The value of large-scale programmes in human genomics
Horn R. et al, (2025), European Journal of Human Genetics
Uptake, utility and resource requirements of a genetic counselling telephone helpline within the BRCA-DIRECT digital pathway for mainstreamed BRCA testing in patients with breast cancer.
Torr B. et al, (2025), Journal of medical genetics
Development of a digital risk-prediction tool based on family health history for the general population: legal and ethical implications.
Dijkstra T. et al, (2024), Journal of community genetics
Ethical considerations in prenatal genomic testing
Horn R. et al, (2024), Best Practice & Research Clinical Obstetrics & Gynaecology, 97, 102548 - 102548
BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial.
Torr B. et al, (2024), British journal of cancer, 131, 1506 - 1515
Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK).
Garrett A. et al, (2024), Genetics in medicine : official journal of the American College of Medical Genetics, 27
The PS4-likelihood ratio calculator: flexible allocation of evidence weighting for case-control data in variant classification.
Rowlands CF. et al, (2024), Journal of medical genetics, 61, 983 - 991
Balancing the rights of the pre-symptomatic child to be found with the risk of harm to others from the screening process
Lucassen A. and Horton R., (2024), European Journal of Human Genetics
Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues
Sahan K. et al, (2024), Journal of Medical Ethics, 50, 517 - 522
Journeys Through Genomics: Co-Producing Visual Resources to Communicate Patient Experiences
Lyle K. et al, (2024), Sociological Research Online
Ethical and social implications of public-private partnerships in the context of genomic/big health data collection.
Horn R. et al, (2024), European journal of human genetics : EJHG, 32, 736 - 741
Focusing attention on physicians’ climate-related duties may risk missing the bigger picture: towards a systems approach to health and climate
Samuel G. et al, (2024), Journal of Medical Ethics, 50, 380 - 381
Why digital innovation may not reduce healthcare's environmental footprint.
Samuel G. et al, (2024), BMJ (Clinical research ed.), 385
Genomics and insurance in the United Kingdom: increasing complexity and emerging challenges
Dixon P. et al, (2024), Health Economics, Policy and Law, 1 - 13
Discussion of off-target and tentative genomic findings may sometimes be necessary to allow evaluation of their clinical significance
Horton RH. et al, (2024), Journal of Medical Ethics, 50, 295 - 298
Predictive genetic testing for Huntington's disease: Exploring participant experiences of uncertainty and ambivalence between clinic appointments.
Ballard LM. et al, (2024), Journal of genetic counseling
Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications.
van der Geest MA. et al, (2024), European journal of human genetics : EJHG, 32, 489 - 497
Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice
Redman MG. et al, (2024), Journal of Medical Genetics, 61, 313 - 318
Glowing gels and pipettes aplenty: how do commercial stock image banks portray genetic tests?
Horton R. et al, (2024), European Journal of Human Genetics, 32, 456 - 460
Advocating for a Context Specific Approach to Tackle Inequities
Samuel G. et al, (2024), The American Journal of Bioethics, 24, 109 - 111