skip to content

Cambridge Public Health

 
Senior Visiting Research Fellow in the Department of Public Health and Primary Care

Dr Richard Milne is Senior Social Scientist in the Society and Ethics Research Group at the Wellcome Genome Campus and Senior Visiting Research Fellow in the Department of Public Health and Primary Care at the University of Cambridge. His research focusses on social and ethical questions associated with the development of new medical technologies, particularly related to dementia and genomic medicine. He is currently working on a Wellcome Trust–funded study of how experts and members of the public address ethical questions associated with the development of data-driven tools for the detection of cognitive decline.

Publications from Elements

Journal articles

2024

  • Costa, A. and Milne, R., 2024. Detecting value(s): Digital biomarkers for Alzheimer's disease and the valuation of new diagnostic technologies. Sociol Health Illn, v. 46
    Doi: 10.1111/1467-9566.13713
  • Costa, A., Atutornu, J., Bircan, T., Boraschi, D., Henriques, S., Milne, R., Okoibhole, L., Patch, C. and Middleton, A., 2024. From "Inclusion in What" to "Equity in What": (Re)Thinking the Question of In/Equity in Precision Medicine and Health. Am J Bioeth, v. 24
    Doi: http://doi.org/10.1080/15265161.2024.2303147
  • 2023

  • Ford, E., Milne, R. and Curlewis, K., 2023. Ethical issues when using digital biomarkers and artificial intelligence for the early detection of dementia. Wiley Interdiscip Rev Data Min Knowl Discov, v. 13
    Doi: 10.1002/widm.1492
  • Graham, M., Milne, R., Fitzsimmons, P. and Sheehan, M., 2023. TREs are still not about trust. J Med Ethics, v. 49
    Doi: 10.1136/jme-2023-109031
  • Staunton, C., Middleton, A., Milne, R., Ó Broin, P. and Calmasini, C., 2023. Governance, access, and harms: perspectives of the Irish public on the use of their genetic data for research
    Doi: http://doi.org/10.12688/wellcomeopenres.19075.1
  • Milne, R. and Patch, C., 2023. Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease. New Bioeth, v. 29
    Doi: http://doi.org/10.1080/20502877.2022.2109697
  • Milne, R., Aidid, U., Atutornu, J., Bircan, T., Boraschi, D., Costa, A., Henriques, S., Patch, C. and Middleton, A., 2023. What Difference Can Public Engagement in Genome Editing Make, and for Whom? Am J Bioeth, v. 23
    Doi: http://doi.org/10.1080/15265161.2023.2207545
  • Graham, M., Milne, R., Fitzsimmons, P. and Sheehan, M., 2023. Trust and the Goldacre Review: why trusted research environments are not about trust. J Med Ethics, v. 49
    Doi: 10.1136/jme-2022-108435
  • Middleton, A., Adams, A., Aidid, H., Atutornu, J., Boraschi, D., Borra, J., Bircan, T., Burch, C., Costa, A., Dickinson, A., Enticknap, A., Galloway, C., Gale, F., Garlick, E., Haydon, E., Henriques, S., Mitchell, M., Milne, R., Monaghan, J., Morley, KI., Muella Santos, M., Olivares Boldu, L., Olumogba, F., Orviss, K., Parry, V., Patch, C., Robarts, L., Shingles, S., Smidt, C., Tomlin, B. and Parkinson, S., 2023. Public engagement with genomics. Wellcome Open Res, v. 8
    Doi: http://doi.org/10.12688/wellcomeopenres.19473.2
  • Frisoni, GB., Altomare, D., Ribaldi, F., Villain, N., Brayne, C., Mukadam, N., Abramowicz, M., Barkhof, F., Berthier, M., Bieler-Aeschlimann, M., Blennow, K., Brioschi Guevara, A., Carrera, E., Chételat, G., Csajka, C., Demonet, J-F., Dodich, A., Garibotto, V., Georges, J., Hurst, S., Jessen, F., Kivipelto, M., Llewellyn, DJ., McWhirter, L., Milne, R., Minguillón, C., Miniussi, C., Molinuevo, JL., Nilsson, PM., Noyce, A., Ranson, JM., Grau-Rivera, O., Schott, JM., Solomon, A., Stephen, R., van der Flier, W., van Duijn, C., Vellas, B., Visser, LNC., Cummings, JL., Scheltens, P., Ritchie, C. and Dubois, B., 2023. Dementia prevention in memory clinics: recommendations from the European task force for brain health services. Lancet Reg Health Eur, v. 26
    Doi: 10.1016/j.lanepe.2022.100576
  • 2022

  • Milne, R., Costa, A. and Brenman, N., 2022. Digital phenotyping and the (data) shadow of Alzheimer's disease. Big Data Soc, v. 9
    Doi: http://doi.org/10.1177/20539517211070748
  • Brenman, NF. and Milne, R., 2022. “Ready for What?”: Timing and Speculation in Alzheimer’s Disease Drug Development Science Technology and Human Values, v. 47
    Doi: http://doi.org/10.1177/01622439211007196
  • Bunnik, EM., Smedinga, M., Milne, R., Georges, J., Richard, E. and Schermer, MHN., 2022. Ethical Frameworks for Disclosure of Alzheimer Disease Biomarkers to Research Participants: Conflicting Norms and a Nuanced Policy. Ethics Hum Res, v. 44
    Doi: http://doi.org/10.1002/eahr.500146
  • Costa, A. and Milne, R., 2022. Understanding 'passivity' in digital health through imaginaries and experiences of coronavirus disease 2019 contact tracing apps. Big Data Soc, v. 9
    Doi: http://doi.org/10.1177/20539517221091138
  • Milne, R., Morley, KI., Almarri, MA., Atutornu, J., Baranova, EE., Bevan, P., Cerezo, M., Cong, Y., Costa, A., Feijao, C., de Freitas, C., Fernow, J., Goodhand, P., Hasan, Q., Hibino, A., Houeland, G., Howard, HC., Hussain Sheikh, Z., Malmgren, CI., Izhevskaya, VL., Jędrzejak, A., Jinhong, C., Kimura, M., Kleiderman, E., Liu, K., Mascalzoni, D., Mendes, Á., Minari, J., Nicol, D., Niemiec, E., Patch, C., Prainsack, B., Rivière, M., Robarts, L., Roberts, J., Romano, V., Sheerah, HA., Smith, J., Soulier, A., Steed, C., Stefànsdóttir, V., Tandre, C., Thorogood, A., Voigt, TH., Wang, N., Yoshizawa, G. and Middleton, A., 2022. Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries Genetics in Medicine, v. 24
    Doi: http://doi.org/10.1016/j.gim.2022.01.002
  • Roberts, J., Milne, R., Middleton, A., Patc, C. and Morley, K., 2022. Opportunities for poaching: using the public’s enjoyment of popular culture to foster dialogues around genetics Journal of Science Communication, v. 21
    Doi: http://doi.org/10.22323/2.21060401
  • Walsh, S., Milne, R. and Brayne, C., 2022. Ethics, evidence, and the environment in dementia risk reduction - Authors' reply. Lancet Healthy Longev, v. 3
    Doi: http://doi.org/10.1016/S2666-7568(22)00037-X
  • Saunders, S., Ritchie, CW., Russ, TC., Muniz-Terrera, G. and Milne, R., 2022. Assessing and disclosing test results for 'mild cognitive impairment': the perspective of old age psychiatrists in Scotland. BMC Geriatr, v. 22
    Doi: http://doi.org/10.1186/s12877-021-02693-x
  • Atutornu, J., Milne, R., Costa, A., Patch, C. and Middleton, A., 2022. Towards equitable and trustworthy genomics research. EBioMedicine, v. 76
    Doi: http://doi.org/10.1016/j.ebiom.2022.103879
  • 2021 (Accepted for publication)

  • Dixon-Woods, M., Milne, R. and Sorbie, A., 2021 (Accepted for publication). What can data trusts for health research learn from participatory governance in biobanks? Journal of Medical Ethics,
  • Dixon-Woods, M., Milne, R. and Sorbie, A., 2021 (Accepted for publication). What can data trusts for health research learn from participatory governance in biobanks? Journal of Medical Ethics,
  • 2021

  • Savić-Kallesøe, S., Middleton, A. and Milne, R., 2021. Public trust and genomic medicine in Canada and the UK. Wellcome Open Res, v. 6
    Doi: http://doi.org/10.12688/wellcomeopenres.16831.2
  • Milne, R., Savić-Kallesøe, S. and Middleton, A., 2021. Public trust and genomic medicine in Canada and the UK Wellcome Open Research, v. 6
    Doi: http://doi.org/10.12688/wellcomeopenres.16831.1
  • Murtagh, MJ., Machirori, M., Gaff, CL., Blell, MT., de Vries, J., Doerr, M., Dove, ES., Duncanson, A., Hastings Ward, J., Hendricks-Sturrup, R., Ho, CWL., Johns, A., Joly, Y., Kato, K., Katsui, K., Kumuthini, J., Maleady-Crowe, F., Middleton, A., Milne, R., Minion, JT., Matshaba, M., Mulrine, S., Patch, C., Ryan, R. and Viney, W., 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, v. 6
    Doi: http://doi.org/10.12688/wellcomeopenres.17233.1
  • Walsh, S., Merrick, R., Milne, R. and Brayne, C., 2021. Aducanumab for Alzheimer's disease? BMJ, v. 374
    Doi: http://doi.org/10.1136/bmj.n1682
  • Milne, R., Morley, KI., Almarri, MA., Anwer, S., Atutornu, J., Baranova, EE., Bevan, P., Cerezo, M., Cong, Y., Costa, A., Critchley, C., Fernow, J., Goodhand, P., Hasan, Q., Hibino, A., Houeland, G., Howard, HC., Hussain, SZ., Malmgren, CI., Izhevskaya, VL., Jędrzejak, A., Jinhong, C., Kimura, M., Kleiderman, E., Leach, B., Liu, K., Mascalzoni, D., Mendes, Á., Minari, J., Nicol, D., Niemiec, E., Patch, C., Pollard, J., Prainsack, B., Rivière, M., Robarts, L., Roberts, J., Romano, V., Sheerah, HA., Smith, J., Soulier, A., Steed, C., Stefànsdóttir, V., Tandre, C., Thorogood, A., Voigt, TH., Wang, N., West, AV., Yoshizawa, G. and Middleton, A., 2021. Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries. Genome Med, v. 13
    Doi: http://doi.org/10.1186/s13073-021-00903-0
  • Rehm, HL., Page, AJH., Smith, L., Adams, JB., Alterovitz, G., Babb, LJ., Barkley, MP., Baudis, M., Beauvais, MJS., Beck, T., Beckmann, JS., Beltran, S., Bernick, D., Bernier, A., Bonfield, JK., Boughtwood, TF., Bourque, G., Bowers, SR., Brookes, AJ., Brudno, M., Brush, MH., Bujold, D., Burdett, T., Buske, OJ., Cabili, MN., Cameron, DL., Carroll, RJ., Casas-Silva, E., Chakravarty, D., Chaudhari, BP., Chen, SH., Cherry, JM., Chung, J., Cline, M., Clissold, HL., Cook-Deegan, RM., Courtot, M., Cunningham, F., Cupak, M., Davies, RM., Denisko, D., Doerr, MJ., Dolman, LI., Dove, ES., Dursi, LJ., Dyke, SOM., Eddy, JA., Eilbeck, K., Ellrott, KP., Fairley, S., Fakhro, KA., Firth, HV., Fitzsimons, MS., Fiume, M., Flicek, P., Fore, IM., Freeberg, MA., Freimuth, RR., Fromont, LA., Fuerth, J., Gaff, CL., Gan, W., Ghanaim, EM., Glazer, D., Green, RC., Griffith, M., Griffith, OL., Grossman, RL., Groza, T., Auvil, JMG., Guigó, R., Gupta, D., Haendel, MA., Hamosh, A., Hansen, DP., Hart, RK., Hartley, DM., Haussler, D., Hendricks-Sturrup, RM., Ho, CWL., Hobb, AE., Hoffman, MM., Hofmann, OM., Holub, P., Hsu, JS., Hubaux, J-P., Hunt, SE., Husami, A., Jacobsen, JO., Jamuar, SS., Janes, EL., Jeanson, F., Jené, A., Johns, AL., Joly, Y., Jones, SJM., Kanitz, A., Kato, K., Keane, TM., Kekesi-Lafrance, K., Kelleher, J., Kerry, G., Khor, S-S., Knoppers, BM., Konopko, MA., Kosaki, K., Kuba, M., Lawson, J., Leinonen, R., Li, S., Lin, MF., Linden, M., Liu, X., Udara Liyanage, I., Lopez, J., Lucassen, AM., Lukowski, M., Mann, AL., Marshall, J., Mattioni, M., Metke-Jimenez, A., Middleton, A., Milne, RJ., Molnár-Gábor, F., Mulder, N., Munoz-Torres, MC., Nag, R., Nakagawa, H., Nasir, J., Navarro, A., Nelson, TH., Niewielska, A., Nisselle, A., Niu, J., Nyrönen, TH., O'Connor, BD., Oesterle, S., Ogishima, S., Wang, VO., Paglione, LAD., Palumbo, E., Parkinson, HE., Philippakis, AA., Pizarro, AD., Prlic, A., Rambla, J., Rendon, A., Rider, RA., Robinson, PN., Rodarmer, KW., Rodriguez, LL., Rubin, AF., Rueda, M., Rushton, GA., Ryan, RS., Saunders, GI., Schuilenburg, H., Schwede, T., Scollen, S., Senf, A., Sheffield, NC., Skantharajah, N., Smith, AV., Sofia, HJ., Spalding, D., Spurdle, AB., Stark, Z., Stein, LD., Suematsu, M., Tan, P., Tedds, JA., Thomson, AA., Thorogood, A., Tickle, TL., Tokunaga, K., Törnroos, J., Torrents, D., Upchurch, S., Valencia, A., Guimera, RV., Vamathevan, J., Varma, S., Vears, DF., Viner, C., Voisin, C., Wagner, AH., Wallace, SE., Walsh, BP., Williams, MS., Winkler, EC., Wold, BJ., Wood, GM., Woolley, JP., Yamasaki, C., Yates, AD., Yung, CK., Zass, LJ., Zaytseva, K., Zhang, J., Goodhand, P., North, K. and Birney, E., 2021. GA4GH: International policies and standards for data sharing across genomic research and healthcare. Cell Genom, v. 1
    Doi: http://doi.org/10.1016/j.xgen.2021.100029
  • Murtagh, MJ., Machirori, M., Gaff, CL., Blell, MT., de Vries, J., Doerr, M., Dove, ES., Duncanson, A., Hastings Ward, J., Hendricks-Sturrup, R., Ho, CWL., Johns, A., Joly, Y., Kato, K., Katsui, K., Kumuthini, J., Maleady-Crowe, F., Middleton, A., Milne, R., Minion, JT., Matshaba, M., Mulrine, S., Patch, C., Ryan, R. and Viney, W., 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 Res, v. 6
    Doi: http://doi.org/10.12688/wellcomeopenres.17233.1
  • Brenman, NF., Milne, R. and Brayne, C., 2021. Trial readiness amongst EPAD longitudinal cohort study participants: Insights from the SPEAR study Alzheimer's & Dementia, v. 17
    Doi: 10.1002/alz.053622
  • Romano, V., Milne, R. and Mascalzoni, D., 2021. Italian public’s views on sharing genetic information and medical information: findings from the ‘Your DNA, Your Say’ study
    Doi: http://doi.org/10.12688/wellcomeopenres.16909.1
  • Milne, R., Altomare, D., Ribaldi, F., Molinuevo, JL., Frisoni, GB., Brayne, C. and European Task Force for Brain Health Services, , 2021. Societal and equity challenges for Brain Health Services. A user manual for Brain Health Services-part 6 of 6. Alzheimers Res Ther, v. 13
    Doi: http://doi.org/10.1186/s13195-021-00885-6
  • Brenman, N. and Milne, R., 2021. Lived time and the affordances of clinical research participation. Sociol Health Illn, v. 43
    Doi: http://doi.org/10.1111/1467-9566.13374
  • Romano, V., Milne, R. and Mascalzoni, D., 2021. Italian public's views on sharing genetic information and medical information: findings from the 'Your DNA, Your Say' study. Wellcome Open Res, v. 6
    Doi: http://doi.org/10.12688/wellcomeopenres.16909.1
  • Solomon, A., Stephen, R., Altomare, D., Carrera, E., Frisoni, GB., Kulmala, J., Molinuevo, JL., Nilsson, P., Ngandu, T., Ribaldi, F., Vellas, B., Scheltens, P., Kivipelto, M. and European Task Force for Brain Health Services, , 2021. Multidomain interventions: state-of-the-art and future directions for protocols to implement precision dementia risk reduction. A user manual for Brain Health Services-part 4 of 6. Alzheimers Res Ther, v. 13
    Doi: http://doi.org/10.1186/s13195-021-00875-8
  • 2020

  • Gregory, S., Bunnik, EM., Callado, AB., Carrie, I., De Boer, C., Duffus, J., Fauria, K., Forster, S., Gove, D., Knezevic, I., Laquidain, A., Pennetier, D., Saunders, S., Sparks, S., Rice, J., Ritchie, CW. and Milne, R., 2020. Involving research participants in a pan-European research initiative: the EPAD participant panel experience. Res Involv Engagem, v. 6
    Doi: http://doi.org/10.1186/s40900-020-00236-z
  • Milne, R. and Latimer, J., 2020. Alzheimer’s disease and the development of a post-genomic science New Genetics and Society, v. 39
    Doi: http://doi.org/10.1080/14636778.2019.1683213
  • Milne, R. and Brayne, C., 2020. We need to think about data governance for dementia research in a digital era. Alzheimers Res Ther, v. 12
    Doi: http://doi.org/10.1186/s13195-020-0584-y
  • Milne, R. and Costa, A., 2020. Disruption and dislocation in post-COVID futures for digital health. Big Data Soc, v. 7
    Doi: http://doi.org/10.1177/2053951720949567
  • Milne, R., 2020. Societal considerations in host genome testing for COVID-19. Genet Med, v. 22
    Doi: http://doi.org/10.1038/s41436-020-0861-y
  • Anna, M., Christine, P., Jonathan, R., Richard, M., Alessia, C., Lauren, R. and Jerome, A., 2020. Professional duties are now considered legal duties of care within genomic medicine. Eur J Hum Genet, v. 28
    Doi: http://doi.org/10.1038/s41431-020-0663-3
  • Middleton, A., Milne, R., Almarri, MA., Anwer, S., Atutornu, J., Baranova, EE., Bevan, P., Cerezo, M., Cong, Y., Critchley, C., Fernow, J., Goodhand, P., Hasan, Q., Hibino, A., Houeland, G., Howard, HC., Hussain, SZ., Malmgren, CI., Izhevskaya, VL., Jędrzejak, A., Jinhong, C., Kimura, M., Kleiderman, E., Leach, B., Liu, K., Mascalzoni, D., Mendes, Á., Minari, J., Wang, N., Nicol, D., Niemiec, E., Patch, C., Pollard, J., Prainsack, B., Rivière, M., Robarts, L., Roberts, J., Romano, V., Sheerah, HA., Smith, J., Soulier, A., Steed, C., Stefànsdóttir, V., Tandre, C., Thorogood, A., Voigt, TH., West, AV., Yoshizawa, G. and Morley, KI., 2020. Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? Am J Hum Genet, v. 107
    Doi: http://doi.org/10.1016/j.ajhg.2020.08.023
  • Middleton, A., Milne, R., Howard, H., Niemiec, E., Robarts, L., Critchley, C., Nicol, D., Prainsack, B., Atutornu, J., Vears, DF., Smith, J., Steed, C., Bevan, P., Scott, ER., Bobe, J., Goodhand, P., Kleiderman, E., Thorogood, A., Morley, KI. and Participant Values Work Stream of the Global Alliance for Genomics and Health, , 2020. Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data. Eur J Hum Genet, v. 28
    Doi: http://doi.org/10.1038/s41431-019-0550-y
  • 2019 (Accepted for publication)

  • Milne, R., 2019 (Accepted for publication). The rare and the common: scale and the genetic imaginary in Alzheimer's disease drug development New Genetics and Society,
    Doi: http://doi.org/10.1080/14636778.2019.1637718
  • 2019

  • Bartlett, R., Milne, R. and Croucher, R., 2019. Strategies to improve recruitment of people with dementia to research studies. Dementia (London), v. 18
    Doi: http://doi.org/10.1177/1471301217748503
  • Milne, R., Morley, KI., Howard, H., Niemiec, E., Nicol, D., Critchley, C., Prainsack, B., Vears, D., Smith, J., Steed, C., Bevan, P., Atutornu, J., Farley, L., Goodhand, P., Thorogood, A., Kleiderman, E., Middleton, A. and Participant Values Work Stream of the Global Alliance for Genomics and Health, , 2019. Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia. Hum Genet, v. 138
    Doi: http://doi.org/10.1007/s00439-019-02062-0
  • Middleton, A., Milne, R., Robarts, L., Roberts, J. and Patch, C., 2019. Should doctors have a legal duty to warn relatives of their genetic risks? Lancet, v. 394
    Doi: http://doi.org/10.1016/S0140-6736(19)32941-1
  • 2018 (Accepted for publication)

  • Milne, RJ., Diaz, A., Badger, S., Bunnik, E., Fauria, K. and Wells, K., 2018 (Accepted for publication). At, with and beyond risk: expectations of living with the possibility of future dementia Sociology of Health and Illness,
  • 2018

  • Bunnik, EM., Richard, E., Milne, R. and Schermer, MHN., 2018. On the personal utility of Alzheimer's disease-related biomarker testing in the research context. J Med Ethics, v. 44
    Doi: http://doi.org/10.1136/medethics-2018-104772
  • Gregory, S., Wells, K., Forysth, K., Latto, C., Szyra, H., Saunders, S., Ritchie, CW. and Milne, R., 2018. Research participants as collaborators: Background, experience and policies from the PREVENT Dementia and EPAD programmes. Dementia (London), v. 17
    Doi: http://doi.org/10.1177/1471301218789307
  • Middleton, A., Milne, R., Thorogood, A., Kleiderman, E., Niemiec, E., Prainsack, B., Farley, L., Bevan, P., Steed, C., Smith, J., Vears, D., Atutornu, J., Howard, HC. and Morley, KI., 2018. Attitudes of publics who are unwilling to donate DNA data for research. European Journal of Medical Genetics,
    Doi: http://doi.org/10.1016/j.ejmg.2018.11.014
  • Stites, SD., Milne, R. and Karlawish, J., 2018. Advances in Alzheimer's imaging are changing the experience of Alzheimer's disease. Alzheimers Dement (Amst), v. 10
    Doi: http://doi.org/10.1016/j.dadm.2018.02.006
  • 2017 (Accepted for publication)

  • Brayne, CEG. and Milne, R., 2017 (Accepted for publication). Perspectives on communicating biomarker-based assessments of Alzheimer’s disease to cognitively healthy individuals Journal of Alzheimer's Disease,
  • Milne, RJ., 2017 (Accepted for publication). From people with dementia to people with data: participation and value in Alzheimer’s disease research BioSocieties,
  • 2017

  • Milne, R., Diaz, A., Bunnik, E., Badger, S., Fauria, K., Molinuevo, JL., Wells, K., Ritchie, CW. and Brayne, C., 2017. [P4–377]: EXPECTATIONS RELATED TO THE IMPLICATIONS OF LEARNING ALZHEIMER's DISEASE RISK AMONG COGNITIVELY HEALTHY RESEARCH PARTICIPANTS Alzheimer's & Dementia, v. 13
    Doi: 10.1016/j.jalz.2017.06.2248
  • Atkinson, S., Milne, R., Badger, S. and Brayne, C., 2017. [P4–379]: RESEARCH PARTICIPANT PERSPECTIVES ON RECRUITMENT FROM EXISTING COHORTS IN DEMENTIAS PLATFORM U.K. Alzheimer's & Dementia, v. 13
    Doi: 10.1016/j.jalz.2017.06.2250
  • Milne, R. and Karlawish, J., 2017. Expanding engagement with the ethical implications of changing definitions of Alzheimer's disease The Lancet Psychiatry, v. 4
    Doi: http://doi.org/10.1016/S2215-0366(17)30089-5
  • 2016 (Accepted for publication)

  • Milne, R., Bunnik, E., Tromp, K., Bemelmans, S., Badger, S., Gove, D., Maman, M., Schermer, M., Truyen, L., Brayne, C. and Richard, E., 2016 (Accepted for publication). Ethical Issues in the Development of Readiness Cohorts in Alzheimer's Disease Research. Journal of Prevention of Alzheimer's Disease, v. 4
    Doi: http://doi.org/10.14283/jpad.2017.5
  • 2016

  • Bemelmans, SASA., Tromp, K., Bunnik, EM., Milne, RJ., Badger, S., Brayne, C., Schermer, MH. and Richard, E., 2016. Psychological, behavioral and social effects of disclosing Alzheimer's disease biomarkers to research participants: a systematic review Alzheimer's research & therapy, v. 8
  • Milne, R., 2016. In search of lost time: age and the promise of induced pluripotent stem cell models of the brain New Genetics and Society, v. 35
    Doi: http://doi.org/10.1080/14636778.2016.1257934
  • Bemelmans, SASA., Tromp, K., Bunnik, EM., Milne, RJ., Badger, S., Brayne, C., Schermer, MH. and Richard, E., 2016. Psychological, behavioral and social effects of disclosing Alzheimer's disease biomarkers to research participants: a systematic review Alzheimer's research & therapy, v. 8
  • 2015

  • Milne, R., 2015. Risk
    Doi: 10.5040/9781350042278-050
  • Milne, R., 2015. Labeling
    Doi: 10.5040/9781350042278-035
  • Milne, R., 2015. Safety
    Doi: 10.5040/9781350042278-051
  • Milne, R., 2015. Quality
    Doi: 10.5040/9781350042278-047
  • Milne, R., 2015. Local-Global
    Doi: 10.5040/9781350042278-036
  • Milne, R., 2015. Taste
    Doi: 10.5040/9781350042278-059
  • 2013

  • Milne, R., 2013. TRUST
  • 2012

  • Milne, R., 2012. Arbiters Of Waste: Date Labels, The Consumer And Knowing Good, Safe Food Sociological Review, v. 60
    Doi: http://doi.org/10.1111/1467-954X.12039
  • Milne, R., 2012. Pharmaceutical prospects: biopharming and the geography of technological expectations. Soc Stud Sci, v. 42
    Doi: http://doi.org/10.1177/0306312711436266
  • 2011

  • Milne, R., 2011. A focus group study of food safety practices in relation to listeriosis among the over-60s Critical Public Health, v. 21
    Doi: http://doi.org/10.1080/09581596.2011.616879
  • Milne, R., Wenzer, J., Brembeck, H. and Brodin, M., 2011. Fraught cuisine: Food scares and the modulation of anxieties Distinktion, v. 12
    Doi: http://doi.org/10.1080/1600910X.2011.576116
  • Milne, R., 2011. Of markets and medicines Science as Culture, v. 20
    Doi: http://doi.org/10.1080/09505431.2010.494720
  • 2010

  • Milne, R., 2010. Drawing bright lines: food and the futures of biopharming Sociological Review, v. 58
    Doi: http://doi.org/10.1111/j.1467-954X.2010.01915.x
  • 2008

  • Milne, R., 2008. Public attitudes toward molecular farming in the UK AgBioForum, v. 11
  • Other publications

    2022

  • Milne, R., Sheehan, M., Barnes, B., Kapper, J., Lea, N., N'Dow, J., Singh, G., Martín-Uranga, A. and Hughes, N., 2022. A concentric circles view of health data relations facilitates understanding of sociotechnical challenges for learning health systems and the role of federated data networks. Front Big Data, v. 5
    Doi: http://doi.org/10.3389/fdata.2022.945739
  • Saunders, S., Ritchie, CW., Russ, TC., Muniz-Terrera, G. and Milne, R., 2022. Correction to: Assessing and disclosing test results for 'mild cognitive impairment': the perspective of old age psychiatrists in Scotland. BMC Geriatr, v. 22
    Doi: http://doi.org/10.1186/s12877-022-02770-9
  • Book chapters

    2017

  • 2017. Emotion
  • 2011

  • Schaffer, SJ. and Schaffer, , 2011. Science