E. Andermann. G. M. Remillard. C. Goyer. L. Blitzer. Andermann - Genetic Mutations

Author Information

Eve Andermann is affiliated with the Neurogenetics Unit and Epilepsy Research Group at the Montreal Neurological Institute and Hospital. She also holds positions in the Departments of Neurology & Neurosurgery and Human Genetics at McGill University, Montreal, QC, Canada. Her extensive research focuses primarily on genetic aspects of neurological conditions, particularly epilepsy.

Research Contributions

Eve Andermann has made significant contributions to the field of neurogenetics, particularly in the study of epilepsy and related neurological disorders. Her research spans various aspects of epilepsy, including its genetic basis, clinical features, and potential treatments. Notable works include studies on the safety and tolerability of eslicarbazepine acetate, the genetic causes of polymicrogyria with epilepsy, and the molecular genetic features of Kufs disease. She has also explored the genetic heterogeneity in progressive myoclonus epilepsies and the implications of de novo mutations in synaptic transmission genes for epileptic encephalopathies.

Aliases

Eve Andermann is also known by several aliases, including E. Andermann, E. Andermann. G. M. Remillard. C. Goyer. L. Blitzer. Andermann, Eva Andermann, and E Andermann.

Publication and Citation Metrics

Metric Value
Citation Count 20,259
h-index 80
Paper Count 313

Publications:

DOI: 10.1111/epi.16854

Year: 2021

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