Karin Anna Wallentin Wadt
Clinical Associate Professor
- 2024
- Published
National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families—The Danish Model
Lindberg, Lars Joachim, Wadt, Karin Anna Wallentin, Therkildsen, C. & Petersen, H. V., 2024, In: Cancers. 16, 8, 13 p., 1577.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The evolutionary impact of childhood cancer on the human gene pool
Stoltze, U. K., Foss-Skiftesvik, J., Hansen, Thomas van Overeem, Rasmussen, Simon, Karczewski, K. J., Wadt, Karin Anna Wallentin & Schmiegelow, Kjeld, 2024, In: Nature Communications. 15, 15 p., 1881.Research output: Contribution to journal › Journal article › Research › peer-review
- 2023
- Published
New pathogenic germline variants identified in mesothelioma
Belcaid, L., Bertelsen, B., Wadt, Karin Anna Wallentin, Tuxen, I., Spanggaard, I., Højgaard, M., Sørensen, Jens Benn, Ravn, J., Lassen, Ulrik Niels, Nielsen, Finn Cilius, Rohrberg, K. & Westmose Yde, C., 2023, In: Lung Cancer. 179, 8 p., 107172.Research output: Contribution to journal › Review › Research › peer-review
- Published
The effect of a single SMARCA4 exon deletion on RNA splicing: Implications for variant classification
Byrjalsen, A., Stoltze, U., Mehrjouy, M., Frederiksen, J. H., Bak, M., Birkedal, U., Hasle, H., Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld, Wadt, Karin Anna Wallentin & Hansen, Thomas van Overeem, 2023, In: Molecular Genetics and Genomic Medicine. 11, 10, 7 p., e2232.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma
Foss-Skiftesvik, J., Mathiasen, René, Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin, Schmiegelow, Kjeld & Stoltze, U. K., 2023, In: Acta Neuropathologica Communications. 11, 1, 94.Research output: Contribution to journal › Comment/debate › Research › peer-review
- Published
TINF2 is a major susceptibility gene in Danish patients with multiple primary melanoma
Jensen, M. R., Jelsig, A. M., Gerdes, Anne-Marie Axø, Hølmich, Lisbet Rosenkrantz, mzt627, mzt627, Lorentzen, H. F., Hansen, M. H., Bak, M., Johansson, P. A., Hayward, N. K., Hansen, Thomas van Overeem & Wadt, Karin Anna Wallentin, 2023, In: Human Genetics and Genomics Advances. 4, 4, 12 p., 100225.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome
Lalloo, F., Kulkarni, A., Chau, C., Nielsen, M., Sheaff, M., Steele, J., van Doorn, R., Wadt, K., Hamill, M., Torr, B., Tischkowitz, M., Ahmed, M., Bajalica-Lagercrantz, S., Blatnik, A., Brunet, J., Cleaver, R., Colas, C., Dabir, T., Evans, D. G., Feshtali, S. & 26 others, , 2023, In: European Journal of Human Genetics. 31, p. 1261–1269 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
RosettaDDGPrediction for high-throughput mutational scans: From stability to binding
Sora, Valentina, Laspiur, A. O., Degn, K., Arnaudi, M., Utichi, M., Beltrame, L., De Menezes, D., Orlandi, M., Stoltze, U. K., Rigina, O., Sackett, P. W., Wadt, Karin Anna Wallentin, Schmiegelow, Kjeld, Tiberti, M. & Papaleo, E., 2023, In: Protein Science. 32, 1, e4527.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants
Stoltze, U. K., Hagen, C. M., Hansen, Thomas van Overeem, Byrjalsen, A., Gerdes, Anne-Marie Axø, Yakimov, V., Rasmussen, Simon, Bækvad-Hansen, M., Hougaard, D. M., Schmiegelow, Kjeld, Hjalgrim, Henrik, Wadt, Karin Anna Wallentin & Bybjerg-Grauholm, J., 2023, In: Genome Medicine. 15, 12 p., 17.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic predisposition & evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors
Stoltze, U. K., Foss-Skiftesvik, J., Hansen, Thomas van Overeem, Byrjalsen, A., Sehested, A., Scheie, David, Mikkelsen, T. S., Rasmussen, Simon, Bak, M., Okkels, H., Callesen, M. T., Skjøth-Rasmussen, J., Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld, Mathiasen, R. & Wadt, Karin Anna Wallentin, 2023, In: Neuro-Oncology. 25, 4, p. 761-773Research output: Contribution to journal › Journal article › Research › peer-review
ID: 212547613
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87
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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
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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
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Exploring the hereditary background of renal cancer in Denmark
Research output: Contribution to journal › Journal article › Research › peer-review
Published