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Clinical, molecular genetics and therapeutic aspects of syndromic obesity

Clinical genetics, 2019-01, Vol.95 (1), p.23-40

2019

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Wnt signaling and the control of human stem cell fate

Stem cell reviews, 2014-04, Vol.10 (2), p.207-229

2014

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Multiple bilateral hip fractures in a patient with dyskeratosis congenita caused by a novel mutation in the PARN gene

Osteoporosis international, 2021-06, Vol.32 (6), p.1227-1231

2021

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A clinical and molecular overview of the human osteopetroses

Calcified tissue international, 2005-11, Vol.77 (5), p.263-274

2005

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Sclerostin in Mineralized Matrices and van Buchem Disease

Journal of dental research, 2009-06, Vol.88 (6), p.569-574

2009

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Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity

International Journal of Obesity, 2014-07, Vol.38 (7), p.1000-1004

2014

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Polymorphisms in the endocannabinoid receptor 1 in relation to fat mass distribution

European journal of endocrinology, 2010-09, Vol.163 (3), p.407-412

2010

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Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover

Nutrients, 2023, Vol.15 (3), p.598

2023

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A gene variant of PNPLA3, but not of APOC3, is associated with histological parameters of NAFLD in an obese population

Obesity (Silver Spring, Md.), 2013-10, Vol.21 (10), p.2138-2145

2013

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Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease

Calcified tissue international, 2004-08, Vol.75 (2), p.144-152

2004

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

Journal of medical genetics, 2002-02, Vol.39 (2), p.91-97

2002

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Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3–Xqter

Bone (New York, N.Y.), 2014-01, Vol.58, p.67-71

2014

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Screening for melanocortin-4 receptor mutations in a cohort of Belgian morbidly obese adults and children

International Journal of Obesity, 2006-02, Vol.30 (2), p.221-225

2006

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The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

Nature genetics, 1992-06, Vol.1 (3), p.171-175

1992

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Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family

Osteoporosis international, 2005-09, Vol.16 (9), p.1167-1170

2005

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Common genetic variation in sFRP5 is associated with fat distribution in men

Endocrine, 2014-08, Vol.46 (3), p.477-484

2014

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Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis

Clinical genetics, 2011-10, Vol.80 (4), p.383-388

2011

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Sclerosing bone dysplasias with involvement of the craniofacial skeleton

Bone (New York, N.Y.), 2014-03, Vol.60, p.48-67

2014

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Localization of the Gene for Hyperostosis Cranialis Interna to Chromosome 8p21 with Analysis of Three Candidate Genes

Calcified tissue international, 2013-07, Vol.93 (1), p.93-100

2013

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Mutations in SFRP1 or SFRP4 are not a common cause of craniotubular hyperostoses

Bone (New York, N.Y.), 2012-05, Vol.50, p.S106-S107

2012

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A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis

British journal of cancer, 2001-07, Vol.85 (2), p.176-181

2001

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Genetic association between WNT10B polymorphisms and obesity in a Belgian case–control population is restricted to males

Molecular genetics and metabolism, 2012-03, Vol.105 (3), p.489-493

2012

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1334 CORRELATION OF HUMAN LIVER PPAR GENE EXPRESSION WITH HISTOLOGICAL SEVERITY OF NASH AND ASSOCIATED METABOLIC DERANGEMENTS: RATIONALE FOR TARGETED THERAPY

Journal of hepatology, 2013-04, Vol.58, p.S538-S538

2013

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Evidence for further genetic heterogeneity of the facio-audio-symphalangism syndrome

Bone (New York, N.Y.), 2010-06, Vol.47, p.S151-S151

2010

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Progressive pseudorheumatoid dysplasia

European radiology, 2000-01, Vol.10 (11), p.1832-1835

2000

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Clinical, molecular genetics and therapeutic aspects of syndromic obesity

Wnt signaling and the control of human stem cell fate

Multiple bilateral hip fractures in a patient with dyskeratosis congenita caused by a novel mutation in the PARN gene

A clinical and molecular overview of the human osteopetroses

Sclerostin in Mineralized Matrices and van Buchem Disease

Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity

Polymorphisms in the endocannabinoid receptor 1 in relation to fat mass distribution

Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover

A gene variant of PNPLA3, but not of APOC3, is associated with histological parameters of NAFLD in an obese population

Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease

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

Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3–Xqter

Screening for melanocortin-4 receptor mutations in a cohort of Belgian morbidly obese adults and children

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family

Common genetic variation in sFRP5 is associated with fat distribution in men

Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis

Sclerosing bone dysplasias with involvement of the craniofacial skeleton

Localization of the Gene for Hyperostosis Cranialis Interna to Chromosome 8p21 with Analysis of Three Candidate Genes

Mutations in SFRP1 or SFRP4 are not a common cause of craniotubular hyperostoses

A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis

Genetic association between WNT10B polymorphisms and obesity in a Belgian case–control population is restricted to males

1334 CORRELATION OF HUMAN LIVER PPAR GENE EXPRESSION WITH HISTOLOGICAL SEVERITY OF NASH AND ASSOCIATED METABOLIC DERANGEMENTS: RATIONALE FOR TARGETED THERAPY

Evidence for further genetic heterogeneity of the facio-audio-symphalangism syndrome

Progressive pseudorheumatoid dysplasia

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