Author Information
Olaug Kristin Rødningen is affiliated with the Department of Medical Genetics at Oslo University Hospital and the University of Oslo, located in Oslo, Norway. Her research expertise lies in the field of genetics, where she has made significant contributions to the understanding of various genetic disorders and their implications.Research Contributions
Olaug Kristin Rødningen has focused her research on a range of genetic topics, including psychiatric assessments in genetic syndromes, mutation analysis, and the genetic underpinnings of various diseases. Notable contributions include her work on Phelan-McDermid Syndrome, hereditary hemorrhagic telangiectasia, and primary immunodeficiency diseases. Her research has also delved into the clinical utility of CNV prediction and mutation analysis in Norwegian families, highlighting founder mutations and novel genetic variants.Aliases
Olaug Kristin Rødningen is known by several aliases in academic publications, including Olaug Rødningen, Olaug K Rødningen, and O. Rødningen, among others. These variations reflect her consistent contribution to the field under slightly different names across various studies and publications.Publication and Citation Metrics
| Metric |
Value |
| Citation Count |
1644 |
| h-index |
22 |
| Paper Count |
61 |
