Featured
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Article |
Identification of potential microRNA–target pairs associated with osteopetrosis by deep sequencing, iTRAQ proteomics and bioinformatics
- Minglin Ou
- , Xiaoqing Zhang
- & Min Ding
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Article |
Allele-specific Col1a1 silencing reduces mutant collagen in fibroblasts from Brtl mouse, a model for classical osteogenesis imperfecta
- Julie Rousseau
- , Roberta Gioia
- & Antonella Forlino
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Clinical Utility Gene Card |
Clinical utility gene card for: osteogenesis imperfecta
- Fleur S van Dijk
- , Raymond Dalgleish
- & Gerard Pals
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Short Report |
Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients
- Edyta Mądry
- , Beata Krasińska
- & Jarosław Walkowiak
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Article |
Single-nucleotide polymorphisms in the P2X7 receptor gene are associated with post-menopausal bone loss and vertebral fractures
- Niklas R Jørgensen
- , Lise B Husted
- & James S Wiley
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Article
| Open Access
Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal women
- Alison Gartland
- , Kristen K Skarratt
- & James S Wiley
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Article |
Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD
- Aude Saint-Pierre
- , Jean-Marc Kaufman
- & Maria Martinez
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Article |
Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG)
- C M Laine
- , B D Chung
- & O Mäkitie
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Article |
Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I
- Frank Rauch
- , Liljana Lalic
- & Francis H Glorieux
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study