Search Results - "Ausems, M G E M"
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Breast cancer risk after salpingo-oophorectomy in healthy BRCA1/2 mutation carriers: revisiting the evidence for risk reduction
Published in JNCI : Journal of the National Cancer Institute (01-05-2015)“…Previous studies have reported a breast cancer (BC) risk reduction of approximately 50% after risk-reducing salpingo-oophorectomy (RRSO) in BRCA1/2 mutation…”
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TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
Published in Journal of medical genetics (01-06-2010)“…BACKGROUND Li-Fraumeni syndrome (LFS) is a rare autosomal dominant cancer predisposition syndrome. Most families fulfilling the classical diagnostic criteria…”
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Development of a plain-language guide for discussing breast cancer genetic counseling and testing with patients with limited health literacy
Published in Supportive care in cancer (01-06-2021)“…Purpose Due to limited health literacy and resulting ineffective communication between healthcare professionals and patients, not all eligible patients are…”
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BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD
Published in Journal of assisted reproduction and genetics (01-11-2017)“…Purpose The aim of this study was to determine whether BRCA1/2 mutation carriers produce fewer mature oocytes after ovarian stimulation for in vitro…”
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Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)
Published in BMJ (Online) (06-09-2012)“…Objective To estimate the risk of breast cancer associated with diagnostic radiation in carriers of BRCA1/2 mutations.Design Retrospective cohort study…”
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Repeated nipple fluid aspiration: compliance and feasibility results from a prospective multicenter study
Published in PloS one (22-05-2015)“…Despite intensive surveillance, a high rate of interval malignancies is still seen in women at increased breast cancer risk. Therefore, novel screening…”
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Referral to cancer genetic counseling: do migrant status and patients’ educational background matter?
Published in Journal of community genetics (01-10-2017)“…Participation rates in cancer genetic counseling differ among populations, as patients with a lower educational background and migrant patients seem to have…”
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Mainstream germline genetic testing in men with metastatic prostate cancer: design and protocol for a multicenter observational study
Published in BMC cancer (30-12-2022)“…In international guidelines, germline genetic testing is recommended for patients with metastatic prostate cancer. Before undergoing germline genetic testing,…”
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Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites
Published in Genes (01-04-2024)“…: Previous studies have suggested that information offered by sellers of health-related direct-to-consumer genetic tests (DTC-GTs) is often incomplete,…”
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Patient-centered research: how do women tolerate nipple fluid aspiration as a potential screening tool for breast cancer?
Published in BMC cancer (27-06-2022)“…Abstract Background Nipple fluid aspiration (NFA) is a technique to acquire nipple aspirate fluid (NAF), which is considered a rich source of breast-specific…”
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Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling
Published in Annals of surgical oncology (01-06-2023)“…Background Pre-test genetic counseling for patients with breast cancer is increasingly being provided by nongenetic healthcare professionals. We evaluated the…”
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Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing
Published in Hereditary cancer in clinical practice (08-09-2022)“…Abstract Background There is a growing need for genetic testing of women with epithelial ovarian cancer. Mainstream genetic testing provides an alternative…”
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Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers
Published in Breast cancer research and treatment (01-10-2019)“…Background In healthy BRCA1/2 mutation carriers, bilateral risk-reducing mastectomy (BRRM) strongly reduces the risk of developing breast cancer (BC); however,…”
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HIF-1α overexpression in ductal carcinoma in situ of the breast in BRCA1 and BRCA2 mutation carriers
Published in PloS one (08-02-2013)“…Recent studies have revealed that BRCA1 and BRCA2 germline mutation-related breast cancers show frequent overexpression of hypoxia inducible factor-1α…”
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Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences
Published in Hereditary cancer in clinical practice (19-01-2021)“…CHEK2 has been recognized as a breast cancer risk gene with moderate effect. Women who have previously tested negative for a BRCA1/2 gene germline pathogenic…”
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Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer
Published in Clinical cancer research (01-02-2004)“…Purpose: Immunohistochemistry (IHC) and microsatellite instability (MSI) analysis can be used to identify patients with a possible DNA mismatch repair defect…”
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ASO Author Reflections: The Role of Surgeons and Nurse Specialists in the Mainstreaming of Genetic Testing for Breast Cancer Patients
Published in Annals of surgical oncology (01-06-2023)Get full text
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Body weight and risk of breast cancer in BRCA1/2 mutation carriers
Published in Breast cancer research and treatment (01-02-2011)“…Obesity is an established risk factor for postmenopausal breast cancer in the general population. However, it is still unclear whether this association also…”
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Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers
Published in Breast cancer research and treatment (01-02-2010)“…BRCA1/2 mutation carriers have a high lifetime risk of developing breast cancer. Differences in penetrance indicate that this risk may be influenced by…”
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Communication in cancer genetic counselling: does it reflect counselees' previsit needs and preferences?
Published in British journal of cancer (09-05-2005)“…This study sought to describe counsellor-counselee interaction during initial cancer genetic counselling consultations and to examine whether the communication…”
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