Coucke, Paul

Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood

Malfait, F., Symoens, S., De Backer, J., Hermanns-Lê, T., Sakalihasan, N., Lapière, C. M., Coucke, P., & De Paepe, A. (2007) · Human Mutation

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 167

Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

Symoens, S., Syx, D., Malfait, F., Callewaert, B., De Backer, J., Vanakker, O., Coucke, P., & De Paepe, A. (2012) · Human Mutation

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 165

Total absence of the α2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems

Malfait, F., Symoens, S., Coucke, P., Nunes, L., De Almeida, S., & De Paepe, A. (2006) · Journal of Medical Genetics

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 124

Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family

Syx, D., Symoens, S., Steyaert, W., De Paepe, A., Coucke, P. J., & Malfait, F. (2015) · Disease Markers

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 34

Genetics of the Ehlers–Danlos syndrome: More than collagen disorders

Van Damme, T., Syx, D., Coucke, P., Symoens, S., De Paepe, A., & Malfait, F. (2015) · Expert Opinion on Orphan Drugs

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 4