Author Information
Kári Stefánsson is a distinguished researcher affiliated with deCODE Genetics/Amgen, Inc., located in Reykjavik, Iceland. His work spans various domains within genetics, particularly focusing on genetic associations and the architecture of complex diseases.Research Contributions
Kári Stefánsson has made significant contributions to the field of genetics through his extensive research on various genetic associations and their implications for human health. In 2022 alone, he has authored papers on topics such as the genetic architecture of asthma-COPD overlap, the role of common genetic variants in human height, intellectual disability syndromes, intervertebral disc disorders, neurodevelopmental syndromes, carpal tunnel syndrome, migraine risk loci, multiple myeloma risk, and the impact of booster vaccinations against COVID-19 variants. His research has provided valuable insights into the genetic underpinnings of these conditions, highlighting potential therapeutic targets and advancing our understanding of human genetics.Aliases
Kári Stefánsson is known by several aliases, including Kári Stefansson, K Stefánsson, Kári Stéfansson, Kári Stefánsson, Kāri Stefánsson, Kari Stefansson, K. Stefansson, K. Stefánsson, Kari Stefánsson, and Káari Stefaánsson.Publication and Citation Metrics
| Metric |
Value |
| Citation Count |
184,988 |
| H-Index |
207 |
| Paper Count |
971 |
