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- 2014
- Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
- 2011
- Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
- Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
- 2004
- One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
- 2001
- Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
- 1998
- BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease
- Analysis of Swedish male breast cancer family data : a simple way to incorporate a common sibling effect
- 1997
- Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer