Life from death: ethical implications of uterus transplantation from deceased donors in global health.
Suwalowska H. et al, (2025), BMJ Glob Health, 10
Determining a role for Patient and Public Involvement and Engagement (PPIE) in genomic data governance for cancer care
Sahan K. et al, (2025), European Journal of Human Genetics
Author Correction: Call for a fairer approach to authorship in publishing biomedical research.
Cheah PY. and Parker M., (2025), Commun Med (Lond), 5
Call for a fairer approach to authorship in publishing biomedical research.
Cheah PY. and Parker M., (2025), Commun Med (Lond), 5
The Rare Therapies Launchpad: a pilot program for individualized medicines in the UK
O’Connor DJ. et al, (2025), Nature Medicine
Artificial intelligence for modelling infectious disease epidemics.
Kraemer MUG. et al, (2025), Nature, 638, 623 - 635
“Looking at the Big Picture”: A Qualitative Study of Ethics in Science Communication and Engagement
Wilkinson C. et al, (2025), Science Communication
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder.
Elkhateeb N. et al, (2024), Genet Med, 27
Is anybody watching: A multi-factor motivational framework for educational video engagement
Parker MJ. et al, (2024), Computers and Education, 222
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable access.
Ellard S. et al, (2024), J Med Genet
Equity and timeliness as factors in the effectiveness of an ethical prenatal sequencing service: reflections from parents and professionals.
Peter M. et al, (2024), Eur J Hum Genet
Ethical issues in Nipah virus control and research: addressing a neglected disease.
Johnson T. et al, (2024), J Med Ethics, 50, 612 - 617
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.
Rots D. et al, (2024), Am J Hum Genet
Ethical implications of disparities in translation genomic medicine: from research to practice.
Suleman M. et al, (2024), J Med Ethics, 50, 435 - 436
Ethical and social implications of public-private partnerships in the context of genomic/big health data collection.
Horn R. et al, (2024), Eur J Hum Genet, 32, 736 - 741
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service.
McInnes-Dean H. et al, (2024), Prenat Diagn, 44, 465 - 479
Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues.
Sahan K. et al, (2024), J Med Ethics