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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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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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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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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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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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism von Germain, Marine, Chasman, Daniel I., de Haan, Hugoline, Tang, Weihong, Lindström, Sara, Weng, Lu-Chen, de Andrade, Mariza, de Visser, Marieke C.H., Wiggins, Kerri L., Suchon, Pierre, Saut, Noémie, Smadja, David M., Le Gal, Grégoire, van Hylckama Vlieg, Astrid, Di Narzo, Antonio, Hao, Ke, Nelson, Christopher P., Rocanin-Arjo, Ares, Folkersen, Lasse, Monajemi, Ramin, Rose, Lynda M., Brody, Jennifer A., Slagboom, Eline, Aïssi, Dylan, Gagnon, France, Deleuze, Jean-Francois, Deloukas, Panos, Tzourio, Christophe, Dartigues, Jean-Francois, Berr, Claudine, Taylor, Kent D., Civelek, Mete, Eriksson, Per, Psaty, Bruce M., Houwing-Duitermaat, Jeanine, Goodall, Alison H., Cambien, François, Kraft, Peter, Amouyel, Philippe, Samani, Nilesh J., Basu, Saonli, Ridker, Paul M., Rosendaal, Frits R., Kabrhel, Christopher, Folsom, Aaron R., Heit, John, Reitsma, Pieter H., Trégouët, David-Alexandre, Smith, Nicholas L., Morange, Pierre-Emmanuel

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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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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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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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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function von Porcu, Eleonora, Medici, Marco, Pistis, Giorgio, Volpato, Claudia B, Wilson, Scott G, Cappola, Anne R, Bos, Steffan D, Deelen, Joris, den Heijer, Martin, Freathy, Rachel M, Lahti, Jari, Liu, Chunyu, Lopez, Lorna M, Nolte, Ilja M, O'Connell, Jeffrey R, Tanaka, Toshiko, Trompet, Stella, Arnold, Alice, Bandinelli, Stefania, Beekman, Marian, Böhringer, Stefan, Brown, Suzanne J, Buckley, Brendan M, Camaschella, Clara, de Craen, Anton J M, Davies, Gail, de Visser, Marieke C H, Ford, Ian, Forsen, Tom, Frayling, Timothy M, Fugazzola, Laura, Gögele, Martin, Hattersley, Andrew T, Hermus, Ad R, Hofman, Albert, Houwing-Duistermaat, Jeanine J, Jensen, Richard A, Kajantie, Eero, Kloppenburg, Margreet, Lim, Ee M, Masciullo, Corrado, Mariotti, Stefano, Minelli, Cosetta, Mitchell, Braxton D, Nagaraja, Ramaiah, Netea-Maier, Romana T, Palotie, Aarno, Persani, Luca, Piras, Maria G, Psaty, Bruce M, Räikkönen, Katri, Richards, J Brent, Rivadeneira, Fernando, Sala, Cinzia, Sabra, Mona M, Sattar, Naveed, Shields, Beverley M, Soranzo, Nicole, Starr, John M, Stott, David J, Sweep, Fred C G J, Usala, Gianluca, van der Klauw, Melanie M, van Heemst, Diana, van Mullem, Alies, Vermeulen, Sita H, Visser, W Edward, Walsh, John P, Westendorp, Rudi G J, Widen, Elisabeth, Zhai, Guangju, Cucca, Francesco, Deary, Ian J, Eriksson, Johan G, Ferrucci, Luigi, Fox, Caroline S, Jukema, J Wouter, Kiemeney, Lambertus A, Pramstaller, Peter P, Schlessinger, David, Shuldiner, Alan R, Slagboom, Eline P, Uitterlinden, André G, Vaidya, Bijay, Visser, Theo J, Wolffenbuttel, Bruce H R, Meulenbelt, Ingrid, Rotter, Jerome I, Spector, Tim D, Hicks, Andrew A, Toniolo, Daniela, Sanna, Serena, Peeters, Robin P, Naitza, Silvia

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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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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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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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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 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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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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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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