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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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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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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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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Discovery of common variants associated with low TSH levels and thyroid cancer risk von Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Jonasson, Jon G, Masson, Gisli, He, Huiling, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Stacey, Simon N, Johannsdottir, Hrefna, Th Helgadottir, Hafdis, Li, Wei, Nagy, Rebecca, Ringel, Matthew D, Kloos, Richard T, de Visser, Marieke C H, Plantinga, Theo S, den Heijer, Martin, Aguillo, Esperanza, Panadero, Angeles, Prats, Enrique, Garcia-Castaño, Almudena, De Juan, Ana, Rivera, Fernando, Walters, G Bragi, Bjarnason, Hjordis, Tryggvadottir, Laufey, Eyjolfsson, Gudmundur I, Bjornsdottir, Unnur S, Holm, Hilma, Olafsson, Isleifur, Kristjansson, Kristleifur, Kristvinsson, Hoskuldur, T Magnusson, Olafur, Thorleifsson, Gudmar, Gulcher, Jeffrey R, Kong, Augustine, Kiemeney, Lambertus ALM, Jonsson, Thorvaldur, Hjartarson, Hannes, Mayordomo, Jose I, Netea-Maier, Romana T, de la Chapelle, Albert, Hrafnkelsson, Jon, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari

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Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study von Pintao, Maria Carolina, Ribeiro, Daniel D., Bezemer, Irene D., Garcia, Andrea A., de Visser, Marieke C.H., Doggen, Carine J.M., Lijfering, Willem M., Reitsma, Pieter H., Rosendaal, Frits R.

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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

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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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Frequency of the TAFI – 438 G/A and factor XIIIA Val34Leu polymorphisms in patients with objectively proven pulmonary embolism von Zidane, Majida, de Visser, Marieke C. H., ten Wolde, Marije, L.Vos, Hans, de Monyé, Wouter, Bertina, Rogier M., Huisman, Menno V.

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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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Annexin A5 haplotypes in familial hypercholesterolemia: Lack of association with carotid intima-media thickness and cardiovascular disease risk von Hiddink, Larissa, Dallinga-Thie, Geesje M, Hovingh, G. Kees, de Visser, Marieke C.H, Peer, Petronella G.M, Stalenhoef, Anton F.H, van Heerde, Waander L

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Polymorphisms in the Annexin A5 gene influence circulating Annexin A5 levels in healthy controls von Hiddink, Larissa, de Visser, Marieke C.H, van Heerde, Waander L

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Factor X Levels, Polymorphisms in the Promoter Region of Factor X, and the Risk of Venous Thrombosis von de Visser, Marieke C. H., Poort, Swibertus R., Vos, Hans L., Rosendaal, Frits R., Bertina, Rogier M.

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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.

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Cerebral small vessel disease genomics and its implications across the lifespan von Sargurupremraj, Muralidharan, Suzuki, Hideaki, Jian, Xueqiu, Sarnowski, Chloé, Evans, Tavia E., Eiriksdottir, Gudny, Sakaue, Saori, Terzikhan, Natalie, Zhao, Wei, Armstrong, Nicola J., Yanek, Lisa R., Kumar, Rajan B., van den Akker, Erik B., McWhirter, Rebekah E., Trompet, Stella, Mishra, Aniket, Saba, Yasaman, Satizabal, Claudia L., Beaudet, Gregory, Petit, Laurent, Tsuchida, Ami, Schilling, Sabrina, Sigurdsson, Sigurdur, Lewis, Cora E., Lopez, Oscar L., Smith, Jennifer A., Valdés Hernández, Maria C., van der Grond, Jeroen, Wright, Margaret J., Knol, Maria J., Thomson, Russell J., Le Grand, Quentin, Duperron, Marie-Gabrielle, Smith, Albert V., Schreiner, Pamela J., Evans, Denis A., Rotter, Jerome I., Beiser, Alexa S., Maniega, Susana Muñoz, Beekman, Marian, Trollor, Julian, Stott, David J., Vernooij, Meike W., Wittfeld, Katharina, Niessen, Wiro J., Soumaré, Aicha, Sidney, Stephen, Turner, Stephen T., Davies, Gail, Thalamuthu, Anbupalam, Völker, Uwe, van Buchem, Mark A., Dupuis, Josée, Bastin, Mark E., Teumer, Alexander, Amouyel, Philippe, Kwok, John B., Bülow, Robin, Deary, Ian J., Schofield, Peter R., Brodaty, Henry, Jiang, Jiyang, Tabara, Yasuharu, Setoh, Kazuya, Miyamoto, Susumu, Yoshida, Kazumichi, Nagata, Manabu, Matsuda, Fumihiko, Psaty, Bruce M., Bennett, David A., De Jager, Philip L., Mosley, Thomas H., Sachdev, Perminder S., Schmidt, Reinhold, Evangelou, Evangelos, Trégouët, David-Alexandre, Ikram, Mohammad A., DeCarli, Charles, Srikanth, Velandai K., Jukema, J. Wouter, Slagboom, Eline P., Kardia, Sharon L. R., Okada, Yukinori, Mazoyer, Bernard, Wardlaw, Joanna M., Nyquist, Paul A., Mather, Karen A., Grabe, Hans J., Schmidt, Helena, Van Duijn, Cornelia M., Gudnason, Vilmundur, Longstreth, William T., Launer, Lenore J., Lathrop, Mark, Seshadri, Sudha, Tzourio, Christophe, Adams, Hieab H., Matthews, Paul M., Fornage, Myriam, Debette, Stéphanie

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The Marburg I polymorphism of factor VII-activating protease is not associated with venous thrombosis von van Minkelen, Rick, de Visser, Marieke C.H., Vos, Hans L., Bertina, Rogier M., Rosendaal, Frits R.

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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.

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The effect of plasma caeruloplasmin levels on the sensitivity for activated protein C von De Visser, Marieke C. H., Souverijn, John H. M., Rosendaal, Frits R., Bertina, Rogier M.

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Haplotypes of VKORC1, NQ01 and GGCX, their effect on activity levels of vitamin K-dependent coagulation factors, and the risk of venous thrombosis von DE VISSER, Marieke C. H, ROSHANI, Sara, RUTTEN, Julie W, VAN HYLCKAMA VLIEG, Astrid, VOS, Hans L, ROSENDAAL, Frits R, REITSMA, Pieter H

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