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genome-wide association study
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Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
The trans-ancestral genomic architecture of glycemic traits
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Multiethnic Meta-Analysis of Genome-Wide Association Studies in > 100 000 Subjects Identifies 23 FibrinogenAssociated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function
FTO genotype is associated with phenotypic variability of body mass index
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults