Optimal selection for BRCA1 and BRCA2 mutation testing using a combination of ‘easy to apply’ probability models

Por Bodmer, D, Ligtenberg, M J L, van der Hout, A H, Gloudemans, S, Ansink, K, Oosterwijk, J C, Hoogerbrugge, N
Publicado em 2006

The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery

Por Hahn, M. M., de Voer, R. M., Hoogerbrugge, N., Ligtenberg, M. J. L., Kuiper, R. P., van Kessel, A. Geurts
Publicado no Cell Oncol (Dordr) (2016)

Reply: Familial ovarian screening: how to address abnormal TVU findings and its influence on the efficacy of screening?

Por Oei, A L M, Massuger, L F A G, Bulten, J, Ligtenberg, M J L, Hoogerbrugge, N, de Hullu, J A
Publicado em 2006

Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability

Por Kets, C M, van Krieken, J H J M, Hebeda, K M, Wezenberg, S J, Goossens, M, Brunner, H G, Ligtenberg, M J L, Hoogerbrugge, N
Publicado em 2006

Deficient mismatch repair system in patients with sporadic advanced colorectal cancer

Por Koopman, M, Kortman, G A M, Mekenkamp, L, Ligtenberg, M J L, Hoogerbrugge, N, Antonini, N F, Punt, C J A, van Krieken, J H J M
Publicado em 2009

Limitations of cytokeratin 20 RT-PCR to detect disseminated tumour cells in blood and bone marrow of patients with colorectal cancer: expression in controls and downregulation in t...

Por Vlems, F A, Diepstra, J H S, Cornelissen, I M H A, Ruers, T J M, Ligtenberg, M J L, Punt, C J A, van Krieken, J H J M, Wobbes, Th, van Muijen, G N P
Publicado em 2002

Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers

Por van der Post, R S, Kiemeney, L A, Ligtenberg, M J L, Witjes, J A, Hulsbergen-van de Kaa, C A, Bodmer, D, Schaap, L, Kets, C M, van Krieken, J H J M, Hoogerbrugge, N
Publicado em 2010

Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer

Por Overbeek, L I H, Kets, C M, Hebeda, K M, Bodmer, D, der Looij, E van, Willems, R, Goossens, M, Arts, N, Brunner, H G, van Krieken, J H J M, Hoogerbrugge, N, Ligtenberg, M J L
Publicado em 2007

Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats

Por 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
Publicado em 2010

Quality control in diagnostic molecular pathology in the Netherlands; proficiency testing for patient identification in tissue samples

Por Thunnissen, F B J M, Tilanus, M G J, Ligtenberg, M J L, Nederlof, P M, Dinjens, W N M, Meulemans, E, Van den Brule, A J C, van Noesel, C J M, de Leeuw, W J F, Schuuring, E
Publicado em 2004

Cost effectiveness of a new strategy to identify HNPCC patients

Por 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
Publicado em 2005

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non‐polyposis colorectal...

Por 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
Publicado em 2006

Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2

Por Ligtenberg, M J L, Hogervorst, F B L, Willems, H W, Arts, P J W, Brink, G, Hageman, S, Bosgoed, E A J, Looij, E Van der, Rookus, M A, Devilee, P, Vos, E M A W, Wigbout, G, Struycken, P M, Menko, F H, Rutgers, E J Th, Hoefsloot, E H, Mariman, E C M, Brunner, H G, Veer, L J Van't
Publicado em 1999

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

Por Peelen, T., van Vliet, M., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., van der Luijt, R., van der Hout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., van Leeuwen, I., Newman, B., Plandsoen, M., van der Est, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., van Asperen, C. J., Meijers-Heijboer, H., Klijn, J. G. M., de Greve, J., King, M.-C., Menko, F. H., Brunner, H. G., Halley, D., van Ommen, G.-J. B., Vasen, H. F. A., Cornelisse, C. J., van 'tVeer, L. J., de Knijff, P., Bakker, E., Devilee, P.
Publicado em 1997