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A reference panel of 64,976 haplotypes for genotype imputation

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Novel genetic determinants of telomere length from a trans-ethnic analysis of 109,122 whole genome sequences in TOPMed

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

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Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts

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