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Current Osteoporosis Reports|April 16, 2018
Human Genetics of Sclerosing Bone DisordersRaphaël De Ridder, Eveline Boudin, Geert Mortier, et al.
Calcified Tissue International|September 20, 2023
Genetic Screening of ZNF687 and PFN1 in a Paget's Disease of Bone Cohort Indicates an Important Role for the Nuclear Localization Signal of ZNF687Yentl Huybrechts, Raphaël De Ridder, Ellen Steenackers, et al.
Calcified Tissue International|February 7, 2019
Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of OnsetRaphaël De Ridder, Eveline Boudin, Geert Vandeweyer, et al.
Bone|May 11, 2020
A multi-omics approach expands the mutational spectrum of MAP2K1-related melorheostosisRaphaël De Ridder, Eveline Boudin, M Carola Zillikens, et al.
Calcified Tissue International|June 26, 2021
A Panel-Based Sequencing Analysis of Patients with Paget's Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importance of the 7q33 LocusRaphaël De Ridder, Geert Vandeweyer, Eveline Boudin, et al.
Bone|August 27, 2019
Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutationsJoséphine J M Peeters, Raphaël De Ridder, Esther C Hamoen, et al.
Calcified Tissue International|March 14, 2025
Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of BoneYentl Huybrechts, Raphaël De Ridder, Dylan Bergen, et al.
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