Aug 15, 2024 | NEWS
Scientists at deCODE genetics, a subsidiary of AMGEN, have discovered rare sequence variants, predicted to cause a loss of function of ITSN1, that are associated with a high risk of Parkinson‘s Disease. The findings also support less studied pathways involved in the...
Jan 3, 2024 | NEWS
In the paper, Obesity variants in the GIPR gene do not associate with risk of fracture or bone mineral density” published in the JCEM, The Journal of Clinical Endocrinology & Metabolism, scientists from deCODE genetics, a subsidiary of Amgen, and...
Oct 26, 2023 | NEWS
A large international study led by deCODE Genetics on the genetics of migraine provides novel insights into the biology of migraine enabling detection of rare variants protecting against migraine, opening an avenue for potential development of novel drug targets. In a...
Oct 4, 2023 | NEWS
In a paper released today, deCODE Genetics’ scientists shared their findings from a plasma proteomics study performed using affinity-based methods. They analyzed the proteins in the context of diseases and diversity in the sequence of the genome and compared...
