1. Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy

   Terlouw, D., Suerink, M., Singh, S. S., Gille, H. J. J. P., Hes, F. J., Langers, A. M. J., Morreau, H., Vasen, H. F. A., Vos, Y. J., van Wezel, T., Tops, C. M., ten Broeke, S. W. & Nielsen, M., Feb-2020, In : European Journal of Human Genetics. 28, 2, p. 222-230 9 p.

   Research output: Contribution to journal › Article › Academic › peer-review

2. An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

   Suerink, M., Rodriguez-Girondo, M., van der Klift, H. M., Colas, C., Brugieres, L., Lavoine, N., Jongmans, M., Capella Munar, G., Evans, D. G., Farrell, M. P., Genuardi, M., Goldberg, Y., Gomez-Garcia, E., Heinimann, K., Hoell, J., Aretz, S., Jasperson, K. W., Kedar, I., Modi, M. B., Nikolaev, S., van Os, T. A. M., Ripperger, T., Rueda, D., Senter, L., Sjursen, W., Sunde, L., Therkildsen, C., Tibiletti, M. G., Trainer, A. H., Vos, Y. J., Wagner, A., Winship, I., Wimmer, K., Zimmermann, S. Y., Vasen, H. F., van Asperen, C. J., Houwing-Duistermaat, J. J., ten Broeke, S. W. & Nielsen, M., Dec-2019, In : Genetics in Medicine. 21, 12, p. 2706-2712 7 p.

   Research output: Contribution to journal › Article › Academic › peer-review

3. The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect

   ten Broeke, S. W., Rodriguez-Girondo, M., Suerink, M., Aretz, S., Bernstein, I., Capella, G., Engel, C., Gomez-Garcia, E. B., van Hest, L. P., Doeberitz, M. V. K., Lagerstedt-Robinson, K., Letteboer, T. G. W., Moller, P., van Os, T. A., Pineda, M., Rahner, N., Olderode-Berends, M. J. W., von Salome, J., Schackert, H. K., Spruijt, L., Steinke-Lange, V., Wagner, A., Tops, C. M. J. & Nielsen, M., Jun-2019, In : CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION. 28, 6, p. 1010-1014 5 p.

   Research output: Contribution to journal › Article › Academic › peer-review

4. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

   Seppala, T. T., Ahadova, A., Dominguez-Valentin, M., Macrae, F., Evans, D. G., Therkildsen, C., Sampson, J., Scott, R., Burn, J., Moeslein, G., Bernstein, I., Holinski-Feder, E., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Lautrup, C. K., Lindblom, A., Plazzer, J-P., Winship, I., Tjandra, D., Katz, L. H., Aretz, S., Hueneburg, R., Holzapfel, S., Heinimann, K., Della Valle, A., Neffa, F., Gluck, N., Cappel, W. H. D. V. T. N., Vasen, H., Morak, M., Steinke-Lange, V., Engel, C., Rahner, N., Schmiegel, W., Vangala, D., Thomas, H., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Capella, G., Pineda, M., Navarro, M., Blanco, I., ten Broeke, S., Nielsen, M., Ljungmann, K., Nakken, S. & Lindor, N., 28-Feb-2019, In : Hereditary cancer in clinical practice. 17, 8 p., 8.

   Research output: Contribution to journal › Article › Academic › peer-review

5. Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

   Grolleman, J. E., de Voer, R. M., Elsayed, F. A., Nielsen, M., Weren, R. D. A., Palles, C., Ligtenberg, M. J. L., Vos, J. R., ten Broeke, S. W., de Miranda, N. F. C. C., Kuiper, R. A., Kamping, E. J., Jansen, E. A. M., Vink-Borger, M. E., Popp, I., Lang, A., Spier, I., Hueneburg, R., James, P. A., Li, N., Staninova, M., Lindsay, H., Cockburn, D., Spasic-Boskovic, O., Clendenning, M., Sweet, K., Capella, G., Sjursen, W., Hoberg-Vetti, H., Jongmans, M. C., Neveling, K., van Kessel, A. G., Morreau, H., Hes, F. J., Sijmons, R. H., Schackert, H. K., Ruiz-Ponte, C., Dymerska, D., Lubinski, J., Rivera, B., Foulkes, W. D., Tomlinson, I. P., Valle, L., Buchanan, D. D., Kenwrick, S., Adlard, J., Dimovski, A. J., Campbell, I. G., Aretz, S. & Kuiper, R. P., 11-Feb-2019, In : Cancer cell. 35, 2, p. 256-266.e5 16 p.

   Research output: Contribution to journal › Article › Academic › peer-review

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