Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience
about
Research participants' perceptions and views on consent for biobank research: a review of empirical data and ethical analysisObtaining informed consent for genomics research in Africa: analysis of H3Africa consent documentsConsent and community engagement in diverse research contextsHuman Heredity and Health (H3) in Africa Kidney Disease Research Network: A Focus on Methods in Sub-Saharan AfricaSharing the Knowledge: Sharing Aggregate Genomic Findings with Research Participants in Developing CountriesUnderstandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.Ethical issues in the export, storage and reuse of human biological samples in biomedical research: perspectives of key stakeholders in Ghana and KenyaA perpetual source of DNA or something really different: ethical issues in the creation of cell lines for African genomics researchKnowing who to trust: exploring the role of 'ethical metadata' in mediating risk of harm in collaborative genomics research in AfricaVoluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in NigeriaEthical and legal implications of whole genome and whole exome sequencing in African populations.Widening participation would be key in enhancing bioinformatics and genomics research in AfricaIs it ethical to prevent secondary use of stored biological samples and data derived from consenting research participants? The case of Malawi.A mixed-methods study on perceptions towards use of Rapid Ethical Assessment to improve informed consent processes for health research in a low-income settingEthical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: protocol for a systematic reviewChallenges in biobank governance in Sub-Saharan Africa.Community engagement strategies for genomic studies in Africa: a review of the literature.Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.Evaluating community engagement in global health research: the need for metrics.Exploring researchers' experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study"The keeping is the problem": A qualitative study of IRB-member perspectives in Botswana on the collection, use, and storage of human biological samples for research.Informed consent in paediatric critical care research--a South African perspective.Rapid Ethical Assessment on Informed Consent Content and Procedure in Hintalo-Wajirat, Northern Ethiopia: A Qualitative StudyCluster randomized trial assessing the effects of rapid ethical assessment on informed consent comprehension in a low-resource setting"I passed the test!" Evidence of diagnostic misconception in the recruitment of population controls for an H3Africa genomic study in Cape Town, South Africa.Neurogenomics: Challenges and opportunities for Ghana.Understanding of research, genetics and genetic research in a rapid ethical assessment in north west Cameroon.Addressing ethical challenges in the Genetics Substudy of the National Eye Survey of Trinidad and Tobago (GSNESTT)."It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.Leaves imitate trees: Minnesota Hmong concepts of heredity and applications to genomics research.Predictors of consent to pharmacogenomics testing in the IDEAL study.Trust me, I'm a researcher!: The role of trust in biomedical research.Complex realities: community engagement for a paediatric randomized controlled malaria vaccine trial in Kilifi, KenyaEngaging Hmong adults in genomic and pharmacogenomic research: Toward reducing health disparities in genomic knowledge using a community-based participatory research approach.Molecular genetics research in ADHD: ethical considerations concerning patients' benefit and resource allocation.Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.Should consent forms used in clinical trials be translated into the local dialects? A survey among past participants in rural Ghana.A Model Approach to Public Engagement Training for Students in Developing Countries.Rules of engagement: perspectives on stakeholder engagement for genomic biobanking research in South Africa.'Researchers have love for life': opportunities and barriers to engage pregnant women in malaria research in post-Ebola Liberia.
P2860
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P2860
Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience
description
2012 nî lūn-bûn
@nan
2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Seeking consent to genetic and ...... y of the MalariaGEN experience
@ast
Seeking consent to genetic and ...... y of the MalariaGEN experience
@en
Seeking consent to genetic and ...... y of the MalariaGEN experience
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type
label
Seeking consent to genetic and ...... y of the MalariaGEN experience
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Seeking consent to genetic and ...... y of the MalariaGEN experience
@en
Seeking consent to genetic and ...... y of the MalariaGEN experience
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prefLabel
Seeking consent to genetic and ...... y of the MalariaGEN experience
@ast
Seeking consent to genetic and ...... y of the MalariaGEN experience
@en
Seeking consent to genetic and ...... y of the MalariaGEN experience
@nl
P2860
P50
P3181
P356
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P1476
Seeking consent to genetic and ...... y of the MalariaGEN experience
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P2093
Kwadwo Koram
Raymond Aborigo
P2860
P2888
P3181
P356
10.1186/1472-6939-13-15
P407
P50
P577
2012-07-02T00:00:00Z
P5875
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1037196363