CEMARA: a Web Dynamic Application Within a N-tier Architecture for Rare Diseases. - Claude Messiaen; Loïc Le Mignot; Ana Rath; Jean-Baptiste Richard; Eric Dufour; Mohamed Ben Saïd; Jean Philippe Jaïs; Alain Verloes; Martine Le Merrer; Christine Bodemer; Geneviève Baujat; Marion Gerard-Blanluet; et al. (MIE, 2008)

CEMARA an information system for rare diseases. - Paul Landais; Claude Messiaen; Ana Rath; Loïc Le Mignot; Eric Dufour; Mohamed Ben Saïd; Jean Philippe Jaïs; Laurent Toubiana; Geneviève Baujat; Eva Bourdon-Lanoy; Marion Gerard-Blanluet; Christine Bodemer; et al. (MedInfo, 2010)

Mapping Orphanet Terminology to UMLS. - Maja Milicic Brandt; Ana Rath; Andrew Devereau; Ségolène Aymé (AIME, 2011)

Dispelling myths about rare disease registry system development. - Matthew I. Bellgard; Christophe Béroud; Kay Parkinson; Tess Harris; Ségolène Aymé; Gareth Baynam; Tarun Weeramanthri; Hugh J. S. Dawkins; Adam Hunter (Source Code Biol. Medicine, 2013)

Correction: Dispelling myths about rare disease registry system development. - Matthew I. Bellgard; Christophe Béroud; Kay Parkinson; Tess Harris; Ségolène Aymé; Gareth Baynam; Tarun Weeramanthri; Hugh J. S. Dawkins; Adam Hunter (Source Code Biol. Medicine, 2014)

The Human Phenotype Ontology in 2017. - Sebastian Köhler 001; Nicole A. Vasilevsky; Mark Engelstad; Erin Foster; Julie A. McMurry; Ségolène Aymé; Gareth Baynam; Susan M. Bello; Cornelius F. Boerkoel; Kym M. Boycott; Michael Brudno; Orion J. Buske; et al. (Nucleic Acids Res., 2017)