This viewer contains all of our work in a citation list view. Each one has several 'tags' so that you may browse as you choose.
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  1. Middleton A, Parry V, Borra J et al (2022) A public backlash towards genomics is a risk all of us working in genomics must share. The Lancet Regional Health - Europe [Online] vol. 15, article 100347. Available at: https://www.sciencedirect.com/science/article/pii/S2666776222000400#cebibl1 [Accessed : 1 Apil 2022]
  2. Hasan Q, Sahoo S (2022). The Role of Awareness in DNA Data Sharing and Public Opinion in India — Challenges Observed. A part of the Engagement & Society Research Seminar Webinar Series. 30 March. Online
  3. Atutornu J, Milne R, Costa A, Patch C, Middleton A (2022) Towards equitable and trustworthy genomics research. eBioMedicine [Online] vol. 76 Available at: https://www.sciencedirect.com/science/article/pii/S2352396422000639 [Accessed: 15 February 2022]
  4. Milne R, Morley KI, Almarri MA ...Atutornu J, Costa A, Howard HC, Patch C, Robarts L, Roberts J, Middleton A et al (2022) Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries. Genetics in Research [Online]  1-10. Available at: https://www.sciencedirect.com/science/article/pii/S1098360022000028 [Accessed: 4 February 2022]
  5. Holmes C (2022) Exploring race, diversity and genomics. [Blog] Wellcome Sanger Institute Blog. [Online] 27th January. Available at: https://sangerinstitute.blog/2022/01/27/exploring-race-diversity-and-genomics/     [Accessed: 27 January 2022]
  6. Government Office for Science (2022). Genomics Beyond Health: What could genomics mean for wider government? Project Report Jamnuary 2022. Foresight, pp. 171
  7. Chavarría-Soley G, Raventós H (2022). The case of Costa Rica (and Latin America): high acceptance of genetic research and data sharing, but low representation. A part of the Engagement & Society Research Seminar Webinar Series. 12 January. Online
  8. India Education Diary (2022) University Of Cambridge: New Centre To Foster Global Conversations About Ethical Issues Raised By Science [online] Available at: https://indiaeducationdiary.in/university-of-cambridge-new-centre-to-foster-global-conversations-about-ethical-issues-raised-by-science/ [Accessed 12 April 2022]
  9. Cambridge Independent (2021) New Kavli Centre for Ethics, Science, and the Public at University of Cambridge will explore ethical implications of scientific discovery [Online] Available at: https://www.cambridgeindependent.co.uk/news/new-kavli-centre-at-cambridge-will-explore-ethical-implicati-9231256/ [Accessed 28 January 2022]
  10. Cambridge Network (2021) New centre to foster global conversations about ethical issues raised by science. [Online] Available at: https://www.cambridgenetwork.co.uk/news/new-centre-foster-global-conversations-about-ethical-issues-raised-science [Accessed 12 January 2022]
  11. Business Wire (2021) The Kavli Foundation Launches Two Kavli Centers for Ethics, Science, and the Public to Engage the Public in Exploring Ethical Implications Born from Scientific Discovery. [Online] Available at: https://www.businesswire.com/news/home/20211209005349/en/The-Kavli-Foundation [Accessed 28 January 2022]
  12. Murtagh JM, Machirori M, Gaff CL ...Middleton A, Milne R, Patch C, et al (2021) Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation. Wellcome Open Research [Online] Vol 6 (Issue 311). Available at: https://wellcomeopenresearch.org/articles/6-311/v1 [Accessed: 12 January 2021]
  13. Knopper BM, Vears D, Ho WLC, ... Middleton A, et al (2021) Voices of GA4GH members: Collaborating in technology and policy development. Cell Genomics, [Online] vol. 1, issue 2, Available at: https://www.cell.com/cell-genomics/fulltext/S2666-979X(21)00043-4?utm [Accessed: 5 January 2022]
  14. Rehm HL, Page AJH, Smith L. ... Middleton A, Milne R, Patch C, et al (2021) GA4GH: International policies and standards for data sharing across genomic research and healthcare. Cell Genomics, [Online] vol. 1, issue 2, Available at: https://www.cell.com/cell-genomics/fulltext/S2666-979X(21)00036-7?utm [Accessed: 5 January 2022]
  15. Voigt T, Prainsack B (2021). “For-profit companies don’t care about patients’ well-being” Data and sharing in Germany. A part of the Engagement & Society Research Seminar Webinar Series. 10 November. Online
  16. Bressman N, Milne R (2021) Lived time and the affordances of clinical research participation. Sociology of Health and Illness, 43(9), pp.2031–2048  
  17. Milne R, Altomare D, Ribaldi F et al (2021) Societal and equity challenges for Brain Health Services. A user manual for Brain Health Services—part 6 of 6. Alzheimer’s Research & Therapy, 13(1)
  18. Cong Y (2021). Public Perspectives on Genetic Information: Is there an essential difference between China and the UK? A part of the Society and Ethics Research Seminar Webinar Series. 5 October. Online
  19. Borra JL (2021) Gnomes, Princess Von Schweetz, and Knocking boots. An exercise in socialising science. [Online] Medium: Bioeconomy.XYZ. 21st September Available at: https://medium.com/bioeconomy-xyz/gnomes-princess-von-schweetz-and-knocking-boots-f13d4aff27b3    [Accessed: 24 September 2021]
  20. Dickinson A (2021) Socialising the genome: building a bridge between the public and the science. Hospital Times, issue 2, pp 56-57
  21. Cosmo Genetics Film Festival (2021) Music of Life: What is a Gene. Online, St Petersburg, Russia. 9 August
  22. Milne R (2021). Trust and trustworthiness in genomic data sharing. A part of the Society and Ethics Research Seminar Webinar Series. 21 July. Online
  23. Roberts J (2021) Op Ed. 'Genetic counselling will be key to help parents navigate changes in prenatal testing.' The Guardian. 13 July. Available at: https://www.theguardian.com/commentisfree/2021/jul/13/genetic-counselling-parents-changes-prenatal-testing?utm_source=dlvr.it&utm_medium=facebook&fbclid=IwAR00ZItFuKpTIaiWhLpn0Vd_1uJftPF0uq-xKlsAR3NnKwa7VcN9k6bI7FQ#comment-150647966  [Accessed: 13 July 2021]
  24. Patch C (2021). Genomic Health Care: Where we are and possible futures. Keynote lecture of the Nursing, Genomics & Healthcare Conference. Wellcome Connecting Sciene Courses and Conferences. 21 July. Online
  25. Walsh S, Merrick R, Milne R & Brayne C (2021) Aducanumab for Alzheimer’s disease? The BMJ, vol. 374, issue 8299
  26. Middleton A, Parry V (2021). Socialising the Genome: Genomics, Communications and Public Trust. Invited speakers by the Public Policy Projects G20 Webinar event. 15 June. Online
  27. Middleton A (2021). ‘Your DNA, Your Say’ - a global public attitudes study on genomic data sharing. A part of the Society and Ethics Research Seminar Webinar Series. 26 May. Online
  28. Milne, R., Morley, K.I., Almarri, M.A. et al (2021). Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries. Genome Medicine [Online]. Volume 13, Article 92. Available at: https://doi.org/10.1186/s13073-021-00903-0.  [Accessed: 26 May 2021]
  29. Savić-Kallesøe S, Middleton A and Milne R (2021) Public trust and genomic medicine in Canada and the UK [version 1; peer review: 2 approved, 1 approved with reservations]. Wellcome Open Research, vol 6, issue 124 [online]. Available at: https://wellcomeopenresearch.org/articles/6-124   [Accessed: 29 June 2021] 
  30. Torres L. with Middleton A (2021) [online]. Interview for the UCLA Genetic Counseling Student Interest Group. University of California, Los Angeles. 4 May

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