Selected Publications

• L Locock and L Smith (2011): Personal experiences of taking part in clinical trials - A qualitative study. - Patient Educ Couns.
• E F France, L Locock, K Hunt, S Ziebland, K Field and S Wyke (2011): Imagined futures: how experiential knowledge of disability affects parents' decision making about foetal abnormality. - Health Expect.
• Louise Locock and Lorraine Smith (2011): Personal benefit, or benefiting others? Deciding whether to take part in clinical trials. - Clin Trials, 8(1):85-93.
• Louise Locock and Janice B Brown (2010): 'All in the same boat'? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND). - Soc Sci Med, 71(8):1498-505.
• Louise Locock, Kate Field, Ann McPherson and Patricia A Boyd (2010): Women's accounts of the physical sensation of chorionic villus sampling and amniocentesis: expectations and experience. - Midwifery, 26(1):64-75.
• Pam Lowe, John Powell, Frances Griffiths, Margaret Thorogood and Louise Locock (2009): Making it all normal: the role of the internet in problematic pregnancy. - Qual Health Res, 19(10):1476-84.
• Louise Locock, Sue Ziebland and Carol Dumelow (2009): Biographical disruption, abruption and repair in the context of motor neurone disease. - Sociol Health Illn, 31(7):1043-58.
• Louise Locock, Jo Alexander and Linda Rozmovits (2008): Women's responses to nausea and vomiting in pregnancy. - Midwifery, 24(2):143-52.
• Louise Locock and Joe Kai (2008): Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics era. - Br J Gen Pract, 58(548):161-8.
• Louise Locock and Jo Alexander (2006): 'Just a bystander'? Men's place in the process of fetal screening and diagnosis. - Soc Sci Med, 62(6):1349-59.
• Louise Locock, Jane Crawford and Jon Crawford (2005): The parents' journey: continuing a pregnancy after a diagnosis of Patau's syndrome. - BMJ, 331(7526):1186-9.