<p>Osteoporosis is a condition of excessive skeletal fragility which results in high risk to low trauma fractures. It is the      most prevalent metabolic bone disease and is a major public health problem which may result in devastating morbidity and mortality.      The most powerful, measurable determinant of fracture risk is bone mineral density (BMD). More than 60% of BMD variation is      attributable to genetic factors. There are gender differences in BMD that contribute to a substantially higher fracture risk      among women than men. Genetic studies demonstrate that some osteoporosis risk genes/genomic regions are gender specific. However,      specific such genes contributing to female BMD and to the sex differences of BMD are largely unknown.</p>     <p>Recent rapid progresses in SNP genotyping technology, in our knowledge about human genome diversity and linkage disequilibrium (LD)      patterns in the human genome as revealed have made it feasible and timely to pursue a powerful whole genome-wide association study (GWAS)      to identify genes for BMD. The major goal of this project is to perform a powerful GWAS study in a large sample of US Caucasian subjects.      Gender specific effects of the genetic variants will be examined. The significant genetic variants discovered will be used to design      diagnostic DNA chips for prognosis for potential health problems of osteoporosis later in life.</p>

Genomic Wide Scans for Female Osteoporosis Genes

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