Magnus Nordenskjöld - Genetic Mutations

Author Information

Magnus Nordenskjöld is a prominent researcher in the field of genetics, affiliated with the Department of Clinical Genetics at Karolinska University Hospital and the Department of Molecular Medicine and Surgery at Karolinska Institutet in Stockholm, Sweden. His work spans several critical areas of genetic research, particularly focusing on the identification and analysis of genetic disorders.

Research Contributions

Magnus Nordenskjöld's research contributions are significant in the field of genetics, particularly in understanding rare genetic disorders and their implications. His work includes studies on Birt-Hogg-Dubé syndrome, severe congenital neutropenia, neurodevelopmental disorders, and cancer genomics. Nordenskjöld has been involved in integrating whole genome sequencing into healthcare settings, highlighting his commitment to applying genetic research in clinical contexts. His research has also explored the cellular mechanisms underlying genetic disorders and identified potential genetic mutations linked to various diseases.

Aliases

Throughout his academic career, Magnus Nordenskjöld has been referenced under various aliases, including M Nordenskjöld, M. Nordenskjöld, and M Nordenskjöld. These variations are often used interchangeably in academic publications and databases.

Publication and Citation Metrics

Metric Value
Total Citation Count 19,271
h-index 72
Total Number of Papers 329

Publications:

Partnered Content Networks

Relevant Topics