Karin Anna Wallentin Wadt
Clinical Associate Professor
- 2022
- Published
Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort
Foss-Skiftesvik, J., Stoltze, U. K., Hansen, Thomas van Overeem, Ahlborn, L. B., Sørensen, E., Ostrowski, Sisse Rye, Kullegaard, S. M. A., Laspiur, A. O., Melchior, L. C., Scheie, David, Kristensen, Bjarne Winther, Skjøth, Jane, Schmiegelow, Kjeld, Wadt, Karin Anna Wallentin & Mathiasen, René, 2022, In: Acta Neuropathologica Communications. 10, 123.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Risk of New Primary Cancer in Patients with Posterior Uveal Melanoma: A National Cohort Study
Bagger, M., Albieri, V., Hindso, T. G., Wadt, Karin Anna Wallentin, Heegaard, Steffen, Andersen, Klaus Kaae & Kiilgaard, Jens Folke, 2022, In: Cancers. 14, 2, 11 p., 284.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Risk of somatic hospitalization in parents after cancer in a child, a nationwide cohort study
von Heymann, A., Alef-Defoe, S., Salem, H., Andersen, Elisabeth Anne Wreford, Dalton, Susanne Oksbjerg, Schmiegelow, Kjeld, Wadt, Karin Anna Wallentin, Winther, J. F., Johansen, Christoffer & Bidstrup, Pernille Envold Hansen, 2022, In: Psycho-Oncology. 31, 7, p. 1196-1203 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance
Louise M Binderup, M., Smerdel, M., Borgwadt, L., Beck Nielsen, S. S., Madsen, M. G., Møller, H. U., Kiilgaard, J. F., Friis-Hansen, L., Harbud, V., Cortnum, S., Owen, H., Gimsing, S., Friis Juhl, H. A., Munthe, S., Geilswijk, M., Rasmussen, Å. K., Møldrup, U., Graumann, O., Donskov, F., Grønbæk, H. & 11 others, , 2022, In: European Journal of Medical Genetics. 65, 8, 104538.Research output: Contribution to journal › Journal article › Research › peer-review
- 2021
- Published
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families
Lacson, J. C. A., Zamani, S. A., Froes, L. A. R., Mitra, N., Qian, L., Doyle, S. H., Azizi, E., Balestrini, C., Bishop, D. T., Bruno, W., Carlos-ortega, B., Cuellar, F., Cust, A. E., Elder, D. E., Gerdes, A., Ghiorzo, P., Grazziotin, T. C., Gruis, N. A., Hansson, J., Hočevar, M. & 18 others, , 1 Dec 2021, In: BMC Public Health. 21, 1, 16 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper
Jelsig, A. M., Jespersen, N., Karstensen, John Gásdal, Ketabi, Z., Rønlund, K., Sunde, L., Thorlacius-Ussing, O., Wadt, Karin Anna Wallentin, Qvist, N. & Lautrup, C. K., 20 Sep 2021, In: Ugeskrift for Laeger. 183, 38, 8 p., :V02210148.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genomforskningsprojekt påviser TP53-mutation hos en pige med rabdomyosarkom
Behrendt-Møller, I., Stoltze, U., Hjalgrim, L. L., Hansen, Thomas van Overeem, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 9 Aug 2021, In: Ugeskrift for Laeger. 183, 32, 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
The International Mismatch Repair Consortium, T. I. M. R. C., Jul 2021, In: The Lancet Oncology. 22, 7, p. 1014-1022 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
Seppälä, T. T., Dominguez-Valentin, M., Crosbie, E. J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R. H., Bertario, L., Bonanni, B., Tibiletti, M. G., Cavestro, G. M., Mints, M., Gluck, N., Katz, L., Heinimann, K. & 66 others, , May 2021, In: European Journal of Cancer. 148, p. 124-133 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome
Winter, G., Kirschner-Schwabe, R., Groeneveld-Krentz, S., Escherich, G., Möricke, A., von Stackelberg, A., Stanulla, M., Bailey, S., Richter, L., Steinemann, D., Ripperger, T., Escudero, A., Farah, R., Lohi, O., Wadt, Karin Anna Wallentin, Jongmans, M., van Engelen, N., Eckert, C. & Kratz, C. P., 2021, In: Leukemia. 35, 5, p. 1475-1479 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 212547613
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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
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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
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