Understanding human linkeropathies: study of the phenotypic and molecular consequences of defective biosynthesis of the glycosaminoglycan tetrasaccharide linker region.

An integrated translational platform to gain insights in and improve diagnosis and management of the Ehlers-Danlos Syndromes.

An integrated translational platform to improve the management and outcome of rare heritable connective tissue disease

Chronic pain in Ehlers-Danlos syndrome: clinical and molecular characterization in human patients and a murine model

From variome to phenome: study of genetic defects underlying the heritable connective tissue disorder Ehlers-Danlos syndrome, and their pathogenic consequences on extracellular matrix organisation and function

Identification of novel genes and pathogenic pathways for osteogenesis imperfecta and Ehlers-Danlos syndrome, paradigm collagen disorders

Identifying a pain signature in classical Ehlers-Danlos syndrome

Linking extracellular matrix defects and chronic pain: the Ehlers-Danlos syndrome as a disease model

Study of mediators and pathways contributing to chronic pain in Ehlers-Danlos syndrome

Study of mediators and pathways contributing to chronic pain in Ehlers-Danlos syndrome 

Transmission Electron Microscopy Expertise Centre

Zebrafish as a model to study pain in Ehlers-Danlos syndromes

Research equipment for behavior analysis in zebrafish disease models.

Study of biological mechanisms involved in heritable connective tissue disorders, using the Ehlers-Danlos Syndrome as a paradigm

Study of the molecular pathogenesis of the Ehlers-Danlos syndrome

Study of molecular pathogenesis of Ehlers-Danlos syndrome/