Yasin Memari
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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
The UK10K project identifies rare variants in health and disease
An interactive genome browser of association results from the UK10K cohorts project
A practical framework and online tool for mutational signature analyses show inter-tissue variation and driver dependencies
Purging of deleterious variants due to drift and founder effect in Italian populations with extended autozygosity
