Anne-Marie Axø Gerdes
Clinical Professor
- 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
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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