Filip Vanhoenacker

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Jan Hellemans, Olena Preobrazhenska, Andy Willaert et al. · Nature Genetics · 2004 · 454 citations · Full text

Lemd3 Result, Developmental Biology, Sclerostin +9

Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

Liesbeth Van Wesenbeeck, Paul R. Odgren, Fraser P. Coxon et al. · Journal of Clinical Investigation · 2007 · 228 citations · Full text

Sclerostin, Bone Resorption, Pathology +16

Mutations in the gene encoding the latency-associated peptide of TGF-β1 cause Camurati-Engelmann disease

Katrien Janssens, Ruth Gershoni‐Baruch, Núria Guañabens et al. · Nature Genetics · 2000 · 211 citations

Latency-associated Peptide, Signal Transduction, Human Growth +5

Consensus document for the diagnosis of prosthetic joint infections: a joint paper by the EANM, EBJIS, and ESR (with ESCMID endorsement)

Alberto Signore, Luca Maria Sconfienza, Olivier Borens et al. · European Journal of Nuclear Medicine and Molecular Imaging · 2019 · 200 citations · Full text

Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

Wim Wuyts, Wim Van Hul, Kristel De Boulle et al. · The American Journal of Human Genetics · 1998 · 196 citations · Full text

Biology, Genetic Disorder, Natural Sciences +7