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

Seminars in arthritis and rheumatism, 2013-10, Vol.43 (2), p.220-240

2013

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

Nature reviews. Rheumatology, 2015-08, Vol.11 (8), p.462-474

2015

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Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis

Obesity reviews, 2020-07, Vol.21 (7), p.e13019-n/a

2020

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MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation

European journal of endocrinology, 2017-08, Vol.177 (2), p.R69-R83

2017

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WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders

Frontiers in endocrinology (Lausanne), 2020-04, Vol.11, p.165-165

2020

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Camurati–Engelmann Disease

Calcified tissue international, 2019-05, Vol.104 (5), p.554-560

2019

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Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M)

Bone Reports, 2020-06, Vol.12, p.100245, Article 100245

2020

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Transforming Growth Factor-β1 to the Bone

Endocrine reviews, 2005-10, Vol.26 (6), p.743-774

2005

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Genetic control of bone mass

Molecular and cellular endocrinology, 2016-09, Vol.432, p.3-13

2016

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

Developmental Biology, 2002-10, Vol.250 (2), p.231-250

2002

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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

Nature (London), 2012-03, Vol.483 (7389), p.350-354

2012

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Minireview : The genetics of low-density Lipoprotein receptor-related protein 5 in bone: A story of extremes

Endocrinology (Philadelphia), 2007-06, Vol.148 (6), p.2622-2629

2007

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

Journal of bone and mineral research, 2016-04, Vol.31 (4), p.874-881

2016

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DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4741

2020

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WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in Osteoblasts

Calcified tissue international, 2020-03, Vol.106 (3), p.294-302

2020

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Bone Overgrowth-associated Mutations in the LRP4 Gene Impair Sclerostin Facilitator Function

The Journal of biological chemistry, 2011-06, Vol.286 (22), p.19489-19500

2011

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Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia

Journal of medical genetics, 2023-05, Vol.60 (5), p.498-504

2023

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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome

American journal of human genetics, 2020-11, Vol.107 (5), p.977-988

2020

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PLEKHM1 Regulates Salmonella-Containing Vacuole Biogenesis and Infection

Cell host & microbe, 2015-01, Vol.17 (1), p.58-71

2015

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Delineation of a new fibrillin-2-opathy with evidence for a role of FBN2 in the pathogenesis of carpal tunnel syndrome

Journal of medical genetics, 2021-11, Vol.58 (11), p.778-782

2021

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

Bone (New York, N.Y.), 2014-02, Vol.59, p.57-65

2014

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

Journal of medical genetics, 2016-08, Vol.53 (8), p.568-574

2016

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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

Calcified tissue international, 2019-06, Vol.104 (6), p.613-621

2019

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High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench

Journal of bone and mineral research, 2023-02, Vol.38 (2), p.229-247

2023

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Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases?

Frontiers in endocrinology (Lausanne), 2022-03, Vol.13, p.892799-892799

2022

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

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

Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis

MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation

WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders

Camurati–Engelmann Disease

Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M)

Transforming Growth Factor-β1 to the Bone

Genetic control of bone mass

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

Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

Minireview : The genetics of low-density Lipoprotein receptor-related protein 5 in bone: A story of extremes

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

DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age

WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in Osteoblasts

Bone Overgrowth-associated Mutations in the LRP4 Gene Impair Sclerostin Facilitator Function

Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia

Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome

PLEKHM1 Regulates Salmonella-Containing Vacuole Biogenesis and Infection

Delineation of a new fibrillin-2-opathy with evidence for a role of FBN2 in the pathogenesis of carpal tunnel syndrome

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

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

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

High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench

Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases?

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