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2020 – today
- 2024
[j3]Carole Faviez, Xiaoyi Chen, Nicolas Garcelon
, Mohamad Zaidan, Katy Billot, Friederike Petzold, Hassan Faour, Maxime Douillet, Jean-Michel Rozet, Valerie Cormier-Daire, Tania Attié-Bitach, Stanislas Lyonnet, Sophie Saunier, Anita Burgun:
Objectivizing issues in the diagnosis of complex rare diseases: lessons learned from testing existing diagnosis support systems on ciliopathies. BMC Medical Informatics Decis. Mak. 24(1): 134 (2024)
2010 – 2019
- 2019
- [j2]Xiaoyi Chen, Nicolas Garcelon, Antoine Neuraz, Katy Billot, Marc Lelarge, Thomas Bonald, Hugo Garcia, Yoann Martin, Vincent Benoit, Marc Vincent, Hassan Faour, Maxime Douillet, Stanislas Lyonnet, Sophie Saunier, Anita Burgun:
Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping. J. Biomed. Informatics 100 (2019)
2000 – 2009
- 2006
- [j1]Nathalie Boddaert, Fanny Mochel, I. Meresse, D. Seidenwurm, Arnaud Cachia, Francis Brunelle, Stanislas Lyonnet, Monica Zilbovicius:
Parieto-occipital grey matter abnormalities in children with Williams syndrome. NeuroImage 30(3): 721-725 (2006)
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