Pages that link to "Q24203650"
Jump to navigation
Jump to search
The following pages link to Cancer genetic risk assessment for individuals at risk of familial breast cancer (Q24203650):
Displaying 41 items.
- Interventions to improve patient access to and utilisation of genetic and genomic counselling services (Q24188203) (← links)
- Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review (Q26744522) (← links)
- Breast Cancer Genetic Counseling: A Surgeon's Perspective (Q26767380) (← links)
- Concerns about unintended negative consequences of informing the public about multifactorial risks may be premature for young adult smokers (Q28395074) (← links)
- What hinders minority ethnic access to cancer genetics services and what may help? (Q33765202) (← links)
- Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group (Q34175545) (← links)
- Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results (Q34351357) (← links)
- A new approach to assessing affect and the emotional implications of personal genomic testing for common disease risk (Q35143295) (← links)
- Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome (Q35348336) (← links)
- General Practitioners and Breast Surgeons in France, Germany, Netherlands and the UK show variable breast cancer risk communication profiles (Q35372433) (← links)
- Impact of Genetic Counseling in Women with a Family History of Breast Cancer in Italy (Q35768618) (← links)
- Psychosocial and Quality of Life in Women Receiving the 21-Gene Recurrence Score Assay: The Impact of Decision Style in Women with Intermediate RS. (Q36147839) (← links)
- Prevalence and detection of psychosocial problems in cancer genetic counseling (Q36240954) (← links)
- Breast Cancer Risk Perceptions among Relatives of Women with Uninformative Negative BRCA1/2 Test Results: The Moderating Effect of the Amount of Shared Information (Q36704494) (← links)
- High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling (Q36906183) (← links)
- Critical research gaps and translational priorities for the successful prevention and treatment of breast cancer (Q37533025) (← links)
- Homologous recombination deficiency (HRD) testing in ovarian cancer clinical practice: a review of the literature. (Q37661436) (← links)
- Patient reported outcomes and patient empowerment in clinical genetics services (Q38259348) (← links)
- Epidemiology of Patients with Ovarian Cancer with and Without a BRCA1/2 Mutation (Q38609944) (← links)
- Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research (Q38730837) (← links)
- Psychological Distress, Anxiety, and Depression of Cancer-Affected BRCA1/2 Mutation Carriers: a Systematic Review (Q38807460) (← links)
- More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling (Q40139758) (← links)
- Evaluation of a pharmacogenetic educational toolkit for community pharmacists (Q40975508) (← links)
- Does rapid genetic counseling and testing in newly diagnosed breast cancer patients cause additional psychosocial distress? results from a randomized clinical trial (Q41024301) (← links)
- Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling (Q41107740) (← links)
- Addressing barriers to uptake of breast cancer chemoprevention for patients and providers (Q41726822) (← links)
- When knowledge of a heritable gene mutation comes out of the blue: treatment-focused genetic testing in women newly diagnosed with breast cancer. (Q42746319) (← links)
- A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer. (Q44259965) (← links)
- Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance (Q44968281) (← links)
- Effect of direct-to-consumer genetic tests on health behaviour and anxiety: a survey of consumers and potential consumers (Q45732623) (← links)
- Women's Perceptions of Journeying Toward an Unknown Future With Breast Cancer: The "Lives at Risk Study". (Q47934410) (← links)
- Germline genetic variants with implications for disease risk and therapeutic outcomes (Q48100807) (← links)
- Genetic assessment wait time indicators in the High Risk Ontario Breast Screening Program (Q48169351) (← links)
- Communication of cancer-related genetic and genomic information: A landscape analysis of reviews (Q49551487) (← links)
- Views of Low-Income Women of Color at Increased Risk for Breast Cancer. (Q53692864) (← links)
- Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain). (Q54300317) (← links)
- Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history (Q61625933) (← links)
- A regional population-based hereditary breast cancer screening tool in Italy: First 5-year results (Q89654302) (← links)
- Association between distress and knowledge among parents of autistic children (Q90306496) (← links)
- Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review (Q91811507) (← links)
- Interventions to improve patient access to and utilisation of genetic and genomic counselling services (Q94347781) (← links)