Variant location is a novel risk factor for individuals with arrhythmogenic cardiomyopathy due to a desmoplakin (DSP) truncating variant von Hoorntje, ET, Burns, C, Marsili, L, Corden, B, Parikh, VN, Te Meerman, GJ, Gray, B, Adiyaman, A, Bagnall, RD, Barge-Schaapveld, DQCM, Van den Berg, MP, Bootsma, M, Bosman, LP, Correnti, G, Duflou, J, Eppinga, RN, Fatkin, D, Fietz, M, Haan, E, Jongbloed, JDH, Hauer, AD, Lam, L, Van Lint, FHM, Lota, A, Marcelis, C, McCarthy, HJ, Van Mil, AM, Oldenburg, RA, Pachter, N, Planken, RN, Reuter, C, Semsarian, C, Van der Smagt, JJ, Thompson, T, Vohra, J, Volders, PGA, Van Waning, JI, Whiffin, N, Van den Wijngaard, A, Amin, AS, Wilde, AAM, Van Woerden, G, Yeates, L, Zentner, D, Ashley, EA, Wheeler, MT, Ware, JS, Van Tintelen, JP, Ingles, J

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Susceptibility to Buruli ulcer is associated with the SLC11A1 (NRAMP1) D543N polymorphism von Stienstra, Y, van der Werf, T S, Oosterom, E, Nolte, I M, van der Graaf, W T A, Etuaful, S, Raghunathan, P L, Whitney, E A S, Ampadu, E O, Asamoa, K, Klutse, E Y, te Meerman, G J, Tappero, J W, Ashford, D A, van der Steege, G

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Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study von Zoodsma, M, Nolte, I M, Schipper, M, Oosterom, E, van der Steege, G, de Vries, E G E, te Meerman, G J, van der Zee, A G J

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Fractional Factorial Design for Optimization of the SELDI Protocol for Human Adipose Tissue Culture Media von Szalowska, Ewa, Van Hijum, Sacha A.F.T., Roelofsen, Han, Hoek, Annemiek, Vonk, Roel J., te Meerman, Gerard J.

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Genetic susceptibility to Hodgkin's lymphoma associated with the human leukocyte antigen region von Diepstra, A., Niens, M., Te Meerman, G. J., Poppema, S., van den Berg, A.

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Methylenetetrahydrofolate reductase (MTHFR) and susceptibility for (pre)neoplastic cervical disease von ZOODSMA, Margreet, NOLTE, Ilja M, SCHIPPER, Martin, OOSTEROM, Elvira, VAN DER STEEGE, Gerrit, DE VRIES, Elisabeth G. E, TE MEERMAN, Gerard J, VAN DER ZEE, Ate G. J

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No increased susceptibility to breast cancer from combined CHEK2 1100delC genotype and the HLA class III region risk factors von de Jong, Mirjam M., Nolte, Ilja M., te Meerman, Gerard J., van der Graaf, Winette T.A., Oosterom, Elvira, Bruinenberg, Marcel, Steege, Gerrit van der, Oosterwijk, Jan C., van der Hout, Annemarie H., Boezen, H. Marike, Schaapveld, Michael, Kleibeuker, Jan H., de Vries, Elisabeth G.E.

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Efficiency control in large-scale genotyping using analysis of variance von SPIJKER, Geert T, BRUINENBERG, Marcel, TE MEERMAN, Gerard J

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Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additive von BOON, Maartje, NOLTE, Ilja M, DE KEYSER, Jacques, BUYS, Charles H. C. M, TE MEERMAN, Gerard J

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Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring von Van der Meulen, Martin A., te Meerman, Gerard J.

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The human leukocyte antigen region and colorectal cancer risk von DE JONG, Mirjam M, NIENS, Marijke, HOFSTRA, Robert M. W, DE VRIES, Elisabeth G. E, KLEIBEUKER, Jan H, NOLTE, Ilja M, TE MEERMAN, Gerard J, VAN DER GRAAF, Winette T. A, MULDER, Marcel J, VAN DER STEEGE, Gerrit, BRUINENBERG, Marcel, SCHAAPVELD, Michael, SIJMONS, Rolf H

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CARD15 in inflammatory bowel disease and Crohn??s disease phenotypes: an association study and pooled analysis von Oostenbrug, LE, Nolte, IM, Oosterom, E, van der Steege, G, te Meerman, GJ, van Dullemen, HM, Drent, JPH, de Jong, DJ, van der Linde, K, Jansen, PLM, Kleibeuker, JH

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Differentiated Thyroid Carcinoma: A Polygenic Disease von Links, Thera P., van Tol, Karin M., te Meerman, Gerard J., de Vries, Elisabeth G.E.

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The HLA class III subregion is responsible for an increased breast cancer risk von de Jong, Mirjam M., Nolte, Ilja M., de Vries, Elisabeth G. E., Schaapveld, Michael, Kleibeuker, Jan H., Oosterom, Elvira, Oosterwijk, Jan C., van der Hout, Annemarie H., van der Steege, Gerrit, Bruinenberg, Marcel, Boezen, H. Marike, te Meerman, Gerad J., van der Graaf, Winette T. A.

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Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in... von de Vries, H G, van der Meulen, M A, Rozen, R, Halley, D J, Scheffer, H, ten Kate, L P, Buys, C H, te Meerman, G J

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Cytogenetic analysis of ten human seminomas von CASTEDO, S. M. M. J, DE JONG, B, OOSTERHUIS, J. W, SERUCA, R, TE MEERMAN, G. J, DAM, A, SCHRAFFORDT KOOPS, H

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BIRTH AND POPULATION PREVALENCE OF DUCHENNE MUSCULAR-DYSTROPHY IN THE NETHERLANDS von VANESSEN, AJ, BUSCH, HFM, TEMEERMAN, GJ, TENKATE, LP

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Linkage analysis by two-dimensional DNA typing von TE MEERMAN, G. J, MULLAART, E, VAN DER MEULEN, M. A, DEN DAAS, J. H. G, MOROLLI, B, UITTERLINDEN, A. G, VIJG, J

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Chromosomal changes in mature residual teratomas following polychemotherapy von CASTEDO, S. M. M. J, DE JONG, B, OOSTERHUIS, J. W, IDENBURG, V. J. S, SERUCA, R, BUIST, J, TE MEERMAN, G. J, SCHRAFFORDT KOOPS, H, SLEIJFER, D. T

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Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RBI gene von SCHEFFER, H, TE MEERMAN, G. J, KRUIZE, Y. C. M, VAN DEN BERG, A. H. M, PENNINGA, D. P, TAN, K. E. W. P, DER KINDEREN, D. J, BUYS, C. H. C. M

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