Leader of the national health network for rare diseases AnDDI-Rares (Health Care for Developmental Anomalies and Intellectual Disability of Rare Causes); General coordinator of the University Hospital Federation TRANSLAD (Translational Medicine for Developmental Disorders) Bourgogne Franche-Comté; Co-coordination of an emerging research team “Genetics of developmental abnormalities” Univ. of Burgundy INSERM labeling in 2017 as part of UMR1231; Coordinator of the Reference Center Anomalies du développement et Syndromes malformatifs de l’Est (Developmental Anomalies and Malformative Syndromes of the East); HealthCare Provider of the European Reference Network ITHACA and Leader of the Teaching and Training WP; Supervisor of the Rare Disease Expertise Platform of the University Hospitals of Dijon and Besançon; Scientific co-director of the Institut de Médecine Génomique et Immunologique (Institute of Genomic and Immunological Medicine) Bourgogne Franche-Comté; Co-coordinator of the inter-univ. diploma Médecine Prédictive et Médecine Personnalisée (Predictive Medicine and Personalized Medicine); Co-coordinator of the inter-univ. diploma Essais Thérapeutiques et Maladies Rares (Therapeutic Trials and Rare Diseases); Coordinator of a patient-partner training (Dijon University).