Whole genome sequencing in nearly 500,000 UK Biobank participants shows that observed rare and common variants now explain ...

Family of woman who died in Shapiro crash slam Delta's "no exceptions" rule Virginia Giuffre's memoir reveals intimate ...

Using full genome sequencing data from more than 347,000 individuals, researchers quantified how much genetic differences explain human traits such as height, body mass index, fertility, and disease ...

A study shows that genome-wide association studies (GWAS) and rare variant burden tests highlight different disease genes.

A large-scale genomic study by researchers at Central South University and King’s College London reveals that rare and common genetic risks interact antagnistically to maintain healthy telomere length ...

However, because infant specimens are extremely rare in the fossil record, scientists were until now unsure if these species-specific traits were present from birth. To find out, the study authors ...