ASHG Journals
Showing 25–28 of 28 results
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The Impact of CNVs on Complex Human Traits
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Tracing decision points in the use of race, ethnicity and genetic ancestry as population descriptors in genomics research
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Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number
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The commonality of TSPEAR-related ARED14 sheds light on human origins
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