From war to the rule of law: peace building after violent conflicts von Voorhoeve, Joris

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From War to the Rule of Law: Peace Building after Violent Conflicts von Raad voor het Regeringsbeleid, Wetenschappelijke, Voorhoeve, Joris

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A Genetic Screen Implicates miRNA-372 and miRNA-373 As Oncogenes in Testicular Germ Cell Tumors von Voorhoeve, P. Mathijs, le Sage, Carlos, Schrier, Mariette, Gillis, Ad J.M., Stoop, Hans, Nagel, Remco, Liu, Ying-Poi, van Duijse, Josyanne, Drost, Jarno, Griekspoor, Alexander, Zlotorynski, Eitan, Yabuta, Norikazu, De Vita, Gabriella, Nojima, Hiroshi, Looijenga, Leendert H.J., Agami, Reuven

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De europese veiligheidsproblematiek von Voorhoeve, J J C

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HINCUTs in cancer: hypoxia-induced noncoding ultraconserved transcripts von Ferdin, J, Nishida, N, Wu, X, Nicoloso, M S, Shah, M Y, Devlin, C, Ling, H, Shimizu, M, Kumar, K, Cortez, M A, Ferracin, M, Bi, Y, Yang, D, Czerniak, B, Zhang, W, Schmittgen, T D, Voorhoeve, M P, Reginato, M J, Negrini, M, Davuluri, R V, Kunej, T, Ivan, M, Calin, G A

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The Raman electron spin-lattice relaxation process for diatomic molecules. II: Experiments in Ca(OH)2:O2 von VAN VELZEN, G. D. F, SPRENKELS, J. C. M, VOORHOEVE, J. C, MEYER, C. H. M, VAN TOLEDO, W, KORSTANJE, L, BOX, P, WENCKEBACH, W. T

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Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study von Groot‐van der Mooren, Maurike, Graaf, Gert, Weijerman, Michel E, Hoffer, Mariette J. V, Knijnenburg, Jeroen, Kevie‐Kersemaekers, Anne‐Marie M. F, Kooper, Angelique J. A, Voorhoeve, Els, Sikkema‐Raddatz, Birgit, Zutven, Laura J. C. M, Srebniak, Malgorzata Ilona, Huijsdens‐van Amsterdam, Karin, Engelen, John J. M, Smeets, Dominique, Kaam, Anton H, Cornel, Martina C

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The European Community's development program von Masoni, Vittorio, Voorhoeve, Joris J C

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Estimates of live birth prevalence of children with Down syndrome in the period 1991–2015 in the Netherlands von Graaf, G., Engelen, J. J. M., Gijsbers, A. C. J., Hochstenbach, R., Hoffer, M. J. V., Kooper, A. J. A., Sikkema‐Raddatz, B., Srebniak, M. I., Kevie‐Kersemaekers, A. M. F., Zutven, L. J. C. M., Voorhoeve, E.

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IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management von Joustra, S. D, Heinen, C. A, Schoenmakers, N, Bonomi, M, Ballieux, B. E. P. B, Turgeon, M.-O, Bernard, D. J, Fliers, E, van Trotsenburg, A. S. P, Losekoot, M, Persani, L, Wit, J. M, Biermasz, N. R, Pereira, A. M, Oostdijk, W

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Copy number variants in patients with short stature von van Duyvenvoorde, Hermine A, Lui, Julian C, Kant, Sarina G, Oostdijk, Wilma, Gijsbers, Antoinet C J, Hoffer, Mariëtte J V, Karperien, Marcel, Walenkamp, Marie J E, Noordam, Cees, Voorhoeve, Paul G, Mericq, Verónica, Pereira, Alberto M, Claahsen-van de Grinten, Hedi L, van Gool, Sandy A, Breuning, Martijn H, Losekoot, Monique, Baron, Jeffrey, Ruivenkamp, Claudia A L, Wit, Jan M

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Towards Next-Generation Sequencing (NGS)-Based Newborn Screening: A Technical Study to Prepare for the Challenges Ahead von Veldman, Abigail, Kiewiet, Mensiena B G, Heiner-Fokkema, Margaretha Rebecca, Nelen, Marcel R, Sinke, Richard J, Sikkema-Raddatz, Birgit, Voorhoeve, Els, Westra, Dineke, Dollé, Martijn E T, Schielen, Peter C J I, van Spronsen, Francjan J

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The ER22/23EK Polymorphism in the Glucocorticoid Receptor Gene Is Associated with a Beneficial Body Composition and Muscle Strength in Young Adults von van Rossum, Elisabeth F. C., Voorhoeve, Paul G., te Velde, Saskia J., Koper, Jan W., Delemarre-van de Waal, Henriette A., Kemper, Han C. G., Lamberts, Steven W. J.

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Effects of a programme of multifactorial home visits on falls and mobility impairments in elderly people at risk: randomised controlled trial von van Haastregt, Jolanda C M, Diederiks, Jos P M, van Rossum, Erik, de Witte, Luc P, Voorhoeve, Peter M, Crebolder, Harry F J M

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RNA-Binding Protein Dnd1 Inhibits MicroRNA Access to Target mRNA von Kedde, Martijn, Strasser, Markus J., Boldajipour, Bijan, Vrielink, Joachim A.F. Oude, Slanchev, Krasimir, le Sage, Carlos, Nagel, Remco, Voorhoeve, P. Mathijs, van Duijse, Josyanne, Ørom, Ulf Andersson, Lund, Anders H., Perrakis, Anastassis, Raz, Erez, Agami, Reuven

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Results of next‐generation sequencing gene panel diagnostics including copy‐number variation analysis in 810 patients suspected of heritable thoracic aortic disorders von Overwater, Eline, Marsili, Luisa, Baars, Marieke J.H., Baas, Annette F., de Beek, Irma, Dulfer, Eelco, Hagen, Johanna M., Hilhorst‐Hofstee, Yvonne, Kempers, Marlies, Krapels, Ingrid P., Menke, Leonie A., Verhagen, Judith M.A., Yeung, Kak K., Zwijnenburg, Petra J.G., Groenink, Maarten, Rijn, Peter, Weiss, Marjan M., Voorhoeve, Els, Tintelen, J. Peter, Houweling, Arjan C., Maugeri, Alessandra

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Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes von Bowman, Pamela, Mathews, Frances, Barbetti, Fabrizio, Shepherd, Maggie H, Sanchez, Janine, Piccini, Barbara, Beltrand, Jacques, Letourneau-Freiberg, Lisa R, Polak, Michel, Greeley, Siri Atma W, Rawlins, Eamon, Babiker, Tarig, Thomas, Nicholas J, De Franco, Elisa, Ellard, Sian, Flanagan, Sarah E, Hattersley, Andrew T

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Phenotypic spectrum of TGFB3 disease‐causing variants in a Dutch‐French cohort and first report of a homozygous patient von Marsili, Luisa, Overwater, Eline, Hanna, Nadine, Baujat, Geneviève, Baars, Marieke J.H., Boileau, Catherine, Bonneau, Dominique, Brehin, Anne Claire, Capri, Yline, Cheung, Ho Y., Dulfer, Eelco, Gerard, Marion, Gouya, Laurent, Hilhorst‐Hofstee, Yvonne, Houweling, Arjan C., Isidor, Bertrand, Le Gloan, Lauriane, Menke, Leonie A., Odent, Sylvie, Morice‐Picard, Fanny, Vanlerberghe, Clemence, Voorhoeve, Els, Tintelen, J. Peter, Maugeri, Alessandra, Arnaud, Pauline

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Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy von Kiewiet, Gea, Westra, Dineke, de Boer, Eddy N, van Berkel, Emma, Hofste, Tom G J, van Zweeden, Martine, Derks, Ronny C, Leijsten, Nico F A, Ruiterkamp-Versteeg, Martina H A, Charbon, Bart, Johansson, Lennart, Bos-Kruizinga, Janneke, Veenstra, Inge J, de Sain-van der Velden, Monique G M, Voorhoeve, Els, Heiner-Fokkema, M Rebecca, van Spronsen, Francjan, Sikkema-Raddatz, Birgit, Nelen, Marcel

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P6497Loeys-Dietz syndrome-5: phenotypic spectrum of TGFB3 mutations in an international cohort and first report of a homozygous patient von Marsili, L, Overwater, E, Hanna, N, Baujat, G, Baars, M J H, Brehin, A C, Gerard, M, Gouya, L, Houweling, A C, Vanlerberghe, C, Voorhoeve, E, Van Tintelen, J P, Maugeri, A, Arnaud, P

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