Focusing attention on physicians' climate-related duties may risk missing the bigger picture: towards a systems approach to health and climate.
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Samuel G. et al, (2024), J Med Ethics
Advocating for a Context Specific Approach to Tackle Inequities.
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Samuel G. et al, (2024), The American journal of bioethics : AJOB, 24, 109 - 111
Challenges of using whole genome sequencing in population newborn screening.
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Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications.
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van der Geest MA. et al, (2024), European journal of human genetics : EJHG
Genomic Data: Building Blocks for Life or Abstract Art?
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Horton R. et al, (2024), Frontiers for Young Minds, 12
Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues
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Sahan K. et al, (2024), Journal of Medical Ethics
Prospective study design and data analysis in UK Biobank.
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Allen NE. et al, (2024), Science translational medicine, 16
Population screening requires robust evidence-genomics is no exception.
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Turnbull C. et al, (2023), Lancet
Glowing gels and pipettes aplenty: how do commercial stock image banks portray genetic tests?
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Horton R. et al, (2023), European journal of human genetics : EJHG
Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure.
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Nolan J. et al, (2023), Genetics in medicine : official journal of the American College of Medical Genetics
Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice.
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Redman MG. et al, (2023), Journal of medical genetics
The ethical challenges of diversifying genomic data: A qualitative evidence synthesis
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Hardcastle F. et al, (2023), Cambridge Prisms: Precision Medicine, 1 - 39
Retrospective Cohort Study on the Limitations of Direct-to-Consumer Genetic Screening in Hereditary Breast and Ovarian Cancer.
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Desai NV. et al, (2023), JCO precision oncology, 7
Discussion of off-target and tentative genomic findings may sometimes be necessary to allow evaluation of their clinical significance.
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Horton RH. et al, (2023), Journal of medical ethics
Ethical preparedness and developments in genomic healthcare.
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Farsides B. and Lucassen AM., (2023), Journal of medical ethics
Facilitating genetic testing after death: the ongoing duty of care to the deceased and their relatives.
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Dennis C. et al, (2023), Journal of the Royal Society of Medicine, 116, 193 - 198
Immortal data: a qualitative exploration of patients’ understandings of genomic data
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Lyle K. et al, (2023), European Journal of Human Genetics, 31, 681 - 686
Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM).
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Ballard LM. et al, (2023), European journal of human genetics : EJHG
Utility of polygenic risk scores in UK cancer screening: a modelling analysis.
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Huntley C. et al, (2023), The Lancet. Oncology
Genomics and Insurance in the United Kingdom: Increasing Complexity and Emerging Challenges
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Dixon P. et al, (2023)