Sue Ziebland

• Core Outcome Sets in Women's and Newborn Health: A Systematic Review.

  Duffy JMN. et al, (2017), BJOG

• Advancing gender equality through the Athena SWAN Charter for Women in Science: An exploratory study of women's and men's perceptions

  Ovseiko PV. et al, (2017), Health Research Policy and Systems, 15

• Do we all agree what “good health care” looks like? Views from those who are “seldom heard” in health research, policy and service improvement

  Ryan SS. et al, (2017), Health Expectations

• Outcome reporting across randomised controlled trials evaluating therapeutic interventions for pre-eclampsia

  Duffy J. et al, (2017), BJOG: An International Journal of Obstetrics and Gynaecology

• Randomised feasibility study of a novel experience-based internet intervention to support self-management in chronic asthma

  Newhouse N. et al, (2016), BMJ Open, 6

• A novel experience-based internet intervention for smoking cessation: feasibility randomised controlled trial

  Powell J. et al, (2016), BMC Public Health, 16, 1 - 9

• Narratives of experience of mental health and illness on healthtalk.org

  Kidd J. and Ziebland S., (2016), Psychiatrist, 40, 273 - 276

• A protocol for developing, disseminating, and implementing a core outcome set for pre-eclampsia

  Duffy JMN. et al, (2016), Pregnancy Hypertension, 6, 274 - 278

• Using alternatives to face-to-face consultations: A survey of prevalence and attitudes in general practice

  Brant H. et al, (2016), British Journal of General Practice, 66, e460 - e466

• Prescribing antibiotics to 'at-risk' children with influenza-like illness in primary care: Qualitative study

  Ashdown HF. et al, (2016), BMJ Open, 6

• What patients do and their impact on implementation: An ethnographic study of participatory quality improvement projects in English acute hospitals

  Boaz A. et al, (2016), Journal of Health, Organisation and Management, 30, 258 - 278

• 'I knew before I was told': Breaches, cues and clues in the diagnostic assemblage

  Locock L. et al, (2016), Social Science and Medicine, 154, 85 - 92

• Proliferation of private online healthcare companies: Should the NHS try to keep up?

  Watson J. et al, (2016), BMJ (Online), 352

• An open letter to the BMJ editors on qualitative research

  Greenhalgh T. et al, (2016), BMJ (Online), 352

• Drawing on Accounts of Long-Term Urinary Catheter Use

  Chapple A. et al, (2016), Qualitative Health Research, 26, 154 - 163

• Do we all agree what "good health care" looks like? Views from those who are "seldom heard" in health research, policy and service improvement

  Ryan S. et al, (2016), Health Expectations

• A joint effort over a period of time: Factors affecting use of urate-lowering therapy for long-Term treatment of gout

  Richardson JC. et al, (2016), BMC Musculoskeletal Disorders, 17

• "Why me? I don't fit the mould ... I am a freak of nature": A qualitative study of women's experience of gout

  Richardson JC. et al, (2015), BMC Women's Health, 15

• Barriers to shared decisions in the most serious of cancers: A qualitative study of patients with pancreatic cancer treated in the UK

  Ziebland S. et al, (2015), Health Expectations, 18, 3302 - 3312

• Barriers to shared decisions in the most serious of cancers: a qualitative study of patients with pancreatic cancer treated in the UK

  Ziebland S. et al, (2015), HEALTH EXPECTATIONS, 18, 3302 - 3312

• Measuring the effects of online health information: Scale validation for the e-Health Impact Questionnaire

  Kelly L. et al, (2015), Patient Education and Counseling, 98, 1418 - 1424

• A database of patient experience: moving beyond anecdote

  Grob R. et al, (2015), PSYCHO-ONCOLOGY, 24, 21 - 22

• Mike Bury: Biographical Disruption and Long-Term and Other Health Conditions

  Locock L. and Ziebland S., (2015), The Palgrave Handbook of Social Theory in Health, Illness and Medicine, 582 - 598

• Taboo and the different death? Perceptions of those bereaved by suicide or other traumatic death

  Chapple A. et al, (2015), Sociology of Health and Illness, 37, 610 - 625

• On interviewing people with pets: Reflections from qualitative research on people with long-term conditions

  Ryan S. and Ziebland S., (2015), Sociology of Health and Illness, 37, 67 - 80

• Mike Bury: Biographical disruption and long-term and other health conditions

  Locock L. and Ziebland S., (2015), The Palgrave Handbook of Social Theory in Health, Illness and Medicine, 582 - 598

• Mapping patients' experiences from initial symptoms to gout diagnosis: A qualitative exploration

  Liddle J. et al, (2015), BMJ Open, 5

• An overview of self-administered health literacy instruments

  O'Neill B. et al, (2014), PLoS ONE, 9

• Informing the development of NICE (National Institute for Health and Care Excellence) quality standards through secondary analysis of qualitative narrative interviews on patients’ experiences

  Ziebland S. et al, (2014), Health Services and Delivery Research, 2, 1 - 206

• Measuring the effects of online health information: Scale validation for the e-Health Impact Questionnaire

  Kelly L. et al, (2014), Patient Education and Counseling

• DEVELOPING A WEB BASED INFORMATION RESOURCE FOR YOUNG PEOPLE LIVING WITH CHRONIC ARTHRITIS AND THEIR CARERS

  McDonagh JE. et al, (2014), RHEUMATOLOGY, 53, 18 - 18

• Collecting data on patient experience is not enough: They must be used to improve care

  Coulter A. et al, (2014), BMJ (Online), 348

• Using secondary analysis of qualitative data of patient experiences of health care to inform health services research and policy

  Ziebland S. and Hunt K., (2014), Journal of Health Services Research and Policy, 19, 177 - 182

• Using a national archive of patient experience narratives to promote local patient-centered quality improvement: An ethnographic process evaluation of ‘accelerated’ experience-based co-design

  Locock L. et al, (2014), Journal of Health Services Research and Policy, 19, 200 - 207

• User-generated online health content: A survey of internet users in the United Kingdom

  O'Neill B. et al, (2014), Journal of Medical Internet Research, 16

• The role of the internet for people with chronic pain: Examples from the DIPEx international project

  Ziebland S. et al, (2014), British Journal of Pain, 9, 62 - 64

• 'I Can Be The Me I Want To Be By Taking an Antidepressant Regularly': People's Feelings About Taking Antidepressants

  Anderson C. et al, (2014), RESEARCH IN SOCIAL & ADMINISTRATIVE PHARMACY, 10, E1 - E1

• "It can't be very important because it comes and goes"-patients' accounts of intermittent symptoms preceding a pancreatic cancer diagnosis: A qualitative study

  Evans J. et al, (2014), BMJ Open, 4

• Measuring the effects of online health information for patients: Item generation for an e-health impact questionnaire

  Kelly L. et al, (2013), Patient Education and Counseling, 93, 433 - 438

• THE E-HEALTH IMPACT QUESTIONNAIRE: DEVELOPING A TOOL TO MEASURE THE EFFECTS OF USING HEALTH-RELATED WEBSITES

  Kelly L. et al, (2013), VALUE IN HEALTH, 16, A605 - A605

• Personal identity and the role of 'carer' among relatives and friends of people with multiple sclerosis

  Hughes N. et al, (2013), Social Science and Medicine, 96, 78 - 85

• Developing a tool to measure the effects of using health-related websites (the e-Health Impact Questionnaire)

  Kelly L. et al, (2013), QUALITY OF LIFE RESEARCH, 22

• How people bereaved by suicide perceive newspaper reporting: Qualitative study

  Chapple A. et al, (2013), British Journal of Psychiatry, 203, 228 - 232

• What parents say about disclosing the end of their pregnancy due to fetal abnormality

  France EF. et al, (2013), Midwifery, 29, 24 - 32

• Understanding and using health experiences

  Ziebland S. et al, (2013)

• Measuring the effects of online health information for patients: Item generation for an e-health impact questionnaire

  Kelly L. et al, (2013), Patient Education and Counseling

• A qualitative exploration of the role of primary care in supporting colorectal cancer patients

  Hall S. et al, (2012), Supportive Care in Cancer, 20, 3071 - 3078

• A proper, fitting explanation? Suicide bereavement and perceptions of the coroner's verdict

  Chapple A. et al, (2012), Crisis, 33, 230 - 238

• Developing and pre-testing an item pool relating to the effects of exposure to health websites

  Kelly L. et al, (2012), QUALITY OF LIFE RESEARCH, 21, 113 - 113

• Talk of frustration in the narratives of people with chronic pain

  Dow CM. et al, (2012), Chronic Illness, 8, 176 - 191

• Emotions and chronic illness

  Ziebland S. and Kokanovic R., (2012), Chronic Illness, 8, 159 - 162

• Understanding depression through a 'coming out' framework

  Ridge D. and Ziebland S., (2012), Sociology of Health and Illness, 34, 730 - 745

• Reassured or fobbed off? Perspectives on infertility consultations in primary care: A qualitative study

  Hinton L. et al, (2012), British Journal of General Practice, 62

• Imagined futures: How experiential knowledge of disability affects parents' decision making about fetal abnormality

  France EF. et al, (2012), Health Expectations, 15, 139 - 156

• Health and illness in a connected world: How might sharing experiences on the internet affect people's health?

  Ziebland S. and Wyke S., (2012), Milbank Quarterly, 90, 219 - 249

• Why listening to health care users really matters

  Ziebland S., (2012), Journal of Health Services Research and Policy, 17, 68 - 69

• An alarming prognosis: How people affected by pancreatic cancer use (and avoid) Internet information

  Chapple A. et al, (2012), Policy and Internet, 4

• Incurable, invisible and inconclusive: Watchful waiting for chronic lymphocytic leukaemia and implications for doctor-patient communication

  Evans J. et al, (2012), European Journal of Cancer Care, 21, 67 - 77

• A qualitative exploration of the role of primary care in supporting colorectal cancer patients

  Hall S. et al, (2012), Supportive Care in Cancer, 1 - 8

• Patients' needs following colorectal cancer diagnosis: Where does primary care fit in?

  Browne S. et al, (2011), British Journal of General Practice, 61

• How information about other people's personal experiences can help with healthcare decision-making: A qualitative study

  Entwistle VA. et al, (2011), Patient Education and Counseling, 85

• Experiences of infertility: where do men fit in?

  Hinton L. et al, (2011), HUMAN REPRODUCTION, 26, I261 - I262

• Qualitative studies of the benefits and adverse effects of the availability of cancer information and support on the internet

  Ziebland SB. et al, (2011), E-Health: The Advent of Online Cancer Information Systems

• Women's distress about unexpected DCIS uncertainties and information provision (response to Pryke et al.)

  Prinjha S. et al, (2011), Journal of Medical Screening, 18, 105 - 106

• Nurses should be encouraged and helped to monitor patients' medicines

  Herxheimer A. and Ziebland S., (2011), Journal of Nursing Management, 19, 393 - 394

• Medical Professionalism in the New Information Age

  Ziebland S., (2011), Sociology of Health and Illness, 33, 505 - 506

• How the internet is changing the experience of bereavement by suicide: A qualitative study in the UK

  Chapple A. and Ziebland S., (2011), Health, 15, 173 - 187

• How personal experiences feature in women's accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality

  France EF. et al, (2011), Social Science and Medicine, 72, 755 - 762

• Exceptionally good? Positive experiences of NHS care and treatment surprises lymphoma patients: a qualitative interview study.

  Ziebland S. et al, (2011), Health Expect, 14, 21 - 28

• 'A mastectomy for something that wasn't even truly invasive cancer.' Women's understandings of having a mastectomy for screen-detected DCIS: A qualitative study

  Prinjha S. et al, (2011), Journal of Medical Screening, 18, 34 - 40

• The role of spirituality and religion for those bereaved due to a traumatic death

  Chapple A. et al, (2011), Mortality, 16, 1 - 19

• Understanding depression through a 'coming out' framework

  Ridge D. and Ziebland S., (2011), Sociology of Health and Illness

• Infertility; isolation and the Internet: A qualitative interview study

  Hinton L. et al, (2010), Patient Education and Counseling, 81, 436 - 441

• Viewing the body after bereavement due to a traumatic death: Qualitative study in the UK

  Chapple A. and Ziebland S., (2010), BMJ (Online), 340

• Encyclopedia of case study research

  Ziebland SB., (2010), Encyclopedia of case study research

• Biographical disruption, abruption and repair in the context of motor neurone disease

  Locock L. et al, (2009), Sociology of Health and Illness, 31, 1043 - 1058

• Depressive disorders

  Ziebland SB., (2009), Depressive disorders

• 'My brain couldn't move from planning a birth to planning a funeral': A qualitative study of parents' experiences of decisions after ending a pregnancy for fetal abnormality

  Hunt K. et al, (2009), International Journal of Nursing Studies, 46, 1111 - 1121

• Patients' views of a multimedia resource featuring experiences of rheumatoid arthritis: Pilot evaluation of www.healthtalkonline.org

  Newman MA. et al, (2009), Health Informatics Journal, 15, 147 - 159

• Breast cancer in young families: A qualitative interview study of fathers and their role and communication with their children following the diagnosis of maternal breast cancer

  Forrest G. et al, (2009), Psycho-Oncology, 18, 96 - 103

• Factors contributing to the time taken to consult with symptoms of lung cancer: A cross-sectional study

  Smith SM. et al, (2009), Thorax, 64, 523 - 531

• Disclosing a cancer diagnosis to friends and family: A gendered analysis of young men's and women's experiences

  Hilton S. et al, (2009), Qualitative Health Research, 19, 744 - 754

• 'Getting through' not 'going under': A qualitative study of gender and spousal support after diagnosis with colorectal cancer

  Emslie C. et al, (2009), Social Science and Medicine, 68, 1169 - 1175

• Men's health

  Ziebland SB., (2009), Men's health

• BMJ

  Ziebland SB., (2009), BMJ

• Perinatal Epidemiology for Public Health Practice

  Ziebland SB., (2008), Perinatal Epidemiology for Public Health Practice

• What affects the uptake of screening for bowel cancer using a faecal occult blood test (FOBt): A qualitative study

  Chapple A. et al, (2008), Social Science and Medicine, 66, 2425 - 2435

• Have men been overlooked? A comparison of young men and women's experiences of chemotherapy-induced alopecia

  Hilton S. et al, (2008), Psycho-Oncology, 17, 577 - 583

• The effect of joint interviewing on the performance of gender

  Seale C. et al, (2008), Field Methods, 20, 107 - 128

• How patients' experiences contribute to decision making: Illustrations from DIPEx (personal experiences of health and illness)

  Ziebland S. and Herxheimer A., (2008), Journal of Nursing Management, 16, 433 - 439

• Collecting personal experiences to help other patients and educate professionals

  Ziebland SB., (2008), Narrative Research in Health and Illness

• The DIPEx Project: Collecting Personal Experiences of Illness and Health Care

  Herxheimer A. and Ziebland S., (2008), Narrative Research in Health and Illness, 115 - 131

• Narrative Research in Health and Illness

  Hurwitz B. et al, (2008), 1 - 446

• Why Men in the United Kingdom still want the prostate specific antigen test

  Chapple A. et al, (2008), Qualitative Health Research, 18, 56 - 64

• The DIPEx project: A systematic collection of personal illness experiences

  Herxheimer A. and Ziebland S., (2008), Neurologie und Rehabilitation, 14, 31 - 40

• Analysing Qualitative Data

  Pope C. et al, (2007), 63 - 81

• Minimising delays in ovarian cancer diagnosis: An expansion of Andersen's model of 'Total patient delay'

  Evans J. et al, (2007), PSYCHO-ONCOLOGY, 16, S158 - S158

• Exploring men's and women's experiences of depression and engagement with health professionals: More similarities than differences? A qualitative interview study

  Emslie C. et al, (2007), BMC Family Practice, 8

• Positive prevention: Contemporary issues facing HIV positive people negotiating sex in the UK

  Ridge D. et al, (2007), Social Science and Medicine, 65, 755 - 770

• Exploring men's and women's experiences of depression and engagement with health professionals: more similarities than differences? A qualitative interview study.

  Emslie C. et al, (2007), BMC Fam Pract, 8

• Patients' perceptions of transrectal prostate biopsy: A qualitative study: Case study

  Chapple AB. et al, (2007), European Journal of Cancer Care, 16, 215 - 221

• Does it matter if clinicians recruiting for a trial don't understand what the trial is really about? Qualitative study of surgeons' experiences of participation in a pragmatic multi-centre RCT

  Ziebland S. et al, (2007), Trials, 8

• Minimizing delays in ovarian cancer diagnosis: An expansion of Andersen's model of 'total patient delay'

  Evans J. et al, (2007), Family Practice, 24, 48 - 55

• Fertility Issues: The Perceptions and Experiences of Young Men Recently Diagnosed and Treated for Cancer

  Chapple A. et al, (2007), Journal of Adolescent Health, 40, 69 - 75

• What people close to death say about euthanasia and assisted suicide: A qualitative study

  Chapple A. et al, (2006), Journal of Medical Ethics, 32, 706 - 710

• 'Can I come off the tablets now?' A qualitative analysis of heart failure patients' understanding of their medication

  Field K. et al, (2006), Family Practice, 23, 624 - 630

• The specialist palliative care nurse: A qualitative study of the patients' perspective

  Chapple A. et al, (2006), International Journal of Nursing Studies, 43, 1011 - 1022

• "The old me could never have done that": How people give meaning to recovery following depression

  Ridge D. and Ziebland S., (2006), Qualitative Health Research, 16, 1038 - 1053

• The choice is yours? How women with ovarian cancer make sense of treatment choices

  Ziebland S. et al, (2006), Patient Education and Counseling, 62, 361 - 367

• Men's accounts of depression: Reconstructing or resisting hegemonic masculinity?

  Emslie C. et al, (2006), Social Science and Medicine, 62, 2246 - 2257

• Making sense of qualitative data analysis: An introduction with illustrations from DIPEx (personal experiences of health and illness)

  Ziebland S. and McPherson A., (2006), Medical Education, 40, 405 - 414

• Gender, cancer experience and internet use: A comparative keyword analysis of interviews and online cancer support groups

  Seale C. et al, (2006), Social Science and Medicine, 62, 2577 - 2590

• Breast cancer in the family-children's perceptions of their mother's cancer and its initial treatment: Qualitative study

  Forrest G. et al, (2006), British Medical Journal, 332, 998 - 1001

• Why do General Practitioners prescribe antibiotics for acute infective conjunctivitis in children? Qualitative interviews with GPs and a questionnaire survey of parents and teachers

  Rose PW. et al, (2006), Family Practice, 23, 226 - 232

• What happened when Scottish women were given advance supplies of emergency contraception? A survey and qualitative study of women's views and experiences

  Ziebland S. et al, (2005), Social Science and Medicine, 60, 1767 - 1779

• Narrative form in accounts of the experience of illness

  Ziebland SB., (2005), The sociolinguistics of narrative

• The role of humor for men with testicular cancer

  Chapple A. and Ziebland S., (2004), Qualitative Health Research, 14, 1123 - 1139

• Expressions of loss of adulthood in the narratives of people with colorectal cancer

  Rozmovits L. and Ziebland S., (2004), Qualitative Health Research, 14, 187 - 203

• The importance of being expert: The quest for cancer information on the Internet

  Ziebland S., (2004), Social Science and Medicine, 59, 1783 - 1793

• Lung cancer patients' perceptions of access to financial benefits: A qualitative study

  Chapple A. et al, (2004), British Journal of General Practice, 54, 589 - 594

• In the absence of evidence, who chooses? A qualitative study of patients' needs after treatment for colorectal cancer

  Rozmovits L. et al, (2004), Journal of Health Services Research and Policy, 9, 159 - 164

• Emergency contraception: Why can't you give it away? Qualitative findings from an evaluation of advance provision of emergency contraception

  Fairhurst K. et al, (2004), Contraception, 70, 25 - 29

• Stigma, shame, and blame experienced by patients with lung cancer: Qualitative study

  Chapple A. et al, (2004), British Medical Journal, 328, 1470 - 1473

• Advanced provision of emergency contraception does not reduce abortion rates

  Glasier A. et al, (2004), Contraception, 69, 361 - 366

• What do patients with prostate or breast cancer want from an Internet site? A qualitative study of information needs

  Rozmovits L. and Ziebland S., (2004), Patient Education and Counseling, 53, 57 - 64

• Reported barriers to eating more fruit and vegetables before and after participation in a randomized controlled trial: A qualitative study

  John JH. and Ziebland S., (2004), Health Education Research, 19, 165 - 174

• How the internet affects patients' experience of cancer: A qualitative study

  Ziebland S. et al, (2004), British Medical Journal, 328, 564 - 567

• What benefit testicular self-examination (multiple letters) [1]

  Hopcroft K. et al, (2004), British Journal of General Practice, 54, 214 - 215

• Qualitative study of men's perceptions of why treatment delays occur in the UK for those with testicular cancer

  Chapple A. et al, (2004), British Journal of General Practice, 54, 25 - 32

• Does stage of change predict outcome in a primary-care intervention to encourage an increase in fruit and vegetable consumption?

  John JH. et al, (2003), Health Education Research, 18, 429 - 438

• DIPEx (Database of Individual Patients' Experience of illness): A multimedia proposal to share experiences and information about illnesses between patients and health professionals

  Herxheimer A. et al, (2003), Atencion Primaria, 31, 386 - 388

• Ethics and dementia: Mapping the literature by bibliometric analysis

  Baldwin C. et al, (2003), International Journal of Geriatric Psychiatry, 18, 41 - 54

• [DIPEx (Database of Individual Patients Experience of illness): a multimedia proposal to share experiences and information about illnesses between patients and health professionals].

  Herxheimer A. et al, (2003), Aten Primaria, 31, 386 - 388

• "People sometimes react funny if they're not told enough": women's views about the risks of diagnostic laparoscopy.

  Moore J. et al, (2002), Health Expect, 5, 302 - 309

• Dietary effect on blood pressure - Reply

  Ziebland S. et al, (2002), LANCET, 360, 1786 - 1786

• Dietary effect on blood pressure [3] (multiple letters)

  Dyer K. et al, (2002), Lancet, 360, 1785 - 1786

• Why men with prostate cancer want wider access to prostate specific antigen testing: Qualitative study

  Chapple A. et al, (2002), British Medical Journal, 325, 737 - 739

• Is 'watchful waiting' a real choice for men with prostate cancer? A qualitative study

  Chapple A. et al, (2002), BJU International, 90, 257 - 264

• Body image and weight change in middle age: A qualitative study

  Ziebland S. et al, (2002), International Journal of Obesity, 26, 1083 - 1091

• Journal of epidemiology and community health

  Ziebland SB., (2002), Journal of epidemiology and community health

• Effects of fruit and vegetable consumption on plasma antioxidant concentrations and blood pressure: A randomised controlled trial

  John JH. et al, (2002), Lancet, 359, 1969 - 1974

• Development and validation of the Day in the Life Questionnaire (DILQ) as a measure of fruit and vegetable questionnaire for 7-9 year olds.

  Edmunds LD. and Ziebland S., (2002), Health Educ Res, 17, 211 - 220

• Carers, ethics and dementia: A survey and review of the literature

  Hughes JC. et al, (2002), International Journal of Geriatric Psychiatry, 17, 35 - 40

• Prostate cancer: Embodied experience and perceptions of masculinity

  Chapple A. and Ziebland S., (2002), Sociology of Health and Illness, 24, 820 - 841

• Smoking cessation in pregnancy: What's a man to do?

  Ziebland S. and Fuller A., (2001), Health Education Journal, 60, 232 - 240

• A database of patients' experiences (DIPEx): A multi-media approach to sharing experiences and information

  Herxheimer A. et al, (2001), Ricerca e Pratica, 17, 181 - 189

• The use of patients' stories by self-help groups: A survey of voluntary organizations in the UK on the register of the College of Health

  Yaphe J. et al, (2000), Health Expectations, 3, 176 - 181

• Database of patients' experiences (DIPEx): A multi-media approach to sharing experiences and information

  Herxheimer A. et al, (2000), Lancet, 355, 1540 - 1543

• Qualitative research in health care. Analysing qualitative data.

  Pope C. et al, (2000), BMJ, 320, 114 - 116

• Analysing qualitative data

  Pope C. et al, (2000), British Medical Journal, 320, 114 - 116

• Emergency contraception: An anomalous position in the family planning repertoire?

  Ziebland S., (1999), Social Science and Medicine, 49, 1409 - 1417

• Computer support for recording and interpreting family histories of breast and ovarian cancer in primary care (RAGs): qualitative evaluation with simulated patients.

  Emery J. et al, (1999), BMJ, 319, 32 - 36

• Process evaluation of a research workshop and follow-up support to help practitioners from 13 weight management projects to carry out evaluations

  Rayner M. and Ziebland S., (1999), Journal of Human Nutrition and Dietetics, 12, 9 - 19

• Current research in Britain

  Ziebland SB., (1999), Current research in Britain

• How important is the smoking status of the Woman's partner as a predictor of smoking cessation in pregnancy? A literature review

  Ziebland S. and Mathews F., (1998), Health Education Journal, 57, 70 - 80

• A 'five-a-day' fruit and vegetable pack for primary school children. Part I: Development and pre-testing

  Boaz A. and Ziebland S., (1998), Health Education Journal, 57, 97 - 104

• Patients' views of routine hospital follow-up: A qualitative study of women with breast cancer in remission

  Adewuyi-Dalton R. et al, (1998), Psycho-Oncology, 7, 436 - 439

• Concerns and cautions about prescribing and deregulating emergency contraception: a qualitative study of GPs using telephone interviews.

  Ziebland S. et al, (1998), Fam Pract, 15, 449 - 456

• Not a 'proper' solution? The gap between professional guidelines and users' views about the safety of using emergency contraception

  Ziebland S. and Maxwell K., (1998), Journal of Health Services Research and Policy, 3, 12 - 19

• Lack of willpower or lack of wherewithal? 'Internal' and 'external' barriers to changing diet and exercise in a three year follow-up of participants in a health check

  Ziebland S. et al, (1998), Social Science and Medicine, 46, 461 - 465

• Smoking cessation interventions for dental patients - Attitudes and reported practices of dentists in the Oxford region

  John JH. et al, (1997), British Dental Journal, 183, 359 - 364

• Qualitative Research Methods in Health and Health Services Research

  Ziebland SB., (1997), Assessment and Evaluation of Health and Medical Care

• 'It's a mega dose of hormones, isn't it?' Why women may be reluctant to use emergency contraception

  Ziebland S. et al, (1996), Journal of Family Planning and Reproductive Health Care, 22, 84 - 86

• Desire for the body normal: Body image and discrepancies between self reported and measured height and weight in a British population

  Ziebland S. et al, (1996), Journal of Epidemiology and Community Health, 50, 105 - 106

• Software for analysing textual data

  Ziebland S., (1996), Journal of Health Services Research & Policy, 1, 247 - 249

• SHORT-FORM-36 QUESTIONNAIRE - REPLY

  ZIEBLAND S., (1995), JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 49, 555 - 555

• QUALITATIVE METHODS IN HEALTH AND MEDICINE - BLOOR,M, TARABORRELLI,P

  ZIEBLAND S., (1995), SOCIOLOGY OF HEALTH & ILLNESS, 17, 430 - 431

• Evaluation of sexual health interventions

  Garcia P. and Ziebland S., (1995), BMJ, 310

• Effectiveness of health checks conducted by nurses in primary care: Final results of the OXCHECK study

  Coulter A. et al, (1995), British Medical Journal, 310, 1099 - 1104

• Emergency contraception.

  Ziebland S. and Garcia P., (1995), Br J Gen Pract, 45, 108 - 109

• The short form 36 health status questionnaire: Clues from the Oxford region's normative data about its usefulness in measuring health gain in population surveys

  Ziebland S., (1995), Journal of Epidemiology and Community Health, 49, 102 - 105

• Could a publicity campaign for emergency contraception reduce the incidence of unwanted pregnancy and how would we know if it did?

  Ziebland S. and Scobie S., (1995), British Journal of Family Planning, 21, 68 - 71

• Measuring Changes in Health Status

  Ziebland S None., (1994), Measuring Health and Medical Outcomes

• Transition questions to assess outcomes in rheumatoid arthritis

  Fitzpatrick R. et al, (1993), Rheumatology, 32, 807 - 811

• A comparison of the sensitivity to change of several health status instruments in rheumatoid arthritis.

  Fitzpatrick R. et al, (1993), J Rheumatol, 20, 429 - 436

• Tacit models of disability underlying health status instruments

  Ziebland S. et al, (1993), Social Science and Medicine, 37, 69 - 75

• Importance of sensitivity to change as a criterion for selecting health status measures.

  Fitzpatrick R. et al, (1992), Quality in health care : QHC, 1, 89 - 93

• A generic health status instrument in the assessment of rheumatoid arthritis

  Fitzpatrick R. et al, (1992), Rheumatology, 31, 87 - 90

• SENSITIVITY TO CHANGE OVER TIME OF 4 HEALTH-STATUS INSTRUMENTS IN RHEUMATOID-ARTHRITIS

  MOWAT A. et al, (1992), BRITISH JOURNAL OF RHEUMATOLOGY, 31, 151 - 151

• Comparison of two approaches to measuring change in health status in rheumatoid arthritis: The Health Assessment Questionnaire (HAQ) and modified HAQ

  Ziebland S. et al, (1992), Annals of the Rheumatic Diseases, 51, 1202 - 1205

• The social dimension of health status measures in rheumatoid arthitis

  Fitzpatrick R. et al, (1991), International Disability Studies, 13, 34 - 37

• What patients do and their impact on implementation process and outcomes during (and after) participatory quality improvement projects in English acute hospitals: Reflections from an ethnographic study

  Boaz A. et al, Journal of Health Organization and Management

• The importance of being expert: cancer information and the Internet

  Ziebland SB.

• The DIPEx project

  Ziebland SB.

• The DIPEx Project

  Ziebland SB.

• The Decision's Yours? How cancer patients make sense of involvement in treatment decisions

  Ziebland SB.

• Stigma Shame and Blame: a qualitative study of patients with lung cancer

  Ziebland SB.

• Primary outcome and outcome measure reporting in randomized trials evaluating treatments for preeclampsia: a systematic review.

  Duffy JMN. et al, International Journal of Gynecology and Obstetrics

• Patients and life changing information

  Ziebland SB.

• Is 'watchful waiting' a real choice for men with prostate cancer? A qualitative study

  Ziebland SB.

• In the absence of evidence who chooses? Follow up for patients with colorectal cancer

  Ziebland SB.

• HTO- Teaching and Learning with shared health experiences

  Ziebland SB.

• How to include patients' perspectives in the development of health promotion strategies for primary care.

  Ziebland SB.

• How the internet affects patients' experience of cancer

  Ziebland S. et al, Understanding health and social care: an introductory reader

• Examining the role of patients' experiences as a resource for choice and decision-making in health care: a creative, inter-disciplinary mixed method study in digital health

  Ziebland S. et al, NIHR Journals library PGfAR

• DIPEx: illness narratives, evidence and primary care

  Ziebland SB.

• DIPEx: enabling patients to learn from each other

  Ziebland SB.

• DIPEx using new technology to give patients/ carers a voice

  Ziebland SB.

• DIPEx patients' experiences of epilepsy

  Ziebland SB.

• DIPEx illness narratives and SDO research

  Ziebland SB.

• Breast cancer in the Family: children's perceptions of their mother's cancer

  Ziebland SB.

• Breast cancer in the Family: children's perceptions of their mother's cancer.

  Ziebland SB.

Key Publications

• Health and illness in a connected world: How might sharing experiences on the internet affect people's health?

  Ziebland S. and Wyke S., (2012), Milbank Quarterly, 90, 219 - 249

• An alarming prognosis: How people affected by pancreatic cancer use (and avoid) Internet information

  Chapple A. et al, (2012), Policy and Internet, 4

• Personal identity and the role of 'carer' among relatives and friends of people with multiple sclerosis

  Hughes N. et al, (2013), Social Science and Medicine, 96, 78 - 85

• Using alternatives to face-to-face consultations: A survey of prevalence and attitudes in general practice

  Brant H. et al, (2016), British Journal of General Practice, 66, e460 - e466

• Collecting data on patient experience is not enough: They must be used to improve care

  Coulter A. et al, (2014), BMJ (Online), 348

Recent Publications

• Core Outcome Sets in Women's and Newborn Health: A Systematic Review.

  Duffy JMN. et al, (2017), BJOG

• Advancing gender equality through the Athena SWAN Charter for Women in Science: An exploratory study of women's and men's perceptions

  Ovseiko PV. et al, (2017), Health Research Policy and Systems, 15

• Do we all agree what “good health care” looks like? Views from those who are “seldom heard” in health research, policy and service improvement

  Ryan SS. et al, (2017), Health Expectations

• Outcome reporting across randomised controlled trials evaluating therapeutic interventions for pre-eclampsia

  Duffy J. et al, (2017), BJOG: An International Journal of Obstetrics and Gynaecology

• Randomised feasibility study of a novel experience-based internet intervention to support self-management in chronic asthma

  Newhouse N. et al, (2016), BMJ Open, 6