Karin Anna Wallentin Wadt

Karin Anna Wallentin Wadt

Clinical Associate Professor

Member of:

  • Clinical Genetics


Publication year:
All
1 - 10 out of 10Page size: 10
  1. 2019
  2. Published

    Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT

    Taylor, N. J., Mitra, N., Qian, L., Avril, M. F., Bishop, D. T., Bressac-de Paillerets, B., Bruno, W., Calista, D., Cuellar, F., Cust, A. E., Demenais, F., Elder, D. E., Gerdes, A. M., Ghiorzo, P., Goldstein, A. M., Grazziotin, T. C., Gruis, N. A., Hansson, J., Harland, M., Hayward, N. K. & 23 others, Hocevar, M., Höiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Landman, G., Larre-Borges, A., Mann, G. J., Nagore, E., Olsson, H., Palmer, J. M., Perić, B., Pjanova, D., Pritchard, A. L., Puig, S., Schmid, H., van der Stoep, N., Tucker, M. A., Wadt, Karin Anna Wallentin, Yang, X. R., Newton-Bishop, J. A., Kanetsky, P. A. & GenoMEL Study Group, G. S. G., Aug 2019, In: Journal of the American Academy of Dermatology. 81, 2, p. 386-394

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?

    Altaraihi, M., Wadt, Karin Anna Wallentin, Ek, J., Gerdes, Anne-Marie Axø & Østergaard, Elsebet, 2019, In: Human Genome Variation. 6, 1, 10.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

    Altaraihi, M., Gerdes, Anne-Marie Axø & Wadt, Karin Anna Wallentin, 2019, In: Human Genome Variation. 6, 3 p., 46.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma

    Johansson, P. A., Nathan, V., Bourke, L. M., Palmer, J. M., Zhang, T., Symmons, J., Howlie, M., Patch, A. M., Read, J., Holland, E. A., Schmid, H., Warrier, S., Glasson, W., Höiom, V., Wadt, K., Jönsson, G., Olsson, H., Ingvar, C., Mann, G., Brown, K. M. & 2 others, Hayward, N. K. & Pritchard, A. L., 2019, In: Melanoma Research. 29, 5, p. 483-490 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Exploring the hereditary background of renal cancer in Denmark

    Christensen, M. B., Wadt, Karin Anna Wallentin, Jensen, U. B., Lautrup, C. K., Bojesen, A., Krogh, L. N., Overeem Hansen, T. V. & Gerdes, Anne-Marie Axø, 2019, In: PLoS ONE. 14, 4, 16 p., e0215725.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma

    Nathan, V., Johansson, P. A., Palmer, J. M., Howlie, M., Hamilton, H. R., Wadt, Karin Anna Wallentin, Jönsson, G., Brooks, K. M., Pritchard, A. L. & Hayward, N. K., 2019, In: Pigment Cell and Melanoma Research. 32, 6, p. 854-863 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Global microRNA profiling of metastatic conjunctival melanoma

    Mikkelsen, Lauge Hjorth, Andersen, M. K., Andreasen, S., Larsen, A., Tan, Q., Toft, Peter Bjerre, Wadt, Karin Anna Wallentin & Heegaard, Steffen, 2019, In: Melanoma Research. 29, 5, p. 465-473 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer

    Bertelsen, B., Tuxen, I. V., Yde, C. W., Gabrielaite, M., Torp, M. H., Kinalis, S., Oestrup, O., Rohrberg, K., Spangaard, I., Santoni Rugiu, Eric, Wadt, Karin Anna Wallentin, Mau-Sorensen, M., Lassen, Ulrik Niels & Nielsen, Finn Cilius, 2019, In: npj Genomic Medicine. 4, 1, 11 p., 13.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome

    Askaner, G., Lei, Ulrikke, Bertelsen, B., Venzo, A. & Wadt, Karin Anna Wallentin, 2019, In: Case Reports in Genetics. 2019, 6 p., 9650184.

    Research output: Contribution to journal › Journal article › Research › peer-review

  11. Published

    The genetic evolution of metastatic uveal melanoma

    Shain, A. H., Bagger, M. M., Yu, R., Chang, D., Liu, S., Vemula, S., Weier, J. F., Wadt, Karin Anna Wallentin, Heegaard, Steffen, Bastian, B. C. & Kiilgaard, Jens Folke, 2019, In: Nature Genetics. 51, p. 1123–1130

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 212547613