(Q34072806)

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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

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Europe PubMed Central

PubMed publication ID

30 July 2017

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

object named as

Wim Van Hul

6

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Marianne Andersen

object named as

Marianne Andersen

4

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5

object named as

Kim Brixen

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Elke Piters

1

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Europe PubMed Central

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30 July 2017

Fenna de Freitas

2

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Europe PubMed Central

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30 July 2017

Torben Leo Nielsen

3

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Europe PubMed Central

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30 July 2017

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publication date

11 November 2011

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Europe PubMed Central

PubMed publication ID

30 July 2017

Calcified Tissue International

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Europe PubMed Central

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30 July 2017

90

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Europe PubMed Central

PubMed publication ID

30 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

30-39

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

An estimate of the worldwide prevalence and disability associated with osteoporotic fractures

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

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Osteoporosis and mortality

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Choice of study phenotype in osteoporosis genetic research

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Human genetics of osteoporosis

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

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Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

New sequence variants associated with bone mineral density

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Analysis of recently identified osteoporosis susceptibility genes in Han Chinese women

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

European bone mineral density loci are also associated with BMD in East-Asian populations

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Sclerostin binds to LRP5/6 and antagonizes canonical Wnt signaling

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

SOST is a ligand for LRP5/LRP6 and a Wnt signaling inhibitor

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Distinct modes of inhibition by sclerostin on bone morphogenetic protein and Wnt signaling pathways

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin function

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

A short treatment with an antibody to sclerostin can inhibit bone loss in an ongoing model of colitis

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Sclerostin antibody treatment increases bone formation, bone mass, and bone strength in a rat model of postmenopausal osteoporosis

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Two doses of sclerostin antibody in cynomolgus monkeys increases bone formation, bone mineral density, and bone strength

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibody

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Hip geometry, bone mineral distribution, and bone strength in European men and women: the EPOS study

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Prevalence of overweight, obesity and physical inactivity in 20- to 29-year-old, Danish men. Relation to sociodemography, physical dysfunction and low socioeconomic status: the Odense Androgen Study

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen study.

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

How to interpret a genome-wide association study

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Multiple genetic loci for bone mineral density and fractures

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Femoral neck BMD is a strong predictor of hip fracture susceptibility in elderly men and women because it detects cortical bone instability: the Rotterdam Study

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Genome-wide association with bone mass and geometry in the Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Pathway-based genome-wide association analysis identified the importance of EphrinA-EphR pathway for femoral neck bone geometry

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Genome-wide association study for femoral neck bone geometry

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Inhibition of adipogenesis by Wnt signaling

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Serum sclerostin levels negatively correlate with parathyroid hormone levels and free estrogen index in postmenopausal women

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Regulation of circulating sclerostin levels by sex steroids in women and in men.

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Effects of parathyroid hormone treatment on circulating sclerostin levels in postmenopausal women

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

Population-based reference values for bone mineral density in young men

1 reference

https://api.crossref.org/works/10.1007%2FS00223-011-9546-5

21 January 2018

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10.1007/S00223-011-9546-5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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