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. Milne R (2021). Trust and trustworthiness in genomic data sharing. A part of the Society and Ethics Research Seminar Webinar Series. 21 July. Online
  2. Roberts J (2021) Op Ed. 'Genetic counselling will be key to help parents navigate changes in prenatal testing.' The Guardian. 13 July. Available at:  [Accessed: 13 July 2021]
  3. Walsh S, Merrick R, Milne R & Brayne C (2021) Aducanumab for Alzheimer’s disease? The BMJ, vol. 374, issue 8299
  4. 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
  5. 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
  6. 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:  [Accessed: 26 May 2021]
  7. 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:   [Accessed: 29 June 2021] 
  8. Torres L. with Middleton A (2021) [online]. Interview for the UCLA Genetic Counseling Student Interest Group. University of California, Los Angeles. 4 May
  9. Middleton A (2021) Your DNA, Your Say: Global public attitudes towards genomic data sharing.Part of the Wellcome Connecting Science Personal Genomics Virtual Conference, 28 April, online. 
  10. Milne R, Sorbie A, Dixon-Woods M, (2021) What can data trusts for health research learn from participatory governance in biobanks. Journal of Medical Ethics. Published Online First: 19 March 2021. doi:10.1136/medethics-2020-107020
  11. Middleton A, (2021) Master multi-stakeholder collaboration, and it will be possible for the EU to master genomic data sharing. EU Reporter Online. Available at: Accessed 15 March 2021.
  12. Middleton A (2021) Your DNA Your Say. 9th Presidency European Personalised Medicine Alliance Conference. 8th May, virtual
  13. Tutty E, Hickerton C, Terrill B, Middleton A (2021) The expectations and realities of nutrigenomic testing in Australia: A qualitative study on-line.  Available at:
  14. J. Hammond, I. Garner, M. Hill, C. Patch, et al., Animation or leaflet: Does it make a difference when educating young people about genome sequencing?, Patient Educ Couns,
  15. Chavarria-Soley G, Francis-Cartin F, Jimenez-Gonzalez F, Ávila-Aguirre A, Castro-Gozez MJ, Robarts L, Middleton A, Raventós H (2021) Attitudes of Costa Rican individuals towards donation of personal genetic data for research. Personalized Medicine. Published online ahead of print, 12 February. Available at:   [Accessed: 15 February 2021]
  16. Archer L (2021). Engaging young people with STEM: A Science Capital approach. Invited speaker as a part of the Society and Ethics Research Seminar Webinar Series. 8 February. Online
  17. Middleton A (2020). Genetic counselling in the future - what are the challenges and what are the existing opportunities. Delivered lecture  on the Genomic Practice for Genetic Counsellors course. Advanced Courses and Scientific Conferences, Wellcome Connecting Science, online, 4 February.
  18. Wigley, Chris (2021). Prof Anna Middleton: Starting genomic conversations with X-Men [The G Word: Genetics England Podcast] Season 1, episode 4, 3rd February. Available at:   [accessed: 19 February]
  19. McEwan A, Patch C, Biesecker B (2021) Second World Congress on Genetic Counseling: An introduction to the special issue. Journal of Genetic Counseling, vol. 30, issue 1, pp 5-6
  20. Milne R, Costa A (2021) Covid, Cognition and the Spaces of Digital Health. Part of the series Health, Medicine and Agency, 19th January, Centre for Research in the Arts, Social Sciences and Humanities (CRASSH) of Cambridge University, online
  21. Roberts J (2020) Genetics and genomics on screen. [Blog] Genomics Education Programme, Health Education England. [Online] 21 December. Available at:   [Accessed: 22 December 2020]
  22. Milne R (2020) Dementia Prediction and Risk Reduction: Socio-cultural Insights, Ethical Reflections and Future Developments. Socio-cultural Insights, Ethical Reflections and Future Developments International Online Symposium, 7th December, University Medical Center Göttingen (UMG), Germany in cooperation with University of Haifa, Israel with funding from the German-Israeli Foundation for Scientific Research and Development (GIF), online
  23. Milne R (2020) Are we ready to fail? Speculation and ‘soft’ failure in Alzheimer’s disease drug development. Part of the Medical Anthropology Webinar Series, 2nd December,  London School of Hygiene and Tropical Medicine, online
  24. Roberts, J (2020). Empowering People [exhibit/stand]. Exhibited at RAREfest2020, 28 November 2020 (online)
  25. Middleton A, Robarts L (2020). Voices of Genetic Counsellors: So Much More Than Just a Test [poster/film]. Exhibited at RAREfest2020, 28 November 2020 (online)
  26. Middleton A et al (2020). Music of Life: What is a Gene [poster/film]. Exhibited at RAREfest2020, 28 November 2020 (online)
  27. Middleton A (2020) Delivered lecture on the Molecular Pathology and Diagnosis of Cancer course. Advanced Courses and Scientific Conferences, Connecting Science, Wellcome Genome Campus. online, 26 November
  28. Milne R (2020) Public perspectives on the donation and sharing of genomic and health information: findings of a global study. Part of the Digital Health webinar series, 24th November,  4th annual meeting of the ÖPPM (Österreichische Plattform Für Personalisierte Meizin in Austria), online
  29. de Wert G, Dondorp W, Clarke A.... Howard H, Patch C, et al. (2020) Opportunistic genomic screening. Recommendations of the European Society of Human Genetics. European Journal of Human Genetics [Online]. Available at:   [Accessed: 3 December 2020]
  30. Lewis C, Hammon J, Hill M, Searle B, Hunter A, Patch C, Chitty LS, Sanderson SC (2020) Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100, 000 Genomes Project. European Journal of Medical Genetics, vol. 63, issue 11, November