NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable target von Hiemcke-Jiwa, L. S., Meister, M. T., Martin, E., Dierselhuis, M. P., Haveman, L. M., Meijers, R. W. J., Tops, B. B. J., Wesseling, P., van Diest, P. J., van Gorp, J. M., Hehir-Kwa, J. Y., van Belzen, I. A. E. M., Bonenkamp, J. J., van Noesel, M. M., Flucke, U., Kester, L. A.

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NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable target von Hiemcke-Jiwa, L S, Meister, M T, Martin, E, Dierselhuis, M P, Haveman, L M, Meijers, R W J, Tops, B B J, Wesseling, P, van Diest, P J, van Gorp, J M, Hehir-Kwa, J Y, van Belzen, I A E M, Bonenkamp, J J, van Noesel, M M, Flucke, U, Kester, L A

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Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGS von van Belzen, Ianthe A E M, Cai, Casey, van Tuil, Marc, Badloe, Shashi, Strengman, Eric, Janse, Alex, Verwiel, Eugène T P, van der Leest, Douwe F M, Kester, Lennart, Molenaar, Jan J, Meijerink, Jules, Drost, Jarno, Peng, Weng Chuan, Kerstens, Hindrik H D, Tops, Bastiaan B J, Holstege, Frank C P, Kemmeren, Patrick, Hehir-Kwa, Jayne Y

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Structural variant detection in cancer genomes: computational challenges and perspectives for precision oncology von van Belzen, Ianthe A. E. M., Schönhuth, Alexander, Kemmeren, Patrick, Hehir-Kwa, Jayne Y.

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Molecular Characterization Reveals Subclasses of 1q Gain in Intermediate Risk Wilms Tumors von van Belzen, Ianthe A E M, van Tuil, Marc, Badloe, Shashi, Strengman, Eric, Janse, Alex, Verwiel, Eugène T P, van der Leest, Douwe F M, de Vos, Sam, Baker-Hernandez, John, Groenendijk, Alissa, de Krijger, Ronald, Kerstens, Hindrik H D, Drost, Jarno, van den Heuvel-Eibrink, Marry M, Tops, Bastiaan B J, Holstege, Frank C P, Kemmeren, Patrick, Hehir-Kwa, Jayne Y

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Immune biomarkers for predicting response to adoptive cell transfer as cancer treatment von van Belzen, Ianthe A. E. M., Kesmir, Can

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A script to highlight hydrophobicity and charge on protein surfaces von Hagemans, Dominique, van Belzen, Ianthe A E M, Morán Luengo, Tania, Rüdiger, Stefan G D

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Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients von Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

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How to quench your thirst. The effect of water-based products varying in temperature and texture, flavour, and sugar content on thirst von van Belzen, L., Postma, E.M., Boesveldt, S.

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Chromatin accessibility landscape of pediatric T‐lymphoblastic leukemia and human T‐cell precursors von Erarslan‐Uysal, Büşra, Kunz, Joachim B, Rausch, Tobias, Richter‐Pechańska, Paulina, van Belzen, Ianthe AEM, Frismantas, Viktoras, Bornhauser, Beat, Ordoñez‐Rueada, Diana, Paulsen, Malte, Benes, Vladimir, Stanulla, Martin, Schrappe, Martin, Cario, Gunnar, Escherich, Gabriele, Bakharevich, Kseniya, Kirschner‐Schwabe, Renate, Eckert, Cornelia, Loukanov, Tsvetomir, Gorenflo, Matthias, Waszak, Sebastian M, Bourquin, Jean‐Pierre, Muckenthaler, Martina U, Korbel, Jan O, Kulozik, Andreas E

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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect von Wijmenga, Cisca, Monsuur, Alienke J, Bakker, Paul I W de, Alizadeh, Behrooz Z, Zhernakova, Alexandra, Bevova, Marianna R, Strengman, Eric, Franke, Lude, Slot, Ruben van't, Belzen, Martine J van, Lavrijsen, Ineke C M, Diosdado, Begoña, Daly, Mark J, Mulder, Chris J J, Mearin, M Luisa, Meijer, Jos W R, Meijer, Gerrit A, Oort, Erica van, Wapenaar, Martin C, Koeleman, Bobby P C

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Noninvasive prenatal diagnosis of Huntington disease: detection of the paternally inherited expanded CAG repeat in maternal plasma von van den Oever, Jessica M. E., Bijlsma, Emilia K., Feenstra, Ilse, Muntjewerff, Nienke, Mathijssen, Inge B., Bakker, Egbert, van Belzen, Martine J., Boon, Elles M. J.

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Changes in diatom patch-size distribution and degradation in a spatially self-organized intertidal mudflat ecosystem von Weerman, E. J, Van Belzen, J, Rietkerk, M, Temmerman, S, Kéfi, S, Herman, P. M. J, de Koppel, J. Van

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A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening von Gerkes, E. H., Fock, J. M., den Dunnen, W. F. A., van Belzen, M. J., van der Lans, C. A., Hoving, E. W., Fakkert, I. E., Smith, M. J., Evans, D. G., Olderode-Berends, M. J. W.

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Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations von Fergelot, Patricia, Van Belzen, Martine, Van Gils, Julien, Afenjar, Alexandra, Armour, Christine M., Arveiler, Benoit, Beets, Lex, Burglen, Lydie, Busa, Tiffany, Collet, Marie, Deforges, Julie, de Vries, Bert B. A., Dominguez Garrido, Elena, Dorison, Nathalie, Dupont, Juliette, Francannet, Christine, Garciá-Minaúr, Sixto, Gabau Vila, Elisabeth, Gebre-Medhin, Samuel, Gener Querol, Blanca, Geneviève, David, Gérard, Marion, Gervasini, Cristina Giovanna, Goldenberg, Alice, Josifova, Dragana, Lachlan, Katherine, Maas, Saskia, Maranda, Bruno, Moilanen, Jukka S., Nordgren, Ann, Parent, Philippe, Rankin, Julia, Reardon, Willie, Rio, Marlène, Roume, Joëlle, Shaw, Adam, Smigiel, Robert, Sojo, Amaia, Solomon, Benjamin, Stembalska, Agnieszka, Stumpel, Constance, Suarez, Francisco, Terhal, Paulien, Thomas, Simon, Touraine, Renaud, Verloes, Alain, Vincent-Delorme, Catherine, Wincent, Josephine, Peters, Dorien J. M., Bartsch, Oliver, Larizza, Lidia, Lacombe, Didier, Hennekam, Raoul C.

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Salt marshes for nature-based flood defense: Sediment type, drainage, and vegetation drive the development of strong sediment beds von Stoorvogel, Marte M., van Belzen, Jim, Temmerman, Stijn, Wiesebron, Lauren E., Fivash, Gregory S., van IJzerloo, Lennart, van de Koppel, Johan, Bouma, Tjeerd J.

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The SNAP-25 gene is associated with cognitive ability : evidence from a family-based study in two independent Dutch cohorts von GOSSO, M. F, DE GEUS, E. J. C, VAN BELZEN, M. J, POLDERMAN, T. J. C, HEUTINK, P, BOOMSMA, D. I, POSTHUMA, D

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Between a rock and a hard place: Environmental and engineering considerations when designing coastal defence structures von Firth, L.B., Thompson, R.C., Bohn, K., Abbiati, M., Airoldi, L., Bouma, T.J., Bozzeda, F., Ceccherelli, V.U., Colangelo, M.A., Evans, A., Ferrario, F., Hanley, M.E., Hinz, H., Hoggart, S.P.G., Jackson, J.E., Moore, P., Morgan, E.H., Perkol-Finkel, S., Skov, M.W., Strain, E.M., van Belzen, J., Hawkins, S.J.

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Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease von Gardiner, Sarah L., Harder, Aster V.E., Campman, Yvonne J.M., Trompet, Stella, Gussekloo, Jacobijn, van Belzen, Martine J., Boogaard, Merel W., Roos, Raymund A.C., Jansen, Iris E., Pijnenburg, Yolande A.L., Scheltens, Philip, van der Flier, Wiesje M., Aziz, N. Ahmad

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The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008) von van Rij, MC, de Koning Gans, PAM, van Belzen, MJ, Roos, RAC, Geraedts, JPM, De Rademaeker, M, Bijlsma, EK, de Die-Smulders, CEM

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