the risk of myocardial infarction von UITTE DE WILLIGE, S., DOGGEN, C. J. M., DE VISSER, M. C. H., BERTINA, R. M., ROSENDAAL, F. R.

Volltext

A Reduced Sensitivity for Activated Protein C in the Absence of Factor V Leiden Increases the Risk of Venous Thrombosis von de Visser, Marieke C.H., Rosendaal, Frits R., Bertina, Rogier M.

Volltext

Polymorphism 10034C>T is located in a region regulating polyadenylation of FGG transcripts and influences the fibrinogen γ′/γA mRNA ratio von UITTE DE WILLIGE, S., RIETVELD, I. M., DE VISSER, M. C. H., VOS, H. L., BERTINA, R. M.

Volltext

The HR2 Haplotype of Factor V: Effects on Factor V Levels, Normalized Activated Protein C Sensitivity Ratios and the Risk of Venous Thrombosis von de Visser, Marieke C. H., Guasch, Joan F., Kamphuisen, Pieter W., Vos, Hans L., Rosendaal, Frits R., Bertina, Rogier M.

Volltext

Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency von Pintao, Maria, Garcia, A A, Borgel, D, Alhenc-Gelas, M, Spek, C A, de Visser, M C H, Gandrille, S, Reitsma, P H

Volltext

Polymorphism 10034C>T is located in a region regulating polyadenylation of FGG transcripts and influences the fibrinogen gamma'/gammaA mRNA ratio von Uitte de Willige, S, Rietveld, I M, De Visser, M C H, Vos, H L, Bertina, R M

Volltext

RYR1-related myopathies: a wide spectrum of phenotypes throughout life von Snoeck, M., van Engelen, B. G. M., Küsters, B., Lammens, M., Meijer, R., Molenaar, J. P. F., Raaphorst, J., Verschuuren-Bemelmans, C. C., Straathof, C. S. M., Sie, L. T. L., de Coo, I. F., van der Pol, W. L., de Visser, M., Scheffer, H., Treves, S., Jungbluth, H., Voermans, N. C., Kamsteeg, E.-J.

Volltext