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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Keloids in Rubinstein-Taybi syndrome: a clinical study von van de Kar, A.L., Houge, G., Shaw, A.C., de Jong, D., van Belzen, M.J., Peters, D.J.M., Hennekam, R.C.M.

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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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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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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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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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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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Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008 von van Rij, MC, de Koning Gans, PAM, Aalfs, CM, Elting, M, Ippel, PF, Maat-Kievit, JA, Vermeer, S, Verschuuren-Bemelmans, CC, van Belzen, MJ, Belfroid, RDM, Losekoot, M, Geraedts, JPM, Roos, RAC, Tibben, A, de Die-Smulders, CEM, Bijlsma, EK

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Methanomicrococcus blatticola gen. nov., sp. nov., a methanol- and methylamine-reducing methanogen from the hindgut of the cockroach Periplaneta americana von Sprenger, WW, van Belzen, MC, Rosenberg, J, Hackstein, JHP, Keltjens, JT

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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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Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients von van Belzen, M J, Koeleman, B P C, Crusius, J B A, Meijer, J W R, Bardoel, A F J, Pearson, P L, Sandkuijl, L A, Houwen, R H J, Wijmenga, C

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Large normal-range TBP and ATXN7 CAG repeat lengths are associated with increased lifetime risk of depression von Gardiner, S L, van Belzen, M J, Boogaard, M W, van Roon-Mom, W M C, Rozing, M P, van Hemert, A M, Smit, J H, Beekman, A T F, van Grootheest, G, Schoevers, R A, Oude Voshaar, R C, Comijs, H C, Penninx, B W J H, van der Mast, R C, Roos, R A C, Aziz, N A

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Intergenerational CAG repeat instability is highly heritable in Huntington's disease von Aziz, N A, van Belzen, M J, Roos, R A C

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CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome von Wincent, Josephine, Luthman, Aron, Belzen, Martine, Lans, Christian, Albert, Johanna, Nordgren, Ann, Anderlid, Britt‐Marie

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Genetic analysis of psychiatric disorders in humans von Van Belzen, M. J., Heutink, P.

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The tissue transglutaminase gene is not a primary factor predisposing to celiac disease von van Belzen, M.J., Mulder, C.J.J., Pearson, P.L., Houwen, R.H.J., Wijmenga, C.

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Association between the CHRM2 gene and intelligence in a sample of 304 Dutch families von Gosso, M. F., Van Belzen, M., De Geus, E. J. C., Polderman, J. C., Heutink, P., Boomsma, D. I., Posthuma, D.

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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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