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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
- 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
- Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
- 2004
-
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
Malander, S LU ; Ridderheim, M LU ; Måsbäck, A LU ; Loman, N LU ; Kristoffersson, U LU ; Olsson, Håkan LU
; Nilbert, M
LU
and Borg, Åke
LU
(2004)
In European Journal of Cancer
40(3).
p.422-428
Mark
- 2001
-
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
Vallon-Christersson, J LU
; Cayanan, C
; Haraldsson, K
LU
; Loman, N
LU
; Bergthorsson, J T
; Brøndum-Nielsen, K
; Gerdes, A M
; Møller, P
; Kristoffersson, U
LU
and Olsson, Håkan
LU
, et al.
(2001)
In Human Molecular Genetics
10(4).
p.60-353
Mark
- 1998
-
BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease
Haraldsson, K LU ; Loman, N LU ; Zhang, Qiu-Xia ; Johannsson, O LU ; Olsson, Håkan LU
and Borg, Åke
LU
(1998)
In Cancer Research
58(7).
p.71-1367
Mark
-
Analysis of Swedish male breast cancer family data : a simple way to incorporate a common sibling effect
Karunaratne, P M ; Elston, R C ; Loman, N LU ; Olsson, H LU
and Ranstam, J
LU
(1998)
In Genetic Epidemiology
15(2).
p.12-201
Mark
- 1997
- Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer