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A reference panel of 64,976 haplotypes for genotype imputation

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes

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