Identification of low-frequency variants associated with gout and serum uric acid levels von Sulem, Patrick, Stefansson, Kari, Gudbjartsson, Daniel F, Walters, G Bragi, Helgadottir, Hafdis T, Helgason, Agnar, Gudjonsson, Sigurjon A, Zanon, Carlo, Besenbacher, Soren, Bjornsdottir, Gyda, Magnusson, Olafur T, Magnusson, Gisli, Hjartarson, Eirikur, Saemundsdottir, Jona, Gylfason, Arnaldur, Jonasdottir, Adalbjorg, Holm, Hilma, Karason, Ari, Rafnar, Thorunn, Stefansson, Hreinn, Andreassen, Ole A, Pedersen, Jesper H, Pack, Allan I, de Visser, Marieke C H, Kiemeney, Lambertus A, Geirsson, Arni J, Eyjolfsson, Gudmundur I, Olafsson, Isleifur, Kong, Augustine, Masson, Gisli, Jonsson, Helgi, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif

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Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen γ′ levels von Uitte de Willige, Shirley, de Visser, Marieke C.H., Houwing-Duistermaat, Jeanine J., Rosendaal, Frits R., Vos, Hans L., Bertina, Rogier M.

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Differential constraints for bounded recursive identification with multivariate splines von de Visser, C.C., Chu, Q.P., Mulder, J.A.

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A sparse collocation method for solving time-dependent HJB equations using multivariate B-splines von Govindarajan, Nithin, de Visser, Cornelis. C., Krishnakumar, Kalmanje

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A new approach to linear regression with multivariate splines von de Visser, C.C., Chu, Q.P., Mulder, J.A.

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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.

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A novel online adaptive kernel method with kernel centers determined by a support vector regression approach von Sun, L.G., de Visser, C.C., Chu, Q.P., Mulder, J.A.

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Anthropometric Measures, Fitness and Habitual Physical Activity in Offspring of Hypertensive Parents Dutch Hypertension and Offspring Study von de Visser, Dianne C., van Hooft, Ingrid M.S., van Doornen, Lorenz J.P., Hofman, Albert, Orlebeke, Jacob F., Grobbee, Diederick E.

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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.

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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.

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ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens von Morelli, Vania M., de Visser, Marieke C. H., van Tilburg, Nico H., Vos, Hans L., Eikenboom, Jeroen C. J., Rosendaal, Frits R., Bertina, Rogier M.

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Fibrinogen gamma gene 3’-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population von Willige, Shirley Uitte de, Pyle, Meridith E., Vos, Hans L., de Visser, Marieke C. H., Lally, Cathy, Dowling, Nicole F., Hooper, W. Craig, Bertina, Rogier M., Austin, Harland

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Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarction von van Minkelen, Rick, Wettinger, Stephanie Bezzina, de Visser, Marieke C.H, Vos, Hans L, Reitsma, Pieter H, Rosendaal, Frits R, Bertina, Rogier M, Doggen, Carine J.M

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Factor IX-R338L (Factor IX Padua) screening in a Dutch population of sibpairs with early onset venous thromboembolism von Koenderman, Jorine S, Bertina, Rogier M, Reitsma, Pieter H, de Visser, Marieke C.H

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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.

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Existing and Training Induced Differences in Aerobic Fitness: Their Relationship to Physiological Response Patterns During Different Types of Stress von DE Geus, Eco J.C., van Doornen, Lorenz J.P., de Visser, Dianne C., Orlebeke, Jacob F.

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Haplotypes of IL1B, IL1RN, IL1R1, and IL1R2 and the Risk of Venous Thrombosis von van Minkelen, Rick, de Visser, Marieke C.H, Houwing-Duistermaat, Jeanine J, Vos, Hans L, Bertina, Rogier M, Rosendaal, Frits R

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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.

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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.

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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.

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