Although our understanding of pathology has grown rapidly in recent decades, the underlying mechanisms of many diseases remain obscure. Genomic research offers a new opportunity for determining how diseases occur, by taking advantage of experiments of nature and a growing array of sophisticated research tools to identify the molecular abnormalities underlying disease processes.1In this review I examine examples in which genomic research has improved our understanding of molecular pathobiology and consider its potential for contributing to the study of common complex diseases.
CITATION STYLE
Burke, W. (2003). Genomics as a Probe for Disease Biology. New England Journal of Medicine, 349(10), 969–974. https://doi.org/10.1056/nejmra012479
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