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10 Most Recent Publications
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Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-result
(Article)
Vos, J. Gómez García, E.B. Oosterwijk, J.C. Menko, F. Stoel, R.D. Asperen, C.J. van Jansen, A.M. Stiggelbout, A.M. Tibben, A. |
2012-01-01
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A counselee-oriented perspective on risk communication in genetic counseling: Explaining the inaccuracy of the counselees' risk perception shortly after BRCA1/2 test result disclosure
(Article)
Vos, J. Stiggelbout, A.M. Oosterwijk, J.C. Gómez García, E.B. Menko, F. Collée, J.M. Asperen, C.J. van Tibben, A. |
2011-09-01
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Exploring the short-term impact of DNA-testing in breast cancer patients: The counselees' perception matters, but the actual BRCA1/2 result does not
(Article)
Vos, J. Oosterwijk, J.C. Gómez García, E.B. Menko, F. Collee, J.M. Asperen, C.J. van Jansen, A.M. Stiggelbout, A.M. Tibben, A. |
2011-06-20
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A whisper-game perspective on the family communication of DNA-test results: A retrospective study on the communication process of BRCA1/2-test results between proband and relatives
(Article)
Vos, J. Menko, F. Jansen, A.M. Asperen, C.J. van Stiggelbout, A.M. Tibben, A. |
2011-03-01
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Perceiving cancer-risks and heredity-likelihood in genetic-counseling: How counselees recall and interpret BRCA 1/2-test results
(Article)
Vos, J. Oosterwijk, J.C. Gómez García, E.B. Menko, F. Jansen, A.M. Stoel, R.D. Asperen, C.J. van Tibben, A. Stiggelbout, A.M. |
2011-03-01
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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
(Article)
Smit, D.L. Mensenkamp, A.R. Hoefsloot, L.H. Moorselaar, R.J.A. van Starink, T.M. Bayley, J.P. Frank, J. Steensel, M.A.M. van Menko, F. Badeloe, S. Breuning, M.H. Simon, M.E.H. Spaendonck, K.Y. van Aalfs, C. Post, J.G. Shanley, S. Krapels, I.P.C. |
2011-01-01
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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
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Chromosome 8q23.3 and 11q23.1 Variants Modify Colorectal Cancer Risk in Lynch Syndrome
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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
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Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
(Article)
Leng, W.W.J. de Jansen, M. Giardiello, F.M. Weterman, M.A.J. Offerhaus, G.J.A. Carvalho, R. Polak, M. Musler, A.R. Milne, A.N.A. Keller, J.J. Menko, F. Rooij, F.W.M. de Iacobuzio-Donahue, C.A. |
2007-12-01
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Biallelic germline mutations of mismatch-repair genes: A possible cause for multiple pediatric malignancies
(Article)
Poley, J.W. Wagner, A. Hoogmans, M.M.C.P. Menko, F. Tops, C. Kros, J.M. Reddingius, R.E. Meijers-Heijboer, E.J. Kuipers, E.J. Dinjens, W.N.M. |
2007-06-01
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