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Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
The UK10K project identifies rare variants in health and disease
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Designing an intuitive web application for drug discovery scientists
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci
