Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study

• Main Authors: Liu Y.-Z., Wilson S.G., Wang L., Liu X.-G., Guo Y.-F., Li J., Yan H., Deloukas P., Soranzo N., Chinnapen-Horsley U., Cervino A., Williams F.M., Xiong D.-H., Zhang Y.-P., Jin T.-B., Levy S., Papasian C.J., Drees B.M., Hamilton J.J., Recker R.R., Spector T.D., Deng H.-W.
• Other Authors: CHEMISTRY
• Format: Article
• Published: 2019
• Subjects: calcium ion; gene product; inositol 1,4,5 trisphosphatase; phospholipase C like 1 protein; unclassified drug; magic factor 1 protein, mouse; magic-factor 1 protein, mouse; recombinant protein; signal transducing adaptor protein; adult; aged; article; bone cell; bone structure; calcium signaling; Caucasian; Chinese; cohort analysis; controlled study; female; gene function; gene identification; gene replication; genetic association; genetic risk; genetic variability; genome analysis; genotype; hip fracture; human; major clinical study; male; pathogenesis; regulatory mechanism; single nucleotide polymorphism; body mass; body size; China; fracture; gene expression regulation; genetics; histology; human genome; metabolism; osteoporosis; pathology; pelvic girdle; physiology; risk factor; United Kingdom; Adaptor Proteins, Signal Transducing; Body Mass Index; Body Size; Female; Fractures, Bone; Gene Expression Regulation; Genome, Human; Great Britain; Humans; Male; Osteoporosis; Pelvic Bones; Polymorphism, Single Nucleotide; Recombinant Proteins; Risk Factors
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/161849
• Institution: National University of Singapore

10.1371/journal.pone.0003160