Pages that link to "Q34077993"

The following pages link to Involving study populations in the review of genetic research (Q34077993):

Displaying 46 items.

• Ethics in public health research: protecting human subjects: the role of community advisory boards (Q24544507) (← links)
• Community involvement in the ethical review of genetic research: lessons from American Indian and Alaska Native populations (Q24811808) (← links)
• Human genetics, environment, and communities of color: ethical and social implications (Q24812213) (← links)
• Will investments in large-scale prospective cohorts and biobanks limit our ability to discover weaker, less common genetic and environmental contributors to complex diseases? (Q24814117) (← links)
• The International HapMap Project (Q27860695) (← links)
• Integrating ethics and science in the International HapMap Project (Q28262651) (← links)
• Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya (Q28749865) (← links)
• GOOD GIFTS FOR THE COMMON GOOD: Blood and Bioethics in the Market of Genetic Research (Q30398074) (← links)
• Sharing Data and Results in Ethnographic Research: Why This Should not be an Ethical Imperative (Q33433649) (← links)
• Caught in Collaboration (Q33789103) (← links)
• Establishing ethical trials for treatment and prevention of AIDS in developing countries (Q33816004) (← links)
• Tailoring the process of informed consent in genetic and genomic research (Q33865729) (← links)
• Ethics in practice: the state of the debate on promoting the social value of global health research in resource poor settings particularly Africa (Q34074948) (← links)
• Human genome diversity: what about the other human genome project? (Q34188156) (← links)
• Ethical and legal implications of pharmacogenomics (Q34188160) (← links)
• Ethical challenges in community-based research (Q34448075) (← links)
• Working with Concepts: The Role of Community in International Collaborative Biomedical Research. (Q34678187) (← links)
• The complex relationship of genetics, groups, and health: what it means for public health (Q34687312) (← links)
• Ethical, legal, and social implications of biobanks for genetics research (Q34763998) (← links)
• Balancing scientific and community interests in community-based participatory research (Q34779804) (← links)
• Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium (Q34960752) (← links)
• Exploring researchers' experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study (Q35680986) (← links)
• Gut Microbiome Diversity among Cheyenne and Arapaho Individuals from Western Oklahoma (Q35869822) (← links)
• Community engagement about genetic variation research (Q35997424) (← links)
• Community engagement in biobanking: Experiences from the eMERGE Network. (Q36210731) (← links)
• Strategies to Build Trust and Recruit African American and Latino Community Residents for Health Research: A Cohort Study (Q36225505) (← links)
• Ethics guidelines for research with the recently dead (Q36306254) (← links)
• A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western Kenya (Q36448171) (← links)
• Protecting communities in biomedical research (Q36497677) (← links)
• The routinisation of genomics and genetics: implications for ethical practices (Q36639329) (← links)
• Recruiting underserved populations to dermatologic research: a systematic review (Q36819871) (← links)
• Beginning community engagement at a busy biomedical research programme: experiences from the KEMRI CGMRC-Wellcome Trust Research Programme, Kilifi, Kenya (Q37192415) (← links)
• Research on environmental health interventions: ethical problems and solutions (Q37615093) (← links)
• Advancing community stakeholder engagement in biomedical HIV prevention trials: principles, practices and evidence (Q38244981) (← links)
• The informed consent aftermath of the genetic revolution. An Italian example of implementation (Q40192133) (← links)
• Informed consent in international health research (Q40347920) (← links)
• Do we need a uniform regulatory system for biobanks across Europe? (Q42674003) (← links)
• Exploitation and community engagement: can community advisory boards successfully assume a role minimising exploitation in international research? (Q43536105) (← links)
• Nondirectiveness and its lay interpretations: the effect of counseling style, ethnicity and culture on attitudes towards genetic counseling among Jewish and Bedouin respondents in Israel (Q47363824) (← links)
• Protecting groups from genetic research (Q47713959) (← links)
• Population genomics and research ethics with socially identifable groups. (Q53179751) (← links)
• Research with groups: group rights, group consent, and collaborative research commentary on "Protecting the Navajo People through tribal regulation of research". (Q53230853) (← links)
• Voluntary participation and informed consent to international genetic research. (Q53248781) (← links)
• The role of IRBs in research involving commercial biobanks. (Q53419595) (← links)
• Community involvement in biomedical research conducted in the global health context; what can be done to make it really matter? (Q55441864) (← links)
• Perspectives on Biological Monitoring in Environmental Health Research: A Focus Group Study in a Native American Community (Q56547215) (← links)