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Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Analysis of protein-coding genetic variation in 60,706 humans
Genome-wide detection and characterization of positive selection in human populations
A second generation human haplotype map of over 3.1 million SNPs
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Support of association between BRD1 and both schizophrenia and bipolar affective disorder.
