| scholarly article | Q13442814 |
| P50 | author | Jada G. Hamilton | Q50633667 |
| P2093 | author name string | Erica S Breslau | |
| Min-Lin Fang | |||
| Heather M Edwards | |||
| Ekland Abdiwahab | |||
| Andrew Jdayani | |||
| P2860 | cites work | Screening for breast cancer: an update for the U.S. Preventive Services Task Force | Q24615837 |
| EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome | Q24655053 | ||
| Cancer screening in the United States, 2015: a review of current American cancer society guidelines and current issues in cancer screening | Q27001043 | ||
| Screening for breast cancer: U.S. Preventive Services Task Force recommendation statement | Q28265041 | ||
| Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine | Q30513982 | ||
| Patient and provider attitudes toward genomic testing for prostate cancer susceptibility: a mixed method study | Q30543371 | ||
| Screening for colorectal cancer: a targeted, updated systematic review for the U.S. Preventive Services Task Force | Q33374239 | ||
| Awareness of cancer susceptibility genetic testing: the 2000, 2005, and 2010 National Health Interview Surveys | Q33703141 | ||
| Familial risk of cancer and knowledge and use of genetic testing | Q33898716 | ||
| Diffusion of breast cancer risk assessment in primary care | Q33902568 | ||
| Screening for prostate cancer: a review of the evidence for the U.S. Preventive Services Task Force | Q34044753 | ||
| Screening for prostate cancer: U.S. Preventive Services Task Force recommendation statement | Q34288506 | ||
| How can polygenic inheritance be used in population screening for common diseases? | Q34327946 | ||
| The role of genome sequencing in personalized breast cancer prevention | Q34458456 | ||
| Screening for colorectal cancer: U.S. Preventive Services Task Force recommendation statement | Q34847160 | ||
| Understanding patient and provider perceptions and expectations of genomic medicine | Q34859653 | ||
| Polygenic susceptibility to prostate and breast cancer: implications for personalised screening | Q34977428 | ||
| Genetic testing and cancer risk management recommendations by physicians for at-risk relatives | Q34985909 | ||
| Educational needs in genetic medicine: primary care perspectives | Q40108592 | ||
| Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers? | Q40540252 | ||
| Prompting Primary Care Providers about Increased Patient Risk As a Result of Family History: Does It Work? | Q40957816 | ||
| An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons | Q42091906 | ||
| Primary care physician management, referral, and relations with specialists concerning patients at risk for cancer due to family history | Q42631551 | ||
| Racial distribution of patient population and family physician endorsed importance of screening patients for inherited predisposition to cancer | Q44236094 | ||
| Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians | Q45122532 | ||
| An agenda for personalized medicine | Q46071434 | ||
| Impact of academic affiliation and training on knowledge of hereditary colorectal cancer. | Q46371367 | ||
| Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians | Q46450515 | ||
| A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians | Q46531911 | ||
| Educational needs and preferred methods of learning among Florida practitioners who order genetic testing for hereditary breast and ovarian cancer | Q46739746 | ||
| Physician Risk Assessment Knowledge Regarding BRCA Genetics Testing. | Q50631227 | ||
| Interactive genetic counseling role-play: a novel educational strategy for family physicians. | Q51966099 | ||
| Genetic assessment of breast cancer risk in primary care practice. | Q53115454 | ||
| Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: U.S. Preventive Services Task Force Recommendation Statement | Q54092157 | ||
| Multiplex Genetic Testing for Cancer Susceptibility: Out on the High Wire Without a Net? | Q56928410 | ||
| Bioethical and Clinical Dilemmas of Direct-to-Consumer Personal Genomic Testing: The Problem of Misattributed Equivalence | Q57590750 | ||
| Knowledge of Lynch syndrome among obstetrician/gynecologists and general surgeons | Q59281170 | ||
| Education and experience with breast health maintenance and breast cancer care: a study of obstetricians and gynecologists | Q82647189 | ||
| Public health implications from COGS and potential for risk stratification and screening | Q86499074 | ||
| Georgia Primary Care Providers' Knowledge of Hereditary Breast and Ovarian Cancer Syndrome | Q86857890 | ||
| Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial | Q35102571 | ||
| Impact of a randomized controlled educational trial to improve physician practice behaviors around screening for inherited breast cancer | Q35152535 | ||
| Direct-to-consumer personalized genomic testing | Q35230171 | ||
| Pre-test genetic counseling services for hereditary breast and ovarian cancer delivered by non-genetics professionals in the state of Florida | Q35375003 | ||
| Prevalence and correlates of receiving and sharing high-penetrance cancer genetic test results: findings from the Health Information National Trends Survey | Q35513354 | ||
| Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis | Q35602297 | ||
| Public Awareness of Direct-to-Consumer Genetic Tests: Findings from the 2013 U.S. Health Information National Trends Survey | Q35868188 | ||
| Cancer risk assessment by rural and Appalachian family medicine physicians | Q35871974 | ||
| Hereditary cancer predisposition syndromes | Q36002146 | ||
| Genetic competencies essential for health care professionals in primary care | Q36128169 | ||
| Increasing Public Awareness of Direct-to-Consumer Genetic Tests: Health Care Access, Internet Use, and Population Density Correlates | Q36147753 | ||
| Attitudes and practices among internists concerning genetic testing | Q36208056 | ||
| Introduction: Understanding and influencing multilevel factors across the cancer care continuum | Q36352867 | ||
| Patterns of cancer genetic testing: a randomized survey of Oregon clinicians. | Q36362526 | ||
| Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study | Q36582758 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| 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 | Q36595729 | ||
| Evidence-based Guidelines for Precision Risk Stratification-Based Screening (PRSBS) for Colorectal Cancer: Lessons learned from the US Armed Forces: Consensus and Future Directions | Q36646520 | ||
| A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer | Q36789430 | ||
| Primary care providers' needs and preferences for information about colorectal cancer survivorship care | Q36969104 | ||
| Delivery of genomic medicine for common chronic adult diseases: a systematic review | Q37113082 | ||
| Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives | Q37345978 | ||
| Impact of web-based case conferencing on cancer genetics training outcomes for community-based clinicians | Q37378178 | ||
| Differential use of available genetic tests among primary care physicians in the United States: results of a national survey | Q37393205 | ||
| Too many referrals of low-risk women for BRCA1/2 genetic services by family physicians | Q37409287 | ||
| Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer. | Q37590728 | ||
| Incorporating genomics into breast and prostate cancer screening: assessing the implications | Q37614763 | ||
| Telegenetics: a systematic review of telemedicine in genetics services | Q38002304 | ||
| Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: a systematic review to update the U.S. Preventive Services Task Force recommendation | Q38173683 | ||
| Primary-care providers' perceived barriers to integration of genetics services: a systematic review of the literature. | Q38248307 | ||
| The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes | Q38967942 | ||
| Academic family physicians' perception of genetic testing and integration into practice: a CERA study | Q39440680 | ||
| Achieving a nationwide learning health system | Q39818571 | ||
| Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndrome | Q39897235 | ||
| Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information | Q40034540 | ||
| P433 | issue | 3 | |
| P921 | main subject | systematic review | Q1504425 |
| research agenda | Q121225075 | ||
| P304 | page(s) | 315-324 | |
| P577 | publication date | 2016-12-19 | |
| P1433 | published in | Journal of General Internal Medicine | Q6295242 |
| P1476 | title | Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda | |
| P478 | volume | 32 |
| Q49685560 | A Research Agenda for Communication Scholars in the Precision Medicine Era. |
| Q92690938 | Challenges and strategies proposed by genetic health professionals to assist with family communication |
| 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 |
| Q92730102 | Differences in referral patterns based on race for women at high-risk for ovarian cancer in the southeast: Results from a Gynecologic Cancer Risk Assessment Clinic |
| Q91923600 | Direct-to-Consumer Genetic Testing Data Privacy: Key Concerns and Recommendations Based on Consumer Perspectives |
| Q52346491 | False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care. |
| Q64234492 | GP attitudes to and expectations for providing personal genomic risk information to the public: a qualitative study |
| Q57052271 | Genetic Testing: Do Cancer Care Nurses Have a Role? |
| Q63753726 | Genetic cancer risk assessment in general practice: systematic review of tools available, clinician attitudes, and patient outcomes |
| Q93387813 | Health beliefs associated with readiness for genetic counseling among high risk breast cancer survivors |
| Q92102522 | Integrating pharmacogenetic testing into primary care |
| Q47117168 | Integrating surgery and genetic testing for the modern surgeon. |
| Q90070074 | Patients' Medical and Psychosocial Experiences After Detection of a CDH1 Variant With Multigene Panel Testing |
| Q64972560 | Patterns and Determinants of Attitudes towards Genetic Risk of Cancer: Case Study in a Malaysian Public University. |
| Q92664348 | Personalized Medicine Implementation with Non-traditional Data Sources: A Conceptual Framework and Survey of the Literature |
| Q57100898 | Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States |
| Q92349490 | Primary Care Physicians' Knowledge, Attitudes, and Experience with Personal Genetic Testing |
| Q89534269 | Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment |
| Q48347469 | When Personal Feels Invasive: Foreseeing Challenges in Precision Medicine Communication. |
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