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- 2020
-
Mark
Willingness to donate genomic and other medical data : results from Germany
(
- Contribution to journal › Article
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Mark
Communicating genetic information to family members : analysis of consent forms for diagnostic genomic sequencing
(
- Contribution to journal › Article
-
Mark
It's much more grey than black and white : clinical geneticists' views on the oversight of consumer genomics in Europe
(
- Contribution to journal › Article
- 2019
-
Mark
«Genethics» and public health genomics
2019) p.243-257(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Consenting patients to genome sequencing
2019) p.31-55(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Attitudes of publics who are unwilling to donate DNA data for research
(
- Contribution to journal › Article
-
Mark
Include egg donors in CRISPR gene-editing debate
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia
(
- Contribution to journal › Article
- 2018
-
Mark
How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis
(
- Contribution to journal › Article
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Mark
Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
(
- Contribution to journal › Article