Un outil de visualisation de classifications et d'intégration de données phénotypiques et génétiques pour faciliter le codage des maladies rares. - Rémy Choquet; Yannick Fonjallaz; Albane de Carrara; Meriem Maaroufi; Pierre-Yves Vandenbussche; Ferdinand Dhombres; Paul Landais (JFIM, 2014)

Formalizing Mappings to Optimize Automated Schema Alignment: Application to Rare Diseases. - Meriem Maaroufi; Rémy Choquet; Paul Landais; Marie-Christine Jaulent (MIE, 2014)

LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems. - Rémy Choquet; Meriem Maaroufi; Yannick Fonjallaz; Albane de Carrara; Pierre-Yves Vandenbussche; Ferdinand Dhombres; Paul Landais (AMIA, 2015)

Towards data integration automation for the French rare disease registry. - Meriem Maaroufi; Rémy Choquet; Paul Landais; Marie-Christine Jaulent (AMIA, 2015)

A methodology for a minimum data set for rare diseases to support national centers of excellence for healthcare and research. - Rémy Choquet; Meriem Maaroufi; Albane de Carrara; Claude Messiaen; Emmanuel Luigi; Paul Landais (J. Am. Medical Informatics Assoc., 2015)