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Lost in translation: why genomic breakthroughs are not reaching patients
by
Field, Matt
, Calcino, Andrew
in
Accreditation
/ Autoimmunity
/ Bioinformatics
/ Biostatistics
/ Clinical trials
/ Disease
/ Editorial
/ FDA approval
/ Funding
/ Genetic markers
/ Genomics
/ Health disparities
/ Health economics
/ Medical research
/ Metabolism
/ Patients
/ Precision medicine
/ Privacy
/ Regulatory approval
/ Success
2026
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Lost in translation: why genomic breakthroughs are not reaching patients
by
Field, Matt
, Calcino, Andrew
in
Accreditation
/ Autoimmunity
/ Bioinformatics
/ Biostatistics
/ Clinical trials
/ Disease
/ Editorial
/ FDA approval
/ Funding
/ Genetic markers
/ Genomics
/ Health disparities
/ Health economics
/ Medical research
/ Metabolism
/ Patients
/ Precision medicine
/ Privacy
/ Regulatory approval
/ Success
2026
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Do you wish to request the book?
Lost in translation: why genomic breakthroughs are not reaching patients
by
Field, Matt
, Calcino, Andrew
in
Accreditation
/ Autoimmunity
/ Bioinformatics
/ Biostatistics
/ Clinical trials
/ Disease
/ Editorial
/ FDA approval
/ Funding
/ Genetic markers
/ Genomics
/ Health disparities
/ Health economics
/ Medical research
/ Metabolism
/ Patients
/ Precision medicine
/ Privacy
/ Regulatory approval
/ Success
2026
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Lost in translation: why genomic breakthroughs are not reaching patients
Journal Article
Lost in translation: why genomic breakthroughs are not reaching patients
2026
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Overview
Despite revolutionary advances in genomic technologies, a persistent disconnect exists between research discoveries and clinical implementation. This translational gap stems from misaligned incentive and funding structures: researchers prioritise publications over clinical uptake, with funding ending at proof-of-concept; clinicians face time constraints and integration challenges; regulators struggle with rapidly evolving technologies and genomics-specific complexities including variant classification and data governance. We propose that dedicated translational medicine centres are essential to bridge this divide. These centres require multidisciplinary teams spanning clinician-scientists, regulatory affairs specialists, health economists, biostatisticians and bioinformaticians, providing end-to-end support from feasibility assessment through to regulatory approval. Success requires government investment, explicit health equity assessments and measuring achievement through clinical uptake rather than traditional academic metrics.
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