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Works
10
Exome-wide association study of plasma lipids in >300,000 individuals
Rare and low-frequency coding variants alter human adult height
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
A first update on mapping the human genetic architecture of COVID-19
Genomic inflation factors under polygenic inheritance
Genome-wide detection and characterization of positive selection in human populations
A second generation human haplotype map of over 3.1 million SNPs
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Erratum
Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies
