Bart Dermaut - Genetic Mutations

Author Information

Bart Dermaut is affiliated with the Department of Biomolecular Medicine and the Center for Medical Genetics at Ghent University, as well as the Department of Neurology at Ghent University Hospital, Ghent, Belgium. His research primarily focuses on complex neurological disorders, including Alzheimer’s disease, frontotemporal dementia, and amyotrophic lateral sclerosis.

Research Contributions

Bart Dermaut has made significant contributions to the field of genetics and neurology, particularly in understanding the molecular mechanisms underlying neurodegenerative diseases. His recent research has explored the roles of various genes such as TDP-43, BIN1, PLAAT3, RNF213, and RBM45 in conditions like Alzheimer's disease, lipodystrophy, and frontotemporal dementia. His work often involves exploring the pathogenic pathways and identifying potential therapeutic targets. Notably, his studies on Alzheimer’s disease susceptibility genes and their isoform-dependent neurotoxic effects have provided valuable insights into the disease's progression and potential interventions.

Aliases

B Dermaut, B. Dermaut, Bart Dermaut

Publication and Citation Metrics

Metric Value
Citation Count 7656
H-index 45
Paper Count 139

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