(Q53248781)

12 May 2018

title

Voluntary participation and informed consent to international genetic research. (English)

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12 May 2018

0 references

2

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12 May 2018

Adebowale A. Adeyemo

3

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12 May 2018

Charles Rotimi

10

Charles N Rotimi

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12 May 2018

Temidayo Ogundiran

4

Temidayo O Ogundiran

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12 May 2018

Teri Strenski

6

Teri Strenski

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12 May 2018

T Elaine Prewitt

8

T Elaine Prewitt

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12 May 2018

author name string

Patricia A Marshall

1

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12 May 2018

Mirjana Vekich

5

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12 May 2018

Jie Zhou

7

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12 May 2018

Richard S Cooper

9

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12 May 2018

language of work or name

English

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publication date

3 October 2006

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12 May 2018

American Journal of Public Health

published in

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12 May 2018

volume

96

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12 May 2018

issue

11

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12 May 2018

page(s)

1989-1995

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12 May 2018

The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research

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1 reference

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25 August 2018

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Stability of parental understanding of random assignment in childhood leukemia trials: an empirical examination of informed consent.

25 August 2018

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Informed consent and collaborative research: perspectives from the developing world

25 August 2018

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Motivations, understanding, and voluntariness in international randomized trials

25 August 2018

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Human rights, cultural pluralism, and international health research

25 August 2018

1 reference

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

25 August 2018

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Trust and informed consent: insights from community members on the Kenyan coast.

25 August 2018

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Views of US researchers about informed consent in international collaborative research

25 August 2018

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A model designed to enhance informed consent: experiences from the HIV prevention trials network.

25 August 2018

1 reference

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Genetic research & human biological samples: some legal and ethical considerations.

25 August 2018

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The ethics of research in developing countries: assessing voluntariness.

25 August 2018

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Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research

25 August 2018

1 reference

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Understanding of informed consent in a low-income setting: three case studies from the Kenyan Coast.

25 August 2018

1 reference

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Ethical issues in identifying and recruiting participants for familial genetic research.

25 August 2018

1 reference

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FACE facts: why human genetics will always provoke bioethics

25 August 2018

1 reference

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Integrating ethics and science in the International HapMap Project

25 August 2018

1 reference

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International ethical guidelines for biomedical research involving human subjects.

25 August 2018

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What makes clinical research in developing countries ethical? The benchmarks of ethical research.

25 August 2018

1 reference

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

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Does informed consent to research require comprehension?

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

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

25 August 2018

1 reference

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Comprehension during informed consent in a less-developed country

25 August 2018

1 reference

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Human rights, politics, and reviews of research ethics

25 August 2018

1 reference

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

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent for population-based research involving genetics

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Involving study populations in the review of genetic research

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Ethics. Protecting communities in biomedical research.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

An evaluation of the informed consent procedure used during a trial of a Haemophilus influenzae type B conjugate vaccine undertaken in The Gambia, West Africa.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

A model agreement for genetic research in socially identifiable populations

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent for HIV testing in a South African hospital: is it truly informed and truly voluntary?

25 August 2018

1 reference

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Communal discourse as a supplement to informed consent for genetic research.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent. Subjects may not understand concept of clinical trials.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Ethical issues of genetic testing and their implications in epidemiologic studies

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Practical experiences in obtaining informed consent for a vaccine trial in rural Africa.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Ethical issues in genetic research: disclosure and informed consent.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Making research consent forms informative and understandable: the experience of the Indian Health Service.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent: some challenges to the universal validity of the Western model

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Issues in Preparing Ethical Guidelines for Epidemiological Studies

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Research and informed consent in Africa--another look

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent: practices and views of investigators in a multinational clinical trial

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Quality of parental consent in a Ugandan malaria study

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

'Even if they ask you to stand by a tree all day, you will have to do it (laughter)...!': community voices on the notion and practice of informed consent for biomedical research in developing countries

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

2 November 2018

Beyond informed consent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Informed consent for a clinical trial in Thailand

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Ethical goals of community consultation in research

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

Obtaining informed consent in Bangladesh

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1751828

The Quality of Informed Consent in a Clinical Research Study in Thailand

30 November 2018

1 reference

12 December 2020

A national dialogue on genetics and minority issues

1 reference

12 December 2020

Communication and miscommunication in informed consent to research

1 reference

12 December 2020

The prevalence of hypertension in seven populations of west African origin

1 reference

12 December 2020

The individual and the community in international genetic research

1 reference

12 December 2020

A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans

1 reference

12 December 2020

"Decoding" informed consent. Insights from women regarding breast cancer susceptibility testing

1 reference

12 December 2020

Identifiers

DOI

10.2105/AJPH.2005.076232

1 reference

12 May 2018

0 references

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12 May 2018