Genetics of osteoporosis
SH Ralston, AG Uitterlinden - Endocrine reviews, 2010 - academic.oup.com
Osteoporosis is a common disease with a strong genetic component characterized by
reduced bone mass, defects in the microarchitecture of bone tissue, and an increased risk of …
reduced bone mass, defects in the microarchitecture of bone tissue, and an increased risk of …
Genetics of osteoporosis from genome-wide association studies: advances and challenges
Osteoporosis is among the most common and costly diseases and is increasing in
prevalence owing to the ageing of our global population. Clinically defined largely through …
prevalence owing to the ageing of our global population. Clinically defined largely through …
Genetics of osteoporosis: accelerating pace in gene identification and validation
Osteoporosis is characterized by low bone mineral density and structural deterioration of
bone tissue, leading to an increased risk of fractures. It is the most common metabolic bone …
bone tissue, leading to an increased risk of fractures. It is the most common metabolic bone …
Molecular genetic studies of gene identification for osteoporosis: the 2009 update
XH Xu, SS Dong, Y Guo, TL Yang, SF Lei… - Endocrine …, 2010 - academic.oup.com
Osteoporosis is a complex human disease that results in increased susceptibility to fragility
fractures. It can be phenotypically characterized using several traits, including bone mineral …
fractures. It can be phenotypically characterized using several traits, including bone mineral …
Powerful Bivariate Genome-Wide Association Analyses Suggest the SOX6 Gene Influencing Both Obesity and Osteoporosis Phenotypes in Males
Background Current genome-wide association studies (GWAS) are normally implemented in
a univariate framework and analyze different phenotypes in isolation. This univariate …
a univariate framework and analyze different phenotypes in isolation. This univariate …
In Vivo Genome‐Wide Expression Study on Human Circulating B Cells Suggests a Novel ESR1 and MAPK3 Network for Postmenopausal Osteoporosis
P **ao, Y Chen, H Jiang, YZ Liu, F Pan… - Journal of Bone and …, 2008 - academic.oup.com
Introduction: Osteoporosis is characterized by low BMD. Studies have shown that B cells
may participate in osteoclastogenesis through expression of osteoclast‐related factors, such …
may participate in osteoclastogenesis through expression of osteoclast‐related factors, such …
Contribution of gender‐specific genetic factors to osteoporosis risk
Common diseases result from the complex relationship between genetic and environmental
factors. The aim of this review is to provide perspective for a conceptual framework aimed at …
factors. The aim of this review is to provide perspective for a conceptual framework aimed at …
Loss of osteoblast Runx3 produces severe congenital osteopenia
O Bauer, A Sharir, A Kimura… - … and Cellular Biology, 2015 - Am Soc Microbiol
Congenital osteopenia is a bone demineralization condition that is associated with elevated
fracture risk in human infants. Here we show that Runx3, like Runx2, is expressed in …
fracture risk in human infants. Here we show that Runx3, like Runx2, is expressed in …
Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians
XD Chen, P **ao, SF Lei, YZ Liu, YF Guo… - Journal of Bone and …, 2010 - academic.oup.com
Osteoporosis is characterized mainly by low bone mineral density (BMD). Many cytokines
and chemokines have been related with bone metabolism. Monocytes in the immune system …
and chemokines have been related with bone metabolism. Monocytes in the immune system …
Identification of PLCL1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study
Osteoporosis, the most prevalent metabolic bone disease among older people, increases
risk for low trauma hip fractures (HF) that are associated with high morbidity and mortality …
risk for low trauma hip fractures (HF) that are associated with high morbidity and mortality …