Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer

Djursby, M., Hansen, T. V. O., Wadt, K. A. W., Madsen, M. B., Berchtold, L. A., Lautrup, C. K., Markholt, S., Jensen, U. B., Krogh, L. N., Lundsgaard, M., Gerdes, A. M., Nilbert, M. & Therkildsen, C., 29 Jul 2022, (E-pub ahead of print) In: Human Genetics.

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Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

Yang, X., Song, H., Leslie, G., Engel, C., Hahnen, E., Auber, B., Horváth, J., Kast, K., Niederacher, D., Turnbull, C., Houlston, R., Hanson, H., Loveday, C., Dolinsky, J. S., LaDuca, H., Ramus, S. J., Menon, U., Rosenthal, A. N., Jacobs, I., Gayther, S. A. & 41 others, Dicks, E., Nevanlinna, H., Aittomäki, K., Pelttari, L. M., Ehrencrona, H., Borg, Å., Kvist, A., Rivera, B., Hansen, T. V. O., Djursby, M., Lee, A., Dennis, J., Bowtell, D. D., Traficante, N., Diez, O., Balmaña, J., Gruber, S. B., Chenevix-Trench, G., Investigators, KC., Jensen, A., Kjær, S. K., Høgdall, E., Castéra, L., Garber, J., Janavicius, R., Osorio, A., Golmard, L., Vega, A., Couch, F. J., Robson, M., Gronwald, J., Domchek, S. M., Culver, J. O., de la Hoya, M., Easton, D. F., Foulkes, W. D., Tischkowitz, M., Meindl, A., Schmutzler, R. K., Pharoah, P. D. P. & Antoniou, A. C., 1 Dec 2020, In: JNCI-Journal of the National Cancer Institute. 112, 12, p. 1242-1250 9 p.

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New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients

Djursby, M., Madsen, M. B., Frederiksen, J. H., Berchtold, L. A., Therkildsen, C., Willemoe, G. L., Hasselby, J. P., Wikman, F., Okkels, H., Skytte, A-B., Nilbert, M., Wadt, K., Gerdes, A-M. & van Overeem Hansen, T., 24 Sep 2020, In: Frontiers in genetics. 11, p. 566266 566266.

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A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

Djursby, M., Wadt, K., Frederiksen, J. H., Madsen, M. B., Berchtold, L. A., Hasselby, J. P., Willemoe, G. L., Hansen, T. V. O. & Gerdes, A-M., 7 Apr 2020, In: Hereditary Cancer in Clinical Practice. 18, 1, p. 1-6 6 p., 8.

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Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer

Jønson, L., Ahlborn, L. B., Steffensen, A. Y., Djursby, M., Ejlertsen, B., Timshel, S., Nielsen, F. C., Gerdes, A-M. & Hansen, T. V. O., Jan 2016, In: Breast Cancer Research and Treatment. 155, 2, p. 215-22 8 p.

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Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations

Ahlborn, L. B., Steffensen, A. Y., Jønson, L., Djursby, M., Nielsen, F. C., Gerdes, A-M. & Hansen, T. V. O., 2015, In: Familial Cancer. 14, 1, p. 129-133

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CDKN2A-mutation hos en familie med arveligt malignt melanom

Djursby, M., Wadt, K., Lorentzen, H., Borg, A., Gerdes, A-M. & Krogh, L., 29 Sep 2014, In: Ugeskrift for læger [online]. 176, 40

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