Researcher
Wim Van Hul
- Research Expertise:Genetic analyses of obesity and comorbidities and skeletal dysplasias
- Keywords:SKELETAL DYSPLASIAS, OBESITY, PAGET DISEASE, GENETIC DISEASE, Biomedical sciences (incl. biochemistry)
- Disciplines:Endocrinology and metabolic diseases, Molecular and cell biology, Metabolic diseases, Genetics
- Research techniques:DNA-sequencing, Next generation sequencing, cloning, expression studies, cell cultures, animal models (mouse and zebrafish)
- Users of research expertise:teams with complementary expertise and interest
Affiliations
- Medical Genetics (MEDGEN) (Research group)
Member
From1 Oct 2022 → Today - Medical genetics of obesity and skeletal disorders (MGENOS) (Research group)
Responsible
From1 Oct 2003 → 30 Sep 2022
Projects
1 - 10 of 27
- Precision Medicine Technologies (PreMeT)From1 Jan 2021 → TodayFunding: IOF - mandates
- Unraveling the Role of Paraoxonase 1 and 3 in the Etiology and Progression of Obesity and Obesity-Associated Liver Disease.From1 Nov 2020 → TodayFunding: FWO fellowships
- GENOmics in MEDicine: From whole genome sequencing towards personalized medicine (GENOMED).From3 Jul 2019 → TodayFunding: BOF - Methusalem, Fund Recuperation Fiscal Exemption
- The role of the paraoxonase gene family in obesity and obesity-associated liver disease following exposure to environmental pollutants or medical intervention strategies.From1 Jan 2019 → 31 Dec 2022Funding: BOF - projects
- Functional evaluation of the role of LRP4 and NPR3 in the regulation of bone metabolism by regulating respectively bone mass and bone growth.From1 Oct 2017 → 30 Sep 2020Funding: FWO fellowships
- Paget's disease of bone: molecular genetic investigation of the NFkB signaling regulating genes CBL, CBLB, and NR4A1 and functional validation in vitro and in Danio rerio.From1 Jan 2017 → 31 Dec 2020Funding: FWO Strategic Basic Research Grant
- Gene identification and zebrafish disease modeling of inherited bone disordersFrom1 Jan 2017 → 31 Dec 2021Funding: FWO scientific research network
- Study on the role of LRP4 in the regulation of Wnt signaling and bone formation.From1 Jan 2015 → 31 Dec 2018Funding: FWO research project (including WEAVE projects)
- GENOMED - Genomics in Medicine.From1 Jan 2015 → 31 Dec 2019Funding: BOF - Other initiatives, Fund Recuperation Fiscal Exemption
- Systems biology for the functional validation of genetic determinants of skeletal diseases (SYBIL).From1 Oct 2013 → 30 Sep 2018Funding: Health
Publications
141 - 150 of 177
- A new familial sclerosing bone dysplasia(2010)
Authors: Eliane Chouery, Alessandra Pangrazio, Annalisa Frattini, Anna Villa, Liesbeth Van Wesenbeeck, Elke Piters, Wim Van Hul, Fraser P. Coxon, Tabitha Schouten, Miep Helfrich, et al.
Pages: 676 - 680 - Common variants in the gene for the serotonin receptor 6 (**HTR6**) do not contribute to obesity(2010)
Authors: Armand Peeters, Sigri Beckers, An Verrijken, Peter Roevens, Pieter J. Peeters, Luc Van Gaal, Wim Van Hul
Pages: 469 - 472 - Albers-Schönberg disease(2009)
Authors: Wim Van Hul
Pages: 70 - Moleculair-genetische oorzaken van de zieke van Paget en aanverwante ziektebeelden(2009)
Authors: Wim Van Hul
Pages: 59 - 62 - Antilichaam tegen sclerostine verhoogt de botvorming bij de rat(2009)
Authors: Wim Van Hul
Pages: 20 - Association study and mutation analysis of adiponectin shows association of variants in **APM1** with complex obesity in women(2009)
Authors: Sigri Beckers, Armand Peeters, Fenna de Freitas, Ilse L. Mertens, Stijn Verhulst, Dominique Haentjens, Kristine Desager, Wim Van Hul
Pages: 492 - 501 - Progressive diaphyseal dysplasia(2009)
Authors: Katrien Janssens, Wim Van Hul
Pages: 272 - Sclerostin in mineralized matrices and van Buchem disease(2009)
Authors: R.L. van Bezooijen, A.L. Bronckers, R.A. Gortzak, P.C.W. Hogendoorn, L. van der Wee-Pals, Wendy Balemans, H.J. Oostenbroek, Wim Van Hul, H. Hamersma, F.G. Dikkers, et al.
Pages: 569 - 574 - TGF-$\beta$ 1-induced migration of bone mesenchymal stem cells couples bone resorption with formation(2009)
Authors: Yi Tang, Xiangwei Wu, Weiqi Lei, Lijuan Pang, Chao Wan, Zhenqi Shi, Ling Zhao, Timothy R. Nagy, Xinyu Peng, Junbo Hu, et al.
Pages: 757 - 765 - Multiple exostoses, hereditary(2009)
Authors: Wim Wuyts, Wim Van Hul
Pages: 791