Somatic APC mosaicism: an underestimated cause of polyposis coli von Hes, F J, Nielsen, M, Bik, E C, Konvalinka, D, Wijnen, J T, Bakker, E, Vasen, H F A, Breuning, M H, Tops, C M J

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MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families von VASEN, H. F. A, STORMORKEN, A, MENKO, F. H, NAGENGAST, F. M, KLEIBEUKER, J. H, GRIFFIOEN, G, TAAL, B. G, MOLLER, P, WIJNEN, J. T

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A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa von van der Merwe, NC, Hamel, N, Schneider, S-R, Apffelstaedt, JP, Wijnen, JT, Foulkes, WD

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Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantation von Lankester, A C, Bierings, M B, van Wering, E R, Wijkhuijs, A J M, de Weger, R A, Wijnen, J T, Vossen, J M, Versluys, B, Egeler, R M, van Tol, M J D, Putter, H, Révész, T, van Dongen, J J M, van der Velden, V H J, Schilham, M W

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis von Vasen, HF, Wijnen, JT, Menko, FH, Kleibeuker, JH, Taal, BG, Griffioen, G, Nagengast, FM, Meijers-Heijboer, EH, Bertario, L, Varesco, L, Bisgaard, ML, Mohr, J, Fodde, R, Khan, PM

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Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing von De Leeneer, K., Van Bockstal, M., De Brouwer, S., Swietek, N., Schietecatte, P., Sabbaghian, N., Van den Ende, J., Willocx, S., Storm, K., Blaumeiser, B., Van Asperen, C. J., Wijnen, J. T., Leunen, K., Legius, E., Michils, G., Matthijs, G., Blok, M. J., Gomez-Garcia, E., De Paepe, A., Tischkowitz, M., Poppe, B., Claes, K.

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Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis von Nielsen, M, Hes, FJ, Nagengast, FM, Weiss, MM, Mathus-Vliegen, EM, Morreau, H, Breuning, MH, Wijnen, JT, Tops, CMJ, Vasen, HFA

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Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations von Johannesma, PC, van der Klift, HM, van Grieken, NCT, Troost, D, te Riele, H, Jacobs, MAJM, Postma, TJ, Heideman, DAM, Tops, CMJ, Wijnen, JT, Menko, FH

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Peutz–Jeghers syndrome: a systematic review and recommendations for management von Beggs, A D, Latchford, A R, Vasen, H F A, Moslein, G, Alonso, A, Aretz, S, Bertario, L, Blanco, I, Bülow, S, Burn, J, Capella, G, Colas, C, Friedl, W, Møller, P, Hes, F J, Järvinen, H, Mecklin, J-P, Nagengast, F M, Parc, Y, Phillips, R K S, Hyer, W, Ponz de Leon, M, Renkonen-Sinisalo, L, Sampson, J R, Stormorken, A, Tejpar, S, Thomas, H J W, Wijnen, J T, Clark, S K, Hodgson, S V

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Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer von Wijnen, Juul T, Vasen, Hans F.A, Khan, P. Meera, Zwinderman, Aeilko H, van der Klift, Heleen, Mulder, Adri, Tops, Carli, Møller, Pål, Fodde, Riccardo, Menko, Fred, Taal, Babs, Nagengast, Fokko, Brunner, Han, Kleibeuker, Jan, Sijmons, Rolf, Griffioen, Gerrit, Bröcker-Vriends, Annette, Bakker, Egbert, van Leeuwen-Cornelisse, Inge, Meijers-Heijboer, Anne, Lindhout, Dick, Breuning, Martijn, Post, Jan, Schaap, Cees, Apold, Jaran, Heimdal, Ketil, Bertario, Lucio, Bisgaard, Marie Luise, Goetz, Petr

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Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation von Wagner, A, Tops, C, Wijnen, J T, Zwinderman, K, van der Meer, C, Kets, M, Niermeijer, M F, Klijn, J G M, Tibben, A, Vasen, H F A, Meijers-Heijboer, H

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Molecular Basis and Enzymatic Properties of Glucose 6-Phosphate Dehydrogenase Volendam, Leading to Chronic Nonspherocytic Anemia, Granulocyte Dysfunction, and Increased Susceptibil... von Roos, Dirk, van Zwieten, Rob, Wijnen, Juul T., Gómez-Gallego, Felix, de Boer, Martin, Stevens, David, Pronk-Admiraal, Claudia J., de Rijk, Thea, van Noorden, Cornelis J.F., Weening, Ron S., Vulliamy, Tom J., Ploem, J. Eduard, Mason, Philip J., Bautista, José M., Khan, P. Meera, Beutler, Ernest

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Gene‐environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testing von Park, Jae‐Gahb, Park, Young Jin, Wijnen, Juul T., Vasen, Hans F.A.

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Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers von Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.

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Performance of BRCA1/2 mutation prediction models in male breast cancer patients von Moghadasi, S., Grundeken, V., Janssen, L.A.M., Dijkstra, N.H., Rodríguez‐Girondo, M., van Zelst‐Stams, W.A.G., Oosterwijk, J.C., Ausems, M.G.E.M., Oldenburg, R.A., Adank, M.A., Blom, E.W., Ruijs, M.W.G., van Os, T.A.M., van Deurzen, C.H.M., Martens, J.W.M., Schroder, C.P., Wijnen, J.T., Vreeswijk, M.P.G., van Asperen, C.J.

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Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP) von Nielsen, M, Franken, P F, Reinards, T H C M, Weiss, M M, Wagner, A, van der Klift, H, Kloosterman, S, Houwing-Duistermaat, J J, Aalfs, C M, Ausems, M G E M, Bröcker-Vriends, A H J T, Gomez Garcia, E B, Hoogerbrugge, N, Menko, F H, Sijmons, R H, Verhoef, S, Kuipers, E J, Morreau, H, Breuning, M H, Tops, C M J, Wijnen, J T, Vasen, H F A, Fodde, R, Hes, F J

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Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach von GILLE, J. J. P, HOGERVORST, F. B. L, MCELGUNN, C. J, SCHOUTEN, J. P, MENKO, F. H, PALS, G, WIJNEN, J. Th, VAN SCHOOTEN, R. J, DOMMERING, C. J, MEIJER, G. A, CRAANEN, M. E, NEDERLOF, P. M, DE JONG, D

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Persistence of host-type hematopoiesis after allogeneic bone marrow transplantation for leukemia is significantly related to the recipient's age and/or the conditioning regimen, bu... von VAN LEEUWEN, J. E. M, VAN TOL, M. J. D, JOOSTEN, A. M, WIJNEN, J. T, VERWEIJ, P. J. M, MEERA KHAN, P, VOSSEN, J. M

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients von de Leeuw, Wiljo J. F., Dierssen, JanWillem, Vasen, Hans F. A., Wijnen, Juul Th, Kenter, Gemma G., Meijers-Heijboer, Hanne, Brocker-Vriends, Annette, Stormorken, Astrid, Moller, Pal, Menko, Fred, Cornelisse, Cees J., Morreau, Hans

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Markers of oxidative stress and antioxidant activity in plasma and erythrocytes in neonatal respiratory distress syndrome von van Zoeren-Grobben, D., Lindeman, JHN, Houdkamp, E., Moison, RMW, Wijnen, JT, Berger, HM

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