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Rigshospitalet - a part of Copenhagen University Hospital

Familial Cancer, ‎1389-9600

Journal

  1. 2021
  2. Published

    Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel

    Byrjalsen, A., Diets, I. J., Bakhuizen, J., Hansen, T. V. O., Schmiegelow, K., Gerdes, A-M., Stoltze, U., Kuiper, R. P., Merks, J. H. M., Wadt, K. & Jongmans, M., Oct 2021, In: Familial Cancer. 20, 4, p. 279-287 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group

    SIOPE Host Genome Working Group, Oct 2021, In: Familial Cancer. 20, 4, p. 337-348 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Two cases of somatic STK11 mosaicism in Danish patients with Peutz-Jeghers syndrome

    Jelsig, A. M., Bertelsen, B., Forss, I. & Karstensen, J. G., Jan 2021, In: Familial Cancer. 20, 1, p. 55-59 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2016
  6. Published

    BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population

    Nielsen, H. R., Nilbert, M., Petersen, J., Ladelund, S., Thomassen, M., Pedersen, I. S., Hansen, T. V. O., Skytte, A-B., Borg, Å. & Therkildsen, C., Oct 2016, In: Familial Cancer. 15, 4, p. 407-12

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Germline TERT promoter mutations are rare in familial melanoma

    Harland, M., Petljak, M., Robles-Espinoza, C. D., Ding, Z., Gruis, N. A., van Doorn, R., Pooley, K. A., Dunning, A. M., Aoude, L. G., Wadt, K. A. W., Gerdes, A-M., Brown, K. M., Hayward, N. K., Newton-Bishop, J. A., Adams, D. J. & Bishop, D. T., 2016, In: Familial Cancer. 15, 1, p. 139-40

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 2015
  9. Published

    High accuracy of family history of melanoma in Danish melanoma cases

    Wadt, K. A. W., Drzewiecki, K. T. & Gerdes, A-M., Dec 2015, In: Familial Cancer. 14, 4, p. 609-13 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    POLE mutations in families predisposed to cutaneous melanoma

    Aoude, L. G., Heitzer, E., Johansson, P., Gartside, M., Wadt, K., Pritchard, A. L., Palmer, J. M., Symmons, J., Gerdes, A-M., Montgomery, G. W., Martin, N. G., Tomlinson, I., Kearsey, S. & Hayward, N. K., Dec 2015, In: Familial Cancer. 14, 4, p. 621-8 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Germline RAD51B truncating mutation in a family with cutaneous melanoma

    Wadt, K. A. W., Aoude, L. G., Golmard, L., Hansen, T. V. O., Sastre-Garau, X., Hayward, N. K. & Gerdes, A-M., Jun 2015, In: Familial Cancer. 14, 2, p. 337-40 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    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

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. 2014
  14. Published
  15. 2013
  16. Published

    Splice site mutations in mismatch repair genes and risk of cancer in the general population

    Thomsen, M., Nordestgaard, B. G., Tybjærg-Hansen, A. & Bojesen, S. E., 18 Jan 2013, In: Familial Cancer. 13, 3, p. 567-72

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. 2012
  18. Published

    Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma

    Wadt, K., Gerdes, A-M., Hansen, T. V. O., Toft, B. G., Friis-Hansen, L. & Andersen, M. K., 2012, In: Familial Cancer. 11, 3, p. 535-7 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. 2011
  20. Published

    A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one

    Kantelinen, J., Hansen, T. V. O., Kansikas, M., Krogh, L. N., Korhonen, M. K., Ollila, S., Nyström, M., Gerdes, A-M. & Kariola, R., 2011, In: Familial Cancer. 10, 3, p. 515-20 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published
  22. 2010
  23. Published

    Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations

    Steffensen, A. Y., Jønson, L., Ejlertsen, B., Gerdes, A-M., Nielsen, F. C. & Hansen, T. V. O., 1 Sep 2010, In: Familial Cancer. 9, 3, p. 283-7 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 106208