-
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.
Journal article
Mackley MP. et al, (2018), Eur J Hum Genet
-
Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.
Journal article
Horn R. and Parker M., (2018), Prenat Diagn, 38, 20 - 25
-
How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.
Journal article
Dheensa S. et al, (2018), Fam Cancer, 17, 155 - 166
-
'It is an entrustment': Broad consent for genomic research and biobanks in Sub-Saharan Africa.
Journal article
Tindana P. et al, (2017), Dev World Bioeth
-
Ethical Translations of Psychiatric Genomics Into Mental Health Practice: Response to Commentaries.
Journal article
Kong C. et al, (2017), Am J Bioeth, 17, W3 - W5
-
Psychiatric Genomics and Mental Health Treatment: Setting the Ethical Agenda.
Journal article
Kong C. et al, (2017), Am J Bioeth, 17, 3 - 12
-
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Journal article
Mackley MP. et al, (2017), Genet Med, 19, 283 - 293
-
Returning genome sequences to research participants: Policy and practice.
Journal article
Wright CF. et al, (2017), Wellcome Open Res, 2
-
Sharing Individual-Level Health Research Data: Experiences, Challenges and a Research Agenda.
Journal article
Cheah PY. et al, (2017), Asian Bioeth Rev, 9, 393 - 400
-
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Journal article
Quinlan-Jones E. et al, (2016), Prenat Diagn, 36, 935 - 941