Ingrid Eileen Scheffer
Impact in
- Psychiatry and Mental health top 0.01%
- Epilepsy research and treatment
- Cellular and Molecular Neuroscience top 0.01%
- Neuroscience and Neuropharmacology Research
Papers in
-
- Epilepsy research and treatment 311
- Genetics 247
- Genetics and Neurodevelopmental Disorders 172
- Genomics and Rare Diseases 143
- Genomic variations and chromosomal abnormalities 65
- Co-authors
- Samuel Frank Berkovic (244 shared papers)Judith Helen Cross (35 shared papers)Solomon L. Moshé (21 shared papers)John C. Mulley (71 shared papers)Jacqueline A. French (22 shared papers)Gary W. Mathern (9 shared papers)Sameer M. Zuberi (28 shared papers)Édouard Hirsch (18 shared papers)
- Journals
- Epilepsia (132 papers)Neurology (81 papers)Annals of Neurology (40 papers)Brain (33 papers)The American Journal of Human Genetics (32 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Ingrid Eileen Scheffer
691 papers receiving 66.0k citations
Ingrid Eileen Scheffer's Hit Papers
Peers
Comparison fields: 5 of 196
- Psychiatry and Mental health 31.5k
- Cellular and Molecular Neuroscience 15.9k
- Genetics 17.6k
- Pediatrics, Perinatology and Child Health 10.3k
- Clinical Biochemistry 3.2k
Countries citing papers authored by Ingrid Eileen Scheffer
This map shows the geographic impact of Ingrid Eileen 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 Eileen 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 Eileen Scheffer more than expected).
Fields of papers citing papers by Ingrid Eileen Scheffer
This network shows the impact of papers produced by Ingrid Eileen 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 Eileen Scheffer. The network helps show where Ingrid Eileen Scheffer may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingrid Eileen Scheffer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 714 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 → | 2014 | 4318 |
| 2 | ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology Hit paper breakdown → | 2017 | 3833 |
| 3 | Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009 Hit paper breakdown → | 2010 | 3399 |
| 4 | Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology Hit paper breakdown → | 2017 | 2543 |
| 5 | A definition and classification of status epilepticus – Report of the ILAE Task Force on Classification of Status Epilepticus Hit paper breakdown → | 2015 | 1761 |
| 6 | Analysis of shared heritability in common disorders of the brain Hit paper breakdown → | 2018 | 1441 |
| 7 | Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome Hit paper breakdown → | 2017 | 1325 |
| 8 | A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy Hit paper breakdown → | 1995 | 940 |
| 9 | doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein Hit paper breakdown → | 1998 | 895 |
| 10 | Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B Hit paper breakdown → | 1998 | 846 |
| 11 | Instruction manual for the ILAE 2017 operational classification of seizure types Hit paper breakdown → | 2017 | 770 |
| 12 | Epilepsy Hit paper breakdown → | 2018 | 742 |
| 13 | Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia Hit paper breakdown → | 1998 | 712 |
| 14 | 2001 | 676 | |
| 15 | 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 Hit paper breakdown → | 2022 | 611 |
| 16 | Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes Hit paper breakdown → | 1997 | 606 |
| 17 | ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions Hit paper breakdown → | 2022 | 597 |
| 18 | Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group Hit paper breakdown → | 2018 | 555 |
| 19 | Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 Hit paper breakdown → | 2013 | 541 |
| 20 | Refining analyses of copy number variation identifies specific genes associated with developmental delay Hit paper breakdown → | 2014 | 533 |
About Ingrid Eileen Scheffer
Ingrid Eileen Scheffer is a scholar working on Psychiatry and Mental health, Genetics, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 714 papers that have together received 69.1k indexed citations. Recurring topics across this work include Epilepsy research and treatment (311 papers), Genetics and Neurodevelopmental Disorders (172 papers), Genomics and Rare Diseases (143 papers), Neuroscience and Neuropharmacology Research (98 papers), Genomic variations and chromosomal abnormalities (65 papers), Ion channel regulation and function (59 papers), Pharmacological Effects and Toxicity Studies (57 papers) and Metabolism and Genetic Disorders (50 papers). The work is most often cited by research in Psychiatry and Mental health (31.5k citations), Cellular and Molecular Neuroscience (15.9k citations), Genetics (17.6k citations), Pediatrics, Perinatology and Child Health (10.3k citations) and Clinical Biochemistry (3.2k citations). Ingrid Eileen Scheffer has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Samuel Frank Berkovic, Judith Helen Cross, Solomon L. Moshé, John C. Mulley, Jacqueline A. French, Gary W. Mathern, Sameer M. Zuberi, Édouard Hirsch, Robert S. Fisher and Samuel Wiebe. Their work appears in journals such as Epilepsia, Neurology, Annals of Neurology, Brain and The American Journal of Human Genetics.
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.