Bertil Johansson - Genetic Mutations

Author Information

Bertil Johansson is a distinguished researcher affiliated with the Department of Clinical Genetics at the University and Regional Laboratories, Region Skåne, located in Lund, Sweden. His work is primarily focused on genetic research, particularly in the context of leukemia, where he has made significant contributions to understanding genetic mutations and their implications in cancer.

Research Contributions

Bertil Johansson has extensively studied mutational signatures in leukemia, contributing to a deeper understanding of genetic alterations associated with various forms of the disease, such as acute myeloid leukemia and acute lymphoblastic leukemia. His research has explored topics like single base substitution mutational signatures, parental origin of monosomies, and enhancer hijacking, which have significant implications for cancer diagnosis and treatment. His work on gene fusions and nomenclature also highlights his involvement in standardizing genetic terminology, which is crucial for advancing genetic research and collaboration.

Aliases

Throughout his career, Bertil Johansson has been known by several aliases, including B Johansson, B-m Johansson, and B. Johansson. These variations appear in different publications and databases, reflecting the common practice of using abbreviated names in scientific literature.

Publication and Citation Metrics

Metric Value
Total Citation Count 16,086
h-index 67
Total Paper Count 306

Publications:

DOI: 10.1111/bjh.17356

Year: 2021

DOI: 10.1080/17474086.2020.1711733

Year: 2020

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