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Rachel Horton
Rachel joined CELS in June 2018 to do a PhD. She is a clinical genetics registrar and is currently spending some time doing dedicated clinical ethics research.
Rachel’s research, funded by a Wellcome Trust Research Award for Health Professionals in Humanities and Social Sciences, explores what we should consider to be a genomic result. Genomic testing identifies the millions of variations that each of us has within our genetic code, and Rachel is interested in how and why decisions are made as to which of these variations should be considered the ‘result’ of a genomic test.
Rachel studied medicine at Oxford, doing an intercalated BA in Molecular Medicine in 2008. She worked as a junior doctor in the Severn deanery before moving to Southampton in 2015 to train in clinical genetics. She completed an MSc in Genomic Medicine at the University of Southampton in 2018.
Rachel was a Junior Research Fellow in Social Sciences at the Centre for Personalised Medicine from September 2021 to September 2025.
Websites
Recent publications
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Balancing the rights of the pre-symptomatic child to be found with the risk of harm to others from the screening process
Journal article
Lucassen A. and Horton R., (2024), European Journal of Human Genetics
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Discussion of off-target and tentative genomic findings may sometimes be necessary to allow evaluation of their clinical significance
Journal article
Horton RH. et al, (2024), Journal of Medical Ethics, 50, 295 - 298
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Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice
Journal article
Redman MG. et al, (2024), Journal of Medical Genetics, 61, 313 - 318
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Glowing gels and pipettes aplenty: how do commercial stock image banks portray genetic tests?
Journal article
Horton R. et al, (2024), European Journal of Human Genetics, 32, 456 - 460
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Challenges of using whole genome sequencing in population newborn screening.
Journal article
Horton R. et al, (2024), BMJ (Clinical research ed.), 384