Torthaí cuardaigh - Van Hul, Wim

Sclerosing bone disorders: a lot of knowns but still some unknowns de réir Van Hul, Wim

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WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders de réir Huybrechts, Yentl, Mortier, Geert, Boudin, Eveline, Van Hul, Wim

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Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases? de réir de Vries, Teun J., Van Hul, Wim, Eekhoff, E. Marelise

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Replication of the SH2B1 rs7498665 Association with Obesity in a Belgian Study Population de réir Beckers, Sigri, Zegers, Doreen, Van Gaal, Luc F., Van Hul, Wim

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Reduced Affinity to and Inhibition by DKK1 Form a Common Mechanism by Which High Bone Mass-Associated Missense Mutations in LRP5 Affect Canonical Wnt Signaling de réir Ai, Minrong, Holmen, Sheri L., Van Hul, Wim, Williams, Bart O., Warman, Matthew L.

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Mapping of Autosomal Dominant Osteopetrosis Type II (Albers-Schönberg Disease) to Chromosome 16p13.3 de réir Bénichou, Olivier, Cleiren, Erna, Gram, Jeppe, Bollerslev, Jens, de Vernejoul, Marie-Christine, Van Hul, Wim

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Editorial: Innovative Therapies in Bone Biology: What Can Be Learned From Rare Bone Diseases? de réir Eekhoff, Elisabeth M. W., de Vries, Teun J., Sakkers, Ralph J. B., Van Hul, Wim

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Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M) de réir Das, Liza, Dhiman, Vandana, Van Hul, Wim, Bhansali, Anil, Gogate, Yashpal, Steenackers, Ellen, Mortier, Geert, Bhadada, Sanjay Kumar

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Copy number variant analysis and expression profiling of the olfactory receptor-rich 11q11 region in obesity predisposition de réir Diels, Sara, Huybreghts, Sander, Van Hoorenbeeck, Kim, Massa, Guy, Verrijken, An, Verhulst, Stijn L., Van Gaal, Luc F., Van Hul, Wim

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Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I de réir Pangrazio, Alessandra, Boudin, Eveline, Piters, Elke, Damante, Giuseppe, Iacono, Nadia Lo, D'Elia, Angela Valentina, Vezzoni, Paolo, Van Hul, Wim, Villa, Anna, Sobacchi, Cristina

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Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates de réir Das, Liza, Dhiman, Vandana, Dutta, Pinaki, Sood, Ashwani, Prakash, Mahesh, Kaur, Simran, Steenackers, Ellen, Hendrickx, Gretl, Dayal, Devi, Van Hul, Wim, Bhadada, Sanjay Kumar

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The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondra... de réir Van Wesenbeeck, Liesbeth, Odgren, Paul R., MacKay, Carole A., D'Angelo, Marina, Safadi, Fayez F., Popoff, Steven N., Van Hul, Wim, Marks, Sandy C.

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Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35 de réir Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, Nicholson, Geoff C., Wuyts, Wim, Van Hul, Wim, Ralston, Stuart H.

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Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis de réir Huybrechts, Yentl, Boudin, Eveline, Hendrickx, Gretl, Steenackers, Ellen, Hamdy, Neveen, Mortier, Geert, Martínez Díaz-Guerra, Guillermo, Bracamonte, Milagros Sierra, Appelman-Dijkstra, Natasha M., Van Hul, Wim

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Identification and Functional Characterization of Novel Mutations in the Melanocortin-4 Receptor de réir Beckers, Sigri, Zegers, Doreen, de Freitas, Fenna, Peeters, Armand V., Verhulst, Stijn L., Massa, Guy, Van Gaal, Luc F., Timmermans, Jean-Pierre, Desager, Kristine N., Van Hul, Wim

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TGF-β1-induced Migration of Bone Mesenchymal Stem Cells Couples Bone Resorption and Formation de réir Tang, Yi, Wu, Xiangwei, Lei, Weiqi, Pang, Lijuan, Wan, Chao, Shi, Zhenqi, Zhao, Ling, Nagy, Timothy R., Peng, Xinyu, Hu, Junbo, Feng, Xu, Van Hul, Wim, Wan, Mei, Cao, Xu

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A targeted multi-omics approach reveals paraoxonase-1 as a determinant of obesity-associated fatty liver disease de réir Diels, Sara, Cuypers, Bart, Tvarijonaviciute, Asta, Derudas, Bruno, Van Dijck, Evelien, Verrijken, An, Van Gaal, Luc F., Laukens, Kris, Lefebvre, Philippe, Ceron, Jose J., Francque, Sven, Vanden Berghe, Wim, Van Hul, Wim

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Functional Assessment of Coding and Regulatory Variants From the DKK1 Locus de réir Martínez‐Gil, Núria, Roca‐Ayats, Neus, Atalay, Nurgül, Pineda‐Moncusí, Marta, Garcia‐Giralt, Natàlia, Van Hul, Wim, Boudin, Eveline, Ovejero, Diana, Mellibovsky, Leonardo, Nogués, Xavier, Díez‐Pérez, Adolfo, Grinberg, Daniel, Balcells, Susanna

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Six Novel Missense Mutations in the LDL Receptor-Related Protein 5 (LRP5) Gene in Different Conditions with an Increased Bone Density de réir Van Wesenbeeck, Liesbeth, Cleiren, Erna, Gram, Jeppe, Beals, Rodney K., Bénichou, Olivier, Scopelliti, Domenico, Key, Lyndon, Renton, Tara, Bartels, Cindy, Gong, Yaoqin, Warman, Matthew L., de Vernejoul, Marie-Christine, Bollerslev, Jens, Van Hul, Wim

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Broadening the Spectrum of Loss-of-Function Variants in NPR-C-Related Extreme Tall Stature de réir Lauffer, Peter, Boudin, Eveline, van der Kaay, Daniëlle C M, Koene, Saskia, van Haeringen, Arie, van Tellingen, Vera, Van Hul, Wim, Prickett, Timothy C R, Mortier, Geert, Espiner, Eric A, van Duyvenvoorde, Hermine A

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