(Q38027020)

27 August 2017

title

Genetics of osteoporosis from genome-wide association studies: advances and challenges (English)

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genome-wide association study

27 August 2017

main subject

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3

Tim D Spector

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27 August 2017

J Brent Richards

1

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27 August 2017

Hou-Feng Zheng

series ordinal

2

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27 August 2017

publication date

18 July 2012

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27 August 2017

published in

Nature Reviews Genetics

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27 August 2017

volume

13

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27 August 2017

issue

8

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27 August 2017

page(s)

576-588

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Diagnosis of osteoporosis.

27 August 2017

cites work

1 reference

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Genetics of osteoporosis

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

31 March 2020

1 reference

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

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31 March 2020

1 reference

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31 March 2020

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31 March 2020

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Matrix-embedded cells control osteoclast formation

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TRANCE is necessary and sufficient for osteoblast-mediated activation of bone resorption in osteoclasts.

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31 March 2020

1 reference

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31 March 2020

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B cells and T cells are critical for the preservation of bone homeostasis and attainment of peak bone mass in vivo

31 March 2020

1 reference

Effects of recombinant leptin therapy in a child with congenital leptin deficiency.

31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

Sox5 and Sox6 are needed to develop and maintain source, columnar, and hypertrophic chondrocytes in the cartilage growth plate

31 March 2020

1 reference

The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation

31 March 2020

1 reference

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

Genetic heterogeneity in human disease

31 March 2020

1 reference

Independent clinical validation of a Canadian FRAX tool: Fracture prediction and model calibration

31 March 2020

1 reference

The potential of genes and other markers to inform about risk

31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

R-Spondin family members regulate the Wnt pathway by a common mechanism

31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

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31 March 2020

1 reference

Sclerostin: a novel target for intervention in the treatment of osteoporosis.

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22805710

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22805710

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRG3228

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Dimensions Publication ID

27 August 2017

1011171235

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