Albrecht, G.L. (1992) The Disability Business. Rehabilitation in America. Newbury Park, CA and London: Sage.
Albrecht, G.L., Seelman, K.D. and Bury, M. (eds.) (2001) The formation of disability studies. In: Handbook of Disability Studies. London: Sage.
Anderson, R. and Bury, M. (eds.) (1988) Living with Chronic Illness. The Experience of Patients and Their Families. London: Unwin Hyman.
Barnes, C. (2012) Understanding the social model of disability: Past, present and future. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 12–29.
Bê, A. (2012) Feminism and disability: A cartography of multiplicity. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 363–375.
Beck, U. (2012) Redefining the sociological project: The cosmopolitan challenge. Sociology 46 (1): 7–12.
Bickenbach, J.E. (2012) The international classification of functioning, disability and health and its relationship to disability studies. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 51–66.
Bilge, S. (2010) Feminist outlooks on intersectionality. Diogenes 225 (1): 58–72.
Blaxter, M. (1976) The Meaning of Disability: A Sociological Study of Impairment. London: Heinemann.
Burawoy, M. (2005) For public sociology. American Sociological Review 7 (February): 4–28.
Bury, M. (1991) The sociology of chronic illness: A review of research and prospects. Sociology of Health and Illness 13 (4): 167–182.
Bury, M. (2010) Chronic illness, self-management and the rhetoric of empowerment. In: G. Scambler and S. Scambler (eds.) New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld. Basingstoke, UK: Palgrave Macmillan, pp. 161–179.
Cabinet Office. (2004) Improving the Life Chances of Disabled People. London: The Prime Minister's Strategy Unit.
Campbell, J. and Oliver, M. (1996) Disability Politics: Understanding Our Past, Changing Our Future. London: Routledge.
Charmaz, K. (1983) Loss of self: A fundamental form of suffering in the chronically ill. Sociology of Health and Illness 5: 168–195.
Cockerham, W.C. (2004) Medical Sociology, 9th edn. London: Pearson Education.
CRPD. (2006) United Nations convention on the rights of people with disabilities, http://www.un.org/disabilities/default.asp?navid=14&pid=150, accessed March 2012.
Durkheim, E. ([1895] 1964) Rules of Sociological Method. New York: Free Press.
Equality & Human Rights Commission. (2010) The United Nations Conventions on the Rights of People with Disabilities: A Guide for Disabled People and Disabled People's Organisations. London: EHRC.
Equality & Human Rights Commission. (2011a) What we do and how we do it, http://www.equalityhumanrights.com/about-us/vision-and-mission/, accessed 3 April 2011.
Equality & Human Rights Commission. (2011b) Vision and mission statement, http://www.equalityhumanrights.com/about-us/, accessed 3 April 2011.
Foucault, M. (1965) Madness and Civilisation. The History of Insanity in the Age of Reason. New York: Random House.
Foucault, M. (1973) The Birth of the Clinic. An Archaeology of Medical Perception. London: Tavistock.
Garland-Thomson, R. (2005) Feminist disability studies. Signs: The Journal of Women in Culture and Society 30 (2): 1577–1587.
Gerhardt, U. (1989) Ideas about Illness: An Intellectual and Political History of Medical Sociology. London: Macmillan.
Goffman, E. (1961) Asylums. Essays on the Social Situation of Mental Patients. New York: Anchor, Doubleday.
Goffman, E. ([1963] 1968) Stigma. Notes on the Management of Spoiled Identity. Harmondsworth, UK: Penguin.
HEFCE. (2006) RAE2008, Panel Criteria and Working Methods, Panel J Bristol: HEFCE, pp. 1–82.
Hunt, P. (ed.) (1966) Stigma: The Experience of Disability. London: Chapman.
Kelleher, D. and Leavey, G. (eds.) (2004) Identity and Health. London: Routledge.
Kelly, M.P. and Field, D. (2004) Medical sociology, chronic illness and the body. In: M. Bury and J. Gabe (eds.) The Sociology of Health and Illness. A Reader. London: Rouledge, First appeared in Sociology of Health and Illness 18(1996): 241–257.
Leonardi, M., Bickenbach, J.E., Üstün, T.B., Kostanjsek, N. and Chatterji, S. (2006) The definition of disability: What's in a name? The Lancet 368 (9543): 1219–1221.
McCall, L. (2005) The complexity of intersectionality. Signs: Journal of Women in Culture and Society 30 (3): 1771–1800.
Oliver, M. (1990) The Politics of Disablement. London: Macmillan.
Oliver, M. (2004) The social model in action: If I had a hammer. In: C. Barnes and G. Mercer (eds.) Implementing the Social Model of Disability: Theory and Research. Leeds, UK: The Disability Press.
Oliver, M. (2009) Understanding Disability. From Theory to Practice, 2nd edn. Basingstoke, UK: Palgrave Macmillan.
Parsons, T. (1951) The Social System. Glencoe, IL: Free Press.
Pearson, C. (2012) Independent living. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 240–252.
Roulestone, A. (2012) Disabled people, work and employment. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 211–224.
Roulestone, A. and Barnes, C. (2005) Working Futures: Disabled People and Social Inclusion. Bristol, UK: Policy Press.
Scambler, G. (1984) Perceiving and coping with stigmatizing illness. In: R. Fitzpatrick, J. Hinton, S. Newman, G. Scambler and J. Thompson (eds.) The Experience of Illness. London: Tavistock.
Scambler, G. (1989) Epilepsy. London: Routledge.
Scambler, G. (2004) Re-framing stigma: Felt and enacted stigma and challenges to the sociology of chronic and disabling conditions. Social Theory and Health 2 (1): 29–46.
Scambler, G. and Scambler, S. (eds.) (2010a) New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld. Basingstoke, UK: Palgrave Macmillan.
Scambler, G. and Scambler, S. (eds.) (2010b) Introduction: The sociology of chronic and disabling conditions; assaults on the lifeworld. In: New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld. Basingstoke, UK: Palgrave Macmillan, pp. 1–7.
Scott, R.A. (1969) The Making of Blind Men. New York: Russell Sage Foundation.
Shakespeare, T. (2006) Disability Rights and Wrongs. London: Routledge.
Shildrick, M. (2012) Critical disability studies: Rethinking the conventions for the age of postmodernity. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 30–41.
Soldatic, K. and Meekosha, H. (2012) Disability and neoliberal state formations. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 195–210.
Stienstra, D. (2012) Race/ethnicity and disability studies: Towards an explicitly intersectoral approach. In: N. Watson, A. Roulestone and C. Thomas (eds.) Routledge Handbook of Disability Studies. London: Routledge, pp. 376–389.
Sussman, M. (ed.) (1966) Sociology of Disability and Rehabilitation. Washington: American Sociological Association.
Thomas, C. (1999) Female Forms: Experiencing and Understanding Disability. Buckingham, UK: Open University Press.
Thomas, C (2007) Sociologies of Disability and Illness. Contested Ideas in Disability Studies and Medical Sociology. Basingstoke, UK: Palgrave Macmillan.
Thomas, C. (2010) Medical sociology and disability theory. In: G. Scambler and S. Scambler (eds.) New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld. Basingstoke, UK: Palgrave Macmillan, pp. 37–56.
Thomas, C. (2011) Disability: Prospects for social inclusion. In: A. Walker, A. Sinfield and C. Walker (eds.) Fighting Poverty, Inequality and Injustice: A Manifesto Inspired by Peter Townsend. Cambridge: Policy Press, pp. 223–240.
Townsend, P. (1979) Poverty in the United Kingdom. Harmondsworth, UK: Penguin.
Tremain, S. (2002) On the subject of impairment. In: M. Corker and T. Shakespeare (eds.) Disability/Postmodernity: Embodying Disability Theory. London: Continuum.
Turner, B.S. (1987) Medical Power and Social Knowledge. London: Sage.
Turner, B.S. (2001) Disability and the sociology of the body. In: G.L. Albrecht, K.D. Seelman and M. Bury (eds.) Handbook of Disability Studies. London: Sage.
Turner, B.S. (2004) The New Medical Sociology. New York and London: W.W. Norton & Co.
Union of the Physically Impaired Against Segregation (UPIAS) and The Disability Alliance (TDA). (1976) Fundamental Principles of Disability. London: UPIAS.
Walby, S. (2007) Complexity theory, systems theory and multiple intersecting inequalities. Philosophy of the Social Sciences 37 (4): 449–470.
Watson, N., Roulestone, A. and Thomas, C. (eds.) (2012) Routledge Handbook of Disability Studies. London: Routledge.
Williams, G.H. (1996) Irving Kenneth Zola, (1935–1994): An appreciation. Sociology of Health and Illness 18 (1): 107–125.
Williams, S. (2010) The biopolitics of chronic illness: Biology, power and personhood. In: G. Scambler and S. Scambler (eds.) New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld. Basingstoke, UK: Palgrave Macmillan, pp. 205–224.
Williams, S.J. (2000) Chronic illness as biographical disruption or biographical disruption as chronic illness? Reflections on a core concept. Sociology of Health and Illness 22 (1): 40–67.
Williams, S.J. (2005) Parsons revisited: From the sick role to … ? Health 9 (2): 123–144.
Wolfensberger, W. (1983) Social role valorisation: A proposed new term for the principle of normalisation. Mental Retardation 21 (6): 234–239.
Wood, P. (1980) International Classification of Impairments, Disabilities and Handicaps. Geneva: World Health Organization.
Zola, I.K. (1982a) Missing Pieces: A Chronicle of Living with a Disability. Philadelphia, PA: Temple University Press..
Zola, I.K. (1982b) Ordinary Lives: Voices of Disease and Disability. Watertown, MA: Applewood Books.
Zola, I.K (1989) Toward the necessary universalizing of disability policy. Milbank Memorial Fund Quarterly 67 (2): 401–428.
Zola, I.K. (1991) Bringing our bodies and ourselves back. In: Reflections on a Past, Present, and Future ‘Medical Sociology’. Journal of Health and Social Behaviour 32 (March): 1–16.
Zola, I.K. (1994) Towards inclusion: The role of people with disabilities in policy and research issues in the United States – A historical and political analysis. In: M. Rioux and M. Bach (eds.) Disability is not Measles. North York, ON: Roeher Institute.