Voluntary participation and informed consent to international genetic research. - Wikidata - awgldk - TriplyDB

Voluntary participation and informed consent to international genetic research.

Voluntary participation and informed consent to international genetic research.

http://www.wikidata.org/entity/Q53248781

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Informed consent comprehension in African research settings Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents Consent and community engagement in diverse research contexts Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.A perpetual source of DNA or something really different: ethical issues in the creation of cell lines for African genomics research Voluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in Nigeria Methodological challenges of genome-wide association analysis in Africa Ethical and legal implications of whole genome and whole exome sequencing in African populations.Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience Recruitment of Yoruba families from Nigeria for genetic research: experience from a multisite keloid study.Consent Under Pressure: The Puzzle of Third Party Coercion.Tailoring the process of informed consent in genetic and genomic research Strengthening the informed consent process in international health research through community engagement: The KEMRI-Wellcome Trust Research Programme Experience.The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countries Perceptions of consent, permission structures and approaches to the community: a rapid ethical assessment performed in North West Cameroon Impact of gender on the decision to participate in a clinical trial: a cross-sectional study.Reported consent processes and demographics: a substudy of the INSIGHT Strategic Timing of AntiRetroviral Treatment (START) trial."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.Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research Motivation and frustration in cardiology trial participation: the patient perspective.Decision-making and motivation to participate in biomedical research in southwest Nigeria.Recruiting underserved populations to dermatologic research: a systematic review Understanding of research, genetics and genetic research in a rapid ethical assessment in north west Cameroon.Informed consent practices in Nigeria.A randomized controlled trial of short and standard-length consent forms for a genetic cohort study: is longer better?Informed consent for human genetic and genomic studies: a systematic review.Measuring voluntariness of consent to research: an instrument review.Cultural aspects related to informed consent in health research: A systematic review.Voluntariness of consent to HIV clinical research: A conceptual and empirical pilot study.Okukkera Ng'omuzungu (lost in translation): understanding the social value of global health research for HIV/AIDS research participants in Uganda.Participants' Understanding of Informed Consent for Biobanking: A Systematic Review.Perspectives of surrogate decision makers for critically ill patients regarding gene variation research.Ethical considerations in conducting research on autism spectrum disorders in low and middle income countries.Relative solidarity: Conceptualising communal participation in genomic research among potential research participants in a developing Sub-Saharan African setting.

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P2860

Voluntary participation and informed consent to international genetic research.

http://www.wikidata.org/entity/Q53248781

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2006 nî lūn-bûn

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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2006年學術文章

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name

Voluntary participation and informed consent to international genetic research.

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Voluntary participation and informed consent to international genetic research.

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type

label

Voluntary participation and informed consent to international genetic research.

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Voluntary participation and informed consent to international genetic research.

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prefLabel

Voluntary participation and informed consent to international genetic research.

@en

Voluntary participation and informed consent to international genetic research.

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Voluntary participation and informed consent to international genetic research.

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Patricia A Marshall

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Richard S Cooper

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P2860

Integrating ethics and science in the International HapMap Project

The challenge of cross-cultural clinical trials research: case report from the Tibetan Autonomous Region, People's Republic of China.

Ethics. Protecting communities in biomedical research.

Involving study populations in the review of genetic research.

Informed consent for population-based research involving genetics.

Science and society: children and incompetent adults in genetic research: consent and safeguards.

Human rights, politics, and reviews of research ethics.

Motivations, understanding, and voluntariness in international randomized trials.

Does the current consent process minimize the risks of genetics research?

Between universalism and relativism: a conceptual exploration of problems in formulating and applying international biomedical ethical guidelines

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