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- 2022
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Mark
Return of genomic results does not motivate intent to participate in research for all : Perspectives across 22 countries
(
- Contribution to journal › Article
- 2021
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Mark
Demonstrating trustworthiness when collecting and sharing genomic data : public views across 22 countries
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- Contribution to journal › Article
- 2020
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Mark
It's much more grey than black and white : clinical geneticists' views on the oversight of consumer genomics in Europe
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- Contribution to journal › Article
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Mark
Willingness to donate genomic and other medical data : results from Germany
(
- Contribution to journal › Article
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Mark
Transparency, consent and trust in the use of customers' data by an online genetic testing company : an Exploratory survey among 23andMe users
(
- Contribution to journal › Article
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Mark
Global Public Perceptions of Genomic Data Sharing : What Shapes the Willingness to Donate DNA and Health Data?
(
- Contribution to journal › Article
- 2019
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Mark
Attitudes of publics who are unwilling to donate DNA data for research
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- Contribution to journal › Article
- 2018
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Mark
'Your DNA, Your Say' : global survey gathering attitudes toward genomics: design, delivery and methods
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- Contribution to journal › Article
- 2015
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Mark
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
2015) In European Journal of Human Genetics(
- Contribution to journal › Article
-
Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
(
- Contribution to journal › Article