Sep 20, 2017 | NEWS
The generation of new mutations is a key driver of evolution but also of susceptibility to rare diseases Fathers pass on four times as many new mutations as mothers do, but the maternal contribution is particularly strong in 10% of the genome that is prone to...
Jul 12, 2017 | NEWS
The American Society of Human Genetics (ASHG) has named Kári Stefánsson, MD, founder of deCODE genetics, the 2017 recipient of the annual William Allan Award. The William Allan Award is the top prize given by the ASHG and recognises a scientist for substantial and...
Jan 17, 2017 | NEWS
In a study published today, scientists at deCODE genetics use genomic and genealogical data from across the population of Iceland over many decades to show that people who carry sequence variations linked to higher levels of education have fewer children than average....
Sep 19, 2016 | NEWS
REYKJAVIK, Iceland, 19 September 2016 – In a new study, researchers at deCODE genetics have used their unique population data resources to shed new light on the processes which continuously shape the diversity of the human genome. In previous studies, they...
May 18, 2016 | NEWS
Analyzes genome, cholesterol and heart disease data from 700,000 people in seven countries Individuals with a rare twelve-letter deletion from a gene on chromosome 17 have significantly reduced non-HDL cholesterol levels and a 35% lower than average risk of heart...
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