dr. S.W. Bajwa-ten Broeke

Telephone:
E-mail:
s.w.ten.broeke umcg.nl
Research
Publications
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
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
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
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
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
ID: 62635075