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
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
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
Challenges of using whole genome sequencing in population newborn screening.
Horton R. et al, (2024), BMJ (Clinical research ed.), 384
Genomic Data: Building Blocks for Life or Abstract Art?
Horton R. et al, (2024), Frontiers for Young Minds, 12
The ethical challenges of diversifying genomic data: A qualitative evidence synthesis
Hardcastle F. et al, (2024), Cambridge Prisms: Precision Medicine, 2
Immortal data: a qualitative exploration of patients’ understandings of genomic data
Lyle K. et al, (2023), European Journal of Human Genetics, 31, 681 - 686
Genomics and Insurance in the United Kingdom: Increasing Complexity and Emerging Challenges
Dixon P. et al, (2023)
Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients.
Hamad A. et al, (2023), European journal of medical genetics, 66
Ethical Considerations in Research with Genomic Data.
Horton R. and Lucassen A., (2023), The New bioethics : a multidisciplinary journal of biotechnology and the body, 29, 37 - 51
Realistic expectations are key to realising the benefits of polygenic scores.
Sud A. et al, (2023), BMJ (Clinical research ed.), 380
Genetic risk scores may compound rather than solve the issue of prostate cancer overdiagnosis.
Horton RH. et al, (2023), British journal of cancer, 128, 1 - 2
Ethical, Legal and Social Issues in Diversifying Genomic Data: Literature Review and Synthesis
Hardcastle F. et al, (2022)
Ethical issues raised by new genomic technologies: the case study of newborn genome screening
Horton R. and Lucassen A., (2022), Cambridge Prisms: Precision Medicine, 1 - 16
Immortal Data: A qualitative exploration of patients’ understandings of genomic data
Lyle K. et al, (2022)
Ectopic vortex veins and varices in Donnai Barrow syndrome.
Higham A. et al, (2022), Ophthalmic genetics, 43, 248 - 252
Care of men with cancer-predisposing BRCA variants.
Horton R. et al, (2021), BMJ (Clinical research ed.), 375
What is the meaning of a 'genomic result' in the context of pregnancy?
Shkedi-Rafid S. et al, (2021), European journal of human genetics : EJHG, 29, 225 - 230
Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study.
Ballard LM. et al, (2020), European journal of human genetics : EJHG, 28, 732 - 741