A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals von Harinck, F, Konings, I C A W, Kluijt, I, Poley, J W, van Hooft, J E, van Dullemen, H M, Nio, C Y, Krak, N C, Hermans, J J, Aalfs, C M, Wagner, A, Sijmons, R H, Biermann, K, van Eijck, C H, Gouma, D J, Dijkgraaf, M G W, Fockens, P, Bruno, M J

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Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling von Bokkers, K., Bleiker, E. M. A., Aalfs, C. M., van Dalen, T., Velthuizen, M. E., Duijveman, P., Sijmons, R. H., Koole, W., Schoenmaeckers, E. J. P., Ausems, M. G. E. M.

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Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing von Johansson, L. F., de Boer, E. N., de Weerd, H. A., van Dijk, F., Elferink, M. G., Schuring-Blom, G. H., Suijkerbuijk, R. F., Sinke, R. J., te Meerman, G. J., Sijmons, R. H., Swertz, M. A., Sikkema-Raddatz, B.

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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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Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal... von Niessen, R C, Berends, M J W, Wu, Y, Sijmons, R H, Hollema, H, Ligtenberg, M J L, de Walle, H E K, de Vries, E G E, Karrenbeld, A, Buys, C H C M, van der Zee, A G J, Hofstra, R M W, Kleibeuker, J H

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TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes von Ruijs, Marielle W G, Verhoef, Senno, Rookus, Matti A, Pruntel, Roelof, van der Hout, Annemarie H, Hogervorst, Frans B L, Kluijt, I, Sijmons, Rolf H, Aalfs, Cora M, Wagner, Anja, Ausems, Margreet G E M, Hoogerbrugge, Nicoline, van Asperen, Christi J, Gomez Garcia, Encarna B, Meijers-Heijboer, Hanne, ten Kate, Leo P, Menko, Fred H, van 't Veer, Laura J

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Cost effectiveness of a new strategy to identify HNPCC patients von Kievit, W, de Bruin, J H F M, Adang, E M M, Severens, J L, Kleibeuker, J H, Sijmons, R H, Ruers, T J, Nagengast, F M, Vasen, H F A, van Krieken, J H J M, Ligtenberg, M J L, Hoogerbrugge, N

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Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study von Van Oostrom, I, Meijers-Heijboer, H, Duivenvoorden, HJ, Bröcker-Vriends, AHJT, Van Asperen, CJ, Sijmons, RH, Seynaeve, C, Van Gool, AR, Klijn, JGM, Tibben, A

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Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress von Lammens, CRM, Bleiker, EMA, Verhoef, S, Hes, FJ, Ausems, MGEM, Majoor-Krakauer, D, Sijmons, RH, Van Der Luijt, RB, Van Den Ouweland, AMW, Van Os, Tam, Hoogerbrugge, N, Gómez García, EB, Dommering, CJ, Gundy, CM, Aaronson, NK

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Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-d... von Hes, FJ, van der Luijt, RB, Janssen, ALW, Zewald, RA, de Jong, GJ, Lenders, JW, Links, TP, Luyten, GPM, Sijmons, RH, Eussen, HJ, Halley, DJJ, Lips, CJM, Pearson, PL, van den Ouweland, AMW, Majoor-Krakauer, DF

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Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations von Wu, Ying, Berends, Maran J.W., Mensink, Rob G.J., Kempinga, Claudia, Sijmons, Rolf H., van der Zee, Ate G.J., Hollema, Harry, Kleibeuker, Jan H., Buys, Charles H.C.M., Hofstra, Robert M.W.

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The introduction of a choice to learn pre-symptomatic DNA test results for BRCA or Lynch syndrome either face-to-face or by letter von Voorwinden, JS, Jaspers, JPC, ter Beest, JG, Kievit, Y, Sijmons, RH, Oosterwijk, JC

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Characteristics of Lynch syndrome associated ovarian cancer von Woolderink, J.M., De Bock, G.H., de Hullu, J.A., Hollema, H., Zweemer, R.P., Slangen, B.F.M., Gaarenstroom, K.N., van Beurden, M., van Doorn, H.C., Sijmons, R.H., Vasen, H.F.A., Mourits, M.J.E.

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The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome von Plazzer, J. P., Sijmons, R. H., Woods, M. O., Peltomäki, P., Thompson, B., Den Dunnen, J. T., Macrae, F.

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Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing von van Oostrom, I., Meijers-Heijboer, H., Duivenvoorden, H.J., Bröcker-Vriends, A.H.J.T., van Asperen, C.J., Sijmons, R.H., Seynaeve, C., Van Gool, A.R., Klijn, J.G.M., Tibben, A.

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Germline Mutations in the PTEN/MMAC1 Gene in Patients With Cowden Disease von Nelen, Marcel R., van Staveren, Wilma C. G., Peeters, Els A. J., Ben Hassel, Mohammed, Gorlin, Robert J., Hamm, Henning, Lindboe, Christian F., Fryns, Jean-Pierre, Sijmons, Rolf H., Woods, D. Geoffrey, Mariman, Edwin C. M., Padberg, George W., Kremer, Hannie

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Genetic predisposition to testicular germ-cell tumours von Holzik, M F Lutke, Rapley, EA, Hoekstra, HJ, Sleijfer, DT, Nolte, IM, Sijmons, RH

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Molecular Evidence Linking Primary Cancer of the Fallopian Tube to BRCA1 Germline Mutations von Zweemer, Ronald P., van Diest, Paul J., Verheijen, René H.M., Ryan, Andy, Gille, Johan J.P., Sijmons, Rolf H., Jacobs, Ian J., Menko, Fred H., Kenemans, Peter

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The additional value of endometrial sampling in the early detection of endometrial cancer in women with Lynch syndrome von Helder-Woolderink, J.M, De Bock, G.H, Sijmons, R.H, Hollema, H, Mourits, M.J.E

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DNA and RNA analysis of intratumour heterogeneity in metastatic clear cell renal cell carcinoma von Ferronika, P., Hof, J., Kats-Ugurlu, G., Terpstra, M., De Lange, K., Leliveld-Kors, A., Sijmons, R.H., Kok, K.

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