The impact of self-harm by young people on parents and families: a qualitative study. Ferrey, A.E., Hughes, N.D., Simkin, S., Locock, L., Stewart, A., Kapur, N., Gunnell, D., Hawton, K. 2016. BMJ Open

Young People’s Experiences of Participation in Clinical Trials: Reasons for Taking Part. Luchtenberg M., Maeckelberghe E., Locock L., Powell L., Verhagen A.A. 2015. Am J Bioeth. 15(11):3-13.

“Why me? I don’t fit the mould … I am a freak of nature”: a qualitative study of women’s experience of gout. Richardson, J., Liddle, J., Mallen, C., Roddy, E., Prinjha, S., Ziebland, S., Hider, S., 2015. BMC Women’s Health. 15:122

Starting antidepressant use: a qualitative synthesis of UK and Australian data. Anderson, C., Kirkpatrick, S., Ridge, D., Kokanovic, R., Tanner, C., 2015. BMJ Open 2015;5:12

‘My dirty little habit’: Patient constructions of antidepressant use and the ‘crisis’ of legitimacy Ridge, D., Kokanovic, R., Broom, A., Kirkpatrick, S., Anderson, C., Tanner, C., 2015.
Social Science & medicine. doi:10.1016/j.socscimed.2015.10.012

Making Sense of an Unknown Terrain: How Parents Understand Self-Harm in Young People
Hughes, N.D., Locock, L., Simkin, S., Stewart, A., Ferrey, A.E., Gunnell, D., Kapur, N., Hawton, K. 2015. Qual Health Res. DOI: 10.1177/1049732315603032

Self-monitoring blood pressure in hypertension, patient and provider perspectives; a systematic review and thematic synthesis.
Fletcher, B.R., Hinton, L., Hartmann-Boyce, J., Roberts, N.W., Bobrovitz, N., McManus, R.J., 2015. Patient Education and Counselling

Support for mothers and their families after life-threatening illness in pregnancy and childbirth: a qualitative study in primary care.
Hinton, L., Locock, L., Knight, M., 2015.
British Journal of General Practice. DOI: 10.3399/bjgp15X686461

“As a parent, there is no rulebook”: A new resource for parents and carers of young people who self-harm.
Ferrey, A.E., Hawton, K., Simkin, S., Hughes, N., Stewart, A., Locock, L. 2015
The Lancet Psychiatry. Volume 2, No.7, p577-579

‘Rule your condition, don’t let it rule you’: young adults’ sense of mastery in their accounts of growing up with a chronic illness.
Heaton, J., Räisänen, U., and Salinas, M., 2015.
Sociology of Health & Illness. doi: 10.1111/1467-9566.12298

Biosamples as gifts? How participants in biobanking projects talk about donation.
Locock, L., Boylan, A-M., 2015.
Health Expectations. doi: 10.1111/hex.12376

The missing piece in antidepressant treatment.
Anderson, C., Kirkpatrick, S., 2015.
Chemist and Druggist.

On interviewing people with pets: reflections from qualitative research on people with long-term conditions.
Ziebland, S., Ryan, S., 2015.
Sociology of Health and Illness. (Wiley Online Library) DOI: 10.1111/1467-9566.12176

The role of the Internet for people with chronic pain: examples from the DIPEx International Project.
Ziebland, S., Lavie-Ajayi, M., and Lucius-Hoene, G., 2015.
British Journal of Pain. Vol. 9(1) 62-64. DOI:10.1177/2049463714555438

Drawing on Accounts of Long-Term Urinary Catheter Use: Design for the ‘Seemingly Mundane’
Chapple, A., Prinjha, S., Feneley, R., and Ziebland, S., 2015.
Sage Pub DOI: 10.1177/1049732315570135

Taboo and the different death? Perceptions of those bereaved by suicide or other traumatic death.
Chapple, A., Ziebland, S., Hawton, K., 2015.
Sociology of Health and Illness. 37. 4 pp 610-625.

‘Biographical disruption’ and its application to long-term conditions and other aspects of health.
Locock, L., Ziebland, S., and Bury, M., 2015. In F Collyer (ed).
Handbook of Social Theory for Health and Medicine’. Basingstoke: Palgrave Macmillan

Maternal critical care: what can we learn from patient experience? A qualitative study
Hinton, L., Locock, L., Knight, M. 2015
BMJ Open