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Ségolène Aymé
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2010 – 2019
- 2017
- [j3]Sebastian Köhler, 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
, Patrick F. Chinnery
, Valentina Cipriani
, Laureen E. Connell, Hugh J. S. Dawkins, Laura E. DeMare, Andrew Devereau, Bert B. A. de Vries, Helen V. Firth, Kathleen Freson
, Daniel Greene, Ada Hamosh, Ingo Helbig, Courtney Hum
, Johanna Jähn, Roger James
, Roland Krause
, Stanley J. F. Laulederkind
, Hanns Lochmüller, Gholson J. Lyon, Soichi Ogishima, Annie Olry, Willem H. Ouwehand, Nikolas Pontikos
, Ana Rath, Franz Schaefer, Richard H. Scott, Michael Segal, Panagiotis I. Sergouniotis, Richard Sever
, Cynthia L. Smith, Volker Straub
, Rachel Thompson
, Catherine Turner
, Ernest Turro
, Marijcke W. M. Veltman, Tom Vulliamy, Jing Yu, Julie von Ziegenweidt, Andreas Zankl, Stephan Züchner, Tomasz Zemojtel, Julius O. B. Jacobsen
, Tudor Groza
, Damian Smedley, Christopher J. Mungall, Melissa A. Haendel
, Peter N. Robinson:
The Human Phenotype Ontology in 2017. Nucleic Acids Res. 45(Database-Issue): D865-D876 (2017) - 2014
- [j2]Matthew I. Bellgard
, Christophe Béroud, Kay Parkinson, Tess Harris, Ségolène Aymé, Gareth Baynam, Tarun Weeramanthri, Hugh J. S. Dawkins, Adam Hunter:
Correction: Dispelling myths about rare disease registry system development. Source Code Biol. Medicine 9: 4 (2014) - 2013
- [j1]Matthew I. Bellgard
, Christophe Béroud
, Kay Parkinson, Tess Harris, Ségolène Aymé, Gareth Baynam, Tarun Weeramanthri, Hugh J. S. Dawkins, Adam Hunter:
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
, 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, Rémi Salomon, Ségolène Aymé, Martine Le Merrer, Alain Verloes
:
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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