Ingrid E. Scheffer

88.6k total citations · 21 hit papers
506 papers, 44.2k citations indexed

About

Ingrid E. Scheffer is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Ingrid E. Scheffer has authored 506 papers receiving a total of 44.2k indexed citations (citations by other indexed papers that have themselves been cited), including 289 papers in Psychiatry and Mental health, 207 papers in Genetics and 168 papers in Molecular Biology. Recurrent topics in Ingrid E. Scheffer's work include Epilepsy research and treatment (286 papers), Genetics and Neurodevelopmental Disorders (152 papers) and Genomics and Rare Diseases (117 papers). Ingrid E. Scheffer is often cited by papers focused on Epilepsy research and treatment (286 papers), Genetics and Neurodevelopmental Disorders (152 papers) and Genomics and Rare Diseases (117 papers). Ingrid E. Scheffer collaborates with scholars based in Australia, United States and United Kingdom. Ingrid E. Scheffer's 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 and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Ingrid E. Scheffer

488 papers receiving 43.0k citations

Hit Papers

ILAE Official Report: A practica... 1995 2026 2005 2015 2014 2017 2010 2017 2015 1000 2.0k 3.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ingrid E. Scheffer Australia 92 26.6k 14.3k 12.9k 12.1k 11.8k 506 44.2k
Samuel F. Berkovic Australia 107 25.5k 1.0× 16.1k 1.1× 11.5k 0.9× 12.4k 1.0× 10.0k 0.8× 606 44.6k
Jacqueline A. French United States 76 26.3k 1.0× 12.3k 0.9× 16.5k 1.3× 4.2k 0.3× 3.4k 0.3× 404 37.6k
J. Helen Cross United Kingdom 71 18.9k 0.7× 7.9k 0.6× 10.9k 0.8× 4.2k 0.3× 4.0k 0.3× 539 31.4k
Solomon L. Moshé United States 69 21.9k 0.8× 11.8k 0.8× 13.4k 1.0× 4.2k 0.3× 3.9k 0.3× 343 31.5k
Gary W. Mathern United States 63 16.8k 0.6× 9.5k 0.7× 9.6k 0.7× 4.2k 0.3× 3.5k 0.3× 189 25.8k
Josemir W. Sander United Kingdom 98 25.6k 1.0× 8.7k 0.6× 18.2k 1.4× 3.3k 0.3× 2.0k 0.2× 621 34.8k
Renzo Guerrini Italy 75 10.3k 0.4× 6.0k 0.4× 8.3k 0.6× 6.0k 0.5× 6.1k 0.5× 556 21.9k
Samuel Wiebe Canada 67 23.0k 0.9× 8.5k 0.6× 14.3k 1.1× 2.1k 0.2× 3.1k 0.3× 293 31.3k
Wolfgang Löscher Germany 88 15.5k 0.6× 16.9k 1.2× 11.2k 0.9× 8.5k 0.7× 1.4k 0.1× 606 34.1k
Orrin Devinsky United States 96 20.3k 0.8× 10.8k 0.8× 9.4k 0.7× 3.5k 0.3× 2.7k 0.2× 743 41.3k

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-authorship network of co-authors of Ingrid E. Scheffer

This figure shows the co-authorship network connecting the top 25 collaborators of Ingrid E. Scheffer. A scholar is included among the top collaborators of Ingrid E. Scheffer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ingrid E. Scheffer. Ingrid E. Scheffer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Chiu, Annie Ting Gee, Mark F. Bennett, Amy Schneider, et al.. (2025). Pathogenic Variants in RNU2‐2 , a Non‐coding Spliceosomal RNA , Cause a Distinctive Developmental and Epileptic Encephalopathy. Annals of Neurology. 99(1). 51–58. 1 indexed citations
2.
Haghshenas, Sadegheh, Michael A. Levy, Raissa Relator, et al.. (2025). Identification of an episignature for the MEF2C-associated syndrome. European Journal of Human Genetics. 34(1). 53–60.
3.
McTague, Amy, Ingrid E. Scheffer, Dimitri M. Kullmann, & Sanjay M. Sisodiya. (2024). Epilepsies. Handbook of clinical neurology. 203. 157–184. 3 indexed citations
4.
Jancovski, Nikola, Kun Zhou, Steve G. Reid, et al.. (2024). Developmental dysfunction in a preclinical model of Kcnq2 developmental and epileptic encephalopathy. Neurobiology of Disease. 205. 106782–106782. 1 indexed citations
5.
Chen, Zhibin, Sarah Barnard, Shobi Sivathamboo, et al.. (2023). Applying the ILAE diagnostic criteria for Lennox‐Gastaut syndrome in the real‐world setting: A multicenter retrospective cohort study. Epilepsia Open. 9(2). 602–612. 6 indexed citations
6.
Specchio, Nicola, Elaine Wirrell, Ingrid E. Scheffer, et al.. (2022). 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. Epilepsia. 63(6). 1398–1442. 447 indexed citations breakdown →
7.
Riney, Kate, Alicia Bogacz, Ernest Somerville, et al.. (2022). International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions. Epilepsia. 63(6). 1443–1474. 132 indexed citations breakdown →
9.
Zuberi, Sameer M., Elaine Wirrell, Elissa Yozawitz, et al.. (2022). ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions. Epilepsia. 63(6). 1349–1397. 455 indexed citations breakdown →
10.
Scheffer, Ingrid E., Katja Boysen, Amy Schneider, et al.. (2019). BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures. Developmental Medicine & Child Neurology. 62(9). 1096–1099. 14 indexed citations
11.
Miller, Ian, Ingrid E. Scheffer, Boudewijn Gunning, et al.. (2019). Cannabidiol (CBD; 10 And 20 MG/KG/Day) Significantly Reduces Convulsive Seizure Frequency In Children And Adolescents With Dravet Syndrome: Results Of A Dose-Ranging, Multi-Center, Randomised, Double-Blind, Placebo-Controlled Trial (GWPCARE2). Epilepsia. 60. 1 indexed citations
12.
Myers, Kenneth A., et al.. (2018). Stiripentol efficacy and safety in Dravet syndrome: a 12‐year observational study. Developmental Medicine & Child Neurology. 60(6). 574–578. 54 indexed citations
13.
Howell, Katherine B., Stefanie Eggers, Kim Dalziel, et al.. (2018). A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy. Epilepsia. 59(6). 1177–1187. 64 indexed citations
14.
Zhu, Xiaolin, Brett Copeland, Joshua Bridgers, et al.. (2017). A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations. PLoS Genetics. 13(11). e1007104–e1007104. 17 indexed citations
15.
Fisher, Robert S., J. Helen Cross, Jacqueline A. French, et al.. (2017). Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology. Epilepsia. 58(4). 522–530. 2161 indexed citations breakdown →
16.
Scheffer, Ingrid E., Samuel F. Berkovic, Giuseppe Capovilla, et al.. (2017). ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology. Epilepsia. 58(4). 512–521. 3282 indexed citations breakdown →
17.
Pisano, Tiziana, Adam L. Numis, Sinéad B. Heavin, et al.. (2015). Early and effective treatment of KCNQ 2 encephalopathy. Epilepsia. 56(5). 685–691. 186 indexed citations
18.
Azmanov, Dimitar N., Veneta Bojinova, Laura V. Flórez, et al.. (2010). Mosaicism of a missenseSCN1Amutation and Dravet syndrome in a Roma/Gypsy family. Epileptic Disorders. 12(2). 117–124. 14 indexed citations
19.
Mullen, Saul A., Arvid Suls, Peter De Jonghe, Samuel F. Berkovic, & Ingrid E. Scheffer. (2010). Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency. Neurology. 75(5). 432–440. 120 indexed citations
20.
Scheffer, Ingrid E., Yuehua Zhang, Floor E. Jansen, & Leanne M. Dibbens. (2009). Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?. Brain and Development. 31(5). 394–400. 122 indexed citations

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