Anne-Marie Axø Gerdes

Anne-Marie Axø Gerdes

Clinical Professor

Member of:

  • Clinical Genetics


Publication year:
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21 - 30 out of 144Page size: 10
  1. 2021
  2. 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.e17

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

  3. Published

    Genetisk screening af kommende forældre

    Smed, V. M., Petersen, Olav Bennike Bjørn, Gerdes, Anne-Marie Axø, Diness, Birgitte Rode & Roos, L. S., 29 Mar 2021, In: Ugeskrift for Laeger. 183, 13, 9 p., V12200933.

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

  4. 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

  5. Published

    Whole genome sequencing identifies rare germline variants enriched in cancer related genes in firstdegree relatives of familial pancreatic cancer patients

    Tan, M., Brusgaard, K., Gerdes, Anne-Marie Axø, Mortensen, M. B., Detlefsen, S., Schaffalitzky de Muckadell, O. B. & Joergensen, M. T., 2021, In: Clinical Genetics. 100, 5, p. 551-562 12 p.

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

  6. 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

  7. Published

    Genetisk screening af adopterede raske individer

    Wriedt, T. R., Gerdes, Anne-Marie Axø, Roos, L. K., Hammer-Hansen, S., Christensen, M. B. & Diness, Birgitte Rode, 29 Mar 2021, In: Ugeskrift for Laeger. 183, 13, 7 p., V11200810.

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

  8. 2020
  9. Published

    Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

    Barnes, D. R., Rookus, M. A., Mcguffog, L., Leslie, G., Mooij, T. M., Dennis, J., Mavaddat, N., Adlard, J., Ahmed, M., Aittomäki, K., Andrieu, N., Andrulis, I. L., Arnold, N., Arun, B. K., Azzollini, J., Balmaña, J., Barkardottir, R. B., Barrowdale, D., Benitez, J., Berthet, P. & 31 others, Białkowska, K., Blanco, A. M., Blok, M. J., Bonanni, B., Boonen, S. E., Borg, Å., Bozsik, A., Bradbury, A. R., Brennan, P., Brewer, C., Brunet, J., Buys, S. S., Caldés, T., Caligo, M. A., Campbell, I., Christensen, L. L., Chung, W. K., Claes, K. B. M., Colas, C., Collonge-rame, M., Cook, J., Daly, M. B., Davidson, R., De La Hoya, M., De Putter, R., Delnatte, C., Devilee, P., Ejlertsen, Bent Laursen, Gerdes, Anne-Marie Axø, Nielsen, Finn Cilius & Consortium of Investigators of Modifiers of BRCA and BRCA2, C. O. I. O. M. O. B. A. B., 1 Oct 2020, In: Genetics in Medicine. 22, 10, p. 1653-1666 14 p.

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

  10. Published

    Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial

    Burn, J., Sheth, H., Elliott, F., Reed, L., Macrae, F., Mecklin, J. P., Möslein, G., McRonald, F. E., Bertario, L., Evans, D. G., Gerdes, A. M., Ho, J. W. C., Lindblom, A., Morrison, P. J., Rashbass, J., Ramesar, R., Seppälä, T., Thomas, H. J. W., Pylvänäinen, K., Borthwick, G. M. & 15 others, Mathers, J. C., Bishop, D. T., Boussioutas, A., Brewer, C., Cook, J., Eccles, D., Ellis, A., Hodgson, S. V., Lubinski, J., Maher, E. R., Porteous, M. E., Sampson, J., Scott, R. J., Side, L. & CAPP2 Investigators, C. I., 2020, In: The Lancet. 395, 10240, p. 1855-1863 9 p.

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

  11. Published

    Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high frequency of cancer prone syndromes

    Byrjalsen, A., Hansen, T. V. O., Stoltze, U. K., Mehrjouy, M. M., Barnkob, N. M., Hjalgrim, L. L., Mathiasen, R., Lautrup, C. K., Gregersen, P. A., Hasle, H., Wehner, P. S., Tuckuviene, R., Sackett, P. W., Laspiur, A. O., Rossing, M., Marvig, R. L., Tommerup, N., Olsen, T. E., Scheie, D., Gupta, R. & 3 others, Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2020, In: PLOS Genetics. 16, 12, e1009231.

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

  12. Published

    A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

    Djursby, M., Wadt, Karin Anna Wallentin, Frederiksen, J. H., Madsen, M. B., Berchtold, L. A., Hasselby, Jane Preuss, Willemoe, G. L., Hansen, T. V. O. & Gerdes, Anne-Marie Axø, 2020, In: Hereditary Cancer in Clinical Practice. 18, 1, 8.

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

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ID: 19459833