Short-term mudflat dynamics drive long-term cyclic salt marsh dynamics von Bouma, T. J., van Belzen, J., Balke, T., van Dalen, J., Klaassen, P., Hartog, A. M., Callaghan, D. P., Hu, Z., Stive, M. J. F., Temmerman, S., Herman, P. 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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Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL von Rutten, Julie W., Dauwerse, Hans G., Gravesteijn, Gido, Belzen, Martine J., Grond, Jeroen, Polke, James M., Bernal‐Quiros, Manuel, Lesnik Oberstein, Saskia A. J.

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Benign and malignant tumors in Rubinstein–Taybi syndrome von Boot, Max V., van Belzen, Martine J., Overbeek, Lucy I., Hijmering, Nathalie, Mendeville, Matias, Waisfisz, Quinten, Wesseling, Pieter, Hennekam, Raoul C., de Jong, Daphne

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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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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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Interactive effects of vegetation and sediment properties on erosion of salt marshes in the Northern Adriatic Sea von Lo, V.B., Bouma, T.J., van Belzen, J., Van Colen, C., Airoldi, L.

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CTLA4+49 A/G and CT60 polymorphisms in Dutch coeliac disease patients von van Belzen, Martine J, Mulder, Chris J J, Zhernakova, Alexandra, Pearson, Peter L, Houwen, Roderick H J, Wijmenga, Cisca

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Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington’s disease von Aziz, N. Ahmad, van Belzen, Martine J, Coops, Ilona D, Belfroid, René D.M, Roos, Raymund A.C

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High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer von Diets, Illja J, Waanders, Esmé, Ligtenberg, Marjolijn J, van Bladel, Diede A G, Kamping, Eveline J, Hoogerbrugge, Peter M, Hopman, Saskia, Olderode-Berends, Maran J, Gerkes, Erica H, Koolen, David A, Marcelis, Carlo, Santen, Gijs W, van Belzen, Martine J, Mordaunt, Dylan, McGregor, Lesley, Thompson, Elizabeth, Kattamis, Antonis, Pastorczak, Agata, Mlynarski, Wojciech, Ilencikova, Denisa, van Silfhout, Anneke Vulto, Gardeitchik, Thatjana, de Bont, Eveline S, Loeffen, Jan, Wagner, Anja, Mensenkamp, Arjen R, Kuiper, Roland P, Hoogerbrugge, Nicoline, Jongmans, Marjolijn C

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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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CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype von Menke, Leonie A., van Belzen, Martine J., Alders, Marielle, Cristofoli, Francesca, Ehmke, Nadja, Fergelot, Patricia, Foster, Alison, Gerkes, Erica H., Hoffer, Mariëtte J. V., Horn, Denise, Kant, Sarina G., Lacombe, Didier, Leon, Eyby, Maas, Saskia M., Melis, Daniela, Muto, Valentina, Park, Soo-Mi, Peeters, Hilde, Peters, Dorien J. M., Pfundt, Rolph, van Ravenswaaij-Arts, Conny M. A., Tartaglia, Marco, Hennekam, Raoul C. M.

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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 major non-HLA locus in celiac disease maps to chromosome 19 von Van Belzen, Martine J, Meijer, Jos W.R, Sandkuijl, Lodewijk A, Bardoel, Alfons F.J, Mulder, Chris J.J, Pearson, Peter L, Houwen, Roderick H.J, Wijmenga, Cisca

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EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease von Losekoot, Monique, van Belzen, Martine J, Seneca, Sara, Bauer, Peter, Stenhouse, Susan A R, Barton, David E

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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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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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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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Two novel cases expanding the phenotype of SETD2‐related overgrowth syndrome von van Rij, Maartje C., Hollink, Iris H. I. M., Terhal, Paulien Anna, Kant, Sarina G., Ruivenkamp, Claudia, van Haeringen, Arie, Kievit, J. Anneke, van Belzen, Martine J.

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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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