(Q28749865)

4

object named as

Thomas N Williams

0 references

author name string

Dorcas M Kamuya

2

0 references

Albert M Mlamba

3

0 references

Sassy S Molyneux

Creative Commons Attribution 2.0 Generic

5

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language of work or name

English

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publication date

15 July 2010

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published in

BMC Medical Ethics

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volume

11

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page(s)

13

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copyright license

start time

15 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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1 reference

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A global network for investigating the genomic epidemiology of malaria

16 March 2017

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From genetic privacy to open consent

16 March 2017

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The complexities of ethical evaluation of genomics research

16 March 2017

1 reference

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Data sharing and intellectual property in a genomic epidemiology network: policies for large-scale research collaboration

16 March 2017

1 reference

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The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenya

16 March 2017

1 reference

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Sickle cell trait and the risk of Plasmodium falciparum malaria and other childhood diseases

16 March 2017

1 reference

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Ethics in public health research: protecting human subjects: the role of community advisory boards

16 March 2017

1 reference

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DNA databanks and consent: a suggested policy option involving an authorization model

16 March 2017

1 reference

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Searching for genetic determinants in the new millennium

16 March 2017

1 reference

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The role of community review in evaluating the risks of human genetic variation research.

16 March 2017

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

16 March 2017

1 reference

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Ethics and the ethnography of medical research in Africa

3 June 2018

1 reference

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'He is now like a brother, I can even give him some blood'--relational ethics and material exchanges in a malaria vaccine 'trial community' in The Gambia

3 June 2018

1 reference

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Beginning community engagement at a busy biomedical research programme: experiences from the KEMRI CGMRC-Wellcome Trust Research Programme, Kilifi, Kenya

3 June 2018

1 reference

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Taking social relationships seriously: lessons learned from the informed consent practices of a vaccine trial on the Kenyan Coast

3 June 2018

1 reference

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Interventions to improve risk communication in clinical genetics: systematic review

3 June 2018

1 reference

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The role of community-based organizations in household ability to pay for health care in Kilifi District, Kenya

3 June 2018

1 reference

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The uneasy ethical and legal underpinnings of large-scale genomic biobanks

3 June 2018

1 reference

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Valid consent for genomic epidemiology in developing countries

3 June 2018

1 reference

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Effectiveness of Haemophilus influenzae type b Conjugate vaccine introduction into routine childhood immunization in Kenya

3 June 2018

1 reference

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Should donors be allowed to give broad consent to future biobank research?

3 June 2018

1 reference

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Exception from informed consent: viewpoint of institutional review boards--balancing risks to subjects, community consultation, and future directions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Protecting communities in pharmacogenetic and pharmacogenomic research

3 June 2018

1 reference

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Genomics and Global Health: Time for a Reappraisal

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Ethical challenges in community-based research

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Involving study populations in the review of genetic research

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Public deliberation and private choice in genetics and reproduction

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Communal discourse as a supplement to informed consent for genetic research

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Eating disorders, serotonin transporter polymorphisms and potential treatment response

3 June 2018

1 reference

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The quest for legitimacy: comment on Cox Macpherson's 'To strengthen consensus, consult the stakeholders'.

21 January 2018

1 reference

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Global voices of science. It takes a village: medical research and ethics in Mali

21 January 2018

1 reference

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

21 January 2018

1 reference

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Shattuck lecture--medical and societal consequences of the Human Genome Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

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

21 January 2018

1 reference

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Screening and counselling for sickle cell disorders and thalassaemia: the experience of parents and health professionals.

21 January 2018

1 reference

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Sweden's answer to genomics ethics

21 January 2018

1 reference

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Ethics of population genomics research.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

The role of community advisory boards: involving communities in the informed consent process.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

Community Members Employed on Research Projects Face Crucial, Often Under-Recognized, Ethical Dilemmas

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

Becoming a father/refusing fatherhood: an empirical bioethics approach to paternal responsibilities and rights

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

'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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

Ethical goals of community consultation in research

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6939-11-13

Public consultation in ethics: an experiment in representative ethics

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918624

Beyond public perceptions of gene technology: community participation in public policy in Australia

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20633282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1472-6939-11-13

1 reference

Dimensions Publication ID

1005702417

0 references

1 reference

1 reference

PubMed publication ID

20633282

1 reference