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Journal article

When screening and diagnosis converge: participant interpretations of additional findings in the 100,000 genomes project

Abstract:
Genomic science is a central feature of the UK government's current 10-year health plan for England, which places significant emphasis on prediction and prevention. Although NHS prevention strategies have long been aimed at catching diseases earlier and at a more treatable stage, genomics until now has focussed largely on diagnosis and treatment. At present, there is limited evidence on how patients and publics engage with uncertain and probabilistic genomic information. While the public health benefits of this turn towards genomic screening may take time to establish, insights can be gained from recent large-scale diagnostic initiatives that also offered a screening element. This article draws on a qualitative longitudinal study of 100,000 Genomes Project participants, within which decision-making around the option to receive Additional Findings (AFs) was discussed. By focusing on future health risks in asymptomatic individuals, AFs can be understood as an opportunistic form of screening. Analysis identified three interrelated themes: ambivalence, reflecting anxiety and uncertainty surrounding decisions to receive AFs; inevitability and participant's own perceptions of patterns of future risk within families; and legacy, capturing motivations framed in collective and relational terms. Participants' accounts reflected enduring expectations of genomic medicine as a source of certainty and clarity, which sits uneasily alongside probabilistic and uncertain forms of knowledge such screening approaches are likely to produce. Understanding how individuals and families conceive of the potential and pitfalls of employing genomic tests in screening contexts is vital as a range of countries pilot or adopt genomic tools in population health services.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41431-026-02139-1

Authors

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-6839-876X
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-3324-4338


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
European Journal of Human Genetics More from this journal
Publication date:
2026-05-22
Acceptance date:
2026-05-05
DOI:
EISSN:
1476-5438
ISSN:
1018-4813


Language:
English
Keywords:
Pubs id:
2423134
Local pid:
pubs:2423134
Source identifiers:
W7162125931
Deposit date:
2026-05-25
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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