Income inequalities in the risk of potentially avoidable hospitalisation for chronic obstructive pulmonary disease

a population data linkage analysis

Indicators of missing Electronic Medical Record (EMR) discharge summaries: A retrospective study on data from a large Canadian cohort

A comparison of Australian chronic disease prevalence estimates using administrative pharmaceutical dispensing data with international and community survey data

Developing a comprehensive database with sensitive health information: A profile of people living with HIV in Newfoundland and Labrador, Canada

Cohort profile: The Secure Anonymised Information Linkage databank Dementia e-cohort (SAIL-DeC)

Immigrant and ethnic neighbourhood concentration and reduced child developmental vulnerability

A Canadian cohort study

Psychosocial disadvantage and residential remoteness is associated with Aboriginal women’s mental health prior to childbirth

Identifying young Aboriginal and Torres Strait Islander children in linked administrative data: A comparison of methods

Prevalence of Down's Syndrome in England, 1998–2013

Comparison of linked surveillance data and electronic health records

Identifying incident cancer cases in dispensing claims

A validation study using Australia’s Repatriation Pharmaceutical Benefits Scheme (PBS) data

Defining a study population using enhanced reporting of Aboriginality and the effects on study outcomes

Is there an agreement between self-reported medical diagnosis in the CARTaGENE cohort and the Québec administrative health databases?

The effect of number of healthcare visits on study sample selection in electronic health record data

Data Resource: population level family justice administrative data with opportunities for data linkage

How effective are population health surveys for estimating prevalence of chronic conditions compared to anonymised clinical data?

Identifying children with Cystic Fibrosis in population-scale routinely collected data in Wales

A Retrospective Review

Development of comparable algorithms to measure primary care indicators using administrative health data across three Canadian provinces

A Privacy Attack on Multiple Dynamic Match-key based Privacy-Preserving Record Linkage

Intercensal and Postcensal Estimation of Population Size for Small Geographic Areas in the United States

A composite neonatal adverse outcome indicator using population-based data: an update

an update

Can Linked Electronic Medical Record and Administrative Data Help Us Identify Those Living with Frailty?

Developing and validating a primary care EMR-based frailty definition using machine learning

Individual and neighbourhood socioeconomic status increase risk of avoidable hospitalizations among Canadian adults: A retrospective cohort study of linked population health data

Guidance for researchers wanting to link NHS data using non-consent approaches: a thematic analysis of feedback from the Health Research Authority Confidentiality Advisory Group

A thematic analysis of feedback from the Health Research Authority Confidentiality Advisory Group

A national initiative in data science for health: an evaluation of the UK Farr Institute

Community-based Health Data Cooperatives Towards Improving the Immigrant Community Health: A Scoping Review to Inform Policy and Practice

The Mortality After Release from Incarceration Consortium (MARIC): Protocol for a multi-national, individual participant data meta-analysis

Parity: A key measure of confounding in data-linkage studies of outcomes after medically assisted reproduction

Evaluation of the effectiveness of the Family Nurse Partnership home visiting programme in first time young mothers in Scotland: a protocol for a natural experiment

Childhood adversity, mental health and suicide (CHASE): a protocol for a longitudinal case-control linked data study

Essential Requirements for Establishing and Operating Data Trusts

Practical Guidance Based on A Working Meeting of Fifteen Canadian Organizations and Initiatives

Empowering knowledge generation through international data network: the IMeCCHI-DATANETWORK

Data Resource: Children and Family Court Advisory and Support Service (Cafcass) public family law administrative records in England

The SPOR-Canadian Data Platform: a national initiative to facilitate data rich multi-jurisdictional research

Using general practice clinical information system data for research: the case in Australia

National data opt out programme: consequences for maternity services in England

Effect of Study Duration and Outcome Measurement Frequency on Estimates of Change for Longitudinal Cohort Studies in Routinely-Collected Administrative Data

Unlocking the Potential of Electronic Health Records for Health Research