Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

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  • 2022

    Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

    Møller, P., Seppälä, T., Dowty, J. G., Haupt, S., Dominguez-Valentin, M., Sunde, L., Bernstein, I., Engel, C., Aretz, S., Nielsen, M., Capella, G., Evans, D. G., Burn, J., Holinski-Feder, E., Bertario, L., Bonanni, B., Lindblom, A., Levi, Z., Macrae, F., Winship, I., & 138 othersPlazzer, J-P., Sijmons, R., Laghi, L., Valle, A. D., Heinimann, K., Half, E., Lopez-Koestner, F., Alvarez-Valenzuela, K., Scott, R. J., Katz, L., Laish, I., Vainer, E., Vaccaro, C. A., Carraro, D. M., Gluck, N., Abu-Freha, N., Stakelum, A., Kennelly, R., Winter, D., Rossi, B. M., Greenblatt, M., Bohorquez, M., Sheth, H., Tibiletti, M. G., Lino-Silva, L. S., Horisberger, K., Portenkirchner, C., Nascimento, I., Rossi, N. T., da Silva, L. A., Thomas, H., Zaránd, A., Mecklin, J-P., Pylvänäinen, K., Renkonen-Sinisalo, L., Lepisto, A., Peltomäki, P., Therkildsen, C., Lindberg, L. J., Thorlacius-Ussing, O., von Knebel Doeberitz, M., Loeffler, M., Rahner, N., Steinke-Lange, V., Schmiegel, W., Vangala, D., Perne, C., Hüneburg, R., de Vargas, A. F., Latchford, A., Gerdes, A-M., Backman, A-S., Guillén-Ponce, C., Snyder, C., Lautrup, C. K., Amor, D., Palmero, E., Stoffel, E., Duijkers, F., Hall, M. J., Hampel, H., Williams, H., Okkels, H., Lubiński, J., Reece, J., Ngeow, J., Guillem, J. G., Arnold, J., Wadt, K., Monahan, K., Senter, L., Rasmussen, L. J., van Hest, L. P., Ricciardiello, L., Kohonen-Corish, M. R. J., Ligtenberg, M. J. L., Southey, M., Aronson, M., Zahary, M. N., Samadder, N. J., Poplawski, N., Hoogerbrugge, N., Morrison, P. J., James, P., Lee, G., Chen-Shtoyerman, R., Ankathil, R., Pai, R., Ward, R., Parry, S., Dębniak, T., John, T., van Overeem Hansen, T., Caldés, T., Yamaguchi, T., Barca-Tierno, V., Garre, P., Cavestro, G. M., Weitz, J., Redler, S., Büttner, R., Heuveline, V., Hopper, J. L., Win, A. K., Lindor, N., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J., Buchanan, D. D., Thibodeau, S. N., Ten Broeke, S. W., Hovig, E., Nakken, S., Pineda, M., Dueñas, N., Brunet, J., Green, K., Lalloo, F., Newton, K., Crosbie, E. J., Mints, M., Tjandra, D., Neffa, F., Esperon, P., Kariv, R., Rosner, G., Pavicic, W. H., Kalfayan, P., Torrezan, G. T., Bassaneze, T., Martin, C., Moslein, G., Ahadova, A., Kloor, M., Sampson, J. R., Jenkins, M. A. & European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC), 1 Oct 2022, In: Hereditary Cancer in Clinical Practice. 20, 1, 36.

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