| Social and ethical issues in mitochondrial donation R Dimond British medical bulletin 115 (1), 173, 2015 | 80 | 2015 |
| Mobile learning devices in the workplace:‘as much a part of the junior doctors’ kit as a stethoscope’? R Dimond, A Bullock, J Lovatt, M Stacey BMC medical education 16 (1), 1-9, 2016 | 78 | 2016 |
| How a mobile app supports the learning and practice of newly qualified doctors in the UK: an intervention study A Bullock, R Dimond, K Webb, J Lovatt, W Hardyman, M Stacey BMC medical education 15 (1), 1-6, 2015 | 70 | 2015 |
| Share and protect our health data: an evidence based approach to rare disease patients’ perspectives on data sharing and data protection-quantitative survey and recommendations S Courbier, R Dimond, V Bros-Facer Orphanet journal of rare diseases 14, 1-15, 2019 | 63 | 2019 |
| Communicating about haemophilia within the family: the importance of context and of experience M Gregory, P Boddington, R Dimond, P Atkinson, A Clarke, P Collins Haemophilia 13 (2), 189-198, 2007 | 42 | 2007 |
| Legalising mitochondrial donation: enacting ethical futures in UK biomedical politics R Dimond, N Stephens Springer, 2018 | 28 | 2018 |
| What binds biosociality? The collective effervescence of the parent-led conference R Dimond, A Bartlett, J Lewis Social Science & Medicine 126, 1-8, 2015 | 26 | 2015 |
| Closure of a human tissue biobank: individual, institutional, and field expectations during cycles of promise and disappointment N Stephens, R Dimond New genetics and society 34 (4), 417-436, 2015 | 25 | 2015 |
| Three persons, three genetic contributors, three parents: Mitochondrial donation, genetic parenting and the immutable grammar of the ‘three x x’ R Dimond, N Stephens Health 22 (3), 240-258, 2018 | 23 | 2018 |
| Medical and scientific conferences as sites of sociological interest: a review of the field S González‐Santos, R Dimond Sociology Compass 9 (3), 235-245, 2015 | 22 | 2015 |
| Mitochondrial donation, patient engagement and narratives of hope C Herbrand, R Dimond Sociology of Health & Illness 40 (4), 623-638, 2018 | 20 | 2018 |
| Negotiating identity at the intersection of paediatric and genetic medicine: the parent as facilitator, narrator and patient R Dimond Sociology of health & illness 36 (1), 1-14, 2014 | 20 | 2014 |
| Narrating the first “three-parent baby”: The initial press reactions from the United Kingdom, the United States, and Mexico SP González Santos, N Stephens, R Dimond Science Communication 40 (4), 419-441, 2018 | 17 | 2018 |
| Can a mobile app improve the quality of patient care provided by trainee doctors? Analysis of trainees’ case reports K Webb, A Bullock, R Dimond, M Stacey BMJ open 6 (9), e013075, 2016 | 15 | 2016 |
| Unexpected tissue and the biobank that closed: an exploration of value and the momentariness of bio-objectification processes N Stephens, R Dimond Life Sciences, Society and Policy 11 (1), 1-15, 2015 | 15 | 2015 |
| Patient and family trajectories of mitochondrial disease: diversity, uncertainty and genetic risk R Dimond Life Sciences, Society and Policy 9 (1), 2, 2013 | 14 | 2013 |
| Techniques of Donation:'Three Parents' Anonymity and Disclosure R Dimond JMLE, Journal of Medical Law and Ethics 3, 165, 2015 | 11 | 2015 |
| Debating CRISPR/cas9 and mitochondrial donation: Continuity and transition performances at scientific conferences N Stephens, R Dimond Engaging Science, Technology, and Society 2, 312-321, 2016 | 9 | 2016 |
| Negotiating blame and responsibility in the context of a “de novo” mutation R Dimond New Genetics and Society 33 (2), 149-166, 2014 | 8 | 2014 |
| “Yeah that made a big difference!”: The importance of the relationship between health professionals and fathers who have a child with Down syndrome F Docherty, R Dimond Journal of genetic counseling 27, 665-674, 2018 | 7 | 2018 |
Neil StephensAssociate Professor in Technology and Society, University of BirminghamVerified email at bham.ac.uk
