A look behind the scenes: the risk and pathogenesis of primary osteoporosis
Hendrickx, Gretl, Boudin, Eveline, Van Hul, Wim
Published in Nature reviews. Rheumatology (01.08.2015)
Published in Nature reviews. Rheumatology (01.08.2015)
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Journal Article
Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M)
Das, Liza, Dhiman, Vandana, Van Hul, Wim, Bhansali, Anil, Gogate, Yashpal, Steenackers, Ellen, Mortier, Geert, Bhadada, Sanjay Kumar
Published in Bone Reports (01.06.2020)
Published in Bone Reports (01.06.2020)
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Journal Article
WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders
Huybrechts, Yentl, Mortier, Geert, Boudin, Eveline, Van Hul, Wim
Published in Frontiers in endocrinology (Lausanne) (09.04.2020)
Published in Frontiers in endocrinology (Lausanne) (09.04.2020)
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Journal Article
Camurati–Engelmann Disease
Van Hul, Wim, Boudin, Eveline, Vanhoenacker, Filip M., Mortier, Geert
Published in Calcified tissue international (01.05.2019)
Published in Calcified tissue international (01.05.2019)
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Journal Article
Transforming Growth Factor-β1 to the Bone
Janssens, Katrien, ten Dijke, Peter, Janssens, Sophie, Van Hul, Wim
Published in Endocrine reviews (01.10.2005)
Published in Endocrine reviews (01.10.2005)
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Journal Article
Genetic control of bone mass
Boudin, Eveline, Fijalkowski, Igor, Hendrickx, Gretl, Van Hul, Wim
Published in Molecular and cellular endocrinology (05.09.2016)
Published in Molecular and cellular endocrinology (05.09.2016)
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Journal Article
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human
Ichimura, Atsuhiko, Hirasawa, Akira, Poulain-Godefroy, Odile, Bonnefond, Amélie, Hara, Takafumi, Yengo, Loïc, Kimura, Ikuo, Leloire, Audrey, Liu, Ning, Iida, Keiko, Choquet, Hélène, Besnard, Philippe, Lecoeur, Cécile, Vivequin, Sidonie, Ayukawa, Kumiko, Takeuchi, Masato, Ozawa, Kentaro, Tauber, Maithé, Maffeis, Claudio, Morandi, Anita, Buzzetti, Raffaella, Elliott, Paul, Pouta, Anneli, Jarvelin, Marjo-Riitta, Körner, Antje, Kiess, Wieland, Pigeyre, Marie, Caiazzo, Roberto, Van Hul, Wim, Van Gaal, Luc, Horber, Fritz, Balkau, Beverley, Lévy-Marchal, Claire, Rouskas, Konstantinos, Kouvatsi, Anastasia, Hebebrand, Johannes, Hinney, Anke, Scherag, Andre, Pattou, François, Meyre, David, Koshimizu, Taka-aki, Wolowczuk, Isabelle, Tsujimoto, Gozoh, Froguel, Philippe
Published in Nature (London) (15.03.2012)
Published in Nature (London) (15.03.2012)
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Journal Article
Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators
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Book Review
Journal Article
A Novel Domain‐Specific Mutation in a Sclerosteosis Patient Suggests a Role of LRP4 as an Anchor for Sclerostin in Human Bone
Fijalkowski, Igor, Geets, Ellen, Steenackers, Ellen, Van Hoof, Viviane, Ramos, Feliciano J, Mortier, Geert, Fortuna, Ana Maria, Van Hul, Wim, Boudin, Eveline
Published in Journal of bone and mineral research (01.04.2016)
Published in Journal of bone and mineral research (01.04.2016)
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Journal Article
WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in Osteoblasts
Hendrickx, Gretl, Boudin, Eveline, Verbeek, Marinus, Fransen, Erik, Mortier, Geert, Van Hul, Wim
Published in Calcified tissue international (01.03.2020)
Published in Calcified tissue international (01.03.2020)
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Journal Article
Bone Overgrowth-associated Mutations in the LRP4 Gene Impair Sclerostin Facilitator Function
Leupin, Olivier, Piters, Elke, Halleux, Christine, Hu, Shouih, Kramer, Ina, Morvan, Frederic, Bouwmeester, Tewis, Schirle, Markus, Bueno-Lozano, Manuel, Ramos Fuentes, Feliciano J., Itin, Peter H., Boudin, Eveline, de Freitas, Fenna, Jennes, Karen, Brannetti, Barbara, Charara, Nadine, Ebersbach, Hilmar, Geisse, Sabine, Lu, Chris X., Bauer, Andreas, Van Hul, Wim, Kneissel, Michaela
Published in The Journal of biological chemistry (03.06.2011)
Published in The Journal of biological chemistry (03.06.2011)
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Journal Article
Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia
Beyltjens, Tessi, Boudin, Eveline, Revencu, Nicole, Boeckx, Nele, Bertrand, Miriam, Schütz, Leon, Haack, Tobias B, Weber, Axel, Biliouri, Eleni, Vinkšel, Mateja, Zagožen, Anja, Peterlin, Borut, Pai, Shashidhar, Telegrafi, Aida, Henderson, Lindsay B, Ells, Courtney, Turner, Lesley, Wuyts, Wim, Van Hul, Wim, Hendrickx, Gretl, Mortier, Geert R
Published in Journal of medical genetics (01.05.2023)
Published in Journal of medical genetics (01.05.2023)
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Journal Article
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
Palencia-Campos, Adrian, Aoto, Phillip C., Machal, Erik M.F., Rivera-Barahona, Ana, Soto-Bielicka, Patricia, Bertinetti, Daniela, Baker, Blaine, Vu, Lily, Piceci-Sparascio, Francesca, Torrente, Isabella, Boudin, Eveline, Peeters, Silke, Van Hul, Wim, Huber, Celine, Bonneau, Dominique, Hildebrand, Michael S., Coleman, Matthew, Bahlo, Melanie, Bennett, Mark F., Schneider, Amy L., Scheffer, Ingrid E., Kibæk, Maria, Kristiansen, Britta S., Issa, Mahmoud Y., Mehrez, Mennat I., Ismail, Samira, Tenorio, Jair, Li, Gaoyang, Skålhegg, Bjørn Steen, Otaify, Ghada A., Temtamy, Samia, Aglan, Mona, Jønch, Aia E., De Luca, Alessandro, Mortier, Geert, Cormier-Daire, Valérie, Ziegler, Alban, Wallis, Mathew, Lapunzina, Pablo, Herberg, Friedrich W., Taylor, Susan S., Ruiz-Perez, Victor L.
Published in American journal of human genetics (05.11.2020)
Published in American journal of human genetics (05.11.2020)
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Journal Article
DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age
Peeters, Silke, Declerck, Ken, Thomas, Muriel, Boudin, Eveline, Beckers, Dominique, Chivu, Olimpia, Heinrichs, Claudine, Devriendt, Koenraad, de Zegher, Francis, Van Hul, Wim, Vanden Berghe, Wim, De Schepper, Jean, Rooman, Raoul, Mortier, Geert
Published in The journal of clinical endocrinology and metabolism (01.12.2020)
Published in The journal of clinical endocrinology and metabolism (01.12.2020)
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Journal Article
PLEKHM1 Regulates Salmonella-Containing Vacuole Biogenesis and Infection
McEwan, David G., Richter, Benjamin, Claudi, Beatrice, Wigge, Christoph, Wild, Philipp, Farhan, Hesso, McGourty, Kieran, Coxon, Fraser P., Franz-Wachtel, Mirita, Perdu, Bram, Akutsu, Masato, Habermann, Anja, Kirchof, Anja, Helfrich, Miep H., Odgren, Paul R., Van Hul, Wim, Frangakis, Achilleas S., Rajalingam, Krishnaraj, Macek, Boris, Holden, David W., Bumann, Dirk, Dikic, Ivan
Published in Cell host & microbe (14.01.2015)
Published in Cell host & microbe (14.01.2015)
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Journal Article
Delineation of a new fibrillin-2-opathy with evidence for a role of FBN2 in the pathogenesis of carpal tunnel syndrome
Peeters, Silke, Decramer, Arne, Cain, Stuart Alan, Houpt, Peter, Verstreken, Frederik, Noyez, Jan, Hermans, Christophe, Jacobs, Werner, Lammens, Martin, Fransen, Erik, Kumar, Ajay Anand, Vandeweyer, Geert, Loeys, Bart, Van Hul, Wim, Baldock, Clair, Boudin, Eveline, Mortier, Geert
Published in Journal of medical genetics (01.11.2021)
Published in Journal of medical genetics (01.11.2021)
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Journal Article