Discovery of cancer risk associations for six novel genes

Scientists at deCODE genetics/Amgen, and their collaborators have discovered six novel genes with rare germline variants that associate with cancer risk. The findings are published today in Nature Genetics under the title “Gene-based burden tests of rare germline...

Sequence variants that affect IgG subclass levels

Kari Stefansson CEO of decode genetics and senior author on the paper with Thorunn A. Olafsdottir first author on the paper. Scientists at deCODE genetics, a subsidiary of Amgen, and collaborators have published a study in Nature Communications reporting sequence...

Variants in the genome affect DNA methylation

A new study by scientists at deCODE Genetics, a subsidiary of Amgen, shows that sequence variants drive the correlation between DNA methylation and gene expression. The same variants are linked to various diseases as well as other human traits. Kari Stefansson, senior...