deCODE GENETICS

FOUNDED IN 1996
OUR RESEARCHPUBLICATIONS
Variants in the genome affect DNA methylation

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.

UNIQUE EXPERTISE

Headquartered in Reykjavik, Iceland, deCODE is a global leader in analyzing and understanding the human genome. Using our unique expertise and population resources, deCODE has discovered key genetic risk factors for dozens of common diseases ranging from cardiovascular disease to cancer.

UNIQUE CAPABILITIES

We operate the most productive human gene discovery engine in the world, employing our discoveries to identify genetic variations associated with human disease.

UNRIVALED CAPABILITIES

OUR PUBLICATIONS

We regularly publish our discoveries in major, peer-reviewed journals, enabling others to further validate and expand upon our findings.

SELECTED PUBLICATIONS

Your Title Goes Here

Your content goes here. Edit or remove this text inline or in the module Content settings. You can also style every aspect of this content in the module Design settings and even apply custom CSS to this text in the module Advanced settings.

Award by the American Society of Human Genetics

At its Annual meeting in October 2017 in Orlando, the American Society of Human Genetics (ASHG), presented Dr. Kári Stefánsson, founder and CEO of deCODE genetics, with the William Allan Award. The award, the top prize given by the society, recognizes a scientist for substantial and far-reaching scientific contributions to human genetics. The ASHG has distributed video footage from the award ceremony. The introduction is given by Professor Mark Daly of Harvard University.