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2010 – 2019
- 2015
[j1]Rémy Choquet, Meriem Maaroufi, Albane de Carrara, Claude Messiaen
, Emmanuel Luigi, Paul Landais:
A methodology for a minimum data set for rare diseases to support national centers of excellence for healthcare and research. J. Am. Medical Informatics Assoc. 22(1): 76-85 (2015)- [c4]Rémy Choquet, Meriem Maaroufi, Yannick Fonjallaz, Albane de Carrara, Pierre-Yves Vandenbussche, Ferdinand Dhombres, Paul Landais:
LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems. AMIA 2015 - [c3]Meriem Maaroufi, Rémy Choquet, Paul Landais, Marie-Christine Jaulent:
Towards data integration automation for the French rare disease registry. AMIA 2015 - 2014
- [c2]Rémy Choquet, Yannick Fonjallaz, Albane de Carrara, Meriem Maaroufi, Pierre-Yves Vandenbussche, Ferdinand Dhombres, Paul Landais:
Un outil de visualisation de classifications et d'intégration de données phénotypiques et génétiques pour faciliter le codage des maladies rares. JFIM 2014: 198-203 - [c1]Meriem Maaroufi, Rémy Choquet, Paul Landais, Marie-Christine Jaulent:
Formalizing Mappings to Optimize Automated Schema Alignment: Application to Rare Diseases. MIE 2014: 283-287
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