Genetics of osteoporosis.

A twin approach to unraveling epigenetics. Trends Genet (2011) 2.38

Genome-wide approaches for identifying genetic risk factors for osteoporosis. Genome Med (2013) 1.09

The genetics of bone loss: challenges and prospects. J Clin Endocrinol Metab (2011) 0.88

Causes, mechanisms and management of paediatric osteoporosis. Nat Rev Rheumatol (2013) 0.88

Epigenetic regulation of fetal bone development and placental transfer of nutrients: progress for osteoporosis. Interdiscip Toxicol (2011) 0.82

Association analysis between g.18873C>T and g.27522G>A genetic polymorphisms of OPG and bone mineral density in Chinese postmenopausal women. Biomed Res Int (2014) 0.77

Evaluation of common variants in CNR2 gene for bone mineral density and osteoporosis susceptibility in postmenopausal women of Han Chinese. Osteoporos Int (2015) 0.77

Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women. Clinics (Sao Paulo) (2012) 0.76

A Candidate Gene Association Study of Bone Mineral Density in an Iranian Population. Front Endocrinol (Lausanne) (2016) 0.75

Association analysis of the COL1A1 polymorphism with bone mineral density and prevalent fractures in Polish postmenopausal women with osteoporosis. Arch Med Sci (2016) 0.75

Lack of Influence of Vitamin D Receptor BsmI (rs1544410) Polymorphism on the Rate of Bone Loss in a Cohort of Postmenopausal Spanish Women Affected by Osteoporosis and Followed for Five Years. PLoS One (2015) 0.75

The influence of vitamin D receptor genetic variants on bone mineral density and osteoporosis in Chinese postmenopausal women. Dis Markers (2015) 0.75

The Glu727 Allele of Thyroid Stimulating Hormone Receptor Gene is Associated with Osteoporosis. N Am J Med Sci (2012) 0.75

Osteoporosis: the current status of mesenchymal stem cell-based therapy. Cell Mol Biol Lett (2016) 0.75

Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility. Curr Osteoporos Rep (2017) 0.75