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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Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients von Hensen, E. F., Siemers, M. D., Jansen, J. C., Corssmit, E. P. M., Romijn, J. A., Tops, C. M. J., van der Mey, A. G. L., Devilee, P., Cornelisse, C. J., Bayley, J. P., Vriends, A. H. J. T.

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Incidence and microbiology of post-operative infections after radical cystectomy and ureteral stent removal; a retrospective cohort study von Kolwijck, E, Seegers, A E M, Tops, S C M, van der Heijden, A G, Sedelaar, J P M, Ten Oever, J

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Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis? von Suerink, M., Potjer, T.P., Versluijs, A.B., ten Broeke, S.W., Tops, C.M., Wimmer, K., Nielsen, M.

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Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients von Terlouw, D., Boot, A., Ducarmon, Q. R., Nooij, S., Jessurun, M. A., Leerdam, M. E., Tops, C. M., Langers, A. M. J., Morreau, H., Wezel, T., Nielsen, M.

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High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands von Hensen, EF, van Duinen, N, Jansen, JC, Corssmit, EPM, Tops, CMJ, Romijn, JA, Vriends, AHJT, van der Mey, AGL, Cornelisse, CJ, Devilee, P, Bayley, JP

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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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Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review von Knopperts, A. P., Nielsen, M., Niessen, R. C., Tops, C. M. J., Jorritsma, B., Varkevisser, J., Wijnen, J., Siezen, C. L. E., Heine-Bröring, R. C., van Kranen, H. J., Vos, Y. J., Westers, H., Kampman, E., Sijmons, R. H., Hes, F. J.

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The diagnostic accuracy of the GeneXpert ESBL- ampC prototype assay for rapid PCR-based detection of extended-spectrum beta-lactamase genes directly from urine von Tops, Sofie C M, Schapendonk, Claire E P, Coolen, Jordy P M, Tenover, Fred C, Tickler, Isabella A, Melchers, Willem J G, Wertheim, Heiman F L

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Prostate biopsy techniques and pre-biopsy prophylactic measures: variation in current practice patterns in the Netherlands von Tops, Sofie C M, Koldewijn, Evert L, Somford, Diederik M, Huis, Anita M P, Kolwijck, Eva, Wertheim, Heiman F L, Hulscher, Marlies E J L, Sedelaar, J P Michiel

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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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Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD‐related paraganglioma von Hoekstra, A.S., Ende, B., Julià, X.P., Breemen, L., Scheurwater, K., Tops, C.M., Malinoc, A., Devilee, P., Neumann, H.P.H., Bayley, J.‐P.

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High frequency of copy-neutral LOH in MUTYH-associated polyposis carcinomas von Middeldorp, A, van Puijenbroek, M, Nielsen, M, Corver, WE, Jordanova, ES, ter Haar, N, Tops, CMJ, Vasen, HFA, Lips, EH, van Eijk, R, Hes, FJ, Oosting, J, Wijnen, J, van Wezel, T, Morreau, H

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Rectal Culture-Based Versus Empirical Antibiotic Prophylaxis to Prevent Infectious Complications in Men Undergoing Transrectal Prostate Biopsy: A Randomized, Nonblinded Multicenter... von Tops, Sofie C M, Kolwijck, Eva, Koldewijn, Evert L, Somford, Diederik M, Delaere, Filip J M, van Leeuwen, Menno A, Breeuwsma, Anthonius J, de Vocht, Thijn F, Broos, Hans J H P, Schipper, Rob A, Steffens, Martijn G, Teerenstra, Steven, Wegdam-Blans, Marjolijn C A, de Brauwer, Els, van den Bijllaardt, Wouter, Leenders, Alexander C A P, Sedelaar, J P Michiel, Wertheim, Heiman F L

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Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians von Hendriks, Yvonne M.C, de Jong, Andrea E, Morreau, Hans, Tops, Carli M.J, Vasen, Hans F, Wijnen, Juul Th, Breuning, Martijn H, Brocker-Vriends, Annette H.J.T

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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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The use of genetic testing in hereditary colorectal cancer syndromes: genetic testing in HNPCC, (A)FAP and MAP von Ramsoekh, D, van Leerdam, ME, Tops, CMJ, Dooijes, D, Steyerberg, EW, Kuipers, EJ, Wagner, A

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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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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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Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations von Leenen, CHM, Geurts-Giele, WRR, Dubbink, HJ, Reddingius, R, van den Ouweland, AM, Tops, CMJ, van de Klift, HM, Kuipers, EJ, van Leerdam, ME, Dinjens, WNM, Wagner, A

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