Pages that link to "Q34441798"
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The following pages link to Disclosing individual results of clinical research: implications of respect for participants (Q34441798):
Displaying 50 items.
- The law of incidental findings in human subjects research: establishing researchers' duties (Q24642724) (← links)
- Patient involvement in clinical research: why, when, and how (Q26750036) (← links)
- The Legal Implications of Report-Back in Household Exposure Studies (Q26751469) (← links)
- Communicating results in post-Belmont era biomonitoring studies: lessons from genetics and neuroimaging research (Q27008196) (← links)
- Participant use and communication of findings from exome sequencing: a mixed-methods study. (Q27324155) (← links)
- Incidental findings in genetics research using archived DNA (Q28283556) (← links)
- Toxic ignorance and right-to-know in biomonitoring results communication: a survey of scientists and study participants (Q28387798) (← links)
- Incidental findings found in "healthy" volunteers during imaging performed for research: current legal and ethical implications (Q28389877) (← links)
- Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting (Q28659644) (← links)
- Ethical, legal, and social considerations in conducting the Human Microbiome Project (Q28660032) (← links)
- Recommendations for the return of research results to study participants and guardians: a report from the Children's Oncology Group (Q28710366) (← links)
- Testing for sexually transmitted infections in a population-based sexual health survey: development of an acceptable ethical approach (Q28729270) (← links)
- Genomic sequencing in clinical trials (Q28732333) (← links)
- Post-genomic clinical trials: the perspective of ACGT (Q28741720) (← links)
- Public expectations for return of results from large-cohort genetic research (Q28754402) (← links)
- Trials and tribulations of protecting children from environmental hazards (Q30398790) (← links)
- Subjects' views of obligations to ensure post-trial access to drugs, care and information: qualitative results from the Experiences of Participants in Clinical Trials (EPIC) study. (Q30498252) (← links)
- Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results (Q30502503) (← links)
- IRB chairs' perspectives on genotype-driven research recruitment (Q30539071) (← links)
- Recommendations for ethical approaches to genotype-driven research recruitment (Q30540771) (← links)
- Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study (Q30572149) (← links)
- When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results (Q33320883) (← links)
- Communicating the results of clinical research to participants: attitudes, practices, and future directions (Q33334605) (← links)
- Considerations for designing a prototype genetic test for use in translational research (Q33724840) (← links)
- Return of results: ethical and legal distinctions between research and clinical care (Q33835535) (← links)
- Ethical challenges in genotype-driven research recruitment (Q33881325) (← links)
- Prospective biorepository participants' perspectives on access to research results (Q33941167) (← links)
- Institutional review board challenges related to community-based participatory research on human exposure to environmental toxins: a case study (Q34036253) (← links)
- A framework for analyzing the ethics of disclosing genetic research findings (Q34081010) (← links)
- Managing incidental findings and research results in genomic research involving biobanks and archived data sets (Q34205284) (← links)
- Teaching health law. (Q34285373) (← links)
- Should we disclose amyloid imaging results to cognitively normal individuals? (Q34286140) (← links)
- Researcher Practices on Returning Genetic Research Results (Q34405755) (← links)
- Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research (Q34436672) (← links)
- Preferences regarding genetic research results: comparing veterans and nonveterans responses (Q34515650) (← links)
- Reciprocity-based reasons for benefiting research participants: most fail, the most plausible is problematic (Q34556648) (← links)
- Disclosing individual genetic results to research participants (Q34579296) (← links)
- Community-based participatory research (CBPR) approach to study children's health in China: Experiences and reflections (Q34585474) (← links)
- Genotype-driven recruitment: a strategy whose time has come? (Q34736416) (← links)
- Ethical, legal, and social implications of biobanks for genetics research (Q34763998) (← links)
- Ethics. Incidental findings in brain imaging research (Q34881764) (← links)
- Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group (Q34960621) (← links)
- Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium (Q34960752) (← links)
- Detecting awareness after severe brain injury (Q35006963) (← links)
- The current impact of incidental findings found during neuroimaging on neurologists' workloads (Q35130180) (← links)
- Returning individual research results: development of a cancer genetics education and risk communication protocol (Q35173889) (← links)
- Opinions and intentions of parents of an autistic child toward genetic research results: two typical profiles (Q35406095) (← links)
- Informed consent in genomics and genetic research (Q35551797) (← links)
- Public Perspectives on Returning Genetics and Genomics Research Results (Q35564757) (← links)
- Compliance with results reporting at ClinicalTrials.gov (Q35575094) (← links)