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List of works by Eveline Boudin

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

scientific article

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

scientific article

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

scientific article published on 21 April 2015

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

article

Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function

scientific article

Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis

scientific article published on 21 May 2015

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

article

Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis.

scientific article

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

scientific article published on 08 September 2020

Functional Assessment of Coding and Regulatory Variants From the <i>DKK1</i> Locus

scientific article published on 02 November 2020

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

scientific article published on 12 January 2017

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

scientific article published on 17 January 2013

Genetic control of bone mass

scientific article

Human Genetics of Sclerosing Bone Disorders.

scientific article published on 14 April 2018

Identification of the first deletion in the LRP5 gene in a patient with autosomal dominant osteopetrosis type I

scientific article

MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation

scientific article published on 5 April 2017

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

scientific article published on 06 October 2012

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

scientific article published on 10 February 2015

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

scientific article published on 3 April 2013

Novel SOST gene mutation in a sclerosteosis patient and her parents

scientific article published on 16 October 2012

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

Sclerosing bone dysplasias: leads toward novel osteoporosis treatments

scientific article

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

scientific article published on 2 May 2012

The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans

scientific article published on 06 May 2017

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

scientific article published on 21 February 2013

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

scientific article published in November 2013

Wnt signaling: a win for bone

scientific article published on 14 March 2008

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