Familial Breast Cancer
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- 2012
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Mark
The retinoblastoma gene undergoes rearrangements in BRCA1-deficient basal-like breast cancer.
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- Contribution to journal › Article
- 2011
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Mark
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2010
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Mark
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
(
- Contribution to journal › Article
- 2008
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Mark
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
(
- Contribution to journal › Article
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Mark
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
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- Contribution to journal › Article
- 2007
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Mark
Tumor genome wide DNA alterations assessed by array CGH in patients with poor and excellent survival following operation for colorectal cancer
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- Contribution to journal › Article
- 2004
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
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- Contribution to journal › Article
- 2001
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Mark
Gene-expression profiles in hereditary breast cancer
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- Contribution to journal › Article
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Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
- 2000
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Mark
A hypersensitive estrogen receptor-alpha mutation in premalignant breast lesions
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- Contribution to journal › Article