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25
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
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 contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies
Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia
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