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  • Cardiff University (98102)
    • Centre for Economic and Social Aspects of Genomics (CESAGen) (114)
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Number of items at this level: 113.

A

Adam, Barbara Elisabeth 2007. Foreword. In: Hassan, Robert and Purser, Ronald E. eds. 24/7: Time and Temporality in the Network Society, Stanford, CA: Stanford University Press, ix-xi.

Adam, Barbara Elisabeth 2007. Mobilität / Verkehr. In: Heitkötter, M. and Schneider, M. eds. Zeitpolitisches Glossar: Grundbegriffe, Felder, Instrumente, Strategien, Tutzinger Materialien, vol. 90. Tutzing: Evangelische Akademie, pp. 51-53.

Adam, Barbara Elisabeth 2008. The timescapes challenge: engagement with the invisible temporal. In: Adam, Barbara Elisabeth, Hockey, Jenny, Thompson, Paul and Edwards, Rosalind eds. Researching Lives Through Time: Time, Generation and Life Stories, Timescapes Working Paper Series, vol. 1. Leeds: University of Leeds, pp. 7-12.

Adam, Barbara Elisabeth 2008. Future matters: futures known, created and minded. Twenty-First Century Society 3 (2) , pp. 111-116. 10.1080/17450140802095102

Adam, Barbara Elisabeth 2009. Zeit ist Geld: Geschwindigkeit aus zeitökonomischer und zeitökologischer Sicht. Presented at: Jenseits der Beschleunigung - Zeitpolitische Perspektiven postfossiler Mobilität, Evangelische Akademie, Tutzing, Germany, 30 April - 2 May 2009.
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Adam, Barbara Elisabeth 2009. Cultural future matters: an exploration in the spirit of Max Weber's methodological writings. Time & Society 18 (1) , pp. 7-25. 10.1177/0961463X08099941

Adam, Barbara Elisabeth 2009. Futures in the making: sociological practice and challenge. In: Jeffries, Vincent ed. Handbook of public sociology, Lanham, MD: Rowman & Littlefield Publishers, pp. 429-474.

Adam, Barbara Elisabeth 2010. Future Matters: Challenge for social theory and social inquiry. Cultura e comunicazione 1 , pp. 47-55.

Adam, Barbara Elisabeth 2010. History of the future: Paradoxes and challenges. Rethinking History 14 (3) , pp. 361-378. 10.1080/13642529.2010.482790

Adam, Barbara Elisabeth 2010. Zeitvielfalt in der Evolution aus gesellschaftstheoretischer Sicht. Presented at: Akademievorlesung: Zeit - Schlüsselvariable der Evolution, Berlin-Brandenburgische Akademie der Wissenschaften, Berlin, Germany, 4 February 2010.
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Adam, Barbara Elisabeth 2011. Wendell Bell and the sociology of the future: challenges past, present and future. Futures 43 (6) , pp. 590-595. 10.1016/j.futures.2011.04.007

Adam, Barbara Elisabeth and Groves, Christopher Robert 2011. Futures tended: care and future-oriented responsibility. Bulletin of Science, Technology & Society 31 (1) , pp. 17-27. 10.1177/0270467610391237

Arribas-Ayllon, Michael 2010. The politics of autonomy in genetic testing of children. In: Wieser, Bernhard and Berger, Wilhelm eds. Assessing life: on the organisation of genetic testing, München: Profil, pp. 17-50.

Arribas-Ayllon, Michael 2010. Beyond pessimism: the dialectic of promise and complexity in genomic research. Genomics, Society, and Policy 6 (2) , pp. 1-12. 10.1186/1746-5354-6-2-1
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Arribas-Ayllon, Michael 2011. The ethics of disclosing genetic diagnosis for Alzheimer's disease: do we need a new paradigm? British Medical Bulletin 100 (1) , pp. 7-21. 10.1093/bmb/ldr023

Arribas-Ayllon, Michael 2012. Personalized medicine and promissory science. In: Chadwick, Ruth ed. Encyclopedia of Applied Ethics (Second Edition), Elsevier, pp. 422-430. (10.1016/B978-0-12-373932-2.00428-2)

Arribas-Ayllon, Michael, Sarangi, Srikant Kumar and Clarke, Angus John 2008. The politics of autonomy in genetic testing of children. [Working Paper]. School of Social Sciences Working Papers Series, vol. 107. Cardiff: Cardiff University. Available at: http://www.caerdydd.ac.uk/socsi/resources/wp107.pd...
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Arribas-Ayllon, Michael, Sarangi, Srikant Kumar and Clarke, Angus John 2008. Professional ambivalence: accounts of ethical practice in childhood genetic testing. [Working Paper]. School of Social Sciences Working Papers Series, vol. 108. Cardiff: Cardiff University. Available at: http://www.caerdydd.ac.uk/socsi/resources/wp108.pd...
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Arribas-Ayllon, Michael, Sarangi, Srikant Kumar and Clarke, Angus John 2011. Genetic testing: accounts of autonomy, responsibility and blame. Genetics and Society, London: Routledge.

Arribas-Ayllon, Michael, Sarangi, Srikant Kumar and Clarke, Angus John 2011. Promissory strategies of personalisation in the commercialisation of genomic knowledge. Communication & Medicine 8 (1) , pp. 53-66. 10.1558/cam.v8i1.53

Arribas-Ayllon, Michael and Walkerdine, Valerie 2008. Foucauldian discourse analysis. In: Willig, Carla and Stainton-Rogers, Wendy eds. The Sage Handbook of Qualitative Research in Psychology, London: Sage, pp. 91-108.

Atkinson, Paul Anthony 2009. Ethics and ethnography. Twenty-First Century Society: Journal of the Academy of Social Sciences 4 (1) , pp. 17-30. 10.1080/17450140802648439

Atkinson, Paul Anthony 2009. The social organisation of aesthetics – a note. MAiA - Music and Arts in Action 2 (1) , pp. 69-72.

Atkinson, Paul Anthony 2009. Illness narratives revisited: the failure of narrative reductionism. Sociological Research Online 14 (5) , 16. 10.5153/sro.2030

Atkinson, Paul Anthony 2010. Making opera work: bricolage and the management of dramaturgy. MAiA - Music and Arts in Action 3 (1) , pp. 3-19.

Atkinson, Paul Anthony 2010. The contested terrain of narrative analysis - an appreciative response [Letter]. Sociology of Health & Illness 32 (4) , pp. 661-662. 10.1111/j.1467-9566.2010.01240_1.x

Atkinson, Paul Anthony and Coffey, Amanda Jane 2011. Analysing documentary realities. In: Silverman, David ed. Qualitative Research, London: Sage Publications Ltd, pp. 56-75.

Atkinson, Paul Anthony and Delamont, Sara 2010. Can the silenced speak? A dialogue for two unvoiced actors. International Review of Qualitative Research 3 (1) , pp. 11-15.
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B

Bhardwaj, Minakshi 2008. Ethics of energy technologies. UNESCO.

Bhardwaj, Minakshi 2008. Eating to order: consumers, business and the media have a big appetite for nutrigenomics. But is it really as nourishing as is claimed? ESRC Genomics Network Newsletter 7 , pp. 33-34.

Bhardwaj, Minakshi 2008. Biobanks and the notion of justice in health. In: Casabona, Romeo and Carlos, María eds. Biotecnología, desarrollo y justicia, Derecho y genoma humano, Bilbao: Editorial Comares, pp. 267-278.

Bhardwaj, Minakshi 2008. Gene-environment interactions and statistical validity: ethical concerns for biobanking. Presented at: Genomics and Society: Setting the Agendas Conference, Amsterdam, Netherlands, 17 - 18 April 2008.

Bhardwaj, Minakshi 2008. Choice, instinct and commercialisation: food rationing based on genes. Presented at: 22nd Annual Meeting of the European Society for Philosophy of Medicine and Healthcare, Tartu, Estonia, 20 - 23 August 2008.

Bhardwaj, Minakshi 2008. Energy: the variability of ethical principles and challenges of environmental governance. Presented at: 9th World Congress of Bioethics, Rijeka-Opatija, Croatia, 3 - 7 September 2008.

Bhardwaj, Minakshi 2008. Nutrigenomics commercialisation. Presented at: 9th World Congress of Bioethics,, Rijeka-Opatija, Croatia, 3 - 7 September 2008.

Bhardwaj, Minakshi 2008. The variability of ethical principles and challenges of environmental governance. Presented at: UNESCO conference on Ethics of Energy Technologies: Energy Equity and Human Security, Chennai, India, 22 - 23 September 2008.

Bhardwaj, Minakshi 2008. Ethical perspectives on the personalization of medicine and public health with special reference to the developments in nutritional genomics. Presented at: International Conference on Bioethics, Kodaikanaal, India, 24 -26 September 2008.

Bhardwaj, Minakshi 2008. Scanning the ethics of genomic technologies: retrospects and prospects. Presented at: International awareness workshop and training course on bioethics education, Karmathur, Tamil Nadu, India, 26-27th September 2008.

Bhardwaj, Minakshi 2008. Ethics of commercialisation of individualism and public health in genomics: some reflections on nutrigenomics. Presented at: 9th Asian Bioethics Congress ‘Bioethics in Asia, Jogyakarta, Indonesia., 3 - 7 November 2008.

C

Calnan, M., Tadd, Winifred, Calnan, S., Hillman, Alexandra, Read, Simon Mark and Bayer, Antony James 2013. 'I often worry about the older person being in that system': exploring the key influences on the provision of dignified care for older people in acute hospitals. Ageing and Society 33 (3) , pp. 465-485. 10.1017/S0144686X12000025
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CESAGEN, . 2008. Inquiry into genomic medicine: Evidence submitted on behalf of the ESRC Centre for Social and Economic Aspects of Genomics (CESAGEN), Cardiff and Lancaster Universities. CESAGEN. Available at: http://www.parliament.uk/business/committees/commi...

Chadwick, Ruth 2004. Nutrigenomics, individualism and public health. Proceedings of the Nutrition Society 63 , pp. 161-166. 10.1079/PNS2003329
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Chadwick, Ruth 2013. Ethical issues in personalized medicine. Drug Discovery Today: Therapeutic Strategies 10 (4) , e171-e174. 10.1016/j.ddstr.2013.05.001

Chadwick, Ruth 2014. The ethics of personalized medicine: a philosopher's perspective. Personalized Medicine 11 (1) , pp. 5-6. 10.2217/pme.13.98

Chadwick, Ruth and O'Connor, Alan 2013. Epigenetics and personalized medicine: prospects and ethical issues. Personalized Medicine 10 (5) , pp. 463-471. 10.2217/pme.13.35

Chadwick, Ruth and Strange, Heather 2015. Biobanking across borders: the challenges of harmonisation. In: Mascalzoni, Deborah ed. Ethics, Law and Governance of Biobanking, New York and London: Springer, pp. 133-139.

Chekar, Choon Key and Haran, Joan 2010. Bioethics in the age of new media [Book Review]. New Genetics and Society 29 (2) , pp. 221-223. 10.1080/14636778.2010.484224

Clarke, Angus J., Cooper, David Neil, Krawczak, Michael, Tyler-Smith, Chris, Wallace, Helen M., Wilkie, Andrew O. M., Raymond, Frances, Chadwick, Ruth, Craddock, Nicholas John, John, Rosalind Margaret, Gallacher, John and Chiano, Mathias 2012. 'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care. Human Genomics 6 , 11. 10.1186/1479-7364-6-11

D

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

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 2014. Negotiating identity at the intersection of paediatric and genetic medicine: the parent as facilitator, narrator and patient. Sociology of Health & Illness 36 (1) , pp. 1-14. 10.1111/1467-9566.12035

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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E

Eriksson, L., Stephens, Neil James and Webster, A. 2008. Stem cell spaces, places and flows [Editorial]. New Genetics and Society 27 (2) , pp. 83-85. 10.1080/14636770802076936

G

Glasner, Peter Egon 2007. Cowboy cloners, mavericks and kings: a cautionary tale of a promissory science. Twenty-First Century Society 2 (3) , pp. 265-274. 10.1080/17450140701631445

Gregory, Margaret Lynne, Middleton, Anna and Atkinson, Paul Anthony 2010. Timescapes and genescapes: the temporal organisation of family communication about genetic conditions. In: Bylund, Carma L. and Gaff, Clara Louise eds. Family Communication about Genetics: Theory and Practice, Oxford: Oxford University Press, pp. 87-101.

Groves, Christopher Robert 2010. The futures of causality: Hans Jonas and Gilles Deleuze. In: Poli, Roberto ed. Causality and Motivation, Philosophische Analyse, vol. 35. Germany: Ontos Verlag, pp. 151-170.

Groves, Christopher Robert 2011. Happiness and uncertainty. OurKingdom 2011 (29 Jun)

Groves, Christopher Robert 2011. The Political imaginary of care: Generic versus singular futures. Journal of International Political Theory 7 (2) , pp. 165-189. 10.3366/jipt.2011.0013
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Guo, Jingli, Liang, Jun, Zhang, Xiaotong, Judge, Paul, Wang, Xiuli and Green, Timothy 2016. Reliability analysis of MMCs considering sub-module designs with individual or series operated IGBTs. IEEE Transactions on Power Delivery Pwrd 32 (2) , pp. 666-677. 10.1109/TPWRD.2016.2572061
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H

Haran, Joan 2007. Managing the boundaries between maverick cloners and mainstream scientists: the life cycle of a news event in a contested field. New Genetics and Society 26 (2) , pp. 203-219. 10.1080/14636770701466980

Haran, Joan 2010. Redefining hope as praxis. Journal for Cultural Research 14 (4) , pp. 393-408. 10.1080/14797581003765341

Haran, Joan 2011. Roisin Ryan-Flood and Rosalind Gill (eds), Secrecy and silence in the research process: Feminist reflections. London and New York: Routledge, 2010. 336 pp (including index). ISBN 9780415452144 (hbk)  80.00; ISBN 9780415605175 (pbk)  22.50 [Book Review]. Qualitative Research 11 (2) , pp. 220-222. 10.1177/14687941110110020605

Hedgecoe, Adam 2009. "A form of practical machinery”: The origins of research ethics committees in the UK. Medical History 53 (3) , pp. 331-350. 10.1017/S0025727300000211
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Hedgecoe, Adam 2010. Bioethics and the reinforcement of socio-technical expectations. Social Studies of Science 40 (2) , pp. 163-186. 10.1177/0306312709349781
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Hedgecoe, Adam 2012. Trust and regulatory organisations: The role of local knowledge and facework in research ethics review. Social Studies of Science 42 (5) , pp. 662-683. 10.1177/0306312712446364
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Hedgecoe, Adam Michael 2008. From resistance to usefulness: sociology and the clinical use of genetic tests. BioSocieties 3 (2) , pp. 183-194. 10.1017/S1745855208006108

Hedgecoe, Adam Michael 2008. Research ethics review and the sociological research relationship. Sociology 42 (5) , pp. 873-886. 10.1177/0038038508094567

Hillman, Alexandra 2014. Why must I wait? Performing legitimacy in a hospital emergency department. Sociology of Health and Illness 36 (485) , pp. 485-499. 10.1111/1467-9566.12072
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Hillman, Alexandra, Tadd, Winifred, Calnan, Sian, Calnan, Michael, Bayer, Antony James and Read, Simon Mark 2013. Risk, governance and the experience of care. Sociology of Health and Illness 35 (6) , pp. 939-955. 10.1111/1467-9566.12017
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Hughes, Jacqueline 2010. After genetics: Huntington's disease, local data, global neuroscience. PhD Thesis, Cardiff University.
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K

Kitzinger, Jenny, Chimba, Mwenya Diana, Williams, Andy, Haran, Joan and Boyce, Tammy 2008. Gender, stereotypes and expertise in the press: how newspapers represent female and male scientists. [Project Report]. UK Resource Centre for Women in Science, Engineering and Technology (UKRC) and Cardiff University. Available at: http://cf.ac.uk/jomec/resources/Kitzinger_Report_2...
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L

Latimer, Joanna Elizabeth 2013. The gene, the clinic & the family: Diagnosing dysmorphology, reviving medical dominance. Genetics and Society, London: Routledge.
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Latimer, Joanna Elizabeth 2014. Guest editorial: Nursing, the politics of organisation and meanings of care. Journal of Research in Nursing 19 (7-8) , pp. 537-545. 10.1177/1744987114562151

Latimer, Joanna Elizabeth, Davis, Terence, Bagley, Mark Christopher and Kipling, David Glyn 2011. Ageing science, health care and social inclusion of older people. Quality in Ageing and Older Adults 12 (1) , pp. 11-16. 10.5042/qiaoa.2011.0140

Latimer, Joanna Elizabeth and Miele, Mara 2013. Naturecultures? Science, affect and the non-human. Theory Culture & Society 30 (7-8) , pp. 5-31. 10.1177/0263276413502088
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Latimer, Joanna Elizabeth and Thomas, Gareth Martin 2015. In/exclusion in the clinic: Down's Syndrome, dysmorphology, and the ethics of everyday medical work. Sociology 49 (5) , pp. 937-954. 10.1177/0038038515588470
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Lewis, Jamie Thornton and Bartlett, Andrew 2013. Inscribing a discipline: tensions in the field of bioinformatics. New Genetics and Society 32 (3) , pp. 243-263. 10.1080/14636778.2013.773172
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Lock, M. and Hedgecoe, Adam 2009. Apoe genotyping, risk estimates, and public understanding of susceptibility genes. In: Ballenger, Jesse F., Whitehouse, Peter, Lyketsos, Constantine, Rabins, Peter and Karlawish, Jason H. T. eds. Treating Dementia : Do We Have a Pill For It?, Baltimore, USA: Johns Hopkins University Press, pp. 231-249.

S

Sampson, Catherine and Atkinson, Paul Anthony 2011. Accounting for discovery: genetic scientists' narratives. Narrative Inquiry 21 (1) , pp. 88-108. 10.1075/ni.21.1.05sam

Scurr, Martin John, Brown, Clare M., Costa Bento, Diana Filipa, Betts, G., Rees, B. I., Hills, Robert Kerrin, Gallimore, Awen Myfanwy and Godkin, Andrew James 2015. Assessing the prognostic value of preoperative carcinoembryonic antigen-specific T-cell responses in colorectal cancer. JNCI Journal of the National Cancer Institute 107 (4) , djv001. 10.1093/jnci/djv001
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Stacey, Glyn and Stephens, Neil James 2012. Social science in a stem cell laboratory: what happened when social and life sciences met. Regenerative Medicine 7 (1) , pp. 117-126. 10.2217/rme.11.107

Stark, Laura and Hedgecoe, Adam 2009. A practical guide to research ethics. In: Bourgeault, Ivy, Dingwall, Robert and de Vries, Ray eds. The SAGE handbook of qualitative methods in health research, London, UK: Sage, pp. 589-607.

Stephens, Neil James 2008. Political interpretative flexibility and the economics of inflation and unemployment. [Working Paper]. School of Social Sciences Working Papers Series, vol. 114. Cardiff: Cardiff University. Available at: http://www.cardiff.ac.uk/socsi/resources/wp114.pdf
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Stephens, Neil James 2008. Closing the 'regulator's regress': making things work in stem cell laboratories. Presented at: Society for the Social Studies of Science conference, Rotterdam, Netherlands, 20 - 23 August 2008.

Stephens, Neil James 2012. Space, place and temporality in stem cell and cancer tissue banking: mediating between patient-donors and biomedical research. Social Theory and Health 10 (3) , pp. 245-264. 10.1057/sth.2012.5

Stephens, Neil James 2013. Growing meat in laboratories: the Promise, ontology, and ethical boundary-work of using muscle cells to make food. Configurations 21 (2) , pp. 159-181. 10.1353/con.2013.0013
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Stephens, Neil James, Atkinson, Paul Anthony and Glasner, Peter Egon 2008. The UK Stem Cell Bank as performative architecture. New Genetics and Society 27 (2) , pp. 87-98. 10.1080/14636770802076977

Stephens, Neil James, Atkinson, Paul Anthony and Glasner, Peter Egon 2008. The UK stem cell bank: securing the past, validating the present, protecting the future. Science as Culture 17 (1) , pp. 43-56. 10.1080/09505430701872970

Stephens, Neil James, Atkinson, Paul Anthony and Glasner, Peter Egon 2011. Internationaliser des standards, mettre en banque avec confiance: la mise en banque de cellules souches dans trois systèmes nationaux. Revue D'Anthropologie des Connaissances 5 (2) , pp. 260-286. 10.3917/rac.013.0260

Stephens, Neil James, Atkinson, Paul Anthony and Glasner, Peter Egon 2011. Documenting the doable and doing the documented: bridging strategies at the UK Stem Cell Bank. Social Studies of Science 41 (6) , pp. 791-813. 10.1177/0306312711423306

Stephens, Neil James, Atkinson, Paul Anthony and Glasner, Peter Egon 2013. Institutional imaginaries of publics in stem cell banking: the cases of the UK and Spain. Science as Culture 22 (4) , pp. 497-515. 10.1080/14636778.2013.764071
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Stephens, Neil James and Delamont, Sara 2009. 'They start to get malicia': teaching tacit and technical knowledge. British Journal of Sociology of Education 30 (5) , pp. 537-548. 10.1080/01425690903101031

Stephens, Neil James and Kanellopoulou, Nadja 2008. Internationalising stem cell banking? : challenges in harmonising the international movement of human embryonic stem cells. ESRC Genomics Network Newsletter 7 , pp. 28-30.

Stephens, Neil James, Lewis, Jamie Thornton and Atkinson, Paul Anthony 2013. Closing the regulatory regress: GMP accreditation in stem cell laboratories. Sociology of Health & Illness 35 (3) , pp. 345-360. 10.1111/j.1467-9566.2012.01482.x
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Strange, Heather 2010. Non-medical sex selection: ethical issues. British Medical Bulletin 94 (1) , pp. 7-20. 10.1093/bmb/ldq002

Strange, Heather 2015. P3-67 Patient and professional experiences with non-invasive prenatal diagnosis (NIPD) and testing (NIPT): social and ethical issues raised. Presented at: ISPD 19th International Conference on Prenatal Diagnosis and Therapy, Washington, DC, USA, 12–15 July 2015. , vol. S1. Prenatal Diagnosis, p. 109. 10.1002/pd.4617

T

Tadd, Winifred and Calnan, Michael 2009. Caring for older people: why dignity matters – the European experience. In: Nordenfelt, Lennart ed. Dignity in Care For Older People, Oxford: Wiley-Blackwell, pp. 119-145. (10.1002/9781444316414.ch6)

Tadd, Winifred, Hillman, Alexandra, Calnan, S., Calnan, M., Bayer, Antony James and Read, Simon Mark 2011. Dignity in practice: An exploration of the care of older adults in acute NHS Trusts. [Project Report]. HMSO. Available at: http://www.bgs.org.uk/pdf_cms/reference/Tadd_Digni...

Tadd, Winifred, Hillman, Alexandra, Calnan, Sian, Calnan, Mike, Bayer, Antony James and Read, Simon Mark 2011. Right place - wrong person: dignity in the acute care of older people. Quality in Ageing and Older Adults 12 (1) , pp. 33-43. 10.5042/qiaoa.2011.0143

Tadd, Winifred, Vanlaera, Linus and Gastmans, Chris 2010. Clarifying the concept of human dignity in the care of the elderly: A dialogue between empirical and philosophical approaches. Ethical Perspectives 17 (2) , pp. 253-281. 10.2143/EP.17.2.2049266

Tadd, Winifred, Woods, Robert, O'Neill, Martin, Windle, Gill, Read, Simon Mark, Seddon, Diane, Hall, Charlotte and Bayer, Anthony 2012. PEACH: Promoting Excellence in All Care Homes. [Project Report]. London: Prevention of Abuse and Neglect in the Institutional Care of Older Adults. Available at: https://www.cfmhas.org.uk/research/completed-proje...
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Thomas, Gareth, Roberts, Julie and Griffiths, Frances 2017. Ultrasound as a technology of reassurance?: How pregnant women and health care professionals articulate ultrasound reassurance and its limitations. Sociology of Health and Illness 39 (6) , pp. 893-907. 10.1111/1467-9566.12554
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Thomas, Gareth Martin 2014. Prenatal screening for down’s syndrome: parent and healthcare practitioner experiences. Sociology Compass 8 (6) , pp. 837-850. 10.1111/soc4.12185
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Thomas, Gareth Martin 2015. Un/inhabitable worlds: the curious case of Down’s syndrome. Somatosphere 2015 (29 Jul)
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Thomas, Gareth Martin 2016. An elephant in the consultation room? Configuring Down Syndrome in British antenatal care. Medical Anthropology Quarterly 30 (2) , pp. 238-258. 10.1111/maq.12222
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Thomas, Gareth Martin 2017. Picture perfect: ‘4D’ ultrasound and the commoditisation of the private prenatal clinic. Journal of Consumer Culture 17 (2) , pp. 359-377. 10.1177/1469540515602300
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Thomas, Gareth Martin and Rothman, Barbara Katz 2016. Keeping the backdoor to eugenics ajar?: Disability and the future of prenatal screening. AMA Journal of Ethics 18 (4) , pp. 406-415. 10.1001/journalofethics.2016.18.04.stas1-1604

Tupasela, Aaro and Stephens, Neil James 2013. The boom and bust cycle of biobanking - thinking through the life cycle of biobanks. Croatian Medical Journal 54 (5) , pp. 501-503. 10.3325/cmj.2013.54.501
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Watermeyer, Richard 2011. Challenges for university engagement in the UK: towards a public academe? Higher Education Quarterly 65 (4) , pp. 386-410. 10.1111/j.1468-2273.2011.00492.x

Watermeyer, Richard 2012. Confirming the legitimacy of female participation in science, technology, engineering and mathematics (STEM): evaluation of a UK STEM initiative for girls. British Journal of Sociology of Education 33 (5) , pp. 679-700. 10.1080/01425692.2012.678751

Watermeyer, Richard 2013. The presentation of science in everyday life: the science show. Cultural Studies of Science Education 8 (3) , pp. 737-751. 10.1007/s11422-013-9484-9

Welsh, Ian, Plows, Alexandra and Evans, Robert John 2007. Human rights and genomics: science, genomics and social movements at the 2004 London Social Forum. New Genetics and Society 26 (2) , pp. 123-135. 10.1080/14636770701466816

This list was generated on Sat Sep 21 13:27:08 2019 BST.