Karin Anna Wallentin Wadt
Clinical Associate Professor
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Prevalence of Pathogenic Germline DICER1 Variants in Young Individuals Thyroidectomised Due to Goitre – A National Danish Cohort
Altaraihi, M., Hansen, T. V. O., Santoni Rugiu, Eric, Rossing, M., Rasmussen, Å. K., Gerdes, A. & Wadt, Karin Anna Wallentin, 2021, In: Frontiers in Endocrinology. 12, 7 p., 727970.Research output: Contribution to journal › Journal article › Research › peer-review
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Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group
Bakhuizen, J. J., Hanson, H., van der Tuin, K., Lalloo, F., Tischkowitz, M., Wadt, Karin Anna Wallentin, Jongmans, M. C. J., SIOPE Host Genome Working Group, S. H. G. W. G., CanGene-CanVar Clinical Guideline Working Group, C. C. G. W. G. & Expert Network Members, E. N. M., 2021, In: Familial Cancer. 20, 4, p. 337-348 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel
Byrjalsen, A., Diets, I. J., Bakhuizen, J., Hansen, Thomas van Overeem, Schmiegelow, Kjeld, Gerdes, Anne-Marie Axø, Stoltze, U., Kuiper, R. P., Merks, J. H. M., Wadt, Karin Anna Wallentin & Jongmans, M., 2021, In: Familial Cancer. 20, 4, p. 279-287 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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Danish guidelines for management of non-APC-associated hereditary polyposis syndromes
Jelsig, A. M., Karstensen, John Gásdal, Jespersen, N., Ketabi, Z., Lautrup, C., Rønlund, K., Sunde, L., Wadt, Karin Anna Wallentin, Thorlacius-Ussing, O. & Qvist, N., 2021, In: Hereditary Cancer in Clinical Practice. 19, 9 p., 41.Research output: Contribution to journal › Review › Research › peer-review
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Novel Genetic Causes of Gastrointestinal Polyposis Syndromes
Jelsig, A. M., Byrjalsen, A., Madsen, M. B., Kuhlmann, Tine Plato, Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin & Karstensen, John Gásdal, 2021, In: Application of Clinical Genetics. 14, p. 455-466 12 p.Research output: Contribution to journal › Review › Research › peer-review
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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
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Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe
extended ERN-GENTURIS Thematic Group 3, E. E. T. G. 3., 2021, In: European Journal of Medical Genetics. 64, 12, 7 p., 104350.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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
Published