Anne-Marie Axø Gerdes

Anne-Marie Axø Gerdes

Clinical Professor

Member of:

  • Clinical Genetics


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  1. Published

    Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome

    Abildgaard, A. B., Stein, Amelie, Nielsen, S. V., Schultz-Knudsen, Katrine, Papaleo, E., Shrikhande, A., Hoffmann, Eva, Bernstein, I., Gerdes, Anne-Marie Axø, Takahashi, M., Ishioka, C., Lindorff-Larsen, Kresten & Hartmann-Petersen, Rasmus, 2019, In: eLife. 8, 28 p., e49138 .

    Research output: Contribution to journal › Journal article › Research › peer-review

  2. Published

    Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations

    Ahlborn, L. B., Steffensen, A. Y., Jønson, L., Djursby, M., Nielsen, Finn Cilius, Gerdes, Anne-Marie Axø & Hansen, T. V. O., 18 Mar 2015, In: Familial Cancer. 14, 1, p. 129-133 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?

    Altaraihi, M., Wadt, Karin Anna Wallentin, Ek, J., Gerdes, Anne-Marie Axø & Østergaard, Elsebet, 2019, In: Human Genome Variation. 6, 1, 10.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. 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

  5. Published

    A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

    Altaraihi, M., Gerdes, Anne-Marie Axø & Wadt, Karin Anna Wallentin, 2019, In: Human Genome Variation. 6, 3 p., 46.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Non-BRCA1/BRCA2 high-risk familial breast cancers are not associated with a high prevalence of BRCAness

    Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, Anne-Marie Axø, Lænkholm, Anne-Vibeke, Kruse, T. A., Nik-Zainal, S. & Thomassen, M., 2023, In: Breast Cancer Research. 25, 1, 10 p., 69.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

    Antoniou, A. C., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., McGuffog, L., Lee, A. R., Barrowdale, D., Healey, S., Sinilnikova, O. M., Caligo, M. A., Loman, N., Harbst, K., Lindblom, A., Arver, B., Rosenquist, R., Karlsson, P. W., Nathanson, K., Domchek, S., Rebbeck, T. & 31 others, Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Złowowcka-Perłowska, E., Osorio, A., Durán, M., Andrés, R., Benítez, J., Hamann, U., Hogervorst, F. B., van Os, T. A., Verhoef, S., Meijers-Heijboer, H. E. J., Wijnen, J., Gómez Garcia, E. B., Ligtenberg, M. J., Kriege, M., Collée, J. M., Ausems, M. G. E. M., Oosterwijk, J. C., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Lalloo, F., Nielsen, Finn Cilius, Gerdes, Anne-Marie Axø & CIMBA, SWE-BRCA, C. S., 2012, In: Breast Cancer Research (Online Edition). 14, 1, p. R33

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

    Antoniou, A. C., Wang, X., Fredericksen, Z. S., McGuffog, L., Tarrell, R., Sinilnikova, O. M., Healey, S., Morrison, J., Kartsonaki, C., Lesnick, T., Ghoussaini, M., Barrowdale, D., Peock, S., Cook, M., Oliver, C., Frost, D., Eccles, D., Evans, D. G., Eeles, R., Izatt, L. & 31 others, Chu, C., Douglas, F., Paterson, J., Stoppa-Lyonnet, D., Houdayer, C., Mazoyer, S., Giraud, S., Lasset, C., Remenieras, A., Caron, O., Hardouin, A., Berthet, P., Hogervorst, F. B. L., Rookus, M. A., Jager, A., van den Ouweland, A., Hoogerbrugge, N., van der Luijt, R. B., Meijers-Heijboer, H., Gómez García, E. B., Devilee, P., Vreeswijk, M. P. G., Lubinski, J., Jakubowska, A., Gronwald, J., Huzarski, T., Byrski, T., Gerdes, Anne-Marie Axø, Hansen, Thomas van Overeem, Nielsen, Finn Cilius & EMBRACE, E., 1 Oct 2010, In: Nature Genetics. 42, 10, p. 885-92 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

    Antoniou, A. C., Kartsonaki, C., Sinilnikova, O. M., Soucy, P., McGuffog, L., Healey, S., Lee, A. R., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Cattaneo, E., Barile, M., Pensotti, V., Pasini, B., Dolcetti, R., Giannini, G., Putignano, A. L., Varesco, L., Radice, P. & 31 others, Mai, P. L., Greene, M. H., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Gerdes, Anne-Marie Axø, Kruse, T. A., Birk Jensen, U., Crüger, D. G., Caligo, M. A., Laitman, Y., Milgrom, R., Kaufman, B., Paluch-Shimon, S., Friedman, E., Loman, N., Harbst, K., Lindblom, A., Arver, B., Ehrencrona, H., Melin, B., Nathanson, K. L., Domchek, S. M., Rebbeck, T., Jakubowska, A., Lubinski, J., Gronwald, J., Huzarski, T., Byrski, T. & SWE-BRCA, S., 2011, In: Human Molecular Genetics. 20, 16, p. 3304-21 18 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    A BAP1 Mutation in a Danish Family Predisposes to Uveal Melanoma and Other Cancers

    Aoude, L. G., Wadt, K., Bojesen, A., Cr�ger, D. G., Borg, A., Trent, J. M., Brown, K. M., Gerdes, Anne-Marie Axø, Jönsson, G. & Hayward, N. K., Aug 2013, In: P L o S One. 8, 8, p. 1-5 5 p., e72144.

    Research output: Contribution to journal › Journal article › Research › peer-review

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ID: 19459833