1. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

   Dominguez-Valentin, M., Crosbie, E. J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Nakken, S., Hovig, E., Nielsen, M., Sijmons, R. H., Bertario, L., Bonanni, B., Tibiletti, M. G., Cavestro, G. M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C. A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H-G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J-P., Plazzer, J-P., Pineda, M., Navarro, M., Brunet Vidal, J., Kariv, R., Rosner, G., Alejandra Pinero, T., Laura Gonzalez, M., Kalfayan, P., Ryan, N., Ten Broeke, S. W., Jenkins, M. A., Sunde, L., Bernstein, I., Burn, J., Greenblatt, M., Cappel, W. H. D. V. T. N., Della Valle, A., Lopez-Koestner, F., Alvarez, K., Buettner, R., Goergens, H., Morak, M., Holzapfel, S., Hueneburg, R., Doeberitz, M. V. K., Loeffler, M., Rahner, N., Weitz, J., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Auranen, A., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Therkildsen, C., Okkels, H., Ketabi, Z., Denton, O. G., Rodland, E. A., Vasen, H., Neffa, F., Esperon, P., Tjandra, D., Moeslein, G., Sampson, J. R., Evans, D. G., Seppala, T. T. & Moller, P., 1-Dec-2020, In : Genetics in Medicine. 8 p.

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

2. The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance

   Ahadova, A., Seppala, T. T., Engel, C., Gallon, R., Burn, J., Holinski-Feder, E., Steinke-Lange, V., Moeslein, G., Nielsen, M., ten Broeke, S. W., Laghi, L., Dominguez-Valentin, M., Capella, G., Macrae, F., Scott, R., Hueneburg, R., Nattermann, J., Hoffmeister, M., Brenner, H., Blaeker, H., Doeberitz, M. V. K., Sampson, J. R., Vasen, H., Mecklin, J-P., Moller, P. & Kloor, M., 3-Aug-2020, In : International Journal of Cancer. 4, p. 800-811 12 p.

   Research output: Contribution to journal › Review article › Academic › peer-review

3. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

   Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Köstner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Büttner, R., Görgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hüneburg, R., Knebel Doeberitz, M. V., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvänäinen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sánchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rødland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Möslein, G., Mecklin, J-P., Nielsen, M. & Møller, P., 1-Sep-2020, In : Genetics in Medicine. 22, 9, p. 1569 1 p.

   Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

4. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

   Dominguez-Valentin, M., Sampson, J. R., Seppala, T. T., ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Kostner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Buettner, R., Goergens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hueneburg, R., von Knebel Doeberitz, M., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvanainen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M. & Gallinger, S., Jan-2020, In : Genetics in Medicine. 22, 1, p. 15-25 11 p.

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

5. 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

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