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Informed consent for human genetic and genomic studies: a systematic review.

Informed consent for human genetic and genomic studies: a systematic review.

http://www.wikidata.org/entity/Q38197382

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ELSI practices in genomic research in East Asia: implications for research collaboration and public participation Research participants' perceptions and views on consent for biobank research: a review of empirical data and ethical analysis Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.Ethical challenges in teaching genetics for medical students.Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond.Expect the unexpected: screening for secondary findings in clinical genomics research.Participant understanding and recall of informed consent for induced pluripotent stem cell biobanking.Towards precision nephrology: the opportunities and challenges of genomic medicine.Communication of cancer-related genetic and genomic information: A landscape analysis of reviews.Recruitment and Participation of Recreational Runners in a Large Epidemiological and Genetic Research Study: Retrospective Data Analysis.

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P2860

Informed consent for human genetic and genomic studies: a systematic review.

http://www.wikidata.org/entity/Q38197382

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article scientifique

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artikel ilmiah

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Informed consent for human genetic and genomic studies: a systematic review.

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Informed consent for human genetic and genomic studies: a systematic review.

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Informed consent for human genetic and genomic studies: a systematic review.

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Clinical Genetics

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Informed consent for human genetic and genomic studies: a systematic review

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A Khan

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B J Capps

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C N Kuswanto

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M Y Sum

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P2860

From genetic privacy to open consent

The genomic and transcriptomic landscape of a HeLa cell line

From patients to partners: participant-centric initiatives in biomedical research

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives

Qualitative thematic analysis of consent forms used in cancer genome sequencing

To share or not to share: a randomized trial of consent for data sharing in genome research

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations

Consent for genetic research in the Framingham Heart Study

Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya

Identifying personal genomes by surname inference

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199-206

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scholarly article

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10.1111/CGE.12384

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3

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86

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2014-04-18T00:00:00Z

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informed consent