390 results on '"Ausems, Margreet G. E. M."'
Search Results
2. Optimizing the detection of hereditary predisposition in women with epithelial ovarian cancer: nationwide implementation of the Tumor-First workflow
3. Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
4. Healthcare professionals’ perspectives on implementation of universal tumor DNA testing in ovarian cancer patients: multidisciplinary focus groups
5. Survival of BRCA1/BRCA2-associated pT1 breast cancer patients, a cohort study
6. Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
7. ASO Visual Abstract: Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling
8. ASO Author Reflections: The Role of Surgeons and Nurse Specialists in the Mainstreaming of Genetic Testing for Breast Cancer Patients
9. Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing
10. Patient-centered research: how do women tolerate nipple fluid aspiration as a potential screening tool for breast cancer?
11. Mainstream germline genetic testing in men with metastatic prostate cancer: design and protocol for a multicenter observational study
12. Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers.
13. A randomized experimental study to test the effects of discussing uncertainty during cancer genetic counseling: different strategies, different outcomes?
14. Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making
15. Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals
16. Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites.
17. Systematic development of a training program for healthcare professionals to improve communication about breast cancer genetic counseling with low health literate patients
18. Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences
19. Increased prevalence of Barrett’s esophagus in patients with MUTYH-associated polyposis (MAP)
20. Genetisch onderzoek bij prostaatkanker: nieuwe ontwikkelingen
21. ‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
22. Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers
23. MRI versus mammography for breast cancer screening in women with familial risk (FaMRIsc): a multicentre, randomised, controlled trial
24. Urinary incontinence more than 15 years after premenopausal risk‐reducing salpingo‐oophorectomy: a multicentre cross‐sectional study
25. Long-Term Morbidity and Health After Early Menopause Due to Oophorectomy in Women at Increased Risk of Ovarian Cancer: Protocol for a Nationwide Cross-Sectional Study With Prospective Follow-Up (HARMOny Study)
26. The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study
27. Contralateral breast cancer risk in patients with breast cancer and a germline-BRCA1/2 pathogenic variant undergoing radiation.
28. Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing
29. Long‐term effects of premenopausal risk‐reducing salpingo‐oophorectomy on cognition in women with high familial risk of ovarian cancer: A cross‐sectional study
30. Additional file 3 of Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
31. Additional file 1 of Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
32. Additional file 5 of Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
33. Additional file 2 of Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
34. Additional file 4 of Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
35. The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
36. Voorwoord bij het themanummer genetische aspecten bij prostaatkanker
37. Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases
38. Rapid genetic counseling and testing in newly diagnosed breast cancer: Patients’ and health professionals’ attitudes, experiences, and evaluation of effects on treatment decision making
39. Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases.
40. Communication Between Breast Cancer Patients Who Received Inconclusive Genetic Test Results and Their Daughters and Sisters Years After Testing
41. Counselees’ Expressed Level of Understanding of the Risk Estimate and Surveillance Recommendation are Not Associated with Breast Cancer Surveillance Adherence
42. The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy
43. Healthcare professionals’ perspectives on implementation of universal tumor DNA testing in ovarian cancer patients: multidisciplinary focus groups
44. Additional file 1 of Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing
45. Additional file 4 of Patient-centered research: how do women tolerate nipple fluid aspiration as a potential screening tool for breast cancer?
46. Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic Cancer
47. The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review
48. Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
49. Does and should breast cancer genetic counselling include lifestyle advice?
50. Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers
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