Anne-Marie Axø Gerdes
Clinical Professor
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TINF2 is a major susceptibility gene in Danish patients with multiple primary melanoma
Jensen, M. R., Jelsig, A. M., Gerdes, Anne-Marie Axø, Hølmich, Lisbet Rosenkrantz, mzt627, mzt627, Lorentzen, H. F., Hansen, M. H., Bak, M., Johansson, P. A., Hayward, N. K., Hansen, Thomas van Overeem & Wadt, Karin Anna Wallentin, 2023, In: Human Genetics and Genomics Advances. 4, 4, 12 p., 100225.Research output: Contribution to journal › Journal article › Research › peer-review
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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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A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing
Thomassen, M., Pedersen, I. S., Vogel, I., Hansen, T. V. O., Brasch-Andersen, C., Brasen, C. L., Crüger, D., Sunde, L. E. M., Nielsen, Finn Cilius, Jensen, U. B., Bisgaard, M. L., Borg, A., Gerdes, Anne-Marie Axø & Kruse, T. A., 1 Jul 2011, In: Breast Cancer Research and Treatment. 128, 1, p. 179-85 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma.
Wadt, K., Choi, J., Chung, J. Y., Kiilgaard, Jens Folke, Heegaard, Steffen, Drzewiecki, K. T. M., Trent, J. M., Hewitt, S. M., Hayward, N. K., Gerdes, Anne-Marie Axø & Brown, K. M., Nov 2012, In: Pigment Cell & Melanoma Research. 25, 6, p. 815-818 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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, , 1 Oct 2010, In: Nature Genetics. 42, 10, p. 885-92 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers
Ding, Y. C., McGuffog, L., Healey, S., Friedman, E., Laitman, Y., Paluch-Shimon, S., Kaufman, B., Liljegren, A., Lindblom, A., Olsson, H., Kristoffersson, U., Stenmark-Askmalm, M., Melin, B., Domchek, S. M., Nathanson, K. L., Rebbeck, T. R., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K. & 31 others, , 2012, In: Cancer Epidemiology, Biomarkers & Prevention. 21, 8, p. 1362-70 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one
Kantelinen, J., Hansen, T. V. O., Kansikas, M., Krogh, L. N., Korhonen, M. K., Ollila, S., Nyström, M., Gerdes, Anne-Marie Axø & Kariola, R., 2011, In: Familial Cancer. 10, 3, p. 515-20 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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255
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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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