Hereditary cancer in clinical practice, 1731-2302

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  1. 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 journalArticleAcademicpeer-review

  2. Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: A Prospective Lynch Syndrome Database report

    Seppala, T., Pylvanainen, K., Evans, D. G., Jarvinen, H., Renkonen-Sinisalo, L., Bernstein, I., Holinski-Feder, E., Sala, P., Lindblom, A., Macrae, F., Blanco, I., Sijmons, R., Jeffries, J., Vasen, H., Burn, J., Nakken, S., Hovig, E., Rodland, E. A., Tharmaratnam, K., Cappel, W. H. D. V. T. N., Hill, J., Wijnen, J., Jenkins, M., Genuardi, M., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Frayling, I. M., Plazzer, J-P., Sampson, J. R., Capella, G., Moslein, G., Mecklin, J-P., Moller, P. & Collaboration Mallorca Grp, 10-Oct-2017, In : Hereditary cancer in clinical practice. 15, 10 p., 18.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. Thank you to all our manuscript reviewers in 2015

    Lubinski, J., Scott, R. J., Sijmons, R. & Theissen, S. M., 29-Feb-2016, In : Hereditary cancer in clinical practice. 14, 2 p., 7.

    Research output: Contribution to journalArticleProfessional

  4. A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

    van Riel, E., Ausems, M. G. E. M., Hogervorst, F. B. L., Kluijt, I., van Gijn, M. E., van Echtelt, J., Scheidel-Jacobse, K., Hennekam, E. F. A. M., Stulp, R. P., Vos, Y. J., Offerhaus, G. J. A., Menko, F. H. & Gille, J. J. P., 12-Aug-2010, In : Hereditary cancer in clinical practice. 8, 9 p., 7.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. Hereditary Cancer in Clinical Practice transfers to BioMed Central

    Lubinski, J., Sijmons, R. H. & Scott, R. J., 26-Jan-2009, In : Hereditary cancer in clinical practice. 7, 1 p., 1.

    Research output: Contribution to journalEditorialAcademicpeer-review

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