Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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A Novel Staging Model for Uveal Melanoma: Combining Tumor Volume, Clinical Factors, and Genetic Alterations in a Danish Cohort
Nissen, K., Hindso, T. G., Faber, C., Wadt, K. A. W., Andersen, M. K., Heegaard, S., Bagger, M. & Kiilgaard, J. F., 2026, In: Ophthalmology. 133, 2, p. 233-247Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile2 Citations (Scopus)12 Downloads (Pure) -
Case report: Onychopapilloma in a patient with BAP1 tumor predisposition syndrome-a useful clinical marker?
Sjostrom, E., Ahlborn, L. B., Eliesen, E. V., Wadt, K., Lei, U. & Byrjalsen, A., 2026, In: Familial Cancer. 25, 2, 4 p., 43.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile1 Downloads (Pure) -
CD19 exon 2 skipping is a potential prognostic correlate of anti-CD19 CAR-T therapy relapse
Dam, S. H., Moranzoni, G., Høie, M. H., Modvig, S., Wadt, K. A. W., Als-Nielsen, B., Schmiegelow, K., Vitting-Seerup, K., Barnkob, M. B. & Olsen, L. R., 2026, In: Frontiers in Molecular Medicine. 6, 10 p., 1763390.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile4 Downloads (Pure) -
Challenges in identifying paediatric cancer predisposition syndromes: international SCOPE survey and SIOPE expert consensus recommendations
Ćavar Pavić, J., Cullinan, N., Jongmans, M., Bourdeaut, F., Wadt, K., LoNigro, L., Davies, M., Michaeli, O., Strang-Karlsson, S., de Putter, R., Sepulchre, E., Cazzaniga, G., Furtwängler, R., Zweier, C., Rössler, J. & Waespe, N., 2 Mar 2026, (E-pub ahead of print) In: European journal of human genetics : EJHG.Research output: Contribution to journal › Journal article › Research › peer-review
Open Access -
DoBSeqWF: A framework for sensitive detection of individual genetic variation in pooled sequencing data
Cort Nielsen, M., Hagen, C. M., Stoltze, U. K., Hansen, T. V. O., Nyegaard, M., Hjalgrim, H., Bækvad-Hansen, M., Byrjalsen, A., Schmiegelow, K., Wadt, K., Bybjerg-Grauholm, J. & Rasmussen, S., 2026, In: NAR Genomics and Bioinformatics. 8, 1, 11 p., lqag021.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile15 Downloads (Pure) -
Exploring the spectrum of central nervous system tumours in carriers of germline POT1 variants
Nielsen, E. N., Jelsig, A. M., Foss-Skiftesvik, J., Lohse, Z., Timshel, S., Borgwardt, L., Hansen, T. V. O. & Wadt, K. A. W., 2026, In: Journal of Medical Genetics. 63, 2, p. 86-92Research output: Contribution to journal › Journal article › Research › peer-review
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Functional Analysis and Clinical Data Reclassify the DICER1 c.4206+1G>C Variant, Leading to Exon 22 Skipping, as Likely Pathogenic
Walpole, S., Santiago-Vela, M. I., Birkedal, U., Hong, Z., Ros, X. B. D., Hansen, T. V. O. & Wadt, K. A. W., 2026, In: Clinical Genetics. 109, 5, p. 931-936Research output: Contribution to journal › Journal article › Research › peer-review
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Novel truncating WT1 germline variant in a case of familial Wilms tumor
Laustsen, M. M., Stoltze, U. K., Larsen, K. B., Olsen, T. E., Wadt, K. A. W., Sørensen, P. L., Klausen, K. G., Brok, J., Winther, T. N. & Ahlborn, L. B., 2026, In: Cancer genetics. 304-305, p. 160-164 5 p.Research output: Contribution to journal › Journal article › Research › peer-review