deCODE GENETICS

FOUNDED IN 1996
OUR RESEARCHPUBLICATIONS
Lethal mutations in pregnancy loss

Lethal mutations in pregnancy loss

In a study published in Nature today “Sequence diversity lost in early pregnancy,” scientists from deCODE genetics, a subsidiary of Amgen, estimate that around one in 136 pregnancies are lost due to new mutations in the fetus. In other words, millions of pregnancies...

DECODE ANNOUNCES NEW LEADERSHIP UPDATES 

DECODE ANNOUNCES NEW LEADERSHIP UPDATES 

Kari Stefánsson, M.D., Dr. Med., Tenure Ends; Two Distinguished Genetic Researchers in Iceland Appointed Co-Managing Directors  deCODE genetics today announced leadership changes. The tenure of Kari Stefánsson, M.D., Dr. Med., founder and chief executive officer of...

A rare missense variant in FRS3 associates with lower body mass index and protection against obesity

A rare missense variant in FRS3 associates with lower body mass index and protection against obesity

Scientists at deCODE genetics, a subsidiary of Amgen, and collaborators have published a study in Nature Communications reporting a rare missense variant in FRS3 that associates with decreased body mass index (BMI) and protection against obesity. This missense variant was discovered in a meta-analysis of genome-wide association studies that included 2 million individuals of diverse ancestries.

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

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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.