Anne-Marie Axø Gerdes
Clinical Professor
- 2019
- Published
Genomisk medicin til præimplantations-, præ- og postnatal diagnostik
Gerdes, Anne-Marie Axø, Risom, L., Kjærgaard, S. & Østergaard, Elsebet, 2019, In: Ugeskrift for Laeger. 181, 7A, 5 p., V11180756.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Parsons, M. T., Tudini, E., Li, H., Hahnen, E., Wappenschmidt, B., Feliubadaló, L., Aalfs, C. M., Agata, S., Aittomäki, K., Alducci, E., Alonso-Cerezo, M. C., Arnold, N., Auber, B., Austin, R., Azzollini, J., Balmaña, J., Barbieri, E., Bartram, C. R., Blanco, A., Blümcke, B. & 31 others, , 2019, In: Human Mutation. 40, 9, p. 1557-1578 22 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Toward mechanistic models for genotype-phenotype correlations in phenylketonuria using protein stability calculations
Scheller, R., Stein, Amelie, Nielsen, S. V., Marin, F. I., Gerdes, Anne-Marie Axø, Di Marco, M., Papaleo, E., Lindorff-Larsen, Kresten & Hartmann-Petersen, Rasmus, 2019, In: Human Mutation. 40, 4, p. 444-457Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer - an European consensus statement and expert recommendations
Singer, C. F., Balmaña, J., Bürki, N., Delaloge, S., Filieri, M. E., Gerdes, Anne-Marie Axø, Grindedal, E. M., Han, S., Johansson, O., Kaufman, B., Krajc, M., Loman, N., Olah, E., Paluch-Shimon, S., Plavetic, N. D., Pohlodek, K., Rhiem, K., Teixeira, M. & Evans, D. G., 2019, In: European Journal of Cancer. 106, p. 54-60 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Evaluation of tumor-infiltrating lymphocytes and association with prognosis in BRCA-mutated breast cancer
Sønderstrup, I. M. H., Jensen, M. B., Ejlertsen, Bent Laursen, Eriksen, J. O., Gerdes, Anne-Marie Axø, Kruse, T. A., Larsen, M. J., Thomassen, M. & Lænkholm, Anne-Vibeke, 2019, In: Acta Oncologica. 58, 3, p. 363-370 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Subtypes in BRCA-mutated breast cancer
Sønderstrup, I. M. H., Jensen, M. R., Ejlertsen, Bent Laursen, Eriksen, J. O., Gerdes, Anne-Marie Axø, Kruse, T. A., Larsen, M. J., Thomassen, M. & Lænkholm, Anne-Vibeke, Feb 2019, In: Human Pathology. 84, p. 192-201 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
Taylor, N. J., Mitra, N., Qian, L., Avril, M. F., Bishop, D. T., Bressac-de Paillerets, B., Bruno, W., Calista, D., Cuellar, F., Cust, A. E., Demenais, F., Elder, D. E., Gerdes, A. M., Ghiorzo, P., Goldstein, A. M., Grazziotin, T. C., Gruis, N. A., Hansson, J., Harland, M., Hayward, N. K. & 23 others, , Aug 2019, In: Journal of the American Academy of Dermatology. 81, 2, p. 386-394Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- Published
En familie med nedarvet DICER1-mutation
Altaraihi, M., Pedersen, J., Rossing, M., Gerdes, Anne-Marie Axø & Wadt, K., 2018, In: Ugeskrift for Laeger. 180, 25, 2 p., V01180063.Research output: Contribution to journal › Letter › Research › peer-review
- Published
Pediatric cancer families' participation in whole-genome sequencing research in Denmark: Parent perspectives
Byrjalsen, A., Stoltze, U., Wadt, K., Hjalgrim, L. L., Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld & Wahlberg, Ayo, 2018, In: European Journal of Cancer Care. 27, 6, p. 1-11 11 p., e12877.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
Moghadasi, S., Meeks, H. D., Vreeswijk, M. P., Janssen, L. A., Borg, Å., Ehrencrona, H., Paulsson-Karlsson, Y., Wappenschmidt, B., Engel, C., Gehrig, A., Arnold, N., Hansen, T. V. O., Thomassen, M., Jensen, U. B., Kruse, T. A., Ejlertsen, B., Gerdes, A-M., Pedersen, I. S., Caputo, S. M., Couch, F. & 20 others, , 2018, In: Journal of Medical Genetics. 55, 1, p. 15-20Research output: Contribution to journal › Journal article › Research › peer-review
ID: 19459833
Most downloads
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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
downloads
Pediatric cancer families' participation in whole-genome sequencing research in Denmark: Parent perspectives
Research output: Contribution to journal › Journal article › Research › peer-review
Published