Reported referral for genetic counseling or BRCA 1/2 testing among United States physicians: a vignette-based study.
about
Clinical utility of a self-administered questionnaire for assessment of hereditary gynecologic cancer.Awareness of cancer susceptibility genetic testing: the 2000, 2005, and 2010 National Health Interview Surveys.Are public health professionals prepared for public health genomics? A cross-sectional survey in Italy.Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.Impact of a randomized controlled educational trial to improve physician practice behaviors around screening for inherited breast cancer.An Effective Multimodal Curriculum to Teach Internal Medicine Residents Evidence-Based Breast Health.Physicians' beliefs about effectiveness of cancer screening tests: a national survey of family physicians, general internists, and obstetrician-gynecologists.Prophylactic oophorectomy rates in relation to a guideline update on referral to genetic counseling.Attitudes and practices among internists concerning genetic testingBarriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.Prevalence and healthcare actions of women in a large health system with a family history meeting the 2005 USPSTF recommendation for BRCA genetic counseling referral.The current use and attitudes towards tumor genome sequencing in breast cancer.A systematic review of factors that act as barriers to patient referral to genetic servicesQuality of cancer family history and referral for genetic counseling and testing among oncology practices: a pilot test of quality measures as part of the American Society of Clinical Oncology Quality Oncology Practice InitiativePublic Health Approaches and Barriers to Educating Providers about Hereditary Breast and Ovarian Cancer Syndrome.Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-UpAge at diagnosis may trump family history in driving BRCA testing in a population of breast cancer patients.Cognitive and psychological impact of BRCA genetic counseling in before and after definitive surgery breast cancer patients.Identification, Evaluation, and Treatment of Patients with Hereditary Cancer Risk within the United States.Genetic risk and gynecologic cancers.Guideline-inconsistent breast cancer screening for women over 50: a vignette-based survey.Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.Challenges in meeting Healthy People 2020 objectives for cancer-related preventive services, National Health Interview Survey, 2008 and 2010.Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer.Accuracy of ovarian and colon cancer risk assessments by U.S. physicians.Use of BRCA Mutation Test in the U.S., 2004-2014.Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes.Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer.The experience of physicians in pharmacogenomic clinical decision support within eight German university hospitals.Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing.Clinical utility of a Web-enabled risk-assessment and clinical decision support program.Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling.All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates.Challenges in managing genetic cancer risk: a long-term qualitative study of unaffected women carrying BRCA1/BRCA2 mutations.Analysis of patient reports on the referral process to two NSW cancer genetic services.Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter.Increasing Appropriate BRCA1/2 Mutation Testing: The Role of Family History Documentation and Genetic Counseling in a Multidisciplinary Clinic.Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.
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P2860
Reported referral for genetic counseling or BRCA 1/2 testing among United States physicians: a vignette-based study.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
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2011年學術文章
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name
Reported referral for genetic ...... cians: a vignette-based study.
@en
Reported referral for genetic ...... cians: a vignette-based study.
@nl
type
label
Reported referral for genetic ...... cians: a vignette-based study.
@en
Reported referral for genetic ...... cians: a vignette-based study.
@nl
prefLabel
Reported referral for genetic ...... cians: a vignette-based study.
@en
Reported referral for genetic ...... cians: a vignette-based study.
@nl
P2093
P2860
P356
P1433
P1476
Reported referral for genetic ...... cians: a vignette-based study.
@en
P2093
Barbara A Goff
Barbara Matthews
C Holly A Andrilla
Denise M Lishner
Jacqueline W Miller
Katrina F Trivers
Laura-Mae Baldwin
P2860
P304
P356
10.1002/CNCR.26166
P407
P577
2011-07-25T00:00:00Z