Annika Bergman


The Jönköping Academy for Improvement of Health and Welfare , Hälsohögskolan


+46 36-10 1237
+46 73-910 18 89
Ändra din information


Engel, C. Versmold, B. Wappenschmidt, B. Simard, J. Easton, D. Peock, S. , ... Schmutzler R. (2010). Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers Cancer Epidemiology, Biomarkers and Prevention, 19(11), 2859-2868. More information
Antoniou, A. Beesley, J. McGuffog, L. Sinilnikova, O. Healey, S. Neuhausen, S. , ... Easton D. (2010). Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction Cancer Research, 70(23), 9742-9754. More information
Thorell, K., Bergman, A., Carén, H., Nilsson, S., Kogner, P., Martinsson, T., Abel, F. (2009). Verification of genes differentially expressed in neuroblastoma tumours: A study of potential tumour suppressor genes BMC Medical Genomics, 2. More information
Bergman, A. Sahlin, P. Emanuelsson, M. Carén, H. Tarnow, P. Martinsson, T. , ... Stenman G. (2009). Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery, 43(5), 251-255. More information
Osorio, A. Milne, R. Pita, G. Peterlongo, P. Heikkinen, T. Simard, J. , ... Benítez J. (2009). Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 (CIMBA) British Journal of Cancer, 101(12), 2048-2054. More information
Johnatty, S. Couch, F. Fredericksen, Z. Tarrell, R. Spurdle, A. Beesley, J. , ... Chenevix-Trench G. (2009). No evidence that GATA3 rs570613 SNP modifies breast cancer risk Breast Cancer Research and Treatment, 117(2), 371-379. More information
Antoniou, A. Sinilnikova, O. McGuffog, L. Healey, S. Nevanlinna, H. Heikkinen, T. , ... Chenevix-Trench G. (2009). Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers Human Molecular Genetics, 18(22), 4442-4456. More information
Bergman, A. Abel, F. Behboudi, A. Yhr, M. Mattsson, J. Svensson, J. , ... Nordling M. (2008). No germline mutations in supposed tumour suppressor genes SAFB1 and SAFB2 in familial breast cancer with linkage to 19p. BMC Medical Genetics, 9. More information
Kanter-Smoler, G. Fritzell, K. Rohlin, A. Engwall, Y. Hallberg, B. Bergman, A. , ... Nordling M. (2008). Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families BMC Medicine, 6. More information
Bergman, A. Karlsson, P. Berggren, J. Martinsson, T. Björck, K. Nilsson, S. , ... Nordling M. (2007). Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3 Genes, Chromosomes and Cancer, 46(3), 302-309. More information
Chenevix-Trench, G., Milne, R., Antoniou, A., Couch, F., Easton, D., Goldgar, D. (2007). An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: The Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA) Breast Cancer Research, 9(2). More information
Bergman, A. Flodin, A. Engwall, Y. Arkblad, E. Berg, K. Einbeigi, Z. , ... Nordling M. (2005). A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques Familial Cancer, 4(2), 89-96. More information
Vujic, M., Bergman, A., Romanus, B., Wahlström, J., Martinsson, T. (2004). Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes. International Journal of Molecular Medicine, 13(1), 47-52. More information
Björk, J. Åkerbrant, H. Iselius, L. Bergman, A. Engwall, Y. Wahlström, J. , ... Hultcrantz R. (2001). Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene Mutations Gastroenterology, 121(5), 1127-1135. More information
Bergman, A. Einbeigi, Z. Olofsson, U. Taib, Z. Wallgren, A. Karlsson, P. , ... Nordling M. (2001). The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation European Journal of Human Genetics, 9(10), 787-793. More information
Einbeigi, Z. Bergman, A. Kindblom, L. Martinsson, T. Meis-Kindblom, J. Nordling, M. , ... Karlsson P. (2001). A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer European Journal of Cancer, 37(15), 1904-1909. More information


Bergman, A. (2006). On the genetics of hereditary breast/ovarian cancer: BRCA1, BRCA2 and beyond (Doctoral thesis, Göteborg: Department of Medical and Clinical Genetics, Institute of Biomedicine, Sahlgrenska Academy at Göteborg University). More information