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Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Rare and low-frequency coding variants alter human adult height
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Exome-chip meta-analysis identifies novel associations of coding variants in BSN and GLRA4 with lumbar spine BMD in 27 339 adults of European descent
Common variants at ten loci influence QT interval duration in the QTGEN Study
Methylation of BoneSOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
