dr. S.W. Bajwa-ten Broeke

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E-mail:
s.w.ten.broeke umcg.nl

Research

Publications
  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 journalArticleAcademicpeer-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 journalReview articleAcademicpeer-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 journalComment/Letter to the editorAcademicpeer-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 journalArticleAcademicpeer-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 journalArticleAcademicpeer-review

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ID: 62635075