Integrating common and rare genetic variation in diverse human populations.


Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide studies that fully examine less common alleles in populations with a wide range of ancestry. To inform the design and interpretation of such studies, we genotyped 1.6 million common… (More)
DOI: 10.1038/nature09298


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