Wim Van Hul

Wim Van Hul

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Wim Van Hul

Publications by authors named "Wim Van Hul"

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Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations.

Bone 2019 Aug 23;128:115044. Epub 2019 Aug 23.

Center for Bone Quality, Leiden University Medical Center, Leiden, the Netherlands; Department of Internal Medicine: Division of Endocrinology, Leiden University Medical Center, Leiden, the Netherlands.

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http://dx.doi.org/10.1016/j.bone.2019.115044DOI Listing
August 2019

Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of Onset.

Calcif Tissue Int 2019 Jun 6;104(6):613-621. Epub 2019 Feb 6.

Center of Medical Genetics, University of Antwerp & Antwerp University Hospital, Prins Boudewijnlaan 43, Edegem, 2650, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00223-019-00530-3DOI Listing
June 2019

Camurati-Engelmann Disease.

Calcif Tissue Int 2019 May 5;104(5):554-560. Epub 2019 Feb 5.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00223-019-00532-1DOI Listing
May 2019

DNA sequencing and copy number variation analysis of MCHR2 in a cohort of Prader Willi like (PWL) patients.

Obes Res Clin Pract 2018 Mar - Apr;12(2):158-166. Epub 2017 Oct 20.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.orcp.2017.10.001DOI Listing
April 2019

Sclerosing bone dysplasias.

Best Pract Res Clin Endocrinol Metab 2018 10 18;32(5):707-723. Epub 2018 Jun 18.

Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.beem.2018.06.003DOI Listing
October 2018

Human Genetics of Sclerosing Bone Disorders.

Curr Osteoporos Rep 2018 06;16(3):256-268

Centre of Medical Genetics, University of Antwerp & University Hospital Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s11914-018-0439-7DOI Listing
June 2018

MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation.

Eur J Endocrinol 2017 Aug 5;177(2):R69-R83. Epub 2017 Apr 5.

Center of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1530/EJE-16-0990DOI Listing
August 2017

Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities.

Calcif Tissue Int 2017 03 12;100(3):244-249. Epub 2017 Jan 12.

Center of Medical Genetics, University of Antwerp and University Hospital of Antwerp, Edegem, Belgium.

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http://dx.doi.org/10.1007/s00223-016-0213-8DOI Listing
March 2017

Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients.

Clin Res Hepatol Gastroenterol 2016 Dec 7;40(6):715-721. Epub 2016 Jun 7.

Department of Endocrinology, Diabetology and Metabolic Diseases, Antwerp University Hospital and University of Antwerp, Wilrijkstraat 10, 2650 Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.clinre.2016.05.004DOI Listing
December 2016

Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents.

Mol Biol Rep 2016 Oct 6;43(10):1041-7. Epub 2016 Aug 6.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s11033-016-4050-7DOI Listing
October 2016

Genetic control of bone mass.

Mol Cell Endocrinol 2016 09 30;432:3-13. Epub 2015 Dec 30.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.mce.2015.12.021DOI Listing
September 2016

Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfecta.

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2016 Sep 27;160(3):442-7. Epub 2016 Apr 27.

Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University in Prague, Czech Republic.

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http://dx.doi.org/10.5507/bp.2016.022DOI Listing
September 2016

Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity.

J Med Genet 2016 08 7;53(8):568-74. Epub 2016 Apr 7.

Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan Department of Orthopaedics, National Rehabilitation Center for Disabled Children, Tokyo, Japan.

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http://dx.doi.org/10.1136/jmedgenet-2016-103756DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769692PMC
August 2016

Association study of PNPLA2 gene with histological parameters of NAFLD in an obese population.

Clin Res Hepatol Gastroenterol 2016 Jun 20;40(3):333-339. Epub 2015 Oct 20.

Department of Endocrinology, Diabetology and Metabolic Diseases, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.clinre.2015.09.001DOI Listing
June 2016

Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss.

Am J Med Genet A 2016 06 20;170(6):1479-84. Epub 2016 Mar 20.

Department of Medical Genetics, University and University Hospital of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.37626DOI Listing
June 2016

Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity.

Endocrine 2016 May 26;52(2):277-86. Epub 2015 Oct 26.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-015-0778-4DOI Listing
May 2016

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

Authors:
Wim Van Hul

Bonekey Rep 2012 6;1:97. Epub 2012 Jun 6.

Department of Medical Genetics, University of Antwerp , Antwerp, Belgium .

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http://dx.doi.org/10.1038/bonekey.2012.97DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816290PMC
April 2016

A Novel Domain-Specific Mutation in a Sclerosteosis Patient Suggests a Role of LRP4 as an Anchor for Sclerostin in Human Bone.

J Bone Miner Res 2016 Apr 24;31(4):874-81. Epub 2016 Jan 24.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1002/jbmr.2782DOI Listing
April 2016

Germline mosaicism in osteopathia striata with cranial sclerosis--recurrence in siblings.

Clin Dysmorphol 2016 Apr;25(2):45-9

Departments of aClinical Genetics bRadiology, Our Lady's Children's Hospital Crumlin, Dublin, Ireland cDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1097/MCD.0000000000000116DOI Listing
April 2016

CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity.

Obesity (Silver Spring) 2016 Apr 27;24(4):970-6. Epub 2016 Feb 27.

Centre of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1002/oby.21435DOI Listing
April 2016

Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.

Mol Genet Metab 2016 Mar 9;117(3):383-8. Epub 2016 Jan 9.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2016.01.003DOI Listing
March 2016

A look behind the scenes: the risk and pathogenesis of primary osteoporosis.

Nat Rev Rheumatol 2015 Aug 21;11(8):462-74. Epub 2015 Apr 21.

Department of Medical Genetics, University of Antwerp, Prins Boudewijnlaan 43B, 2650 Edegem, Belgium.

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http://dx.doi.org/10.1038/nrrheum.2015.48DOI Listing
August 2015

Genetic and structural variation in the SH2B1 gene in the Belgian population.

Mol Genet Metab 2015 Aug 27;115(4):193-8. Epub 2015 May 27.

Centre of Medical Genetics, University of Antwerp, Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2015.05.010DOI Listing
August 2015

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.

Hum Mol Genet 2015 Jun 10;24(11):3038-49. Epub 2015 Feb 10.

Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France

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http://dx.doi.org/10.1093/hmg/ddv053DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424950PMC
June 2015

Prenatal diagnosis of osteopathia striata with cranial sclerosis.

Prenat Diagn 2015 Mar 26;35(3):302-4. Epub 2014 Nov 26.

Laboratoire de Pathologie, Hôpital Femme Mère Enfant, Université Claude Bernard Lyon I, Lyon, France.

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http://doi.wiley.com/10.1002/pd.4513
Publisher Site
http://dx.doi.org/10.1002/pd.4513DOI Listing
March 2015

PLEKHM1 regulates Salmonella-containing vacuole biogenesis and infection.

Cell Host Microbe 2015 Jan 11;17(1):58-71. Epub 2014 Dec 11.

Institute of Biochemistry II, Goethe University School of Medicine, Theodor-Stern-Kai 7, D-60590 Frankfurt (Main), Germany; Buchmann Institute for Molecular Life Sciences, Max-von-Laue-Str. 15, Goethe University 60438 Frankfurt am Main, Germany; University of Split, School of Medicine, Department of Immunology and Medical Genetics, Soltanska 2, 21 000 Split, Croatia. Electronic address:

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http://dx.doi.org/10.1016/j.chom.2014.11.011DOI Listing
January 2015

Sclerosing bone dysplasias: leads toward novel osteoporosis treatments.

Curr Osteoporos Rep 2014 Sep;12(3):243-51

Department of Medical Genetics, University and University Hospital of Antwerp, Edegem, Belgium.

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http://dx.doi.org/10.1007/s11914-014-0220-5DOI Listing
September 2014

Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred.

Calcif Tissue Int 2014 Feb 24;94(2):240-7. Epub 2013 Oct 24.

Department of Endocrinology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India,

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http://dx.doi.org/10.1007/s00223-013-9804-9DOI Listing
February 2014

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

Bone 2014 Feb 1;59:57-65. Epub 2013 Nov 1.

Department of Medical Genetics, University of Antwerp, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2013.10.022DOI Listing
February 2014

Prevalence of rare MC3R variants in obese cases and lean controls.

Endocrine 2013 Oct 24;44(2):386-90. Epub 2012 Dec 24.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, B-2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-012-9862-1DOI Listing
October 2013

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

Semin Arthritis Rheum 2013 Oct 21;43(2):220-40. Epub 2013 Feb 21.

Department of Medical Genetics, University of Antwerp, Edegem, Belgium.

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http://dx.doi.org/10.1016/j.semarthrit.2013.01.004DOI Listing
October 2013

Mutation analysis of WNT10B in obese children, adolescents and adults.

Endocrine 2013 Aug 27;44(1):107-13. Epub 2012 Oct 27.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-012-9824-7DOI Listing
August 2013

Genetic association study of WNT10B polymorphisms with BMD and adiposity parameters in Danish and Belgian males.

Endocrine 2013 Aug 17;44(1):247-54. Epub 2013 Jan 17.

Department of Medical Genetics, University of Antwerp, Prins Boudewijnlaan 43, 2650, Edegem, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-012-9869-7DOI Listing
August 2013

Autosomal dominant osteopetrosis revisited: lessons from recent studies.

Eur J Endocrinol 2013 Aug 13;169(2):R39-57. Epub 2013 Jul 13.

Section of Specialized Endocrinology, Medical Clinic B, Rikshospitalet, Oslo University Hospital, N-0027 Oslo, Norway.

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http://dx.doi.org/10.1530/EJE-13-0136DOI Listing
August 2013

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

Bone 2013 Jul 3;55(1):52-6. Epub 2013 Apr 3.

Department of Medical Genetics, University and University Hospital of Antwerp, Edegem, Belgium.

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http://dx.doi.org/10.1016/j.bone.2013.03.015DOI Listing
July 2013

No important role for genetic variation in the Chibby gene in monogenic and complex obesity.

Mol Biol Rep 2013 Jul 5;40(7):4491-8. Epub 2013 May 5.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s11033-013-2541-3DOI Listing
July 2013

Monogenic and complex forms of obesity: insights from genetics reveal the leptin-melanocortin signaling pathway as a common player.

Crit Rev Eukaryot Gene Expr 2012 ;22(4):325-43

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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June 2013

Resistin polymorphisms show associations with obesity, but not with bone parameters in men: results from the Odense Androgen Study.

Mol Biol Rep 2013 Mar 1;40(3):2467-72. Epub 2012 Dec 1.

Centre for Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s11033-012-2327-zDOI Listing
March 2013

Novel SOST gene mutation in a sclerosteosis patient and her parents.

Bone 2013 Feb 16;52(2):707-10. Epub 2012 Oct 16.

Dept. of Endocrinology and Metabolism, PGIMER, Chandigarh-160012, India.

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http://dx.doi.org/10.1016/j.bone.2012.10.009DOI Listing
February 2013

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

Clin Dysmorphol 2013 Jan;22(1):1-6

Department of Medical Genetics, University Hospital Antwerp, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1097/MCD.0b013e3283590986DOI Listing
January 2013

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

Bone 2013 Jan 6;52(1):292-5. Epub 2012 Oct 6.

Department of Medical Genetics, University and University Hospital of Antwerp, Edegem, Belgium.

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http://dx.doi.org/10.1016/j.bone.2012.09.034DOI Listing
January 2013

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

Mol Genet Metab 2012 Dec 22;107(4):729-34. Epub 2012 Oct 22.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1-2610 Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2012.10.014DOI Listing
December 2012

Assessment of gene-by-sex interaction effect on bone mineral density.

J Bone Miner Res 2012 Oct;27(10):2051-64

Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue CT3, Boston,MA 02118, USA.

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http://dx.doi.org/10.1002/jbmr.1679DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447125PMC
October 2012

Replication of the SH2B1 rs7498665 association with obesity in a Belgian study population.

Obes Facts 2011 6;4(6):473-7. Epub 2011 Dec 6.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1159/000335305DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444515PMC
June 2012

Paget's disease of bone: evidence for complex pathogenetic interactions.

Semin Arthritis Rheum 2012 Apr 29;41(5):619-41. Epub 2011 Sep 29.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.semarthrit.2011.07.005DOI Listing
April 2012

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.

Authors:
Karol Estrada Unnur Styrkarsdottir Evangelos Evangelou Yi-Hsiang Hsu Emma L Duncan Evangelia E Ntzani Ling Oei Omar M E Albagha Najaf Amin John P Kemp Daniel L Koller Guo Li Ching-Ti Liu Ryan L Minster Alireza Moayyeri Liesbeth Vandenput Dana Willner Su-Mei Xiao Laura M Yerges-Armstrong Hou-Feng Zheng Nerea Alonso Joel Eriksson Candace M Kammerer Stephen K Kaptoge Paul J Leo Gudmar Thorleifsson Scott G Wilson James F Wilson Ville Aalto Markku Alen Aaron K Aragaki Thor Aspelund Jacqueline R Center Zoe Dailiana David J Duggan Melissa Garcia Natàlia Garcia-Giralt Sylvie Giroux Göran Hallmans Lynne J Hocking Lise Bjerre Husted Karen A Jameson Rita Khusainova Ghi Su Kim Charles Kooperberg Theodora Koromila Marcin Kruk Marika Laaksonen Andrea Z Lacroix Seung Hun Lee Ping C Leung Joshua R Lewis Laura Masi Simona Mencej-Bedrac Tuan V Nguyen Xavier Nogues Millan S Patel Janez Prezelj Lynda M Rose Serena Scollen Kristin Siggeirsdottir Albert V Smith Olle Svensson Stella Trompet Olivia Trummer Natasja M van Schoor Jean Woo Kun Zhu Susana Balcells Maria Luisa Brandi Brendan M Buckley Sulin Cheng Claus Christiansen Cyrus Cooper George Dedoussis Ian Ford Morten Frost David Goltzman Jesús González-Macías Mika Kähönen Magnus Karlsson Elza Khusnutdinova Jung-Min Koh Panagoula Kollia Bente Lomholt Langdahl William D Leslie Paul Lips Östen Ljunggren Roman S Lorenc Janja Marc Dan Mellström Barbara Obermayer-Pietsch José M Olmos Ulrika Pettersson-Kymmer David M Reid José A Riancho Paul M Ridker François Rousseau P Eline Slagboom Nelson L S Tang Roser Urreizti Wim Van Hul Jorma Viikari María T Zarrabeitia Yurii S Aulchenko Martha Castano-Betancourt Elin Grundberg Lizbeth Herrera Thorvaldur Ingvarsson Hrefna Johannsdottir Tony Kwan Rui Li Robert Luben Carolina Medina-Gómez Stefan Th Palsson Sjur Reppe Jerome I Rotter Gunnar Sigurdsson Joyce B J van Meurs Dominique Verlaan Frances M K Williams Andrew R Wood Yanhua Zhou Kaare M Gautvik Tomi Pastinen Soumya Raychaudhuri Jane A Cauley Daniel I Chasman Graeme R Clark Steven R Cummings Patrick Danoy Elaine M Dennison Richard Eastell John A Eisman Vilmundur Gudnason Albert Hofman Rebecca D Jackson Graeme Jones J Wouter Jukema Kay-Tee Khaw Terho Lehtimäki Yongmei Liu Mattias Lorentzon Eugene McCloskey Braxton D Mitchell Kannabiran Nandakumar Geoffrey C Nicholson Ben A Oostra Munro Peacock Huibert A P Pols Richard L Prince Olli Raitakari Ian R Reid John Robbins Philip N Sambrook Pak Chung Sham Alan R Shuldiner Frances A Tylavsky Cornelia M van Duijn Nick J Wareham L Adrienne Cupples Michael J Econs David M Evans Tamara B Harris Annie Wai Chee Kung Bruce M Psaty Jonathan Reeve Timothy D Spector Elizabeth A Streeten M Carola Zillikens Unnur Thorsteinsdottir Claes Ohlsson David Karasik J Brent Richards Matthew A Brown Kari Stefansson André G Uitterlinden Stuart H Ralston John P A Ioannidis Douglas P Kiel Fernando Rivadeneira

Nat Genet 2012 Apr 15;44(5):491-501. Epub 2012 Apr 15.

Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://kooperberg.fhcrc.org/papers/2012estrada.pdf
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http://www.nature.com/doifinder/10.1038/ng.2249
Publisher Site
http://dx.doi.org/10.1038/ng.2249DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338864PMC
April 2012

Association study of polymorphisms in the SOST gene region and parameters of bone strength and body composition in both young and elderly men: data from the Odense Androgen Study.

Calcif Tissue Int 2012 Jan 11;90(1):30-9. Epub 2011 Nov 11.

Department of Medical Genetics, University and University Hospital of Antwerp, Prins Boudewijnlaan 43B, 2650 Edegem, Belgium.

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http://dx.doi.org/10.1007/s00223-011-9546-5DOI Listing
January 2012

The neurology of carbonic anhydrase type II deficiency syndrome.

Brain 2011 Dec 26;134(Pt 12):3502-15. Epub 2011 Nov 26.

Department of Ophthalmology and Paediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1093/brain/awr302DOI Listing
December 2011

[Osteopathia striata with cranial sclerosis].

Acta Med Port 2010 Nov-Dec;23(6):1147-50. Epub 2010 Dec 28.

Centro de Genética Médica Dr. Jacinto Magalhães, Departamento de Genética, Instituto Nacional de Saúde Dr. Ricardo Jorge, Porto.

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October 2011

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

Mol Genet Metab 2011 Jul 11;103(3):282-6. Epub 2011 Mar 11.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2011.03.007DOI Listing
July 2011

Identification and functional characterization of a missense mutation in resistin in two patients with severe obesity and insulin resistance.

Eur J Endocrinol 2011 Jun 25;164(6):927-36. Epub 2011 Mar 25.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, B-2610 Antwerp, Belgium.

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http://dx.doi.org/10.1530/EJE-10-1080DOI Listing
June 2011

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

Mol Genet Metab 2011 May 22;103(1):71-5. Epub 2011 Jan 22.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2011.01.007DOI Listing
May 2011

Identification of genetic modifiers of monogenic (bone) diseases: new tools available, but with limitations.

Authors:
Wim Van Hul

J Bone Miner Res 2011 May;26(5):918-9

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1002/jbmr.391DOI Listing
May 2011

Sclerosing bone disorders: too much of a good thing.

Crit Rev Eukaryot Gene Expr 2010 ;20(3):195-212

Department of Medical Genetics, University and University Hospital Antwerp, Belgium.

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February 2011

Identification of three novel genetic variants in the melanocortin-3 receptor of obese children.

Obesity (Silver Spring) 2011 Jan 10;19(1):152-9. Epub 2010 Jun 10.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1038/oby.2010.127DOI Listing
January 2011

Common variants in the gene for the serotonin receptor 6 (HTR6) do not contribute to obesity.

J Genet 2010 Dec;89(4):469-72

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12041-010-0066-2DOI Listing
December 2010

Common melanocortin-3 receptor variants are not associated with obesity, although rs3746619 does influence weight in obese individuals.

Endocrine 2010 Oct 23;38(2):289-93. Epub 2010 Oct 23.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-010-9386-5DOI Listing
October 2010

Identification and functional characterization of novel mutations in the melanocortin-4 receptor.

Obes Facts 2010 Oct 15;3(5):304-11. Epub 2010 Oct 15.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1159/000321565DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452105PMC
October 2010

A new familial sclerosing bone dysplasia.

J Bone Miner Res 2010 Mar;25(3):676-80

Unité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.

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http://dx.doi.org/10.1359/jbmr.090733DOI Listing
March 2010

The role of the leptin-melanocortin signalling pathway in the control of food intake.

Crit Rev Eukaryot Gene Expr 2009 ;19(4):267-87

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://www.dl.begellhouse.com/download/article/65f7f95a79ca0
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December 2009

Association study and mutation analysis of adiponectin shows association of variants in APM1 with complex obesity in women.

Ann Hum Genet 2009 Sep 1;73(Pt 5):492-501. Epub 2009 Jul 1.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, B-2610 Antwerp, Belgium.

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http://doi.wiley.com/10.1111/j.1469-1809.2009.00532.x
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http://dx.doi.org/10.1111/j.1469-1809.2009.00532.xDOI Listing
September 2009

Possible role for ENPP1 polymorphism in obesity but not for INSIG2 and PLIN variants.

Endocrine 2009 Aug 28;36(1):103-9. Epub 2009 Apr 28.

Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, Wilrijk, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s12020-009-9194-yDOI Listing
August 2009

TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation.

Nat Med 2009 Jul 5;15(7):757-65. Epub 2009 Jul 5.

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://dx.doi.org/10.1038/nm.1979DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727637PMC
July 2009

Association of the BDNF Val66Met variation with obesity in women.

Mol Genet Metab 2008 Sep-Oct;95(1-2):110-2. Epub 2008 Jul 29.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2008.06.008DOI Listing
November 2008

Association of SIRT1 gene variation with visceral obesity.

Hum Genet 2008 Nov 27;124(4):431-6. Epub 2008 Sep 27.

Department of Biomedical Sciences, Center for Medical Genetics, University of Antwerp, Universiteitsplein 1, Wilrijk, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00439-008-0567-8DOI Listing
November 2008

Recurrent sclerosing dysplasia of bone: report of a case.

J Oral Maxillofac Surg 2008 Nov;66(11):2372-4

Maxillofacial Unit, University Hospital Aintree, Liverpool, United Kingdom.

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http://dx.doi.org/10.1016/j.joms.2007.12.034DOI Listing
November 2008

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

Bone 2008 Aug 29;43(2):405-9. Epub 2008 Apr 29.

Department of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

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http://dx.doi.org/10.1016/j.bone.2008.04.011DOI Listing
August 2008

The binding between sclerostin and LRP5 is altered by DKK1 and by high-bone mass LRP5 mutations.

Calcif Tissue Int 2008 Jun;82(6):445-53

Department of Medical Genetics, University and University Hospital of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00223-008-9130-9DOI Listing
June 2008

Wnt signaling: a win for bone.

Arch Biochem Biophys 2008 May 14;473(2):112-6. Epub 2008 Mar 14.

Department of Medical Genetics, University and University Hospital Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.abb.2008.03.006DOI Listing
May 2008

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

Mol Genet Metab 2008 Apr 4;93(4):481-4. Epub 2007 Dec 4.

Center for Medical Genetics, Department of Biomedical Sciences, University of Antwerp (UA) and University of Antwerp Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ymgme.2007.10.011DOI Listing
April 2008

Analysis of genetic variations in the resistin gene shows no associations with obesity in women.

Obesity (Silver Spring) 2008 Apr 24;16(4):905-7. Epub 2008 Jan 24.

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1038/oby.2007.131DOI Listing
April 2008

Lessons from sclerosing bone dysplasias.

Authors:
Wim Van Hul

Horm Res 2007 10;68 Suppl 5:37-9. Epub 2007 Dec 10.

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1159/000110472DOI Listing
March 2008