Kerina H. Jones

发表

The Good, the Bad, the Clunky: Improving the Use of Administrative Data for Research

Paul Jackson, Kerina H. Jones, Sharon Heys, 2018, International journal of population data science.

Identifying and Addressing the Barriers to the Use of an Internet-Register for Multiple Sclerosis

Simon Thompson, Kerina H. Jones, David V. Ford, 2013, Int. J. Heal. Inf. Syst. Informatics.

A 3-dimensional balanced scorecard model for R&D

Kerina H. Jones, K. Jones, 2007 .

Desirability and expectations of the UK MS Register: Views of people with MS

Kerina H. Jones, David V. Ford, Lisa A. Osborne, 2013, Int. J. Medical Informatics.

The Good, the Bad, the Clunky and . . . the Outcomes

Kerina H. Jones, Sharon Heys, Karen Tingay, 2018 .

Sources of Discovery, Reasons for Registration, and Expectations of an Internet-Based Register for Multiple Sclerosis: Visualisations and Explorations of Word Uses and Contexts

Simon Thompson, Kerina H. Jones, David V. Ford, 2012, Int. J. Heal. Inf. Syst. Informatics.

A case study of the Secure Anonymous Information Linkage (SAIL) Gateway: A privacy-protecting remote access system for health-related research and evaluation☆

Simon Thompson, Chris Jones, Kerina H. Jones, 2014, J. Biomed. Informatics.

The other side of the coin: harm due to the non-use of health-related data

Kerina H. Jones, David V. Ford, Graeme Laurie, 2016, Int. J. Medical Informatics.

LINKAGE: Factors in selecting a data linkage approach

Kerina H. Jones, David V. Ford, 2019 .

Secure data analysis environments: can we agree on criteria for “Appropriate secure access” to linked health data?

J. Charles Victor, Kerina H. Jones, David V. Ford, 2018 .

On moving targets and magic bullets: Can the UK lead the way with responsible data linkage for health research?

Dipak Kalra, John D. Ainsworth, James A. Cunningham, 2015, Int. J. Medical Informatics.

Data safe havens to combine health and genomic data: benefits and challenges

Kerina H. Jones, Arron Lacey, Mark I. Rees, 2017 .

The feasibility of collecting information from people with Multiple Sclerosis for the UK MS Register via a web portal: characterising a cohort of people with MS

Kerina H. Jones, David V. Ford, Inocencio D. C. Maramba, 2012, BMC Medical Informatics and Decision Making.

The SAIL databank: linking multiple health and social care datasets

Kerina H. Jones, Caroline J. Brooks, David V. Ford, 2009, BMC Medical Informatics Decis. Mak..

The Potential of Research Drawing on Clinical Free Text to Bring Benefits to Patients in the United Kingdom: A Systematic Review of the Literature

Kerina H. Jones, Elizabeth Ford, Emma Squires, 2021, Frontiers in Digital Health.

A Review of Evidence Relating to Harm Resulting from Uses of Health and Biomedical Data

Kerina H. Jones, Graeme Laurie, Leslie Stevens, 1970 .

Involving consumers in the work of a data linkage research unit

Kerina H. Jones, David V. Ford, Cynthia L. McNerney, 2014 .

Outcome measures for multiple sclerosis

Phil Reed, Kerina H. Jones, David V. Ford, 2014 .