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51

Localization of the Gene Causing the Osteopetrotic Phenotype in the Incisors Absent (Ia) Rat on Chromosome 10q32.1

Liesbeth van Wesenbeeck, Paul R Odgren, Carole A Mackay, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2004

Language:

english

File:

PDF, 194 KB

english, 2004

52

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids

Guy Van Camp, Wim Van Hul, Hubert Backhovens, Piet Stinissen, Anita Wehnert, David Patterson, Antoon Vandenberghe, Christine Van Broeckhoven

Journal:

Somatic Cell and Molecular Genetics

Year:

1990

Language:

english

File:

PDF, 843 KB

english, 1990

53

Recurrent Sclerosing Dysplasia of Bone: Report of a Case

Martin Druce Batstone, Gary Walton, Anthony Lynham, Frank Monsour, Wendy Balemans, Wim Van Hul

Journal:

Journal of Oral and Maxillofacial Surgery

Year:

2008

Language:

english

File:

PDF, 309 KB

english, 2008

54

Exclusion of the chromosomal 1p21 region in a large pedigree with a phenotypic variant of type II autosomal dominant osteopetrosis

Olivier David Bénichou, Els Van Hul, Wim Van Hul, Marie-Christine de Vernejoul

Journal:

Joint Bone Spine

Year:

2001

Language:

english

File:

PDF, 243 KB

english, 2001

55

Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators

Wendy Balemans, Wim Van Hul

Journal:

Developmental Biology

Year:

2002

Language:

english

File:

PDF, 537 KB

english, 2002

56

A Contiguous Physical Map of the Pericentromeric Region of Chromosome 21q between D21Z1 and D21S13E

Wim Van Hul, Guy Van Camp, Lieven Stuyver, Jean M. Delabar, Melvin G. McInnis, Andrew C. Warren, Stylianos E. Antonarakis, Christine Van Broeckhoven

Journal:

Year:

1993

File:

PDF, 397 KB

1993

57

The Human Extracellular Matrix Gene 1 (ECM1): Genomic Structure, cDNA Cloning, Expression Pattern, and Chromosomal Localization

Patrick Smits, Jian Ni, Ping Feng, Jan Wauters, Wim Van Hul, Mohamed El Boutaibi, Patrick J. Dillon, Joseph Merregaert

Journal:

Year:

1997

Language:

english

File:

PDF, 439 KB

english, 1997

58

Identification of a Third EXT-like Gene (EXTL3) Belonging to the EXT Gene Family

Wim Van Hul, Wim Wuyts, Jan Hendrickx, Frank Speleman, Jan Wauters, Kristel De Boulle, Nadine Van Roy, Paul Bossuyt, Patrick J. Willems

Journal:

Year:

1998

Language:

english

File:

PDF, 568 KB

english, 1998

59

Wnt signaling: A win for bone

Elke Piters, Eveline Boudin, Wim Van Hul

Journal:

Archives of Biochemistry and Biophysics

Year:

2008

Language:

english

File:

PDF, 525 KB

english, 2008

60

A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene

Wendy Balemans, Erna Cleiren, Ulrike Siebers, Jürgen Horst, Wim Van Hul

Journal:

Year:

2005

Language:

english

File:

PDF, 1.23 MB

english, 2005

61

Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis

José M. López, Wendy Balemans, Elke Piters, Wim Van Hul, Gilberto González

Journal:

Year:

2008

Language:

english

File:

PDF, 552 KB

english, 2008

62

Identification and characterization of 2 missense mutations in the LRP4 gene causing increased bone mineral density

Elke Piters, Olivier Leupin, Eveline Boudin, Fenna De Freitas, Manuel Bueno, Feliciano Ramos, Peter Itin, Michaela Kneissel, Wim Van Hul

Journal:

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

63

Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I

Alessandra Pangrazio, Eveline Boudin, Elke Piters, Giuseppe Damante, Nadia Lo Iacono, Angela Valentina D'Elia, Paolo Vezzoni, Wim Van Hul, Anna Villa, Cristina Sobacchi

Journal:

Year:

2011

Language:

english

File:

PDF, 259 KB

english, 2011

64

Variants in the FTO gene are associated with common obesity in the Belgian population

Armand Peeters, Sigri Beckers, An Verrijken, Peter Roevens, Pieter Peeters, Luc Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 104 KB

english, 2008

65

Association of the BDNF Val66Met variation with obesity in women

Sigri Beckers, Armand Peeters, Doreen Zegers, Ilse Mertens, Luc Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 574 KB

english, 2008

66

Association study of MC4R with complex obesity and replication of the rs17782313 association signal

Sigri Beckers, Doreen Zegers, Fenna de Freitas, Ilse L. Mertens, Luc F. Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 161 KB

english, 2011

67

Association between polymorphisms of the Nesfatin gene, NUCB2, and obesity in men

Doreen Zegers, Sigri Beckers, Ilse L. Mertens, Luc F. Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 255 KB

english, 2011

68

Association study of common variants in the sFRP1 gene region and parameters of bone strength and body composition in two independent healthy Caucasian male cohorts

Eveline Boudin, Elke Piters, Erik Fransen, Torben Leo Nielsen, Marianne Andersen, Greet Roef, Youri Taes, Kim Brixen, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 239 KB

english, 2012

69

Single nucleotide polymorphisms in sFRP4 are associated with bone and body composition related parameters in Danish but not in Belgian men

Eveline Boudin, Elke Piters, Torben Leo Nielsen, Marianne Andersen, Greet Roef, Youri Taes, Kim Brixen, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 209 KB

english, 2012

70

Hereditary multiple exostoses: from genetics to clinical syndrome and complications

Filip M Vanhoenacker, Wim Van Hul, Wim Wuyts, P.J Willems, Arthur M De Schepper

Journal:

European Journal of Radiology

Year:

2001

Language:

english

File:

PDF, 1.39 MB

english, 2001

71

Molecular and radiological diagnosis of sclerosing bone dysplasias

Wim Van Hul, Filip Vanhoenacker, Wendy Balemans, Katrien Janssens, A.M De Schepper

Journal:

European Journal of Radiology

Year:

2001

Language:

english

File:

PDF, 335 KB

english, 2001

72

Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21

Wim Van Hul, Wendy Balemans, Els Van Hul, Frederik G. Dikkers, Henk Obee, Robert J. Stokroos, Peter Hildering, Filip Vanhoenacker, Guy Van Camp, Patrick J. Willems

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 736 KB

english, 1998

73

Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, Florindo Mollica, Hermann-Josef Lüdecke, Bekir Sitki Sayli, Ugo E. Pazzaglia, Geert Mortier, Ben Hamel, Ern

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 327 KB

english, 1998

74

EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas

Judith V.M.G. Bovée, Anne-Marie Cleton-Jansen, Wim Wuyts, Goedele Caethoven, Antonie H.M. Taminiau, Egbert Bakker, Wim Van Hul, Cees J. Cornelisse, Pancras C.W. Hogendoorn

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 349 KB

english, 1999

75

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35

Lynne J. Hocking, Craig A. Herbert, Rosie K. Nicholls, Fiona Williams, Simon T. Bennett, Tim Cundy, Geoff C. Nicholson, Wim Wuyts, Wim Van Hul, Stuart H. Ralston

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 755 KB

english, 2001

76

Mapping of Autosomal Dominant Osteopetrosis Type II (Albers-Schönberg Disease) to Chromosome 16p13.3

Olivier Bénichou, Erna Cleiren, Jeppe Gram, Jens Bollerslev, Marie-Christine de Vernejoul, Wim Van Hul

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 1.54 MB

english, 2001

77

Localization of a Gene for Autosomal Dominant Osteopetrosis (Albers-Schönberg Disease) to Chromosome 1p21

Wim Van Hul, Jens Bollerslev, Jeppe Gram, Els Van Hul, Wim Wuyts, Olivier Benichou, Filip Vanhoenacker, Patrick J. Willems

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 260 KB

english, 1997

78

The Genetics of Low-Density Lipoprotein Receptor-Related Protein 5 in Bone: A Story of Extremes

Balemans, Wendy, Van Hul, Wim

Journal:

Year:

2007

Language:

english

File:

PDF, 209 KB

english, 2007

79

Identification of mutations in the NUCB2/nesfatin gene in children with severe obesity

Doreen Zegers, Sigri Beckers, Fenna de Freitas, Karen Jennes, Jasmijn K. Van Camp, Ilse L. Mertens, Kim Van Hoorenbeeck, Raoul P. Rooman, Kristine N. Desager, Guy Massa, Luc F. Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 417 KB

english, 2012

80

Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis

Eveline Boudin, Elke Piters, Igor Fijalkowski, Gino Stevenheydens, Ellen Steenackers, Outi Kuismin, Jukka S. Moilanen, Geert Mortier, Wim Van Hul

Journal:

Year:

2013

Language:

english

File:

PDF, 257 KB

english, 2013

81

Novel SOST gene mutation in a sclerosteosis patient and her parents

Sanjay Kumar Bhadada, Ashu Rastogi, Ellen Steenackers, Eveline Boudin, Ashutosh Arya, Vandana Dhiman, Anil Bhansali, Wim Van Hul

Journal:

Year:

2013

Language:

english

File:

PDF, 647 KB

english, 2013

82

Mutation analysis ofWNT10Bin obese children, adolescents and adults

Camp, Jasmijn K., Zegers, Doreen, Verhulst, Stijn L., Hoorenbeeck, Kim, Massa, Guy, Verrijken, An, Desager, Kristine N., Gaal, Luc F., Hul, Wim, Beckers, Sigri

Journal:

Endocrine (Springer)

Year:

2013

Language:

english

File:

PDF, 230 KB

english, 2013

83

Replication of the SH2B1 rs7498665 Association with Obesity in a Belgian Study Population

Beckers, Sigri, Zegers, Doreen, Van Gaal, Luc F., Van Hul, Wim

Journal:

Year:

2011

Language:

english

File:

PDF, 155 KB

english, 2011

84

Mutation Screening of EXT1 and EXT2 by Denaturing High-Performance Liquid Chromatography, Direct Sequencing Analysis, Fluorescence in Situ Hybridization, and a New Multiplex Ligation-Dependent Probe Amplification Probe Set in Patients with Multiple Osteochondromas

Jennes, Ivy, Entius, Mark M., Van Hul, Els, Parra, Alessandro, Sangiorgi, Luca, Wuyts, Wim

Journal:

The Journal of Molecular Diagnostics

Year:

2008

Language:

english

File:

PDF, 355 KB

english, 2008

85

The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases

Boudin, Eveline, Fijalkowski, Igor, Piters, Elke, Van Hul, Wim

Journal:

Seminars in Arthritis and Rheumatism

Year:

2013

Language:

english

File:

PDF, 855 KB

english, 2013

86

A Known SOST Gene Mutation Causes Sclerosteosis in a Familial and an Isolated Case from Brazilian Origin

Kim, Chong Ae, Honjo, Rachel, Bertola, Débora, Albano, Lílian, Oliveira, Luiz, Jales, Sumatra, Siqueira, José, Castilho, Arthur, Balemans, Wendy, Piters, Elke, Jennes, Karen, Van Hul, Wim

Journal:

Genetic Testing

Year:

2008

Language:

english

File:

PDF, 7.73 MB

english, 2008

87

Transforming Growth Factor-β1 to the Bone

Janssens, Katrien, ten Dijke, Peter, Janssens, Sophie, Van Hul, Wim

Journal:

Endocrine Reviews

Year:

2005

Language:

english

File:

PDF, 485 KB

english, 2005

88

The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island

Stinissen, Piet, Van Hul, Wim, Van Camp, Guy, Backhovens, Hubert, Wehnert, Anita, Vandenberghe, Antoon, Van Broeckhoven, Christine

Journal:

Year:

1990

Language:

english

File:

PDF, 565 KB

english, 1990

89

Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters

Hendrickx, Gretl, Boudin, Eveline, Fijałkowski, Igor, Nielsen, Torben Leo, Andersen, Marianne, Brixen, Kim, Van Hul, Wim

Journal:

Year:

2014

Language:

english

File:

PDF, 612 KB

english, 2014

90

D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21

Warren, Andrew C., Petersen, Michael B., Van Hul, Wim, McInnis, Melvin G., Van Broeckhoven, Christine, Cox, Tara K., Chakravarti, Aravinda, Antonarakis, Stylianos E.

Journal:

Year:

1992

Language:

english

File:

PDF, 461 KB

english, 1992

91

A common LRP4 haplotype is associated with bone mineral density and hip geometry in men—Data from the Odense Androgen Study (OAS)

Boudin, Eveline, Steenackers, Ellen, Freitas, Fenna de, Nielsen, Torben Leo, Andersen, Marianne, Brixen, Kim, Hul, Wim Van, Piters, Elke

Journal:

Year:

2013

Language:

english

File:

PDF, 226 KB

english, 2013

92

No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders

Boudin, Eveline, Jennes, Karen, de Freitas, Fenna, Tegay, David, Mortier, Geert, Van Hul, Wim

Journal:

Year:

2013

Language:

english

File:

PDF, 171 KB

english, 2013

93

Camurati–Engelmann Disease (Progressive Diaphyseal Dysplasia): Reports of an Indian Kindred

Bhadada, Sanjay Kumar, Sridhar, Subbiah, Steenackers, Ellen, Dhiman, Vandana, Mortier, Geert, Bhansali, Anil, Hul, Wim

Journal:

Calcified Tissue International

Year:

2014

Language:

english

File:

PDF, 485 KB

english, 2014

94

Sclerosing Bone Dysplasias: Leads Toward Novel Osteoporosis Treatments

Fijalkowski, Igor, Boudin, Eveline, Mortier, Geert, Van Hul, Wim

Journal:

Current Osteoporosis Reports

Year:

2014

Language:

english

File:

PDF, 427 KB

english, 2014

95

Adipose Triglyceride Lipase and Hormone-Sensitive Lipase Protein Expression Is Decreased in the Obese Insulin-Resistant State

Jocken, Johan W. E., Langin, Dominique, Smit, Egbert, Saris, Wim H. M., Valle, Carine, Hul, Gabby B., Holm, Cecilia, Arner, Peter, Blaak, Ellen E.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2007

Language:

english

File:

PDF, 281 KB

english, 2007

96

PPARα gene expression correlates with severity and histological treatment response in patients with non-alcoholic steatohepatitis

Francque, Sven, Verrijken, An, Caron, Sandrine, Prawitt, Janne, Paumelle, Réjane, Derudas, Bruno, Lefebvre, Philippe, Taskinen, Marja-Riitta, Van Hul, Wim, Mertens, Ilse, Hubens, Guy, Van Marck, Eric,

Journal:

Journal of Hepatology

Year:

2015

Language:

english

File:

PDF, 965 KB

english, 2015

97

Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome

van den Ende, Jenneke J., Borra, Vere, Van Hul, Wim

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 365 KB

english, 2013

98

Lessons from Sclerosing Bone Dysplasias

Journal:

Hormone Research

Year:

2007

Language:

english

File:

PDF, 85 KB

english, 2007

99

A Mutation Affecting the Latency-Associated Peptide of TGFβ1 in Camurati-Engelmann Disease Enhances Osteoclast Formation in Vitro

McGowan, Neil W. A., MacPherson, Heather, Janssens, Katrien, Van Hul, Wim, Frith, Julie C., Fraser, William D., Ralston, Stuart H., Helfrich, Miep H.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2003

Language:

english

File:

PDF, 287 KB

english, 2003

100

Sclerosing bone disorders: a lot of knowns but still some unknowns

Journal:

BoneKEy Reports

Year:

2012

Language:

english

File:

PDF, 205 KB

english, 2012