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2008
Mark The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
Antoniou, A. C. ; Cunningham, A. P. ; Peto, J. ; Evans, D. G. ; Lalloo, F. ; Narod, S. A. ; Risch, H. A. ; Eyfjord, J. E. ; Hopper, J. L. and Southey, M. C. , et al. (2008) In British Journal of Cancer 98(8). p.1457-1466
- Contribution to journal › Article
2006
Mark Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
Karppinen, S. -M. ; Barkardottir, R. B. ; Harbst, Katja ^LU ; Sydenham, T. ; Syrjakoski, K. ; Schleutker, J. ; Ikonen, T. ; Pylkas, K. ; Rapakko, K. and Erkko, H. , et al. (2006) In Journal of Medical Genetics 43(11). p.856-862
- Contribution to journal › Article
2005
Mark Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
Antoniou, A C ; Pharoah, P D P ; Narod, S ; Risch, H A ; Eyfjord, J E ; Hopper, J L ; Olsson, Håkan ^LU ; Johannsson, O ; Borg, Åke ^LU and Pasini, B , et al. (2005) In Journal of Medical Genetics 42(7). p.602-603
- Contribution to journal › Article
2004
Mark BRCA2 mutations in 154 Finnish male breast cancer patients
Syrjakoski, K ; Kuukasjarvi, T ; Waltering, K ; Haraldsson, Karin ^LU ; Auvinen, A ; Borg, Åke ^LU ; Kainu, T ; Kallioniemi, OP and Koivisto, PA (2004) In Neoplasia 6(5). p.541-545
- Contribution to journal › Article
2003
Mark Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
Antoniou, A ; Pharoah, PDP ; Narod, S ; Risch, HA ; Eyfjord, JE ; Hopper, JL ; Loman, Niklas ^LU ; Olsson, H ^LU ; Johannsson, O and Borg, Åke ^LU , et al. (2003) In American Journal of Human Genetics 72(5). p.1117-1130
- Contribution to journal › Article
2002
Mark A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
Rozenblum, E ; Vahteristo, P ; Törngren, Therese ^LU ; Bergthorsson, JT ; Syrjakoski, K ; Weaver, D ; Haraldsson, Karin ^LU ; Johannsdottir, HK ; Vehmanen, P and Nigam, S , et al. (2002) In Human Genetics 110(2). p.111-121
- Contribution to journal › Article
2000
Mark Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Kainu, T ; Juo, S H ; Desper, R ; Schaffer, A A ; Gillanders, E ; Rozenblum, E ; Freas-Lutz, D ; Weaver, D ; Stephan, D and Bailey-Wilson, J , et al. (2000) In Proceedings of the National Academy of Sciences 97(17). p.9603-9608
- Contribution to journal › Article