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scopus: 6602903359

Hes, F.J.

(Frederik Hes)


cancer mutation patient family colorectal variant study mutyh colorectal cancer pms 2 disease distress carrier sequence surveillance level netherland table analysis partner tumor polyposi genetic germline department signi ficantly individual von hippel-lindau disease university pms 2cl allele signi syndrome result control member mutyh-associated genet control patients support carcinoma score survival advice repair deletion region examination sample genomic msh 6 family members leiden worry hippel-lindau crc risk ficantly guideline vhl-related database sequence transfer probe scale protein screening genotype identi fied rt-pcr number mutyh-associated polyposis hospital cell carcinoma vhl disease vhl family members colon center population transfer health 165cy




10 Most Recent Publications

Compliance with periodic surveillance for Von-Hippel-Lindau disease (Article)
Lammens, C.R.M. Aaronson, N.K. Luijt, R.B. van der Ouweland, A.M.W. van den Hest, L.P. van Verhoef, S. Bleiker, E.M.A. Hes, F.J. Links, T.P. Zonnenberg, B.A. Lenders, J.W.M. Majoor-Krakauer, D.F. Os, T.A.M. van Gómez García, E.B. Herder, W.W. de
2011-06-01
Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes (Article)
Lammens, C.R.M. Bleiker, E.M.A. Luijt, R.B. van der Ouweland, A.M.W. van den Ruijs, M.W.G. Gundy, C. Nagtegaal, T. Aaronson, N.K. Verhoef, S. Ausems, M.G.E.M. Majoor-Krakauer, D.F. Sijmons, R.H. Hes, F.J. Gómez García, E.B. Os, T.A.M. van Spruijt, L.
2011-06-01
Survival of MUTYH-associated polyposis patients with colorectal cancer and matched control colorectal cancer patients (Article)
Nielsen, M. Steenbergen, L.N. van Hes, F.J. Jones, N. Vogt, S. Vasen, H.F. Morreau, H. Aretz, S. Sampson, J. Dekkers, O.M. Janssen-Heijnen, M.L.G.
2010-11-01
Reproducibility, accuracy, and predictors of accuracy for the detection of coronary atherosclerotic plaque composition by computed tomography: An ex vivo comparison to intravascular ultrasound (Article)
Out, A.A. Tops, C.M.J. Fostira, F. Franken, P.F. Gaustadnes, M. Heinimann, K. Hodgson, S.V. Hogervorst, F.B.L. Holinski-Feder, E. Lagerstedt, K. Olschwang, S. Ouweland, A.M.W. van den Nielsen, M. Redeker, E.J.W. Scott, R.J. Vankeirsbilck, B. Gronlund, R.V. Wijnen, J.T. Wikman, F.P. Aretz, S. Sampson, J. Devilee, P. Dunnen, J.T. den Weiss, M.M. Hes, F.J. Minderhout, I.J.H.M. van Fokkema, I.F.A.C. Buisine, M-P. Claes, K. Colas, C. Fodde, R.
2010-11-01
Psychosocial impact of Von Hippel-Lindau disease: Levels and sources of distress (Article)
Lammens, C.R.M. Bleiker, E.M.A. Hoogerbrugge, N. Gómez García, E.B. Dommering, C.J. Gundy, C.M. Aaronson, N.K. Verhoef, S. Hes, F.J. Ausems, M.G.E.M. Majoor-Krakauer, D.F. Sijmons, R.H. Luijt, R.B. van der Ouweland, A.M.W. van den Os, T.A.M. van
2010-05-01
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients (Article)
Klift, H.M. van der Tops, C. Izatt, L. Hest, L.P. Alonso, A.M. Vriends, A.H.J.T. Wagner, A. Zelst-Stams, W.A. van Vasen, H. Morreau, H. Devilee, P. Wijnen, J.T. Bik, E.C. Boogaard, M.W. Borgstein, A.M. Hansson, K.B. Ausems, M.G.E.M. Garcia, E.G. Green, A. Hes, F.J.
2010-05-01
Multiple genomic aberrations in a patient with mental retardation and hypogonadism: 45,X/46,X,psu dic(Y) karyotype, thyroid hormone receptor beta (THRB) mutation and heterozygosity for Wilson disease (Article)
Hes, F.J. Madan, K. Rombout-Liem, I.S. Szuhai, K. Sørensen, H. Amstel, H.K.P. van Bakker, E. Visser, T.J. Smit, J.W.A. Hansson, K.B.
2009-10-01
Chromosome 8q23.3 and 11q23.1 Variants Modify Colorectal Cancer Risk in Lynch Syndrome (Article)
Wijnen, J.T. Brohet, R.M. Hoogerbrugge, N. Menko, F. Os, T.A.M. van Sijmons, R.H. Verhoef, S. Wagner, A. Nagengast, F.M. Kleibeuker, J.H. Devilee, P. Morreau, H. Eijk, R. van Goldgar, D. Tomlinson, I.P. Houlston, R. Wezel, T. van Vasen, H. Jagmohan-Changur, S. Middeldorp, A. Tops, C. Puijenbroek, M. van Ausems, M.G.E.M. Gómez García, E.B. Hes, F.J.
2009-01-01
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-dependent probe amplification (Article)
Hes, F.J. Luijt, R.B. van der Halley, D. Lips, C.J.M. Pearson, P.L. Ouweland, A.M.W. van den Majoor-Krakauer, D.F. Janssen, A.L.W. Zewald, R.A. Jong, G.J. de Lenders, J.W. Links, T.P. Luyten, G.P.M. Sijmons, R.H. Eussen, B.H.J.
2007-08-01
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family (Article)
Puijenbroek, M. van Nielsen, M. Hes, F.J. Morreau, H. Reinards, T.H.C.M. Weiss, M.M. Wagner, A. Hendriks, Y. Vasen, H. Tops, C. Wijnen, J.T. Wezel, T. van
2007-03-01