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Trends in Molecular Medicine|August 15, 2024
Pathogenic mechanisms in genetically defined Ehlers-Danlos syndromesDelfien Syx, Fransiska MalfaitGenes|February 25, 2022
The Ehlers-Danlos Syndromes against the Backdrop of Inborn Errors of MetabolismTim Van Damme, Marlies Colman, Delfien Syx, et al.Clinical and Experimental Rheumatology|October 3, 2017
Hypermobility, the Ehlers-Danlos syndromes and chronic painDelfien Syx, Inge De Wandele, Lies Rombaut, et al.JBMR Plus|March 29, 2021
Loss of TANGO1 Leads to Absence of Bone MineralizationBrecht Guillemyn, Sheela Nampoothiri, Delfien Syx, et al.Genes & Diseases|August 21, 2025
ADAMTS2: More than a procollagen N-proteinaseRuben Vanlerberghe, Alain Colige, Anne-Marie Malfait, et al.Current Rheumatology Reports|February 27, 2018
Peripheral Mechanisms Contributing to Osteoarthritis PainDelfien Syx, Phuong B Tran, Rachel E Miller, et al.Frontiers in Genetics|October 29, 2021
Animal Models of Ehlers-Danlos Syndromes: Phenotype, Pathogenesis, and Translational PotentialRobin Vroman, Anne-Marie Malfait, Rachel E Miller, et al.Pain|June 20, 2025
The influence of genetic and epigenetic variations on dynamic experimental pain measures in adults with and without chronic musculoskeletal pain: a systematic reviewAmber Billens, Amber De Groote, Delfien Syx, et al.Human Mutation|July 15, 2021
Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers-Danlos syndromeMarlies Colman, Delfien Syx, Inge De Wandele, et al.Disease Markers|October 28, 2015
Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian FamilyDelfien Syx, Sofie Symoens, Wouter Steyaert, et al.Pageof 6