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Ingrid E. Scheffer | Researchclopedia

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Ingrid E. Scheffer

Royal Children's Hospital ORCID

1,043

Works

88,612

Citations

141

h-index

568

i10-index

Research Topics

Epilepsy research and treatment Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases

Affiliations

Université Claude Bernard Lyon 12017–2017

Semmelweis University2019–2019

University of Foggia2015–2015

Northwestern University2022–2022

Western University2023–2024

Top Works

ILAE Official Report: A practical clinical definition of epilepsy

Robert S. Fisher,Carlos Alberto Acevedo,et al.

20145,755 citations

Neuroscience and Neuropharmacology Research

Metabolism and Genetic Disorders

<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology

Ingrid E. Scheffer,Samuel F. Berkovic,et al.

20174,769 citations

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009

Anne T. Berg,Samuel F. Berkovic,et al.

20104,342 citations

Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

Robert S. Fisher,J. Helen Cross,et al.

20173,312 citations

A definition and classification of status epilepticus – Report of the <scp>ILAE</scp> Task Force on Classification of Status Epilepticus

Eugen Trinka,Hannah R. Cock,et al.

20152,288 citations

Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome

Orrin Devinsky,J. Helen Cross,et al.

20171,631 citations

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Ortrud K. Steinlein,John C. Mulley,et al.

19951,131 citations

doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

Joseph G. Gleeson,Kristina M. Allen,et al.

19981,083 citations

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

Robyn H. Wallace,Dao Wen Wang,et al.

19981,000 citations