The RaDiCo information system for rare disease cohorts
RaDiCo provides a robust IS, compatible with the French Data Hub and RDs ERNs, integrated on a RD platform that enables e-cohorts creation, monitoring and analysis.
Authors
- Serge Amselem (ORCID: https://orcid.org/0000-0001-9506-3968)
- Paul Landais (ORCID: https://orcid.org/0000-0002-4166-8432)
- Sonia Guéguen
- Annick Clément
Institutions
- Inserm (FR)
- Université de Montpellier (FR)
- Sorbonne Université (FR)
- Hôpital Armand-Trousseau (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Maladies génétiques d’expression pédiatrique
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2025-04-08
- DOI
- https://doi.org/10.1186/s13023-025-03629-z
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Vanderbilt University
- Agence Nationale de la Recherche
- Institut National de la Santé et de la Recherche Médicale
- Sorbonne Université