Anne-Marie Axø Gerdes
Clinical Professor
- 2013
- Published
Von Hippel-Lindau disease (vHL)
Binderup, M. L. M., Bisgaard, S. M. L., Harbud, V., Møller, H. U., Gimsing, S., Friis-Hansen, Lennart Jan, Hansen, Thomas van Overeem, Bagi, P., Knigge, Ulrich, Kosteljanetz, M., Bøgeskov, L., Thomsen, C., Gerdes, Anne-Marie Axø, Ousager, L. B. & Sunde, L., Dec 2013, In: Danish Medical Journal. 60, 12, p. B4763Research output: Contribution to journal › Journal article › Research › peer-review
- 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
- Published
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Bojesen, S. E., Pooley, K. A., Johnatty, S. E., Beesley, J., Michailidou, K., Tyrer, J. P., Edwards, S. L., Pickett, H. A., Shen, H. C., Smart, C. E., Hillman, K. M., Mai, P. L., Lawrenson, K., Stutz, M. D., Lu, Y., Karevan, R., Woods, N., Johnston, R. L., French, J. D., Chen, X. & 31 others, , Apr 2013, In: Nature Genetics. 45, 4, p. 371-84, 384e1-2Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genomsekventering – klinisk anvendelse
Hertz, J. M., Gerdes, Anne-Marie Axø, Grønskov, K., Thomassen, M. & Vogel, I., 18 Mar 2013, In: Ugeskrift for Laeger. 175, 12, p. 818 1 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Couch, F. J., Gerdes, Anne-Marie Axø, Nielsen, Finn Cilius & al., E., Mar 2013, In: P L o S Genetics. 9, 3, p. 1-21 21 p., e1003212.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Classifications within molecular subtypes enables identification of BRCA1/BRCA2 mutation carriers by RNA tumor profiling
Larsen, M. J., Kruse, T. A., Tan, Q., Lænkholm, Anne-Vibeke, Bak, M., Lykkesfeldt, A. E., Sørensen, K. P., Hansen, Thomas van Overeem, Ejlertsen, Bent Laursen, Gerdes, Anne-Marie Axø & Thomassen, M., 2013, In: P L o S One. 8, 5, 12 p., e64268.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients
Petersen, S. M., Dandanell, M., Rasmussen, Lene Juel, Gerdes, Anne-Marie Axø, Krogh, L. N., Bernstein, I., Okkels, H., Wikman, F., Nielsen, Finn Cilius & Hansen, Thomas van Overeem, 2013, In: BMC Medical Genetics. 14, p. 103Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Phillips, K-A., Milne, R. L., Rookus, M. A., Daly, M. B., Antoniou, A. C., Peock, S., Frost, D., Easton, D. F., Ellis, S., Friedlander, M. L., Buys, S. S., Andrieu, N., Noguès, C., Stoppa-Lyonnet, D., Bonadona, V., Pujol, P., McLachlan, S. A., John, E. M., Hooning, M. J., Seynaeve, C. & 16 others, , 2013, In: Journal of Clinical Oncology. 31, 25, p. 3091-3099 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- Published
Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
Mathers, J. C., Movahedi, M., Macrae, F., Mecklin, J-P., Moeslein, G., Olschwang, S., Eccles, D., Evans, G., Maher, E. R., Bertario, L., Bisgaard, S. M. L., Dunlop, M., Ho, J. W., Hodgson, S., Lindblom, A., Lubinski, J., Morrison, P. J., Murday, V., Ramesar, R., Side, L. & 14 others, , Dec 2012, In: The Lancet Oncology. 13, 12, p. 1242-1249 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
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
- Published
Multiple self-healing squamous epithelioma er en arvelig tilstand med selvhelende hudkræft
Broesby-Olsen, S., Frandsen, S. K., Thomassen, M., Brandrup, F. & Gerdes, Anne-Marie Axø, 23 Apr 2012, In: Ugeskrift for Laeger. 174, 17, p. 1149-51 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
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
- Published
Awareness of endometrial cancer risk and compliance with screening in hereditary nonpolyposis colorectal cancer
Ketabi, Z., Mosgaard, B. J., Gerdes, Anne-Marie Axø, Ladelund, S. & Bernstein, I. T., 2012, In: Obstetrics and Gynecology. 120, 5, p. 1005-12 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cancergenetik - arvelig disposition for cancer
Gerdes, Anne-Marie Axø, 2012, Medicinsk genetik. Nørby, S. & Jensen, P. K. A. (eds.). 2 ed. København, p. 231-254Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research
- Published
Clinical genetics in Denmark
Gerdes, Anne-Marie Axø, 2012, In: BSHG News. 46, p. 61-62Research output: Contribution to journal › Journal article › Research
- 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, , 2012, In: Breast Cancer Research (Online Edition). 14, 1, p. R33Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Couch, F. J., Gaudet, M. M., Antoniou, A. C., Ramus, S. J., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., Wang, X., Kirchhoff, T., McGuffog, L., Barrowdale, D., Lee, A. R., Healey, S., Sinilnikova, O. M., Andrulis, I. L., Ozcelik, H., Mulligan, A. M., Thomassen, M., Gerdes, A-M. & 31 others, , 2012, In: Cancer Epidemiology, Biomarkers & Prevention. 21, 4, p. 645-57 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetiske fund giver nye muligheder for udredning af arveligt malignt melanom
Wadt, K. A. W., Drzewiecki, K. T. & Gerdes, Anne-Marie Axø, 2012, In: Ugeskrift for Laeger. 174, 8, p. 493-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Is the SPINK1 variant p.N34S overrepresented in patients with acute pancreatitis?
Jøergensen, M. T., Brusgaard, K., Novovic, S., Andersen, A. M., Hansen, M. B., Gerdes, Anne-Marie Axø & de Muckadell, O. B. S., 2012, In: European Journal of Gastroenterology and Hepatology. 24, 3, p. 309-15 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Klinisk genetik
Skovby, F., Gerdes, Anne-Marie Axø & Hertz, J. M., 2012, Basisbog i diagnostiske fag. Thomsen, H. S. (ed.). 1 ed. København, p. 167-196Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research
- Published
Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma
Wadt, K., Gerdes, Anne-Marie Axø, Hansen, T. V. O., Toft, B. G., Friis-Hansen, L. & Andersen, M. K., 2012, In: Familial Cancer. 11, 3, p. 535-7 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ny genteknologisk diagnostik af familiær gastrointestinal stromal tumor
Wadt, K., Andersen, M. K., Hansen, T. V. O. & Gerdes, Anne-Marie Axø, 2012, In: Ugeskrift for Laeger. 174, 21, p. 1462-4 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
Ramus, S. J., Antoniou, A. C., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., McGuffog, L., Sinilnikova, O. M., Healey, S., Barrowdale, D., Lee, A. R., Thomassen, M., Gerdes, A-M., Kruse, T. A., Jensen, U. B., Skytte, A-B., Caligo, M. A., Liljegren, A., Lindblom, A., Olsson, H. & 31 others, , 2012, In: Human Mutation. 33, 4, p. 690-702 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Mavaddat, N., Barrowdale, D., Andrulis, I. L., Domchek, S. M., Eccles, D., Nevanlinna, H., Ramus, S. J., Spurdle, A., Robson, M., Sherman, M., Mulligan, A. M., Couch, F. J., Engel, C., McGuffog, L., Healey, S., Sinilnikova, O. M., Southey, M. C., Terry, M. B., Goldgar, D., O'Malley, F. & 31 others, , 2012, In: Cancer Epidemiology, Biomarkers & Prevention. 21, 1, p. 134-147 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2011
- Published
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
- Published
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
- Published
Arvelige cancersyndromer
Gerdes, Anne-Marie Axø, 2011, In: Ugeskrift for Laeger. 173, 34, p. 2035-8 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Biomedical informatics as support to individual healthcare in hereditary colon cancer: the Danish HNPCC system
Bernstein, I. T., Lindorff-Larsen, K., Timshel, S., Brandt, C., Dinesen, B., Fenger, M., Gerdes, Anne-Marie Axø, Iversen, L. H., Madsen, M. R., Okkels, H., Sunde, L. E. M., Rahr, H., Wikman, F. P. & Rossing, N. N., 2011, In: Human Mutation. 32, 5, p. 551-6 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Breast cancer after bilateral risk-reducing mastectomy
Skytte, A., Crüger, D. G., Gerster, M., Laenkholm, A., Lang, C., Brøndum-Nielsen, K., Andersen, M. K., Sunde, L. E. M., Kølvraa, S. & Gerdes, Anne-Marie Axø, 2011, In: Clinical Genetics. 79, 5, p. 431-7 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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, , 2011, In: Human Molecular Genetics. 20, 16, p. 3304-21 18 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
Mulligan, A. M., Couch, F. J., Barrowdale, D., Domchek, S. M., Eccles, D., Nevanlinna, H., Ramus, S. J., Robson, M., Sherman, M., Spurdle, A. B., Wappenschmidt, B., Lee, A. R., McGuffog, L., Healey, S., Sinilnikova, O. M., Janavicius, R., Hansen, T. V. O., Nielsen, F. C., Ejlertsen, B., Osorio, A. & 169 others, , 2011, In: Breast Cancer Research (Online Edition). 13, 6, p. R110Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Cox, D. G., Simard, J., Sinnett, D., Hamdi, Y., Soucy, P., Ouimet, M., Barjhoux, L., Verny-Pierre, C., McGuffog, L., Healey, S., Szabo, C., Greene, M. H., Mai, P. L., Andrulis, I. L., Thomassen, M., Gerdes, A-M., Caligo, M. A., Friedman, E., Laitman, Y., Kaufman, B. & 31 others, , 2011, In: Human Molecular Genetics. 20, 23, p. 4732-47 16 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Ramus, S. J., Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J., Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., Allavena, A. & 31 others, , 2011, In: National Cancer Institute. Journal (Print). 103, 2, p. 105-16 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation
Peixoto, A., Santos, C., Pinheiro, M., Pinto, P., Soares, M. J., Rocha, P., Gusmão, L., Amorim, A., van der Hout, A., Gerdes, A-M., Thomassen, M., Kruse, T. A., Cruger, D., Sunde, L. E. M., Bignon, Y-J., Uhrhammer, N., Cornil, L., Rouleau, E., Lidereau, R., Yannoukakos, D. & 47 others, , 2011, In: Breast Cancer Research and Treatment. 127, 3, p. 671-9 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Intragenic duplication: a novel mutational mechanism in hereditary pancreatitis
Joergensen, M. T., Geisz, A., Brusgaard, K., Schaffalitzky de Muckadell, O. B., Hegyi, P., Gerdes, Anne-Marie Axø & Sahin-Tóth, M., 2011, In: Pancreas. 40, 4, p. 540-6 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
Burn, J., Gerdes, A-M., Macrae, F., Mecklin, J-P., Moeslein, G., Olschwang, S., Eccles, D., Evans, D. G., Maher, E. R., Bertario, L., Bisgaard, S. M. L., Dunlop, M. G., Ho, J. W. C., Hodgson, S. V., Lindblom, A., Lubinski, J., Morrison, P. J., Murday, V., Ramesar, R., Side, L. & 14 others, , 2011, In: Lancet. 378, 9809, p. 2081-7 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1
Goudie, D. R., D'Alessandro, M., Merriman, B., Lee, H., Szeverényi, I., Avery, S., O'Connor, B. D., Nelson, S. F., Coats, S. E., Stewart, A., Christie, L., Pichert, G., Friedel, J., Hayes, I., Burrows, N., Whittaker, S., Gerdes, A-M. A., Broesby-Olsen, S., Ferguson-Smith, M. A., Verma, C. & 3 others, , 2011, In: Nature Genetics. 43, 4, p. 365-9 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations
Hansen, T. V. O., Jønson, L., Steffensen, A. Y., Andersen, M. K., Kjaergaard, S., Gerdes, Anne-Marie Axø, Ejlertsen, B. & Nielsen, Finn Cilius, 2011, In: Familial Cancer. 10, 2, p. 207-12 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2010
- 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, , 1 Oct 2010, In: Nature Genetics. 42, 10, p. 885-92 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations
Steffensen, A. Y., Jønson, L., Ejlertsen, B., Gerdes, Anne-Marie Axø, Nielsen, Finn Cilius & Hansen, Thomas van Overeem, 1 Sep 2010, In: Familial Cancer. 9, 3, p. 283-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Medullary thyroid cancer: RET testing of an archival material
Godballe, C., Jørgensen, G., Gerdes, Anne-Marie Axø, Krogdahl, A. S., Tybjærg-Hansen, Anne & Nielsen, Finn Cilius, 1 Apr 2010, In: European Archives of Oto-Rhino-Laryngology. 267, 4, p. 613-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Risk-reducing mastectomy and salpingo-oophorectomy in unaffected BRCA mutation carriers: uptake and timing
Skytte, A., Gerdes, Anne-Marie Axø, Andersen, M. K., Sunde, L., Brøndum-Nielsen, K., Waldstrøm, M., Kølvraa, S., Crüger, D., Skytte, A., Gerdes, Anne-Marie Axø, Andersen, M. K., Sunde, L., Brøndum-Nielsen, K., Waldstrøm, M., Kølvraa, S. & Crüger, D., 1 Apr 2010, In: Clinical Genetics. 77, 4, p. 342-9 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2009
- Published
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients
Christensen, L. L., Kariola, R., Korhonen, M. K., Wikman, F. P., Sunde, L., Gerdes, A-M., Okkels, H., Brandt, C. A., Bernstein, I., Hansen, T. V. O., Hagemann-Madsen, R., Andersen, C. L., Nyström, M., Ørntoft, T. F., Christensen, L., Kariola, R., Korhonen, M., Wikman, F., Sunde, L., Gerdes, A-M. & 8 others, , 2009, In: Familial Cancer. 8, 4, p. 489-500 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2000
- Published
Frequent disruption of the RB1 pathway in diffuse large B cell lymphoma: prognostic significance of E2F-1 and p16INK4A
Møller, M. B., Kania, Per, Ino, Y., Gerdes, Anne-Marie Axø, Nielsen, Olaf, Louis, D. N., Skjødt, K. & Pedersen, N. T., May 2000, In: Leukemia. 14, 5, p. 898-904 7 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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