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Raphaël De Ridder

University of Antwerp

7

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16

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

2021 European Journal of Human Genetics
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A multi-omics approach expands the mutational spectrum of MAP2K1-related melorheostosis.

2020 Bone
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Gene set enrichment analysis reveals a first somatic mutation in the catalytic domain of MAP2K1 in a melorheostosis patient

2020 Bone reports
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Human Genetics of Sclerosing Bone Disorders

2018 Current Osteoporosis Reports
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Citations (7)