Karin Anna Wallentin Wadt
Clinical Associate Professor
- 2024
- E-pub ahead of print
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort
Hammer-Hansen, S., Stoltze, U., Bartels, Emil Daniel, Hansen, Thomas van Overeem, Byrjalsen, A., Tybjærg-Hansen, Anne, Juul, K., Schmiegelow, Kjeld, Tfelt-Hansen, Jacob, Bundgård, Henning, Wadt, Karin Anna Wallentin & Diness, Birgitte Rode, 2024, (E-pub ahead of print) In: European Journal of Human Genetics. 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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
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
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
- Published
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
Stoltze, U. K., Hildonen, M., Hansen, Thomas van Overeem, Foss-Skiftesvik, J., Byrjalsen, A., Lundsgaard, M., Pignata, L., Grønskov, K., Tümer, Asuman Zeynep, Schmiegelow, Kjeld, Brok, J. S. & Wadt, Karin Anna Wallentin, 2023, In: Journal of Medical Genetics. 60, 9, p. 842-849Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes
Stoltze, U. K., Hansen, Thomas van Overeem, Brok, J. S., Gronskov, K., Tümer, Asuman Zeynep, Ahlborn, L. B., Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2023, In: Journal of Medical Genetics. 60, 2, p. 128-130 3 p., 108335.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
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
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
- 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
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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A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis
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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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