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Number of items: 35.

Courbier, Sandra, Dimond, Rebecca and Bros-Facer, Virginie 2019. 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. Orphanet Journal of Rare Diseases 14 , 175. 10.1186/s13023-019-1123-4
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Dimond, Rebecca, Machin, Laura and Frith, Lucy 2019. Editorial: Towards a sociology of donation. Sociology of Health and Illness 41 (3) , pp. 549-552. 10.1111/1467-9566.12840
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Dimond, Rebecca 2018. Ethics of mitochondrial gene replacement therapy. In: Hostiuc, Sorin ed. Clinical Ethics at the Crossroads of Genetic and Reproductive Technologies, Academic,

González Santos, Sandra P., Stephens, Neil and Dimond, Rebecca 2018. Narrating the first "three-parent baby": The initial press reactions from the United Kingdom, the United States, and Mexico. Science Communication 40 (4) , pp. 419-441. 10.1177/1075547018772312
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Pond, Emily and Dimond, Rebecca 2018. Reproductive decision making: interviews with mothers of children with undiagnosed developmental delay. Journal of Community Genetics 9 (3) , pp. 315-325. 10.1007/s12687-017-0354-0
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Docherty, Freyja and Dimond, Rebecca 2018. 'Yeah that made a big difference!': The importance of the relationship between health professionals and fathers who have a child with Down Syndrome. Journal of Genetic Counseling 27 (3) , pp. 665-674. 10.1007/s10897-017-0171-y
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Dimond, Rebecca and Stephens, Neil 2018. Three persons, three genetic contributors, three parents: Mitochondrial donation, genetic parenting and the immutable grammar of the 'three x x'. Health 22 (3) , pp. 240-258. 10.1177/1363459316689380

Herbrand, Cathy and Dimond, Rebecca 2018. Mitochondrial donation, patient engagement and narratives of hope. Sociology of Health and Illness 40 (4) , pp. 623-638. 10.1111/1467-9566.12631
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Dimond, Rebecca and Stephens, Neil 2018. Legalising mitochondrial donation: Enacting ethical futures in UK biomedical politics. Cham, Switzerland: Palgrave Pivot. 10.1007/978-3-319-74645-6

Dimond, Rebecca and Krajewska, Atina 2017. Comment on mitochondrial replacement techniques and the birth of the 'first'. Journal of Law and the Biosciences 4 (3) , pp. 599-604. 10.1093/jlb/lsx021
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Dimond, Rebecca and Lewis, Jamie Thornton 2017. Paul Atkinson Festschrift: editorial. Qualitative Research 17 (2) , pp. 139-142. 10.1177/1468794116688414

Webb, Katie Louise, Bullock, Alison Deborah, Dimond, Rebecca and Stacey, M. 2016. Can a mobile app improve the quality of patient care provided by trainee doctors? Analysis of trainees case reports. BMJ Open 6 , 10.1136/bmjopen-2016-013075. 10.1136/bmjopen-2016-013075
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Dimond, Rebecca, Bullock, Alison Deborah, Lovatt, Joseph and Stacey, Mark Reginald William 2016. Mobile learning devices in the workplace: 'as much a part of the junior doctors' kit as a stethoscope'? BMC Medical Education 16 , 207. 10.1186/s12909-016-0732-z
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Stephens, Neil James and Dimond, Rebecca 2016. Debating CRISPR/cas9 and mitochondrial donation: continuity and transition performances at scientific conferences. Engaging Science, Technology, and Society 2 , pp. 312-321. 10.17351/ests2016.080
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Stephens, Neil James and Dimond, Rebecca 2015. Unexpected tissue and the biobank that closed: an exploration of value and the momentariness of bio-objectification processes. Life Sciences, Society and Policy 11 , 14. 10.1186/s40504-015-0032-0
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Stephens, Neil and Dimond, Rebecca 2015. Closure of a human tissue biobank: individual, institutional, and field expectations during cycles of promise and disappointment. New Genetics and Society 34 (4) , pp. 417-436. 10.1080/14636778.2015.1107469
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Dimond, Rebecca 2015. Social and ethical issues in mitochondrial donation. British Medical Bulletin 115 (1) , pp. 173-182. 10.1093/bmb/ldv037
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Dimond, Rebecca 2015. Techniques of donation: ‘three parents’, anonymity and disclosure. Journal of Medical Law and Ethics 3 (3) , pp. 165-173. 10.7590/221354015X14488767262831
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Bullock, Alison Deborah, Dimond, Rebecca, Webb, Katie Louise, Lovatt, Joseph, Hardyman, Wendy and Stacey, Mark Reginald William 2015. How a mobile app supports the learning and practice of newly qualified doctors in the UK: an intervention study. BMC Medical Education 15 (1) , 71. 10.1186/s12909-015-0356-8
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González-Santos, Sandra and Dimond, Rebecca 2015. Medical and scientific conferences as sites of sociological interest: A review of the field. Sociology Compass 9 (3) , pp. 235-245. 10.1111/soc4.12250
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Dimond, Rebecca, Bartlett, Andrew and Lewis, Jamie 2015. What binds biosociality? The collective effervescence of the parent conference. Social Science and Medicine 126 , pp. 1-8. 10.1016/j.socscimed.2014.12.005
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Dimond, Rebecca 2014. Parent-led conferences as sites of medical work. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 18 (6) , pp. 631-645. 10.1177/1363459314524806
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Dimond, Rebecca 2014. Dimond views on consultation process. Cardiff University.
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Dimond, Rebecca 2014. Dimond response to Department of Health mitochondria consultation. [Project Report]. Unpublished.
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Dimond, Rebecca 2014. Negotiating identity at the intersection of paediatric and genetic medicine: the parent as facilitator, narrator and patient. Sociology of Health and Illness 36 (1) , pp. 1-14. 10.1111/1467-9566.12035

Dimond, Rebecca 2014. Negotiating blame and responsibility in the context of a 'de novo' mutation. New Genetics and Society 33 (2) , pp. 149-166. 10.1080/14636778.2014.910450
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Banks, Timothy and Dimond, Rebecca 2013. Nettleton, Sarah: The Sociology of Health and Illness 3rd. ed [Book Review]. Medical Sociology Online 7 (2) , pp. 78-79.
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Dimond, Rebecca 2013. Patient and family trajectories of mitochondrial disease: diversity, uncertainty and genetic risk. Life Sciences, Society and Policy 9 (1) , 2. 10.1186/2195-7819-9-2
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Dimond, Rebecca 2013. Telecare technologies and the transformation of healthcare [Book Review]. New Genetics and Society 32 (1) , pp. 97-99. 10.1080/14636778.2012.743275

Dimond, Rebecca 2013. Managing the mutations. Britain in 2013 2013 , pp. 90-91.

Dimond, Rebecca and Hughes, Jacqueline 2013. Geneticization. In: Gabe, J. and Monaghan, L. eds. Key Concepts of Medical Sociology (2nd ed.), SAGE Key Concepts series, London: SAGE Publications, pp. 136-140.

Dimond, Rebecca 2012. Preventing mitochondrial disease: What about the patients? [Comment]. [Online]. BioNews 678: BioNews. Available at: http://www.bionews.org.uk/page_196131.asp

Dimond, Rebecca 2012. Ethical issues in treating mitochondrial disease [Comment]. [Online]. ESRC Genomics Network: ESRC. Available at: http://www.genomicsnetwork.ac.uk/cesagen/news/

Grant, Aimee, Mannay, Dawn, Alberti, Gabriella, Needs, Jackie and Dimond, Rebecca 2009. Postgraduate café papers 2008-9. [Working Paper]. School of Social Sciences Working Papers Series, vol. 122. Cardiff: Cardiff University.
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Gregory, M., Boddington, P., Dimond, Rebecca, Atkinson, P., Clarke, A. and Collins, Peter William 2007. Communicating about haemophilia within the family: the importance of context and of experience. Haemophilia 13 (2) , pp. 189-198. 10.1111/j.1365-2516.2006.01417.x

This list was generated on Wed Apr 8 04:20:46 2020 BST.