Jerome Atutornu
Research Subjects
Research Interests
Jerome Atutornu has a total of 43 co-authors. Here are the top co-authors by number of shared publications:
- Anna Middleton
Faculty of Education, University of Cambridge, Cambridge, UK
7 shared publications - Richard Milne
Wellcome Sanger Institute
7 shared publications - Christopher M. Hayre
School of Dentistry and Medical Sciences, Faculty of Science and Health, Charles Sturt University, Wagga Wagga, NSW 2650, Australia
5 shared publications Adrian Thorogood
Centre of Genomics and Policy, McGill University, Montreal, Canada
3 shared publications- Christine Patch
Genomics England, Queen Mary University of London, Dawson Hall, London, UK
3 shared publications Claire Steed
Web Team, Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK
3 shared publications
Latest Publications
- 23 February 2024
- Published by Taylor & Francis in The American Journal of Bioethics
- Vol. 24 (3) , 89-91
From “Inclusion in What” to “Equity in What”: (Re)Thinking the Question of In/Equity in Precision Medicine and Health
- 23 February 2024
- Published by Taylor & Francis in The American Journal of Bioethics
- Vol. 24 (3) , 89-91
From “Inclusion in What” to “Equity in What”: (Re)Thinking the Question of In/Equity in Precision Medicine and Health
- 20 June 2023
- Published by Taylor & Francis in The American Journal of Bioethics
- Vol. 23 (7) , 58-60
What Difference Can Public Engagement in Genome Editing Make, and for Whom?
- 20 June 2023
- Published by Taylor & Francis in The American Journal of Bioethics
- Vol. 23 (7) , 58-60
What Difference Can Public Engagement in Genome Editing Make, and for Whom?
- Open Access
- 12 February 2022
- Published by Elsevier in EBioMedicine
- Vol. 76, 103879
Towards equitable and trustworthy genomics research
- 12 February 2022
- Published by Elsevier in EBioMedicine
- Vol. 76, 103879
Open AccessTowards equitable and trustworthy genomics research
- Open Access
- 1 September 2020
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 51 (3) , 443-450
A Survey Exploring Personalised Medicine amongst Radiography Academics within the United Kingdom
- 1 September 2020
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 51 (3) , 443-450
Open AccessA Survey Exploring Personalised Medicine amongst Radiography Academics within the United Kingdom
- Open Access
- 8 June 2020
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 28 (10) , 1301-1304
Professional duties are now considered legal duties of care within genomic medicine
The legal duty to protect patient confidentiality is common knowledge amongst healthcare professionals. However, what may not be widely known, is that this duty is not always absolute. In the United Kingdom, both the General Medical Council governing the practice of all doctors, as well as many other professional codes of practice recognise that, under certain circumstances, it may be appropriate to break confidentiality. This arises when there is a wider duty to protect the health of others, and when the risk of non-disclosure outweighs the potential harm from breaking confidentiality. We discuss this situation specifically in relation to genomic medicine where relatives in a family may have differing views on the sharing of familial genetic information. Overruling a patient’s wishes is predicated on balancing the duty of care towards the patient versus protecting their relative from serious harm. We discuss the practice implications of a pivotal legal case that concluded recently in the High Court of Justice in England and Wales, ABC v St Georges Healthcare NHS Trust & Ors. Professional guidance is already clear that genetic healthcare professionals must undertake a balancing exercise to weigh up contradictory duties of care. However, the judge has provided a new legal weighting to these professional duties: ‘The scope of the duty extends not only to conducting the necessary balancing exercise but also to acting in accordance with its outcome’ [1: 189]. In the context of genomic medicine, this has important consequences for clinical practice.
- 8 June 2020
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 28 (10) , 1301-1304
Open AccessProfessional duties are now considered legal duties of care within genomic medicine
The legal duty to protect patient confidentiality is common knowledge amongst healthcare professionals. However, what may not be widely known, is that this duty is not always absolute. In the United Kingdom, both the General Medical Council governing the practice of all doctors, as well as many other professional codes of practice recognise that, under certain circumstances, it may be appropriate to break confidentiality. This arises when there is a wider duty to protect the health of others, and when the risk of non-disclosure outweighs the potential harm from breaking confidentiality. We discuss this situation specifically in relation to genomic medicine where relatives in a family may have differing views on the sharing of familial genetic information. Overruling a patient’s wishes is predicated on balancing the duty of care towards the patient versus protecting their relative from serious harm. We discuss the practice implications of a pivotal legal case that concluded recently in the High Court of Justice in England and Wales, ABC v St Georges Healthcare NHS Trust & Ors. Professional guidance is already clear that genetic healthcare professionals must undertake a balancing exercise to weigh up contradictory duties of care. However, the judge has provided a new legal weighting to these professional duties: ‘The scope of the duty extends not only to conducting the necessary balancing exercise but also to acting in accordance with its outcome’ [1: 189]. In the context of genomic medicine, this has important consequences for clinical practice.
- Open Access
- 29 November 2019
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 28 (4) , 424-434
Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data
Public acceptance is critical for sharing of genomic data at scale. This paper examines how acceptance of data sharing pertains to the perceived similarities and differences between DNA and other forms of personal data. It explores the perceptions of representative publics from the USA, Canada, the UK and Australia (n = 8967) towards the donation of DNA and health data. Fifty-two percent of this public held ‘exceptionalist’ views about genetics (i.e., believed DNA is different or ‘special’ compared to other types of medical information). This group was more likely to be familiar with or have had personal experience with genomics and to perceive DNA information as having personal as well as clinical and scientific value. Those with personal experience with genetics and genetic exceptionalist views were nearly six times more likely to be willing to donate their anonymous DNA and medical information for research than other respondents. Perceived harms from re-identification did not appear to dissuade publics from being willing to participate in research. The interplay between exceptionalist views about genetics and the personal, scientific and clinical value attributed to data would be a valuable focus for future research.
- 29 November 2019
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 28 (4) , 424-434
Open AccessMembers of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data
Public acceptance is critical for sharing of genomic data at scale. This paper examines how acceptance of data sharing pertains to the perceived similarities and differences between DNA and other forms of personal data. It explores the perceptions of representative publics from the USA, Canada, the UK and Australia (n = 8967) towards the donation of DNA and health data. Fifty-two percent of this public held ‘exceptionalist’ views about genetics (i.e., believed DNA is different or ‘special’ compared to other types of medical information). This group was more likely to be familiar with or have had personal experience with genomics and to perceive DNA information as having personal as well as clinical and scientific value. Those with personal experience with genetics and genetic exceptionalist views were nearly six times more likely to be willing to donate their anonymous DNA and medical information for research than other respondents. Perceived harms from re-identification did not appear to dissuade publics from being willing to participate in research. The interplay between exceptionalist views about genetics and the personal, scientific and clinical value attributed to data would be a valuable focus for future research.
- Open Access
- 17 September 2019
- Published by Springer Nature in Human Genetics
- Vol. 138 (11-12) , 1237-1246
Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia
Trust may be important in shaping public attitudes to genetics and intentions to participate in genomics research and big data initiatives. As such, we examined trust in data sharing among the general public. A cross-sectional online survey collected responses from representative publics in the USA, Canada, UK and Australia (n = 8967). Participants were most likely to trust their medical doctor and less likely to trust other entities named. Company researchers were least likely to be trusted. Low, Variable and High Trust classes were defined using latent class analysis. Members of the High Trust class were more likely to be under 50 years, male, with children, hold religious beliefs, have personal experience of genetics and be from the USA. They were most likely to be willing to donate their genomic and health data for clinical and research uses. The Low Trust class were less reassured than other respondents by laws preventing exploitation of donated information. Variation in trust, its relation to areas of concern about the use of genomic data and potential of legislation are considered. These findings have relevance for efforts to expand genomic medicine and data sharing beyond those with personal experience of genetics or research participants.
- 17 September 2019
- Published by Springer Nature in Human Genetics
- Vol. 138 (11-12) , 1237-1246
Open AccessTrust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia
Trust may be important in shaping public attitudes to genetics and intentions to participate in genomics research and big data initiatives. As such, we examined trust in data sharing among the general public. A cross-sectional online survey collected responses from representative publics in the USA, Canada, UK and Australia (n = 8967). Participants were most likely to trust their medical doctor and less likely to trust other entities named. Company researchers were least likely to be trusted. Low, Variable and High Trust classes were defined using latent class analysis. Members of the High Trust class were more likely to be under 50 years, male, with children, hold religious beliefs, have personal experience of genetics and be from the USA. They were most likely to be willing to donate their genomic and health data for clinical and research uses. The Low Trust class were less reassured than other respondents by laws preventing exploitation of donated information. Variation in trust, its relation to areas of concern about the use of genomic data and potential of legislation are considered. These findings have relevance for efforts to expand genomic medicine and data sharing beyond those with personal experience of genetics or research participants.
- 1 June 2019
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 50 (2) , 345-347
Is Image Interpretation a Sustainable Form of Advanced Practice in Medical Imaging?
- 1 June 2019
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 50 (2) , 345-347
Is Image Interpretation a Sustainable Form of Advanced Practice in Medical Imaging?
- Top Cited PapersOpen Access
- 1 May 2019
- Published by Elsevier in European Journal of Medical Genetics
- Vol. 62 (5) , 316-323
Attitudes of publics who are unwilling to donate DNA data for research
- 1 May 2019
- Published by Elsevier in European Journal of Medical Genetics
- Vol. 62 (5) , 316-323
Top Cited PapersOpen AccessAttitudes of publics who are unwilling to donate DNA data for research
- 1 December 2018
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 49 (4) , 352-359
Personalised Medicine and Medical Imaging: Opportunities and Challenges for Contemporary Health Care
- 1 December 2018
- Published by Elsevier in Journal of Medical Imaging and Radiation Sciences
- Vol. 49 (4) , 352-359
Personalised Medicine and Medical Imaging: Opportunities and Challenges for Contemporary Health Care