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scopus: 13906703700

Ruijs, M.W.G.

(Marielle Ruijs)


cancer family mutation breast cancer breast syndrome partner germline surveillance netherland study distress patient member carrier tumour signi ficantly level tumours table criteria family members advice individual tumor li-fraumeni syndrome genetic signi analysis testing diagnosis li-fraumeni risk family members chompret criteria sarcoma history chompret spouse support worry number department centre score disease attitude dutch genet bene fits ficantly children scale brain fi rst sample family history lfl criteria amsterdam phenotype carcinoma screening women index tp 53 gene chek 2 respondent sequence fraumeni jf jr tp 53-positive families chek 2 gene c-revised .1100delc variable control brain tumour sf -36 scales questionnaire lfs family members vhl family members intron




6 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
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: Mutation detection rate and relative frequency of cancers in different familial phenotypes (Article)
Ruijs, M.W.G.
2010-06-01
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
The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype (Article)
Ruijs, M.W.G. Broeks, A. Menko, F. Ausems, M.G.E.M. Wagner, A. Oldenburg, R. Meijers-Heijboer, H. Veer, L.J. van 't Verhoef, S.
2009-02-17
Two TP53 germline mutations in a classical Li-Fraumeni syndrome family (Article)
Hest, L.P. Ruijs, M.W.G. Wagner, A. Meer, C.A. van der Verhoef, S. Veer, L.J. van 't Meijers-Heijboer, E.J.
2007-09-01