(Q28730767)

2

0 references

T Wang

3

0 references

P A Kelly

4

0 references

S G Hilsenbeck

5

0 references

A L McGuire

Towards a data sharing Code of Conduct for international genomic research

6

0 references

language of work or name

English

0 references

publication date

2012

0 references

published in

Public Health Genomics

0 references

volume

15

0 references

issue

2

0 references

page(s)

106-14

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3318928

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

17 March 2017

1 reference

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Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience

17 March 2017

1 reference

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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays

17 March 2017

1 reference

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DNA data sharing: research participants' perspectives

17 March 2017

1 reference

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Genetics. No longer de-identified

17 March 2017

1 reference

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Three approaches to qualitative content analysis

17 March 2017

1 reference

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Channeling consumers to preferred providers and the impact of status quo bias: does type of provider matter?

7 April 2017

1 reference

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Predicting intention to biobank: a national survey.

3 June 2018

1 reference

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Glad you asked: participants' opinions of re-consent for dbGap data submission

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3318928

Public and biobank participant attitudes toward genetic research participation and data sharing

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3318928

Hypothetical and factual willingness to participate in biobank 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=3318928

The role of race and trust in tissue/blood donation 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=3318928

Public opinion about the importance of privacy in biobank 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=3318928

Informed consent for biorepositories: assessing prospective participants' understanding and opinions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3318928

Genetics. Genomic research and human subject privacy

3 June 2018

1 reference

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When choice is demotivating: can one desire too much of a good thing?

3 June 2018

2 references

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3 June 2018

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Validation of a decisional conflict scale

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3318928

Measuring trust in medical researchers

3 June 2018

1 reference

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Assessing the understanding of biobank participants.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1159%2F000334718

Protection of human subjects

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22213783

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Personal privacy, public benefits, and biobanks: A conjoint analysis of policy priorities and public perceptions

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22213783

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Medical decision making in situations that offer multiple alternatives

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22213783