Johnson SB. and Parker M., (2019), Nat Rev Genet
Dunn M., (2019), J Med Ethics, 45, 149 - 150
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J. et al, (2019), Lancet, 393, 747 - 757
Negotiating jurisdictional boundaries in response to new genetic possibilities in breast cancer care: The creation of an ‘oncogenetic taskscape’
Wright S. et al, (2019), Social Science & Medicine
Moving into the mainstream: healthcare professionals' views of implementing treatment focussed genetic testing in breast cancer care.
Hallowell N. et al, (2019), Familial cancer
Chan EYY. et al, (2019), Lancet, 393, 112 - 113
The NeuroDev Study: Phenotypic and Genetic Characterization of Neurodevelopmental Disorders in Kenya and South Africa.
de Menil V. et al, (2019), Neuron, 101, 15 - 19
Pratt B. et al, (2018), BMC Med Ethics, 19
Kimberly LL. et al, (2018), Pediatrics, 142
Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.
Cheah PY. et al, (2018), BMC Med Ethics, 19
Friesen P. and Blease C., (2018), J Med Ethics, 44, 774 - 781
McCoy MS. et al, (2018), Journal of medical ethics
Reasonable disagreement and the justification of pre-emptive ethics governance in social research: a response to Hammersley.
Sheehan M. et al, (2018), J Med Ethics, 44, 719 - 720
Ethical understandings of proxy decision making for research involving adults lacking capacity: A systematic review (framework synthesis) of empirical research.
Shepherd V. et al, (2018), AJOB Empir Bioeth, 9, 267 - 286