We mapped the gene regulatory network of key immune disease genes in primary CD4+ T cells using causal inference methods
We discovered thousands of unexpectedly common somatic mutations in blood
We identified TCL1A as a key mediator of clonal expansion in CHIP clones
We performed a GWAS meta-analysis of lab derived phenotypes from the Michigan Genomics Initiative (Umich) and BioVU (Vanderbilt)
We discovered the genetic determinants of CHIP in ~97,000 TOPMed whole genomes