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Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies
Rare coding variants in ten genes confer substantial risk for schizophrenia
Analysis of protein-coding genetic variation in 60,706 humans
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
An atlas of genetic correlations across human diseases and traits
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders