Raphael De Ridder

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 8 publications

Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.

Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.

Journal: Calcified tissue international

Published: November 14, 2024

Genetic Screening of ZNF687 and PFN1 in a Paget's Disease of Bone Cohort Indicates an Important Role for the Nuclear Localization Signal of ZNF687.

Genetic Screening of ZNF687 and PFN1 in a Paget's Disease of Bone Cohort Indicates an Important Role for the Nuclear Localization Signal of ZNF687.

Journal: Calcified tissue international

Published: July 19, 2023

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 Locus.

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 Locus.

Journal: Calcified tissue international

Published: April 07, 2021

A multi-omics approach expands the mutational spectrum of MAP2K1-related melorheostosis.

A multi-omics approach expands the mutational spectrum of MAP2K1-related melorheostosis.

Journal: Bone

Published: April 07, 2020

Resequencing of candidate genes for Keratoconus reveals a role for Ehlers-Danlos Syndrome genes.

Resequencing of candidate genes for Keratoconus reveals a role for Ehlers-Danlos Syndrome genes.

Journal: European journal of human genetics : EJHG

Published: August 06, 2019

Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations.

Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations.

Journal: Bone

Published: June 11, 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 Onset.

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 Onset.

Journal: Calcified tissue international

Published: November 05, 2018

Human Genetics of Sclerosing Bone Disorders.

Human Genetics of Sclerosing Bone Disorders.

Journal: Current osteoporosis reports

Published: April 16, 2018

Showing 1-8 of 8

Last Updated: 09/26/2026