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...
Jun 22, 2021 | NEWS
Scientists at deCODE genetics have found a new biomarker for osteoarthritis, that outperforms previously reported biomarkers and is an independent predictor of disease. Kari Stefansson and Unnur Styrkarsdpttir. In a study published in the medical journal,...
