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scopus: 7003695826

Sijmons, R.H.

(Rolf Sijmons)


cancer family mutation distress study testing individual carrier disease partner genetic result support university database patient cancer distress brca 1/2 level netherland 1/2 scale participant health syndrome hnpcc table signi ficantly member signi department variant breast relationship genet breast cancer surveillance center system children illness impact research laboratory family members representation characteristic result disclosure family system characteristics population test result hnpcc mutation families tumor variable variation communication status perception women model relative susceptibility group analysis project susceptibility testing disclosure ficantly number germline cancer status score advice gender counseling erasmus mc illness representations parent von hippel-lindau disease worry




10 Most Recent Publications

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
Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits (Article)
Lammens, C.R.M. Bleiker, E.M.A. Gómez García, E.B. Cats, A. Nagtegaal, T. Verhoef, S. Aaronson, N.K. Wagner, A. Sijmons, R.H. Ausems, M.G.E.M. Vriends, A.H.J.T. Ruijs, M.W.G. Os, T.A.M. van Spruijt, L.
2010-12-01
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
Attitude towards pre-implantation genetic diagnosis for hereditary cancer (Article)
Lammens, C.R.M. Bleiker, E.M.A. Spruijt, L. Verhoef, S. Gómez García, E.B. Ruijs, M.W.G. Aaronson, N.K. Vriends, A.H.J.T. Jansweijer, M. Ausems, M.G.E.M. Wagner, A. Sijmons, R.H. Ouweland, A.M.W. van den Luijt, R.B. van der
2009-12-01
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project (Article)
Cotton, R.G.H. Al Aqeel, A.I. Patrinos, G.P. Qi, M. Ramesar, R.S. Scott, R.J. Sijmons, R.H. Sobrido, M.J. Vihinen, M. Al-Mulla, F. Carrera, P. Claustres, M. Ekong, R. Hyland, V.J. Macrae, F.A. Marafie, M.J. Paalman, M.H.
2009-12-01
Planning the human variome project: The Spain report (Article)
Kaput, J. Cotton, R.G.H. Bapat, B. Yim, S.H. Yoo, H.S. Bernstein, I.T. Bhak, J. Bleoo, S.L. Blöcer, H. Brenner, S.E. Burn, J. Bustamante, M. Calzone, R. Cambon-Thomsen, A. Hardman, L. Cargill, M. Carrera, P. Cavedon, L. Cho, Y.S. Chung, Y.J. Claustres, M. Cutting, G. Dalgleish, R. Dunnen, J.T. den Diaz, C. Watson, M. Dobrowolski, S. Santos, M.R.N.D. Ekong, R. Flanagan, S.B. Flicek, P. Furukawa, Y. Genuardi, M. Ghang, H. Golubenko, M.V. Greenblatt, M.S. Ageel, A.I.A. Hamosh, A. Hancock, J.M. Hardison, R. Harrison, T.M. Hoffmann, R. Horaitis, R. Howard, H.J. Barash, C.I. Izagirre, N. Jung, J. Al-Aama, J.Y. Kojima, T. Laradi, S. Lee, Y.S. Lee, J.Y. Gil-da-Silva-Lopes, V.L. Macrae, F.A. Maglott, D. Marafie, M.J. Marsh, S. Matsubara, Y. Al-Mulla, F. Messiaen, L.M. Möslein, G. Netea, M.G. Norton, M.L. Oefner, P.J. Oetting, W.S. O'Leary, J.C. Ramirez, A.M.O. de Paalman, M.H. Parboosingh, J. Alonso, S. Patrinos, G.P. Perozzi, G. Phillips, I.R. Povey, S. Prasad, S. Qi, M. Quin, D.J. Ramesar, R.S. Richards, C.S. Savige, J. Aretz, S. Scheible, D.G. Scott, R.J. Seminara, D. Shephard, E.A. Sijmons, R.H. Smith, T.D. Sobrido, M.J. Tanaka, T. Tavtigian, S.V. Taylor, G.R. Auerbach, A.D. Teague, J. Töpel, T. Ullman-Cullere, M. Utsunomiya, J. Kranen, H. van Vihinen, M. Webb, E. Weber, T.K. Yeager, M. Yeom, Y.I.
2009-04-01
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
The common sense model of self-regulation and psychological adjustment to predictive genetic testing: A prospective study (Article)
Oostrom, I.I.H. van Meijers-Heijboer, E.J. Duivenvoorden, H.J. Bröcker-vriends, A.H.J.T. Asperen, C.J. van Sijmons, R.H. Seynaeve, C.M. Gool, A.R. van Klijn, J.G.M. Tibben, A.
2007-12-01
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
A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships (Article)
Oostrom, I.I.H. van Meijers-Heijboer, E.J. Dooren, S. van Tibben, A. Duivenvoorden, H.J. Bröcker-vriends, A.H.J.T. Asperen, C.J. van Sijmons, R.H. Seynaeve, C.M. Gool, A.R. van Klijn, J.G.M. Riedijk, S.R.
2007-04-01