Karin Anna Wallentin Wadt
Clinical Associate Professor
51 - 55 out of 55Page size: 10
- 2019
- 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
- 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
- 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
- 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. 1123–1130Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- Published
Putative new childhood leukemia cancer predisposition syndrome caused by germline bi-allelic missense mutations in DDX41
Diness, Birgitte Rode, Risom, L., Frandsen, T. L., Hansen, B., Andersen, M. K., Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2018, In: Genes Chromosomes and Cancer. 57, 12, p. 670-674 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 212547613
Most downloads
-
87
downloads
High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
79
downloads
A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
64
downloads
Exploring the hereditary background of renal cancer in Denmark
Research output: Contribution to journal › Journal article › Research › peer-review
Published