Karin Anna Wallentin Wadt
Clinical Associate Professor
- 2023
- 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
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
- 2022
- Published
9p21.3 Microdeletion involving CDKN2A/2B in a young patient with multiple primary cancers and review of the literature
Jensen, M. R., Stoltze, U., Hansen, Thomas van Overeem, Bak, M., Sehested, A., Rechnitzer, C., Mathiasen, René, Scheie, David, Larsen, K. B., Olsen, T. E., Muhic, A., Skjøth, Jane, Rossing, Caroline Maria, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2022, In: Cold Spring Harbor molecular case studies. 8, 4, a006164.Research output: Contribution to journal › Review › Research › peer-review
- Published
Background sensitivity to chemotherapy-induced nausea and vomiting and response to antiemetics in paediatric patients: a genetic association study
Eliasen, A., Kornholt, J., Mathiasen, R., Wadt, Karin Anna Wallentin, Stoltze, U., Brok, J., Rechnitzer, C., Schmiegelow, Kjeld & Dalhoff, Kim, 2022, In: Pharmacogenetics and Genomics. 32, 2, p. 72-78 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cancer-related Mutations with Local or Long-range Effects on an Allosteric Loop of p53
Degn, K., Beltrame, L., Dahl Hede, F., Sora, V., Nicolaci, V., Vabistsevits, M., Schmiegelow, Kjeld, Wadt, Karin Anna Wallentin, Tiberti, M., Lambrughi, M. & Papaleo, E., 2022, In: Journal of Molecular Biology. 434, 17, 33 p., 167663.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer
Djursby, M., Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin, Madsen, M. B., Berchtold, L. A., Lautrup, C. K., Markholt, S., Jensen, U. B., Krogh, L. N., Lundsgaard, M., Gerdes, Anne-Marie Axø, Nilbert, Mef Christina & Therkildsen, C., 2022, In: Human Genetics. 141, p. 1925–1933Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC), T. E. H. T. G. (. A. T. I. M. R. C. (., 2022, In: Hereditary Cancer in Clinical Practice. 20, 36.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review
Beck, S. H., Jelsig, A. M., Yassin, H. M., Lindberg, L. J., Wadt, Karin Anna Wallentin & Karstensen, John Gásdal, 2022, In: Familial Cancer. 21, 4, p. 453-462Research output: Contribution to journal › Review › Research › peer-review
- Published
Onkogenetik I: Arvelig disposition til cancer
Wadt, Karin Anna Wallentin & Lautrup, C. K., 2022, Medicinsk genetik. 3 ed. FADL's Forlag, p. 291-317Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Education
- Published
Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma
Schedel, A., Friedrich, U. A., Morcos, M. N. F., Wagener, R., Mehtonen, J., Watrin, T., Saitta, C., Brozou, T., Michler, P., Walter, C., Försti, A., Baksi, A., Menzel, M., Horak, P., Paramasivam, N., Fazio, G., Autry, R. J., Fröhling, S., Suttorp, M., Gertzen, C. & 13 others, , 2022, In: International Journal of Molecular Sciences. 23, 9, 5174.Research 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
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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