(Q38197382)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

review article

1 reference

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

0 references

1 reference

5

1 reference

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11 March 2020

author name string

A Khan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

B J Capps

2

1 reference

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11 March 2020

M Y Sum

3

1 reference

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11 March 2020

C N Kuswanto

4

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11 March 2020

publication date

18 April 2014

1 reference

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11 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

volume

86

1 reference

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11 March 2020

issue

3

1 reference

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11 March 2020

page(s)

199-206

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

Qualitative thematic analysis of consent forms used in cancer genome sequencing

11 March 2020

cites work

1 reference

Ethical, legal, and social implications of biobanks for genetics research

21 January 2018

1 reference

Identifying personal genomes by surname inference

21 January 2018

1 reference

From genetic privacy to open consent

21 January 2018

1 reference

The genomic and transcriptomic landscape of a HeLa cell line

21 January 2018

1 reference

Icelandic database shelved as court judges privacy in peril

21 January 2018

1 reference

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

21 January 2018

1 reference

Sampling populations of humans across the world: ELSI issues

21 January 2018

1 reference

Using thematic analysis in psychology

21 January 2018

1 reference

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

21 January 2018

1 reference

Simplifying informed consent for biorepositories: stakeholder perspectives

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience

21 January 2018

1 reference

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis

21 January 2018

1 reference

Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent.

21 January 2018

1 reference

Consent for genetic research in the Framingham Heart Study

21 January 2018

1 reference

Biobanking, consent, and commercialization in international genetics research: the Type 1 Diabetes Genetics Consortium

21 January 2018

1 reference

Informed consent for genetic research on blood stored for more than a decade: a population based study

21 January 2018

1 reference

Recommendations for ethical approaches to genotype-driven research recruitment

21 January 2018

1 reference

The adequacy of informed consent forms in genetic research in Oman: a pilot study

21 January 2018

1 reference

Voluntary participation and informed consent to international genetic research.

21 January 2018

1 reference

Researcher and institutional review board chair perspectives on incidental findings in genomic research

21 January 2018

1 reference

Closure of population biobanks and direct-to-consumer genetic testing companies

21 January 2018

1 reference

Ethical issues arising from the participation of children in genetic research

21 January 2018

1 reference

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

21 January 2018

1 reference

Analysis of informed consent document utilization in a minimal-risk genetic study

21 January 2018

1 reference

Informed consent and patient's rights documents: a right, a rite, or a rewrite?

21 January 2018

1 reference

Consent for genetics studies among clinical trial participants: findings from Action for Health in Diabetes (Look AHEAD).

21 January 2018

1 reference

Informed consent in genomics and genetic research

21 January 2018

1 reference

Tailoring the process of informed consent in genetic and genomic research

21 January 2018

1 reference

Effects of informed consent for individual genome sequencing on relevant knowledge

21 January 2018

1 reference

Obtaining informed consent for genetic studies: The multiethnic study of atherosclerosis

21 January 2018

1 reference

What research participants want to know about genetic research results: the impact of "genetic exceptionalism".

21 January 2018

1 reference

Captious certainties: makings, meanings and misreadings of consumer-oriented genetic testing

21 January 2018

1 reference

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

21 January 2018

1 reference

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

21 January 2018

1 reference

Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study

21 January 2018

1 reference

Ethical and practical challenges surrounding genetic and genomic research in developing countries

21 January 2018

1 reference

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials

21 January 2018

1 reference

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research

21 January 2018

1 reference

Patients' views on identifiability of samples and informed consent for genetic research

21 January 2018

1 reference

Informed consent, participation in, and withdrawal from a population based cohort study involving genetic analysis

21 January 2018

1 reference

International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accreditation system.

21 January 2018

1 reference

Consent Forms in Genomics: The Difference between Law and Practice

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12384

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24646408%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

1 reference