ADVANCES IN GENETICS AND GENOMICS ARE REVOLUtionizing biomedical science and providing great promise for the future of clinical practice. The magnitude, scope, and pace of discovery in genetics and genomics research are at unprecedented levels and continue to increase exponentially. Progress in basic science resulting from the sequencing of the human genome and new approaches for genomics analyses have accelerated and continue to expand, resulting in new knowledge, mechanisms, and techniques for examining the genetic basis of disease. These discoveries have important implications for understanding disease processes and pathophysiology, for predicting disease susceptibility and progression, and for refining and individualizing treatments—all of which ultimately have the potential to improve health and to increase both quality of life and longevity. Given the pace of discovery and the promise in translating these scientific discoveries to clinical application, physicians and other health care professionals must have a keen awareness about ongoing research and advances in genetics and genomics. This theme issue of JAMA is intended to provide information on genetics and genomics that is relevant and accessible for clinicians, yet also should be of interest to physician-scientists and other investigators involved in genetics and genomics research. A total of 121 manuscripts were submitted for this theme issue, resulting in far too many articles to publish in one issue. Therefore, a number of articles on genetics and genomics will be published in upcoming issues of JAMA. In addition, several members of our family of Archives Journals also are publishing theme issues on genetics and genomics, including the March and April issues of Archives of Neurology and the March issues of Archives of Dermatology, Archives of Ophthalmology, and Archives of Surgery. Additional articles on genomics and genetics are included in the March issues of Archives of General Psychiatry, Archives of Internal Medicine, and Archives of Otolaryngology–Head & Neck Surgery. In this issue of JAMA, 5 articles provide new information on genetics and genomics for common diseases and conditions, including cardiovascular disease, osteoporosis, posttraumatic stress disorder, venous thromboembolism, and cancer. In an elegant, comprehensive study, Bhattacharyya and colleagues examined the relationship among genotype, generelated functional activity, and clinical outcomes in 1399 patients who had undergone coronary angiography. The authors found consistent associations among paraoxonase 1 (PON1) genotypes, levels of PON1 activity and systemic indices of oxidant stress, and prevalent cardiovascular disease as well as recurrent and incident cardiovascular events. In an ambitious multicenter collaborative investigation that included individual-level data from 37 534 individuals from Europe and North America, van Meurs and colleagues studied the relationship between polymorphisms of the gene encoding low-density lipoprotein receptorrelated protein 5 (LRP5) and bone mineral density and fracture risk. The authors report evidence for an association of common variants of the LRP5 gene with alterations in bone mineral density and risk of lumbar spine fractures and femoral neck fractures. In an investigation designed to increase understanding of genetic and environmental risk factors and their potential interactions with development of posttraumatic stress disorder (PTSD) symptoms, Binder and colleagues examined psychological risk factors combined with single nucleotide polymorphism (SNP) genotyping in 762 primarily lowincome, African American men and women. Four SNPs of the FKBP5 gene had significant interactions with severity of child abuse as a predictor of symptoms of PTSD in adults, suggesting the possibility of a gene–childhood environment interaction for adult PTSD. In an analysis designed to examine genetic factors associated with deep vein thrombosis, Bezemer and colleagues analyzed 3 large case-control studies. SNPs in several genes, including CYP4V2, were associated with deep vein thrombosis and with coagulation factor XI levels, suggesting that common genetic variation is an important factor in venous thrombotic disease. As Bovill points out in an insightful accompanying editorial, studies such as this hold the promise that risk profiles with significant predictive value ultimately may be developed to help guide clinical practice.