| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/CGE.12868 |
| P698 | PubMed publication ID | 27643459 |
| P50 | author | Mandy L Ballinger | Q52900795 |
| David M Thomas | Q64605553 | ||
| Amanda Willis | Q85264878 | ||
| P2093 | author name string | B Meiser | |
| S K Smith | |||
| M-A Young | |||
| P2860 | cites work | Comprehensive molecular portraits of human breast tumours | Q24630844 |
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| Consequences of universal MSI/IHC in screening ENDOMETRIAL cancer patients for Lynch syndrome | Q34017044 | ||
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| African American women's limited knowledge and experiences with genetic counseling for hereditary breast cancer | Q34630227 | ||
| What is the impact of genetic counselling in women at increased risk of developing hereditary breast cancer? A meta-analytic review | Q34682125 | ||
| Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS). | Q34980887 | ||
| Factors influencing cancer risk perception in high risk populations: a systematic review. | Q35056613 | ||
| Predictors of perceived breast cancer risk and the relation between perceived risk and breast cancer screening: a meta-analytic review | Q35690900 | ||
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| BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group | Q36145443 | ||
| Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors | Q36361079 | ||
| Timing and context: important considerations in the return of genetic results to research participants | Q36470928 | ||
| Uptake rates for breast cancer genetic testing: a systematic review | Q36479647 | ||
| Underutilization of BRCA1/2 testing to guide breast cancer treatment: black and Hispanic women particularly at risk | Q36706640 | ||
| Most patients with colorectal tumors at young age do not visit a cancer genetics clinic | Q36800267 | ||
| The withdrawal from oncogenetic counselling and testing for hereditary and familial breast and ovarian cancer. A descriptive study of an Italian sample | Q37040188 | ||
| Low rates of African American participation in genetic counseling and testing for BRCA1/2 mutations: racial disparities or just a difference? | Q37172955 | ||
| Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up | Q37234775 | ||
| Awareness of genetic counseling and perceptions of its purpose: a survey of the Canadian public | Q37302605 | ||
| A systematic review of the impact of genetic counseling on risk perception accuracy. | Q37416415 | ||
| Reflex testing for Lynch syndrome: if we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC). | Q37589534 | ||
| What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research | Q37727863 | ||
| 100 years Lynch syndrome: what have we learned about psychosocial issues? | Q38106642 | ||
| Predictors of genetic testing decisions: a systematic review and critique of the literature | Q38203489 | ||
| Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer | Q40153778 | ||
| Referral to cancer genetic counseling: are there stages of readiness? | Q40275273 | ||
| Proband family uptake of familial-genetic counselling. | Q40727080 | ||
| Recall of and reactions to a surgeon referral letter for BRCA genetic counseling among high-risk breast cancer patients | Q42619409 | ||
| Australian study on public knowledge of human genetics and health. | Q43569660 | ||
| Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families | Q46735021 | ||
| Inequality of use of cancer genetics services by members of breast, ovarian and colorectal cancer families in South East Scotland | Q46774592 | ||
| Genetic testing in familial melanoma: uptake and implications. | Q48332903 | ||
| Are videoconferenced consultations as effective as face-to-face consultations for hereditary breast and ovarian cancer genetic counseling? | Q48821165 | ||
| Determinants of genetic counseling uptake and its impact on breast cancer outcome: a population-based study. | Q50722910 | ||
| Psychosocial consequences of genetic counseling: a population-based follow-up study. | Q50762334 | ||
| Socioeconomic status and quality of life of women with family history of breast cancer attending an oncogenetic counseling clinic: a comparison with general population. | Q50779450 | ||
| Acceptance of and attitude toward genetic testing for hereditary nonpolyposis colorectal cancer: a comparison of participants and nonparticipants in genetic counseling. | Q51005039 | ||
| Endometrial cancer patients and compliance with genetic counseling: room for improvement. | Q51526342 | ||
| Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members | Q57567514 | ||
| “For All My Family's Sake, I Should Go and Find Out”: An Australian Report on Genetic Counseling and Testing Uptake in Individuals at High Risk of Breast and/or Ovarian Cancer | Q57910567 | ||
| P433 | issue | 2 | |
| P921 | main subject | sociodemography | Q3487479 |
| P304 | page(s) | 121-133 | |
| P577 | publication date | 2016-09-19 | |
| P1433 | published in | Clinical Genetics | Q5133760 |
| P1476 | title | Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review | |
| P478 | volume | 92 |
| Q91989395 | An Applied Framework in Support of Shared Decision Making about BRCA Genetic Testing |
| Q91989403 | Automatic Genetic Risk Assessment Calculation Using Breast Cancer Family History Data from the EHR compared to Self-Report |
| Q49551487 | Communication of cancer-related genetic and genomic information: A landscape analysis of reviews |
| Q88709734 | Creation and Implementation of an Environmental Scan to Assess Cancer Genetics Services at Three Oncology Care Settings |
| Q49892558 | Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk |
| Q52660922 | Gaps in Receipt of Clinically Indicated Genetic Counseling After Diagnosis of Breast Cancer. |
| Q92008556 | Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey |
| Q93387813 | Health beliefs associated with readiness for genetic counseling among high risk breast cancer survivors |
| Q92303085 | Is immunohistochemistry-based screening for Lynch syndrome in endometrial cancer effective? The consent's the thing |
| Q47350873 | Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial |
| Q64279958 | Painting a portrait: Analysis of national health survey data for cancer genetic counseling |
| Q58786293 | Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
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