Highly accurate DNA-based detection and treatment results of MET exon 14 skipping mutations in lung cancer von Pruis, M.A., Geurts-Giele, W.R.R., von der, Thüsen J.H., Meijssen, I.C., Dinjens, W.N.M., Aerts, J.G.J.V., Dingemans, A.M.C., Lolkema, M.P., Paats, M.S., Dubbink, H.J.

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IDH1 mutations in low-grade astrocytomas predict survival but not response to temozolomide von DUBBINK, H. J, TAAL, W, BOOGERD, W, GROENENDIJK, F. H, SILLEVIS SMITT, PA. E, DINJENS, W. N. M, VAN DEN BENT, M. J, VAN MARION, R, KROS, J. M, VAN HEUVEL, I, BROMBERG, J. E, ZONNENBERG, B. A, ZONNENBERG, C. B. L, POSTMA, T. J, GIJTENBEEK, J. M. M

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Retrospective study of a 16 year cohort of BRCA1 and BRCA2 carriers presenting for RRSO: Prevalence of invasive and in-situ carcinoma, with follow-up von Blok, F., Dasgupta, S., Dinjens, W.N.M., Roes, E.M., van Beekhuizen, H.J., Ewing-Graham, P.C.

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E-cadherin-catenin cell-cell adhesion complex and human cancer von Wijnhoven, B. P. L., Dinjens, W. N. M., Pignatelli, M.

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Evaluation of a nationwide Dutch guideline to detect Lynch syndrome in patients with endometrial cancer von Tjalsma, A.S., Wagner, A., Dinjens, W.N.M., Ewing-Graham, P.C., Alcalá, L.S.M., de Groot, M.E.R., Hamoen, K.E., van Hof, A.C., Hofhuis, W., Hofman, L.N., Hoogduin, K.J., Kaijser, J., Makkus, A.C.F., Mol, S.J.J., Plaisier, G.M., Schelfhout, K., Smedts, H.P.M., Smit, R.A., Timmers, P.J., Vencken, P.M.L.H., Visschers, B., van der Wurff, A.A.M., van Doorn, H.C.

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Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats von You, J-F, Buhard, O, Ligtenberg, M J L, Kets, C M, Niessen, R C, Hofstra, R M W, Wagner, A, Dinjens, W N M, Colas, C, Lascols, O, Collura, A, Flejou, J-F, Duval, A, Hamelin, R

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Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencing von Doebar, S. C., Krol, N. M., van Marion, R., Brouwer, R. W. W., van Ijcken, W. F. J., Martens, J. M., Dinjens, W. N. M., van Deurzen, C. H. M.

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Granular dot-like staining with MLH1 immunohistochemistry is a clone-dependent artefact von Dasgupta, S., Ewing-Graham, P.C., Groenendijk, F.H., Stam, O., Biermann, K.E., Doukas, M., Dubbink, H.J., van Velthuysen, M.F., Dinjens, W.N.M., Van Bockstal, M.R.

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TuBaFrost 2: Standardising tissue collection and quality control procedures for a European virtual frozen tissue bank network von Morente, M.M., Mager, R., Alonso, S., Pezzella, F., Spatz, A., Knox, K., Kerr, D., Dinjens, W.N.M., Oosterhuis, J.W., Lam, K.H., Oomen, M.H.A., van Damme, B., van de Vijver, M., van Boven, H., Kerjaschki, D., Pammer, J., Lopez-Guerrero, J.A., Llombart Bosch, A., Carbone, A., Gloghini, A., Teodorovic, I., Isabelle, M., Passioukov, A., Lejeune, S., Therasse, P., van Veen, E.-B., Ratcliffe, C., Riegman, P.H.J.

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Immunohistochemical expression of stem cell markers in pheochromocytomas/paragangliomas is associated with SDHx mutations von Oudijk, L, Neuhofer, C M, Lichtenauer, U D, Papathomas, T G, Korpershoek, E, Stoop, H, Oosterhuis, J W, Smid, M, Restuccia, D F, Robledo, M, de Cubas, A A, Mannelli, M, Gimenez-Roqueplo, A P, Dinjens, W N M, Beuschlein, F, de Krijger, R R

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Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers von Goverde, A., Spaander, M. C. W., Nieboer, D., van den Ouweland, A. M. W., Dinjens, W. N. M., Dubbink, H. J., Tops, C. J., ten Broeke, S. W., Bruno, M. J., Hofstra, R. M. W., Steyerberg, E. W., Wagner, A.

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Translational research on esophageal adenocarcinoma: from cell line to clinic von Boonstra, J. J., Tilanus, H. W., Dinjens, W. N. M.

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Absence of TERT promoter mutations in esophageal adenocarcinoma von Nistelrooij, A.M.J., Zwarthoff, E.C., Post, E., Lurkin, I., Marion, R., Kopershoek, E., Biermann, K., Wijnhoven, B.P.L., Dinjens, W.N.M.

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TuBaFrost 3: Regulatory and ethical issues on the exchange of residual tissue for research across Europe von van Veen, E.-B., Riegman, P.H.J., Dinjens, W.N.M., Lam, K.H., Oomen, M.H.A., Spatz, A., Mager, R., Ratcliffe, C., Knox, K., Kerr, D., van Damme, B., van de Vijver, M., van Boven, H., Morente, M.M., Alonso, S., Kerjaschki, D., Pammer, J., Lopez-Guerrero, J.A., Llombart Bosch, A., Carbone, A., Gloghini, A., Teodorovic, I., Isabelle, M., Passioukov, A., Lejeune, S., Therasse, P., Oosterhuis, J.W.

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Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma von van Nistelrooij, A. M. J., van Marion, R., van Ijcken, W. F. J., de Klein, A., Wagner, A., Biermann, K., Spaander, M. C. W., van Lanschot, J. J. B., Dinjens, W. N. M., Wijnhoven, B. P. L.

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Specific detection of OCT3/4 isoform A/B/B1 expression in solid (germ cell) tumours and cell lines: confirmation of OCT3/4 specificity for germ cell tumours von Rijlaarsdam, M A, van Herk, H A D M, Gillis, A J M, Stoop, H, Jenster, G, Martens, J, van Leenders, G J L H, Dinjens, W, Hoogland, A M, Timmermans, M, Looijenga, L H J

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Biobanking for Interdisciplinary Clinical Research von Riegman, P.H.J., Dinjens, W.N.M., Oosterhuis, J.W.

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A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting von Ramsoekh, D, Wagner, A, van Leerdam, M E, Dinjens, W N M, Steyerberg, E W, Halley, D J J, Kuipers, E J, Dooijes, D

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TuBaFrost 6: Virtual microscopy in virtual tumour banking von Teodorovic, I., Isabelle, M., Carbone, A., Passioukov, A., Lejeune, S., Jaminé, D., Therasse, P., Gloghini, A., Dinjens, W.N.M., Lam, K.H., Oomen, M.H.A., Spatz, A., Ratcliffe, C., Knox, K., Mager, R., Kerr, D., Pezzella, F., van Damme, B., van de Vijver, M., van Boven, H., Morente, M.M., Alonso, S., Kerjaschki, D., Pammer, J., Lopez-Guerrero, J.A., Llombart Bosch, A., van Veen, E.-B., Oosterhuis, J.W., Riegman, P.H.J.

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PTEN in colorectal cancer: a report on two Cowden syndrome patients von Kersseboom, R, Dubbink, HJ, Corver, WE, van Tilburg, AJP, Poley, JW, van Leerdam, ME, Atmodimedjo, PN, van de Laar, IMBH, Collée, JM, Dinjens, WNM, Morreau, H, Wagner, A

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