W. Balemans

J. Gille, W. Van Hul, W. Balemans, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Polymorphisms in the Low-Density Lipoprotein Receptor-Related Protein 5 (LRP5) Gene Are Associated with Peak Bone Mass in Non-sedentary Men: Results from the Odense Androgen Study

M. Andersen, K. Brixen, B. Abrahamsen, 2007, Calcified Tissue International.

Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men

J. Kaufman, Minrong Ai, A. De Paepe, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Molecular and radiological diagnosis of sclerosing bone dysplasias.

A. D. De Schepper, K. Janssens, F. Vanhoenacker, 2001, European journal of radiology.

Identification of the disease-causing gene in sclerosteosis--discovery of a novel bone anabolic target?

W. Hul, W. Van Hul, W. Balemans, 2004, Journal of musculoskeletal & neuronal interactions.

The Binding Between Sclerostin and LRP5 is Altered by DKK1 and by High-Bone Mass LRP5 Mutations

Minrong Ai, M. Warman, W. Hul, 2008, Calcified Tissue International.

Novel LRP5 Missense Mutation in a Patient With a High Bone Mass Phenotype Results in Decreased DKK1‐Mediated Inhibition of Wnt Signaling*

J. Devogelaer, W. Van Hul, W. Balemans, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin.

C. Kim, W. Van Hul, D. Bertola, 2008, Genetic testing.

Patients with Van Buchem disease, an osteosclerotic genetic disease, have elevated bone formation markers, higher bone density, and greater derived polar moment of inertia than normal.

J. Wergedal, F. Vanhoenacker, W. Van Hul, 2003, The Journal of clinical endocrinology and metabolism.

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

M Dioszegi, K Lindpaintner, P. Tacconi, 2001, Human molecular genetics.

The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q.

C. Cremers, A. Parving, P. Willems, 1997, Genomics.

Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea

E. Green, P. Van de Heyning, P. Willems, 1997, European journal of human genetics : EJHG.

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.

R. Frants, P. Willems, D. van Velzen, 1995, Human molecular genetics.

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease

K. Lindpaintner, W. Hul, W. Wuyts, 2002, Journal of medical genetics.

A Clinical and Molecular Overview of the Human Osteopetroses

W. Hul, W. Balemans, L. V. Wesenbeeck, 2005, Calcified Tissue International.

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

F. E. Offeciers, K. Verhoeven, P. Govaerts, 1997, American journal of human genetics.

Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

W. Hul, R. Stokroos, P. Willems, 1998, American journal of human genetics.

Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

C. Stratakis, W. Hul, J. van den Ende, 1999, American journal of human genetics.

Van Buchem disease and sclerosteosis

W. Hul, W. Balemans, 2009 .

Human genetics of SOST.

W. Van Hul, W. Balemans, 2006, Journal of musculoskeletal & neuronal interactions.

Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms.

K. Lindpaintner, D. Reid, W. Hul, 2002, Bone.

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

S. Ralston, N. Haites, P. Willems, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Localisation of the gene for Van Buchem disease to a candidate region of less than 1 cM on chromosome 17.

W. Hul, R. Stokroos, P. Willems, 1997 .

Sclerosing bone dysplasias: genetic and radioclinical features

A. D. De Schepper, W. Hul, F. Vanhoenacker, 2000, European Radiology.

Essentiality of FASII pathway for Staphylococcus aureus

Koen Andries, K. Andries, N. Lounis, 2010, Nature.

Common Genetic Variation in the DKK1 Gene is Associated with Hip Axis Length but not with Bone Mineral Density and Bone Turnover Markers in Young Adult Men: Results from the Odense Androgen Study

M. Andersen, K. Brixen, W. Van Hul, 2010, Calcified Tissue International.

Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome

F. Eyskens, W. Van Hul, W. Courtens, 2007, American journal of medical genetics. Part A.

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

T. Fagerheim, K. Verhoeven, Richard J. H. Smith, 2000, Human Genetics.

Design, Synthesis, and Biological Evaluation of Novel Indoles Targeting the Influenza PB2 Cap Binding Region.

Christophe Buyck, J. Grimes, J. Keown, 2019, Journal of medicinal chemistry.

Linkage Designer and Linkage Reporter software for automated gene localization studies

P. Willems, G. Camp, W. Balemans, 1996 .

A novel LRP5 mutation in a patient with increased bone mass results in reduced DKK1-inhibition

W. Hul, J. Devogelaer, W. Balemans, 2006 .