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Ready for Genomic Medicine? Perspectives of Health Care Decision Makers

Paul R. Billings, MD, PhD; Rick J. Carlson, JD; Josh Carlson, MPH; Mary Cain, MPH; Charles Wilson, MD, MSHA, ScD; Peter Shorett, BA; Wendy Everett, ScD
Arch Intern Med. 2005;165(16):1917-1919. doi:10.1001/archinte.165.16.1917.
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Remarkable progress has been made in establishing the field of genomic medicine during the past decade. A host of therapeutic and diagnostic tools—such as the use of molecular simulations to identify new drug pathways1 and gene expression profiles to predict the course of breast cancer2—are moving from the laboratory to the marketplace. Amid the speculation about possible applications and effects of this new medical discipline, 2 major projections have emerged. One predicts that genomic medicine will disrupt many aspects of health care, making current models of its delivery obsolete. Recent reports by the UK National Health Service3 and the US National Human Genome Research Institute4,5 reflect this view. The other is less radical, projecting an initial enhancement of current uses of DNA and genetic information, followed by a gradual diffusion of new genomic medical information and technologies throughout the health care system.68

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Individuals receiving certificates during years when tests were offered by the American Board of Medical Genetics (ABMG).14

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The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
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