Ingrid E. Scheffer

88.6k citations
506 papers · 44.2k · 21 hit papers · h-index 92

Impact in

Papers in

    • Epilepsy research and treatment 286
    • Genetics and Neurodevelopmental Disorders 152
    • Genomics and Rare Diseases 117
    • Genomic variations and chromosomal abnormalities 49

Ingrid E. Scheffer

488 papers receiving 43.0k citations

Ingrid E. Scheffer's Hit Papers

International consensus on diagnosis and management of Dravet syndrome 2022 · 129 citations
1290+5+10Years since publication10002.0k3.0k

Peers

Ingrid E. Scheffer
Comparison fields: 5 of 181
  • Psychiatry and Mental health 26.6k
  • Cellular and Molecular Neuroscience 14.3k
  • Pediatrics, Perinatology and Child Health 12.9k
  • Genetics 11.8k
  • Clinical Biochemistry 2.7k
Replace Samuel F. Berkovic with:
Samuel F. Berkovic Australia
Solomon L. Moshé United States
Jacqueline A. French United States
Gary W. Mathern United States
J. Helen Cross United Kingdom
Renzo Guerrini Italy
Josemir W. Sander United Kingdom
Jerome Engel United States
Samuel Wiebe Canada
Orrin Devinsky United States
Ingrid E. Scheffer relative to Samuel F. Berkovic Australia Samuel F. Berkovic's profile →
Citations per field
00.5×1.5×2.4×
Samuel F. Berkovic · 1×
Citations per year

Countries citing papers authored by Ingrid E. Scheffer

Since Specialization
Citations

This map shows the geographic impact of Ingrid E. Scheffer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ingrid E. Scheffer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid E. Scheffer more than expected).

Fields of papers citing papers by Ingrid E. Scheffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ingrid E. Scheffer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ingrid E. Scheffer. The network helps show where Ingrid E. Scheffer may publish in the future.

Co-authors

The 25 scholars most cited alongside Ingrid E. Scheffer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ingrid E. Scheffer Line = papers co-authored together Ingrid E. Scheffer links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 506 papers — load more, or switch the sort, to bring in the rest.

#Work
1
ILAE Official Report: A practical clinical definition of epilepsy
Hit paper breakdown →
20143768
2
ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology
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20173282
3
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
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20103023
4
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology
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20172161
5
A definition and classification of status epilepticus – Report of the ILAE Task Force on Classification of Status Epilepticus
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20151514
6
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
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20171167
7
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
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1995843
8
doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
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1998801
9
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
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1998783
10
Instruction manual for the ILAE 2017 operational classification of seizure types
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2017678
11
Epilepsy
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2018650
12
Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia
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1998625
13
Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures
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2001590
14
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
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1997543
15
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
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2022455
16
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
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2022447
17 1995376
18
The genetic landscape of the epileptic encephalopathies of infancy and childhood
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2015370
19 2002331
20 2002317

About Ingrid E. Scheffer

Ingrid E. Scheffer is a scholar working on Psychiatry and Mental health, Genetics, Molecular Biology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 506 papers that have together received 44.2k indexed citations. Recurring topics across this work include Epilepsy research and treatment (286 papers), Genetics and Neurodevelopmental Disorders (152 papers), Genomics and Rare Diseases (117 papers), Neuroscience and Neuropharmacology Research (111 papers), Pharmacological Effects and Toxicity Studies (73 papers), Ion channel regulation and function (67 papers), Genomic variations and chromosomal abnormalities (49 papers) and Metabolism and Genetic Disorders (45 papers). The work is most often cited by research in Psychiatry and Mental health (26.6k citations), Cellular and Molecular Neuroscience (14.3k citations), Pediatrics, Perinatology and Child Health (12.9k citations), Genetics (11.8k citations) and Clinical Biochemistry (2.7k citations). Ingrid E. Scheffer has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Samuel F. Berkovic, J. Helen Cross, Solomon L. Moshé, Jacqueline A. French, John C. Mulley, Gary W. Mathern, Sameer M. Zuberi, Robert S. Fisher, Édouard Hirsch and Samuel Wiebe. Their work appears in journals such as Epilepsia, Neurology, Annals of Neurology, Epilepsy Research and Developmental Medicine & Child Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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