EUROCAT: an update on its functions and activities View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-10

AUTHORS

F. D. Tucker, J. K. Morris, on behalf of the JRC Management Committee, A. Neville, E. Garne, A. Kinsner-Ovaskainen, M. Lanzoni, M. A. Loane, S. Martin, C. Nicholl, J. Rankin, A. K. Rissmann

ABSTRACT

This paper provides an outline of the development and growth of EUROCAT, the European network of congenital anomaly registers. In recent years the network has been through a period of transition and change. The Central Register of data has transferred from the Ulster University to the EU Joint-Research-Centre, Ispra, Italy.The benefits of combining data from across Europe, from different populations and countries are described by the uses to which these data can be put. These uses include:. surveillance of anomalies at a local, regional or pan-European level. pharmacovigilance. registration of rare diseasesNew studies and projects are underway, including EUROlinkCAT (a Horizon 2020 funded data-linkage project), promising a fruitful future in further research of congenital anomalies. More... »

PAGES

407-410

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s12687-018-0367-3

DOI

http://dx.doi.org/10.1007/s12687-018-0367-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1103837006

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29736796


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