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All Outputs (3)

Factors that influence public engagement with eHealth: a literature review (2011)
Journal Article
Hardiker, N., & Grant, M. (2011). Factors that influence public engagement with eHealth: a literature review. International Journal of Medical Informatics, 80(1), 1-12. https://doi.org/10.1016/j.ijmedinf.2010.10.017

Purpose: Public engagement with eHealth is generally viewed as beneficial. However, despite the potential benefits, public engagement with eHealth services remains variable. This article explores reasons for this variability through a review of publi... Read More about Factors that influence public engagement with eHealth: a literature review.

Semantic mappings and locality of nursing diagnostic concepts in UMLS (2011)
Journal Article
Kim, T., Coenen, A., & Hardiker, N. (2012). Semantic mappings and locality of nursing diagnostic concepts in UMLS. Journal of Biomedical Informatics, 45(1), 93-100. https://doi.org/10.1016/j.jbi.2011.09.002

One solution for enhancing the interoperability between nursing information systems, given the availability of multiple nursing terminologies, is to cross-map existing nursing concepts. The Unified Medical Language System (UMLS) developed and distrib... Read More about Semantic mappings and locality of nursing diagnostic concepts in UMLS.

Incorporating personalized gene sequence variants, molecular genetics knowledge, and health knowledge into an EHR prototype based on the continuity of care record standard (2011)
Journal Article
Jing, X., Kay, S., Marley, T., Hardiker, N., & Cimino, J. (2011). Incorporating personalized gene sequence variants, molecular genetics knowledge, and health knowledge into an EHR prototype based on the continuity of care record standard. Journal of Biomedical Informatics, 45(1), 82-92. https://doi.org/10.1016/j.jbi.2011.09.001

Objectives: the current volume and complexity of genetic tests, and the molecular genetics knowledge and health knowledge related to interpretation of the results of those tests, are rapidly outstripping the ability of individual clinicians to recall... Read More about Incorporating personalized gene sequence variants, molecular genetics knowledge, and health knowledge into an EHR prototype based on the continuity of care record standard.