Mef Christina Nilbert

Mef Christina Nilbert

Affiliate Professor


  1. 2009
  2. Published

    Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.

    Nilbert, M., Wikman, F. P., Hansen, T. V. O., Krarup, H. B., Orntoft, T. F., Nielsen, F. C., Sunde, L., Gerdes, A-M., Cruger, D., Timshel, S., Bisgaard, S. M. L., Bernstein, I., Okkels, H., Nilbert, M., Wikman, F., Hansen, T., Krarup, H., Orntoft, T., Nielsen, F., Sunde, L. & 6 others, Gerdes, A., Cruger, D., Timshel, S., Bisgaard, M., Bernstein, I. & Okkels, H., 2009, In: Familial Cancer. 8, 1, p. 75-83 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Role for Genetic Anticipation in Lynch Syndrome

    Nilbert, Mef Christina, Timshel, S., Bernstein, I. & Larsen, K., 2009, In: Journal of Clinical Oncology. 27, 3, p. 360-64 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

    Nilbert, Mef Christina, Therkildsen, C., Nissen, A., Akerman, M., Bernstein, I., Nilbert, Mef Christina, Therkildsen, C., Nissen, A., Akerman, M. & Bernstein, I., 2009, In: Familial Cancer. 8, 3, p. 209-13

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2008
  6. Published

    A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome

    Clendenning, M., Senter, L., Hampel, H., Robinson, K. L., Sun, S., Buchanan, D., Walsh, M. D., Nilbert, Mef Christina, Green, J. S., Potter, J., Lindblom, A. & de la Chapelle, A., 2008, In: Journal of Medical Genetics. 45, p. 340-45

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Book review.

    Nilbert, Mef Christina, 2008, In: Acta Oncologica. 47, 8, p. 1619 1 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72

    Nilbert, Mef Christina, Kristoffersson, U., Ericsson, M., Johannsson, O., Rambech, E. & Mangell, P., 2008, In: BMC Medical Genetics. 9, 1, p. 101

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Clinicopathologic factors identify sporadic mismatch repair-defective colon cancers.

    Halvarsson, B., Anderson, H., Domanska, K., Lindmark, G. & Nilbert, Mef Christina, 2008, In: American Journal of Clinical Pathology. 129, 2, p. 238-44 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).

    Staaf, J., Törngren, T., Rambech, E., Johansson, U., Persson, C., Sellberg, G., Tellhed, L., Nilbert, Mef Christina & Borg, A., 2008, In: Human Mutation. 29, 4, p. 555-64 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Genetic profiling differentiates second primary tumors from metastases in adult metachronous soft tissue sarcoma

    Fernebro, J., Carneiro, A., Rydholm, A., Domanski, H. A., Karlsson, A., Borg, A. & Nilbert, Mef Christina, 2008, In: Sarcoma. 2008, p. 431019

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

    Magnusson, Stig Peter, Borg, A., Kristoffersson, U., Nilbert, M., Wiebe, T., Olsson, H., Magnusson, S., Borg, A., Kristoffersson, U., Nilbert, Mef Christina, Wiebe, T. & Olsson, H., 2008, In: Familial Cancer. 7, 4, p. 331-7 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 339579003