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.
Please use the options below if you are searching for something specific! Alternatively, see the more visual catalogue viewer

  1. Milne R, and Costa A (2020) Disruption and Dislocation in Post-COVID Futures for Digital Health. Big Data & Society, vol. 7, issue 2
  2. Patch C (2020). How do we ‘do’ consent? Clinical & research models in genomic medicine 100,000 Genomes Project and beyond. Invited speaker as a part of the Society and Ethics Research Seminar Webinar Series. 12 August. Online
  3. Connecting Science. (2020) Immunology and identity: The implications of immunity passports. [Blog] Medium. [Online] Available at: https://medium.com/@connectingscience/immunology-and-identity-the-implications-of-immunity-passports-9d7d307cd292 [Accessed: 23 October 2020]
  4. Roberts J (2020). Problematic concepts in science communication: deficits, dialogues and expertise. Invited speaker as a part of the Society and Ethics Research Seminar Webinar Series. 28 July. Online
  5. Middleton A, Machirori M, Mabuka-Maroa J et al (2020) We need to talk about big data and genomics. Here's why – and how [Blog] World Economic Forum [Online] Available at: https://www.weforum.org/agenda/2020/07/why-we-need-a-public-conversation-about-big-data-and-genomics [Accessed: 25 September 2020]
  6. Middleton A, Machirori M, Mabuka-Maroa J et al (2020) Why it's time to bring genomics into the mainstream [Blog] World Economic Forum [Online] Available at: https://www.weforum.org/agenda/2020/07/bring-genomics-into-the-mainstream [Accessed: 25 September 2020]
  7. Middleton A, Machiori M, Mabuka-Maroa J 2020. We need to talk about big data and genomics. Here’s why – and how. The European Sting [Online]. 27th July. Available at: https://europeansting.com/2020/07/27/we-need-to-talk-about-big-data-and-genomics-heres-why-and-how/ [Accessed: 28 July 2020]
  8. Milne R (2020). Covid and Society: The implications of immunity passports. Invited speaker as a part of the Society and Ethics Research Seminar Webinar Series. 9 July. Online
  9. Middleton A. (2020) Ethics and genomic data sharing: global public attitudes. In: Board of Genetic Counselling India 5th Annual e-Conference 2020. 02 June. Online
  10. Tonkin E, Calzone K, Badzek L… Middleton, A, Patch C, et al (2020) A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery. Journal of Nursing Scholarship. Published online ahead of print, 27 June.
  11. Patch, C (2020). The impact of Covid-19 on rare disease communities. [Blog] Genomics Education Programme. 16h June. Available at: https://www.genomicseducation.hee.nhs.uk/blog/the-impact-of-covid-19-on-rare-disease-communities/ [Accessed: 24 June 2020].
  12. Milne R (2020) Societal considerations in host genome testing for COVID-19. Genetics in Medicine. Published online ahead of print, 8 June
  13. Patch C (2020). Implementing a hybrid clinical/research model in genomic medicine: post 100,000 Genomes Project. Spoken presentation. European Society of Human Genetics 2020 Virtual Conference. 8 June. Online
  14. Middleton A, Patch C, Roberts J, Milne R, Costa A, Robarts L, Atutornu J (2020) Professional duties are now considered legal duties of care within genomic medicine. European Journal of Human Genetics, vol. 28, pp 1301-1304
  15. Middleton A (2020). How to help society interact with genomic technology. Invited plenary speaker. European Society of Human Genetics 2020 Virtual Conference. 8 June. Online
  16. Cantú C, Cheng G, Doerr S, Frost J, Gambacorta L for the Bank for International Settlement (2020) On health and privacy: technology to combat the pandemic. BIS bulletin no. 17. 19th May
  17. Film made by Lauren Robarts. Society and Ethics Research Wellcome Genome Campus (2020) AGNC chair’s message to the AGNC membership on changes to the genomic medicine service in England. Available at:https://youtu.be/hxc3jJ60bHQ [Accessed: 19 May 2020]
  18. Patch C, Roberts L (2020). A conversation between Christine Patch of Genomics England and Lauren Roberts of SWAN. Session 0103: Diagnosing Undiagnosed Rare Disease Patients: Tools and Resources to strengthen the voice of the undiagnosed Rare Disease Community at the 10th European Conference on Rare Diseases & Orphan Products. Online, 15th May.
  19. Regulatory and Ethics Work Stream of the Global Alliance for Genomics and Health (2020) Responsible Data Sharing to Respond to the COVID-19 Pandemic: Ethical and Legal Considerations. [Online] 15 May. Available at: https://docs.google.com/document/d/1wK_NoNYXKy0ttTQ-ySHh3ZRpvPrLV4uPwV8FSq6BQ60/edit# [Accessed: 16 July 2020]
  20. Costa A, Frankova V (2020). What next after the search for a diagnosis? Hearing families’ experiences. Spoken presentation. Session 0104: What’s Next After the Search for a Diagnosis? The Future of Specialised Health Services at the 10th European Conference on Rare Diseases & Orphan Products. Online, 15th May.
  21. Eurordis Rare Diseases Europe (2020), The 10th European Conference on Rare Diseases & Orphan Products, 14 - 15 May. Online.
  22. Parkhill J, Lindsay SJ, Jones P... Roberts J, et al (2020) Oxford Biology Primers: Genomics. Oxford: Oxford University Press, pp 47-64
  23. Tonkin E, Calzone KA, Badzek L... Middleton A, Patch C, et al (2020) A Roadmap for Global Acceleration of Genomics Integration Across Nursing. Journal of Nursing Scholarship, vol. 52, issue 3, pp 329-338, May
  24. Raw Science Film Festival (2020) Music of Life: What is a Gene. The Shrine Auditorium, Los Angeles, USA. 16 April  
  25. Arney K (2020) Interview with Richard Milne and Anna Middleton. The Alzheimer’s Gene [Ingenious, BBC Radio 4] 9 April. Available at: https://www.bbc.co.uk/programmes/m000h0v8
  26. The Tulane Public Health & Social Justice Film Festival (2020) Voices of Genetic Counsellors: So Much More Than Just a Test. The Tidewater Building, Tulane University, New Orleans, USA. 3 April  
  27. Voight TH, Holtz V, Niemiec E, Howard HC, Middleton A, Prainsack B (2020) Willingness to donate genomic and other medical data: results from Germany. European Journal of Human Genetics, vol. 28, issue 4, pp 1000-1009
  28. Middleton A, Milne R, et al (2020) Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data. European Journal of Human Genetics, vol. 28, issue 4, pp 424-434, April
  29. Milne R, Middleton A (2020).  Your DNA, Your Say: Global public views on sharing genomic data. Invited presentation at Genomics in Health Implementation Forum. Online. 23rd March.
  30. Genetics Literacy Project 2020. Podcast: Can you inherit more than half your genes from one parent? Debunking genomic myths and misconceptions. Genetic Literacy Project: Science Not Ideology [Online]. Available at:https://geneticliteracyproject.org/2020/03/16/podcast-can-you-inherit-more-than-half-your-genes-from-one-parent-debunking-genomic-myths-and-misconceptions/ [Accessed: 17 March 2020]

Pages