“Let’s get the best quality research we can”: public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study

The effect of seeking consent on the representativeness of patient cohorts: iron-deficiency anaemia and colorectal cancer

(2011) S. Damery et al.   Colorectal Disease

What Do People Affected by Cancer Think About Electronic Health Information Exchange? Results From the 2010 LIVESTRONG Electronic Health Information Exchange Survey and the 2008 Health Information National Trends Survey

(2011) Ellen B. Beckjord et al.   Journal of Oncology Practice

Latest results from the UK trials evaluating prostate cancer screening and treatment: The CAP and ProtecT studies

(2010) J.A. Lane et al.   EUROPEAN JOURNAL OF CANCER

Views on health information sharing and privacy from primary care practices using electronic medical records

(2010) Gihan Perera et al.   INTERNATIONAL JOURNAL OF MEDICAL INFORMATICS

Public attitudes to the use in research of personal health information from general practitioners' records: a survey of the Irish general public

(2010) B. S. Buckley et al.   JOURNAL OF MEDICAL ETHICS

Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?

(2009) Donald J Willison et al.   BMC Medical Ethics

Measuring morbidity: self-report or health care records?

(2009) J. Barber et al.   FAMILY PRACTICE

Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue

(2008) Donald J Willison et al.   BMC Medical Ethics

The impact of consent on observational research: a comparison of outcomes from consenters and non consenters to an observational study

(2008) Una Macleod et al.   BMC Medical Research Methodology

Research on Medical Records without Informed Consent

(2008) Franklin G. Miller   JOURNAL OF LAW MEDICINE & ETHICS

Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group

(2007) C Metcalfe et al.   JOURNAL OF MEDICAL ETHICS