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Author Correction: Perspectives on ENCODE
Partitioning heritability by functional annotation using genome-wide association summary statistics
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes
Pathologically expanded peripheral T helper cell subset drives B cells in rheumatoid arthritis
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Genes with High Network Connectivity Are Enriched for Disease Heritability
Using chromatin marks to interpret and localize genetic associations to complex human traits and diseases.
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery
