Anne-Marie Axø Gerdes
Clinical Professor
- 2022
- Published
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
ENIGMA Consortium, E. C. & CIMBA Consortium, C. C., 2022, In: Genetics in Medicine. 24, 1, p. 119-129 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up
the CAPP2 Investigators, T. C. I., 2022, In: Cancer Prevention Research. 15, 9, p. 623-634Research 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
Etik og jura
Ousager, L. B., Gerdes, Anne-Marie Axø & Kristensen, K., 2022, Medicinsk genetik. FADL's Forlag, p. 477-500Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication
- Published
Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients
Tan, M., Brusgaard, K., Gerdes, Anne-Marie Axø, Larsen, M. J., Mortensen, M. B., Detlefsen, S., de Muckadell, O. B. S. & Joergensen, M. T., 2022, In: Annals of Human Genetics. 86, 4, p. 195-206 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2021
- Published
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
- Published
Direct to consumer genetic testing in Denmark—public knowledge, use, and attitudes
Gerdes, Anne-Marie Axø, Nicolaisen, L., Husum, E., Andersen, J. B., Gantzhorn, M. D., Roos, L. & Diness, Birgitte Rode, May 2021, In: European Journal of Human Genetics. 29, 5, p. 851-860 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Tumour-infiltrating CD4-, CD8- and FOXP3-positive immune cells as predictive markers of mortality in BRCA1- and BRCA2-associated breast cancer
Jørgensen, N., Hviid, Thomas Vauvert F., Nielsen, L. B., Sønderstrup, I. M. H., Eriksen, J. O., Ejlertsen, Bent Laursen, Gerdes, Anne-Marie Axø, Kruse, T. A., Thomassen, M., Jensen, M. & Lænkholm, Anne-Vibeke, Aug 2021, In: British Journal of Cancer. 125, p. 1388–1398Research output: Contribution to journal › Journal article › Research › peer-review
- 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
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
GEMO Study Collaborators, G. S. C., EMBRACE Collaborators, E. C., OCGN Investigators, O. I., HEBON Investigators, H. I. & kConFab Investigators, K. I., 2021, In: Genetics in Medicine. 23, 9, p. 1726-1737Research output: Contribution to journal › Journal article › Research › peer-review
ID: 19459833
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346
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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
256
downloads
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
237
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Pediatric cancer families' participation in whole-genome sequencing research in Denmark: Parent perspectives
Research output: Contribution to journal › Journal article › Research › peer-review
Published