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Ségolène Aymé
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2010 – 2019
- 2017
- [j3]Sebastian Köhler, Nicole A. Vasilevsky
, Mark Engelstad, Erin Foster
The Human Phenotype Ontology in 2017. Nucleic Acids Res. 45(Database-Issue): D865-D876 (2017) - 2014
- [j2]Matthew I. Bellgard
Correction: Dispelling myths about rare disease registry system development. Source Code Biol. Medicine 9: 4 (2014) - 2013
- [j1]Matthew I. Bellgard
Dispelling myths about rare disease registry system development. Source Code Biol. Medicine 8: 21 (2013) - 2011
- [c3]Maja Milicic Brandt, Ana Rath, Andrew Devereau, Ségolène Aymé:
Mapping Orphanet Terminology to UMLS. AIME 2011: 194-203 - 2010
- [c2]Paul Landais, Claude Messiaen
CEMARA an information system for rare diseases. MedInfo 2010: 481-485
2000 – 2009
- 2008
- [c1]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, Eva Bourdon-Lanoy, Rémi Salomon, Ségolène Aymé, Paul Landais:
CEMARA: a Web Dynamic Application Within a N-tier Architecture for Rare Diseases. MIE 2008: 51-56
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