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Anneke Lucassen

Professor of Genomic Medicine. Director of the Centre for Personalised Medicine


My research career started by investigating the molecular genetics of common diseases in the 1990s (during my DPhil in Oxford) with an ambition to translate laboratory findings into the clinic to improve the identification and management of heritable diseases. I soon realised that in order to do so effectively, we first needed to know how to address some of the ethical and legal issues that arise in genetic- and genomic- medicine, and this has been the focus of my research ever since.

As professor of Clinical Genetics at the University of Southampton I set up a translational research group with expertise in molecular research, social science research, and direct contact with patients to provide an effective translation pipeline, focusing on the anticipation -and removal - of barriers to implementation. It functioned as an ELSA lab: addressing the ethical, legal and social aspects of developments in big data relevant to health, and I co-led one of 5 themes within the Southampton NIHR Biomedical Research Centre [Data, Health and Society] until 2023

I was delighted to move [back] to Oxford in September 2021 and bring this research to the Centre for Human Genetics, where our research programme addresses what needs to happen to ensure the benefits of genomic discovery have direct relevance to patients and society. We have made field changing contributions to understanding the ethical aspects of for example: misattributed genetic relationships; familial contact tracing in genetics; unanticipated clinical predictions from genomic findings genetic testing of children for adult diseases; high rates of spurious results from direct to consumer genetic tests; the hybrid territory between research and clinical practice.  These have been incorporated into clinical guidelines and position statements.

Our research outputs have helped initiate and shape policy via various national roles. For example, I was a Nuffield Council of Bioethics member from 2009-2015; I sat on the Genomics England Ethics Advisory committee from 2014 to 2024. I was the inaugural chair of the British Society for Genetic Medicine (BSGM) Ethics and Policy committee, and chaired the society from 2016-2020. I chaired the ethics advisory committee of UK Biobank (from 2019-2025) and the joint committee of genomic medicine- JCGM (a royal college of physician/ pathology/ BSGM committee) from 2021-2025). Since 2022 I have been a member for the National Screening Committee.

I am an Honorary Consultant in Clinical Genetics (anneke.lucassen@ouh.nhs.uk) 

 

 

Recent publications

Determining a role for Patient and Public Involvement and Engagement (PPIE) in genomic data governance for cancer care

Journal article

Sahan K. et al, (2026), European Journal of Human Genetics, 34, 1081 - 1086

Missed cases or unreported signals? Genomic newborn screening and the architecture of what counts.

Journal article

Carley HM. and Lucassen AM., (2026), European journal of human genetics : EJHG

Who and how we engage: A systemic mapping of stakeholder perspectives on genomic newborn screening.

Journal article

Phillips A. et al, (2026), European journal of human genetics : EJHG

Reducing the diagnostic odyssey in rare disease: why screening is not the only answer.

Journal article

Wright CF. et al, (2026), Nature medicine

From Scale to Situated: Sociotechnical Imaginaries and the Configuration of Algorithmic Health Research

Journal article

Lyle K. et al, (2026), Sociology of Health & Illness, 48

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

Journal article

Weller S. and Lucassen A., (2026), European journal of human genetics : EJHG