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Six centers around the country come together to uncover the genetic causes of single-gene disorders.

An international collaboration uncovers several genetic markers associated with SARS-CoV-2 infection and COVID-19 severity.

Studies document extent to which common and rare genetic variants work in concert to shape blood traits and disease risk

In people with a single-gene variant that puts them at high risk for heart disease, breast cancer, or colorectal cancer, the rest of the genome can alter that risk.

COVID-19 test insights, an expanded elemental encyclopedia, where food choice and genetics meet, and more.

Pooled screening in human cells and molecular understanding of Huntington’s disease and pediatric brain cancers. 

Analyses of the largest publicly available catalog of human genomic data reveal new details on rare types of genetic variation and provide better tools for genetic disease diagnosis and drug development.

Analyzing cardiac measurements from large biobanks can uncover genetic predisposition to diseases like heart failure and arrhythmias.