ASHG Journals

Showing 25–33 of 33 results

Regulatory features aid interpretation of 3’UTR variants
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Stability of Polygenic Scores Across Discovery GWAS
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Stakeholders’ Views on Returning Polygenic Risk Scores
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Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding
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The impact of clinical genome sequencing in a global population with suspected rare genetic disease
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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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