Professor Janice McLaughlin
Professor of Sociology
- Email: firstname.lastname@example.org
- Telephone: +44 (0) 191 208 7511
- Fax: +44 (0) 191 208 7497
- Address: Sociology
Claremont Bridge Building
University of Newcastle
Newcastle upon Tyne
I have been at Newcastle University since 2001, when I joined as a lecturer. During my time here I have played various roles, including running our undergraduate degree programmes, being Executive Director of the Policy, Ethics and Life Sciences Research Centre and until recently Head of the Sociology Subject Area.
My research examines various aspects of childhood disability via empirical research and in partnership with families and disability organisations.
My google scholar profile can be found here:
1996 PhD Department of Government, University of Manchester.
1993 MA Political Science, Virginia Polytechnic Institute and State University.
1990 BA Politics Honours (2:1), University of Strathclyde.
I am both a member and a Trustee of the British Sociological Association
I am also co-editor of the Scandinavian Journal of Disability Research
My current primary research interest can be briefly represented as: exploring how childhood disability or illness is framed from within the worlds of medicine, community and family. Through this research interest crucial insights are being generated on the importance of the relationships between these different worlds in the production of meaning. In the process the work challenges existing perceptions within disability studies that children and their families are simple objects of medical inquiry, alongside challenging perceptions in medical sociology that disability is interesting when it happens to previously ‘normal’ adult bodies. Clearly explorations of family and kinship are central to such explorations and I am increasingly pursuing an interest in both the fluidity of kinship relations, which are not framed by biology, and the significance of genetics in ascribing particular narratives of what family is based on biological ties.
An additional long term research activity involves writing on contemporary feminist social theory, in particular in relation to identities, materiality and critical theory. These two areas of work come together at various points, particularly when exploring experiences of and ideas about kinship and care.
A wide selection of my publications can be downloaded from Newcastle University's 'e-prints service'.
Current and Recent Work
With Emma Clavering, Erica Haimes and Michael Wright I ran an ESRC project examining the intersections between genetics and kinship from a social anthropological perspective (https://www.ncl.ac.uk/peals/research/currentprojects/item/kinshipandgeneticjourneysastudyoftheexperiencesoffamilieswhoareref.html) between 2008 and 2011. The focus was on families who have a child referred to genetic services and examining over time how varied family members, including children themselves, incorporate and don't incorporate genetic meanings into their family narratives and vice versa. While the project is concluded we are still actively developing our publications from the project.
With Edmund Coleman-Fountain, Patrick Olivier, and Allan Colver I also led an ESRC project examining the embodied transitions disabled young people make as they move towards adulthood (https://www.ncl.ac.uk/peals/research/currentprojects/item/embodiedselvesintransitiondisabledyoungbodies.html). The project examined whether disability makes a difference in such transitions and if it does what kind of difference is that. We also examined whether pain is a meaningful concept to disabled young people and influential to how they think about their bodies. The work involved both qualitative interviews and alongside, creative work with both photography and artefact making with the research participants. Some of findings can also be found here: http://research.ncl.ac.uk/thebodymatters/
I have successfully supervised 14 PhD students to the completion of their studies and currently supervise 6 PhD students. The majority of these past and current students are ESRC funded.
I am happy to discuss potential PhD topics in the areas of disability, kinship and care, medical innovation and feminist social theory.
British Sociological Association Elected Trustee
Co-Editor of the Scandinavian Journal of Disability Studies Research
Previous member of the Editorial Board of Sociology.
ESRC, Referee Fellowship and Grant Proposals and End of Award Reports
Book Proposal Reviews for Routledge, Palgrave and Polity.
Journal Article Reviews for Sociology, Sociology of Health and Illness, Theory, Culture and Society, Social Science and Medicine, Social Research Methodology: Theory and Practice, European Journal of Health Management, Sociology of Health and Illness, Science Technology and Human Values and Feminist Theory, Women’s Studies International Forum, Community, Work and Family, Social Policy and Society, Journal of Applied Research, Diabetic Medicine, Health.
Interdependencies of Care in Families with Disabled Children and their Significance for Citizenship, International Interdisciplinary Symposium, Families, Rights, & Disability: Interdisciplinary, Innsbruck University, June 2017
Kinship and Childhood Disability: Exploring Shared Memories of the Past and Present, Society for the Study of Childhood in the Past, Annual Conference Durham University, September 2016.
The responsibility to build capability in the context of disability, Pluralities of Health Workshop, Tubingen, Germany, October 2016.
The Medical Reshaping of Disabled Bodies as a Response to Stigma and a Route to Normality, Shame, Stigma and Medicine Symposium, Trinity College Dublin, September 2015
Making the Good Life Via The Medical and Social Reshaping of Disabled Young Bodies’, Reappraising the Good Life Workshop, Gottingen University, February 2015.
(With Edmund Coleman-Fountain) ‘Unfinished Young Disabled Bodies: Practices and Stories of Body Intervention’, College of Education, Otago University, New Zealand, February 2014.
‘Who is Family?’ The Ethics of Family Involvement in Healthcare Conference, Centre for Bioethics, Singapore University, February 2013
‘About Care and Family’, The Ethics of Family Involvement in Healthcare Conference, Centre for Bioethics, Singapore University, February 2013.
'Families’ experiences of paediatric genetics: Findings from an ethnographic study'. British Society for Human Genetics Conference, 5th – 7th September, Warwick University, 2011
‘Potential familial and patient responses to gene therapy: lessons from current genetics provision in healthcare’ TREAT-NMD 2011 International Conference, Geneva, Nov, 2011
‘Working across disciplinary and institutional boundaries in health and social research.’ BSA Regional Postgraduate Workshop: Bridging the Gap: Translating knowledge into action in Health and Social Research. Newcastle University. 3rd June, 2010.
‘Modes of care and mothering: How does citizenship and care intersect in the lives of mothers of disabled children’?, ESRC Seminar Series ‘Parenting Cultures’, University of Kent, January, 2009.
Parental perspectives on evidence: When are parents experts?, European Academy of Childhood Disability, Vilnius, Lithuania, June, 2009
(with Emma Clavering) ‘How inclusion is operationalised in early year settings. Findings from a research study undertaken in Newcastle and Sheffield’. Twelfth Conference and Annual Meeting of the North of England Collaborative Cerebral Palsy Survey, Trevalyan College, University of Durham, 21st of March, 2007
'What makes looking after a baby with complex needs challenging? The perspective of parents’, North of England Paediatric Society, Centre for Life, Newcastle, 15th of June, 2007
‘The social, ethical and political exploration of genetics and the new life sciences’, Launch of the Institute of Health and Society, Newcastle University, 27th of October, 2006.
'Gendering the user and technological innovation,' International Summer Academy on Technology Studies, Austria, July. 2001
I teach a Stage 3 Module called 'Investigating the Body' within the BA Sociology undergraduate Programme
I have until recently taught the module 'Social Divisions' on the MA Sociology and Social Research
- Bertilsdotter Rosqvist H, Katsui H, McLaughlin J. Editorial review: Touring the archive 1999-2017 and mapping the future of Scandinavian Journal of Disability Research. Scandinavian Journal of Disability Research 2018, 20(1), 1-5.
- McLaughlin J. The Child in the Paediatric Genetics Clinic. Chichester: John Wiley & Sons Ltd, 2018. Available at: https://doi.org/10.1002/9780470015902.a0028017.
- Jackson K, Finch T, Kaner E, McLaughlin J. Understanding alcohol as an element of 'care practices' in adult White British women's everyday personal relationships: A qualitative study. BMC Women's Health 2018, 18(1), 137.
- McLaughlin J, Coleman-Fountain E. Visual Methods and Voice in Disabled Childhoods Research: Troubling Narrative Authenticity. Qualitative Research 2018, (ePub ahead of Print).
- McLaughlin J. The medical reshaping of disabled bodies as a response to stigma and a route to normality. Medical Humanities 2017, 43, 244-250.
- Rosqvist HB, Katsui H, McLaughlin J. Change and continuity in journal priorities. Scandinavian Journal of Disability Research 2016, 18(4), 281-283.
- McLaughlin J, Coleman-Fountain E, Clavering E. Disabled childhoods: Monitoring differences and emerging identities. London: Taylor and Francis Inc, 2016.
- McLaughlin J, Coleman-Fountain E, Clavering E. Disabled Childhoods: Monitoring Differences and Emerging Identities. Routledge, 2016.
- McLaughlin J. Family ties in genes and stories: The importance of value and recognition in the narratives people tell of family. Sociological Review 2015, 63(3), 626–643.
- McLaughlin J. The Gene, the Clinic and the Family: Diagnosing Dysmorphology, Reviving Medical Dominance [Book Review]. Sociology of Health and Illness 2015, 37(3), 485-486.
- Verkerk MA, Lindemann H, McLaughlin J, Scully JL, Kihlbom U, Nelson J, Chin J. Where families and healthcare meet. Journal of Medical Ethics 2015, 41(2), 183-185.
- McLaughlin J. Digital Imagery and Child Embodiment in Paediatric Genetics: Sources and Relationships of Meaning. Sociology 2014, 48(2), 216-232.
- McLaughlin J, Coleman-Fountain E. The Unfinished Body: The Medical and Social Reshaping of Disabled Young Bodies. Social Science & Medicine 2014, 120, 76-84.
- Coleman-Fountain E, McLaughlin J. The Interactions of Disability and Impairment. Social Theory and Health 2013, 11(2), 133-150.
- McLaughlin J. Understanding disabled families: Replacing tales of burden with ties of interdependency. In: Watson, N., Roulstone, A., Thomas, C, ed. Routledge Handbook of Disability Studies. Abingdon, Oxon, UK: Routledge, 2012, pp.402-413.
- McLaughlin J, Clavering EK. Visualising difference, similarity and belonging in paediatric genetics. Sociology of Health and Illness 2012, 34(3), 459-474.
- McLaughlin J, Phillimore P, Richardson D, ed. Contesting Recognition: Culture, Identity and Citizenship. Basingstoke: Palgrave Macmillan, 2011.
- McLaughlin J, Phillimore P, Richardson D. Introduction: Why Contesting Recognition?. In: McLaughlin, J., Phillimore, P., Richardson, D, ed. Contesting Recognition: Culture, Identity and Citizenship. Basingstoke: Palgrave Macmillan, 2011, pp.1-19.
- McLaughlin J. Modes of care and mothering: How does citizenship and care intersect in the lives of mothers of disabled children?. In: Dahl, HM; Keränen, M; Kovalainen, A, ed. Europeanization, Care and Gender: Global Complexities. Basingstoke, UK: Palgrave Macmillan, 2011, pp.94-107.
- McLaughlin J, Clavering EK. Questions of kinship and inheritance in pediatric genetics: substance and responsibility. New Genetics and Society 2011, 30(4), 399-413.
- Clavering EK, McLaughlin J. Children's participation in health research: from objects to agents?. Child: Care, Health and Development 2010, 36(5), 603-611.
- McLaughlin J. Where's the Harm? Challenging Bioethical Support of Prenatal Selection for Sexual Orientation. In: Scully, JS; Baldwin-Ragaven, LE; Fitzpatrick, P, ed. Feminist Bioethics: At the Centre, On the Margins. Baltimore, MD: The John Hopkins University Press, 2010, pp.174-189.
- McLaughlin J, Goodley D, Clavering E, Fisher P. Families Raising Disabled Children: Enabling Care and Social Justice. Basingstoke: Palgrave, 2008.
- McLaughlin J, Goodley D. Seeking and rejecting certainty: Exposing the sophisticated lifeworlds of parents of disabled babies. Sociology 2008, 42(2), 317-335.
- Clavering EK, McLaughlin J. Crossing multidisciplinary divides: Exploring professional hierarchies and boundaries in focus groups. Qualitative Health Research 2007, 17(3), 400-410.
- McLaughlin J. Conceptualising Intensive Caring Activities: the Changing Lives of Families with Young Disabled Children. Sociological Research Online 2006, 11(1).
- Richardson D, McLaughlin J, Casey ME, ed. Intersections between feminist and queer theory. Basingstoke: Palgrave Macmillan, 2006.
- McLaughlin J, Casey ME, Richardson D. Introduction: At the intersections of feminist and queer debates. In: Richardson, D; McLaughlin, J; Casey, ME, ed. Intersections Between Feminist and Queer Theory. Basingstoke: Palgrave Macmillan, 2006, pp.1-18.
- McLaughlin J. The return of the material: Cycles of theoretical fashion in lesbian, gay and queer studies. In: Diane Richardson, Janice McLaughlin and Mark E. Casey, ed. Intersections between feminist and queer theory. Basingstoke: Palgrave Macmillan, 2006, pp.59-77.
- McLaughlin J. Exploring diagnostic processes: Social science perspectives. Archives of Disease in Childhood 2005, 90(3), 284-287.
- McLaughlin J. Gendering Technological Change in Organisations. In: Rohracher H, ed. User Involvement in Innovation Processes. Profil-Verlag: Munich, 2005, pp.127-146.
- Casey ME, McLaughlin J, Richardson D. Locating sexualities: politics, identities and space. Sexualities 2004, 7(4), 387-390.
- McLaughlin J. Professional Translations of Evidence Based Medicine. In: Learmonth M; Harding N, ed. Unmasking Health Management: A Critical Text. Hauppauge, New York: Nova Science Publishers, 2004, pp.75-90.
- McLaughlin J. Feminist Social and Political Theory : Contemporary Debates and Dialogues . Basingstoke: Palgrave Macmillan, 2003.
- McLaughlin J. Risky Professional Boundaries: Articulations of the Personal Self by Antenatal Screening Professionals’. Journal of Health, Organization and Management 2003, 17(4), 264-279.
- McLaughlin J. Screening networks: Shared agendas in feminist and disability movement challenges to antenatal screening and abortion. Disability and Society 2003, 18(3), 297-310.
- McLaughlin J. EBM and risk : Rhetorical resources in the articulation of professional identity. Journal of Management in Medicine 2001, 15(5), 352-363.
- McLaughlin J, Rosen P, Skinner D, Webster A. Valuing Technology: Organisations, Culture and Change. London: Routledge, 1999.