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Open AccessLow-risk susceptibility alleles in 40 human breast cancer cell lines
Low-risk breast cancer susceptibility alleles or SNPs confer only modest breast cancer risks ranging from just over 1.0 to1.3 fold. Yet, they are common among most populations and therefore are involved in the...
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Article
Open AccessStandard psychological consultations and follow up for women at increased risk of hereditary breast cancer considering prophylactic mastectomy
Women at increased (genetic) risk of breast cancer have to weigh the personal pros and cons of prophylactic mastectomy (PM) as an option to reduce their cancer risk. So far, no routine referral to a psychologi...
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Article
Open AccessA family history of breast cancer will not predict female early onset breast cancer in a population-based setting
An increased risk of breast cancer for relatives of breast cancer patients has been demonstrated in many studies, and having a relative diagnosed with breast cancer at an early age is an indication for breast ...
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Open AccessClinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases
Seven SNPs in five genomic loci were recently found to confer a mildly increased risk of breast cancer.
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Open AccessPathway analysis of gene signatures predicting metastasis of node-negative primary breast cancer
Published prognostic gene signatures in breast cancer have few genes in common. Here we provide a rationale for this observation by studying the prognostic power and the underlying biological pathways of diffe...
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Article
Open AccessGnRH and LHRgene variants predict adverse outcome in premenopausal breast cancer patients
Breast cancer development and progression are dependent on estrogen activity. In premenopausal women, estrogen production is mainly regulated through the hypothalamic-pituitary-gonadal (HPG) axis.
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Open AccessIdentification of women with an increased risk of develo** radiation-induced breast cancer: a case only study
Radiation exposure at a young age is one of the strongest risk factors for breast cancer. Germline mutations in genes involved in the DNA-damage repair pathway (DDRP) may render women more susceptible to radia...
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The impact of having relatives affected with breast cancer on psychological distress in women at increased risk for hereditary breast cancer
Purpose.Being at hereditary risk of breast cancer (BC) may lead to elevated levels of distress because of the impact of the BC-process in relatives.
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Open AccessComment on Screening by MRI Mentioned in the Reviews by Narod and Møller
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One Year Follow-Up of Women Opting for Presymptomatic Testing for BRCA1 and BRCA2: Emotional Impact of the Test Outcome and Decisions on Risk Management (Surveillance or Prophylactic Surgery)
Genetic testing enables women at risk for hereditary breast and/or ovarian cancer to find out whether they have inherited the gene mutation (BRCA1/BRCA2), and if so, to opt for frequent surveillance and/or pro...