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scopus: 35411281400

Wijnen, J.

(Juul Wijnen)


cancer family breast mutation colorectal breast cancer colorectal cancer hnpcc colorectal cancer cases genetic carrier study genetics service breast cancer risk cohort msh 6 mutation university patient analysis table department nonpolyposis colorectal cancer criteria phenotype genet susceptibility netherland endometrial cancer allele 1.00 endometrial carcinoma dutch tumor brca 1 service colorectal cancer risk meijers-heijboer association variant germline hospital tumour centre polyps chek 2 microsatellite instability colorectal cancer families control vasen tumours center nonpolyposi hnpcc-like disease status presence age 50 y /hnpcc expression foundation research instability rotterdam brca 2 carriers mlh 1 amsterdam colon msh 2 index gata 3 hbcc phenotype wijnen onset population fodde article leiden university prevalence vasen hf age !60 years




4 Most Recent Publications

No evidence that GATA3 rs570613 SNP modifies breast cancer risk (Article)
Johnatty, S.E. Couch, F.J. Fink-Retter, A. Domchek, S.M. Nathanson, K.L. Pankratz, V.S. Lindor, N.M. Godwin, A.K. Caligo, M.A. Hopper, J. Southey, M.C. Giles, G.G. Fredericksen, Z. Justenhoven, C. Brauch, H. Hamann, U. Ko, Y.D. Heikkinen, T. Aaltonen, K. Aittomäki, K. Blomgvist, C. Nevanlinna, H. Hall, P. Tarrell, R. Czene, k. Liu, J. Peock, S. Cook, M. Platte, R. Gareth Evans, D. Lalloo, F. Eeles, R. Pichert, G. Eccles, D. Spurdle, A.B. Davidson, R. Cole, T.J. Cook, J. Douglas, F. Chu, C. Paterson, J. Hodgson, S.V. Hogervorst, F.B.L. Rookus, M.A. Seynaeve, C.M. Beesley, J. Wijnen, J. Vreeswijk, M.P. Ligtenberg, M. Luijt, R.B. van der Os, T.A.M. van Gille, H.J.P. Blok, M.J. Issacs, C. Humphreys, M.K. McGuffog, L. Chen, X. Healey, S. Sinilnikova, O. Antoniou, A.C. Easton, D.F. Chenevix-Trench, G. Gschwantler-Kaulich, D. Singer, C.F. Fuerhauser, C.
2009-09-01
CHEK2 1100delC is a susceptibility allele for HNPCC-related colorectal cancer (Article)
Wasielewski, M. Vasen, H. Wijnen, J. Hooning, M. Dooijes, D. Tops, C. Klijn, J.G.M. Meijers-Heijboer, E.J. Schutte, M.
2008-08-01
The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype (Article)
Meijers-Heijboer, E.J. Moslein, G. Bos, R.R. van den Snoo, A. de Schutte, A.E.M. Franken, P.F. Fat, G.T. Jagmohan, S. Chapman, P. Brekelmans, C.T. Wijnen, J. Vasen, H. Lynch, H. Ouweland, A.M.W. van den Klijn, J.G.M. Hollestelle, A. Wasielewski, M. Fodde, R. Wagner, A. Elstrodt, F. Verkuijlen, P. Tops, C. Burn, J.
2003-01-01
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree (Article)
Wagner, A. Krimpen, C. van Breuning, M.H. Meer, C. van der Vasen, H.F. Niermeijer, M.F. Lindhout, D. Hendriks, Y. Meijers-Heijboer, E.J. Wijnen, J. Leeuw, W.J. de Morreau, H. Hofstra, R. Tops, C. Cornelisse, C.J. Zwinderman, A.H. Bik, E. Brocker-Vriends, A.H. Fodde, R.
2001-01-01