G. Hendrickx

发表

Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters.

M. Andersen, K. Brixen, Igor Fijałkowski, 2014, Bone.

The Lrp4R1170Q Homozygous Knock‐In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans

G. Mortier, P. D’Haese, Igor Fijałkowski, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities

M. Andersen, K. Brixen, W. Van Hul, 2017, Calcified Tissue International.

WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in Osteoblasts

G. Mortier, E. Fransen, W. Van Hul, 2019, Calcified Tissue International.

Enzyme replacement therapy in mice lacking arylsulfatase B targets bone-remodeling cells, but not chondrocytes

M. Schweizer, C. Meyer-Schwesinger, M. Amling, 2020, Human molecular genetics.

Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis

G. Mortier, W. Van Hul, N. Hamdy, 2021, Genes.

Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia

G. Mortier, B. Peterlin, T. Haack, 2022, Journal of Medical Genetics.

A recessive form of craniodiaphyseal dysplasia caused by a homozygous missense variant in SP7/Osterix.

G. Mortier, W. Van Hul, D. Geneviève, 2022, Bone.

Piezo1 Inactivation in Chondrocytes Impairs Trabecular Bone Formation

U. Schumacher, M. Schweizer, M. Amling, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Lysosomal Protein Arylsulfatase B Is a Key Enzyme Involved in Skeletal Turnover

Georgia Makrypidi-Fraune, P. Saftig, M. Schweizer, 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetic control of bone mass

W. Hul, Igor Fijałkowski, G. Hendrickx, 2016, Molecular and Cellular Endocrinology.

Imbalanced cellular metabolism compromises cartilage homeostasis and joint function in a mouse model of mucolipidosis type III gamma

J. Simon Wiegert, H. Clausen‐Schaumann, M. Schweizer, 2020, Disease Models & Mechanisms.

High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench

D. Kiel, F. Rivadeneira, O. Mäkitie, 2022, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A look behind the scenes: the risk and pathogenesis of primary osteoporosis

W. Hul, G. Hendrickx, E. Boudin, 2015, Nature Reviews Rheumatology.

Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis

G. Mortier, R. Cousins, R. Stokroos, 2018, PLoS genetics.

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

Tycho Canter Cremers, G. Mortier, E. Fransen, 2021, Calcified Tissue International.

Transgenic inhibition of interleukin-6 trans-signaling does not prevent skeletal pathologies in mucolipidosis type II mice

J. Schwartz, S. Rose-John, M. Amling, 2021, Scientific Reports.

Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates

S. Bhadada, W. Van Hul, D. Dayal, 2021, AACE clinical case reports.

WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in Osteoblasts

G. Mortier, E. Fransen, W. Van Hul, 2019, Calcified Tissue International.

The Lrp4R1170Q Homozygous Knock‐In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans

G. Mortier, Igor Fijałkowski, W. Van Hul, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.