Anne-Marie Axø Gerdes
Clinical Professor
- 2022
- 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
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
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
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
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
Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study
Tan, M., Brusgaard, K., Gerdes, Anne-Marie Axø, Mortensen, M. B., Detlefsen, S., Schaffalitzky De Muckadell, O. B. & Joergensen, M. T., 3 Aug 2021, In: Scandinavian Journal of Gastroenterology. 56, 8, p. 965-971 7 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
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study
Epidemiological Study of Familial Breast Cancer, Gene Etude Prospective Sein Ovaire Sein, Hereditary Breast and Ovarian Cancer Research Group Netherlands, and International BRCA1/2 Carrier Cohort Study, E. S. O. F. B. C. G. E. P. S. O. S. H. B. A. O. C. R. G. N. A. I. B. C. C. S., Jul 2021, In: American Journal of Obstetrics and Gynecology. 225, 1, p. 51.e1-51.e17Research 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
ID: 19459833
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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
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256
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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
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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
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