Andreas Brunklaus

4.2k total citations
47 papers, 1.8k citations indexed

About

Andreas Brunklaus is a scholar working on Psychiatry and Mental health, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andreas Brunklaus has authored 47 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Psychiatry and Mental health, 20 papers in Genetics and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andreas Brunklaus's work include Epilepsy research and treatment (26 papers), Genomics and Rare Diseases (15 papers) and Genetics and Neurodevelopmental Disorders (15 papers). Andreas Brunklaus is often cited by papers focused on Epilepsy research and treatment (26 papers), Genomics and Rare Diseases (15 papers) and Genetics and Neurodevelopmental Disorders (15 papers). Andreas Brunklaus collaborates with scholars based in United Kingdom, United States and Germany. Andreas Brunklaus's co-authors include Sameer M. Zuberi, Eleanor Reavey, Rachael Ellis, Joseph D. Symonds, Liam Dorris, Dennis Lal, Dora Steel, John S. Duncan, Rachael Birch and Keith Pohl and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Brain.

In The Last Decade

Andreas Brunklaus

43 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Brunklaus United Kingdom 22 1.0k 622 560 458 358 47 1.8k
Kazumaru Wada Japan 22 942 0.9× 319 0.5× 875 1.6× 321 0.7× 972 2.7× 43 1.8k
Erik Taubøll Norway 34 2.1k 2.0× 188 0.3× 708 1.3× 1.8k 3.9× 779 2.2× 145 3.6k
Katherine Nickels United States 28 1.7k 1.7× 408 0.7× 294 0.5× 956 2.1× 634 1.8× 79 2.6k
Mario Mastrangelo Italy 23 292 0.3× 330 0.5× 594 1.1× 187 0.4× 279 0.8× 99 1.7k
Stanley R. Resor United States 30 1.4k 1.4× 331 0.5× 246 0.4× 1.0k 2.2× 498 1.4× 45 2.5k
Patricia Gassó Spain 26 490 0.5× 283 0.5× 426 0.8× 116 0.3× 276 0.8× 94 1.6k
Sara Matricardi Italy 23 825 0.8× 216 0.3× 198 0.4× 493 1.1× 393 1.1× 68 1.4k
Johan Lundgren Sweden 20 271 0.3× 180 0.3× 333 0.6× 226 0.5× 312 0.9× 28 1.3k
R. Canger Italy 24 1.5k 1.5× 319 0.5× 235 0.4× 1.1k 2.5× 464 1.3× 62 2.1k
Rocío Sánchez‐Carpintero Spain 15 787 0.8× 159 0.3× 191 0.3× 360 0.8× 288 0.8× 63 1.2k

Countries citing papers authored by Andreas Brunklaus

Since Specialization
Citations

This map shows the geographic impact of Andreas Brunklaus'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 Andreas Brunklaus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Brunklaus more than expected).

Fields of papers citing papers by Andreas Brunklaus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas Brunklaus. 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 Andreas Brunklaus. The network helps show where Andreas Brunklaus may publish in the future.

Co-authorship network of co-authors of Andreas Brunklaus

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Brunklaus. A scholar is included among the top collaborators of Andreas Brunklaus 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 Andreas Brunklaus. Andreas Brunklaus 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.
Brunklaus, Andreas, et al.. (2026). Zorevunersen in Children and Adolescents with Dravet Syndrome. New England Journal of Medicine. 394(10). 969–982.
2.
Schneider, Amy, Gaëtan Lesca, Joseph D. Symonds, et al.. (2025). SCN1A pathogenic variants do not have a distinctive blood‐derived DNA methylation signature. Epilepsia. 66(4). e66–e72.
3.
Brunklaus, Andreas, Susanne Schubert‐Bast, Francesca Darra, et al.. (2025). Communicating a diagnosis of Dravet syndrome to parents/caregivers: An international Delphi consensus. Epilepsia Open. 10(2). 450–465. 1 indexed citations
4.
Specchio, Nicola, Eleonora Aronica, Stéphane Auvin, et al.. (2025). The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options. Epilepsia. 66(4). 970–987. 4 indexed citations
5.
Schubert‐Bast, Susanne, Susanne Knake, Felix von Podewils, et al.. (2025). A multicenter cohort study on the efficacy, retention, and tolerability of cenobamate in patients with developmental and epileptic encephalopathies. Epilepsia. 66(5). 1519–1528. 9 indexed citations
6.
Strzelczyk, Adam, Felix von Podewils, Hajo M. Hamer, et al.. (2025). Post-marketing Experience with Cenobamate in the Treatment of Focal Epilepsies: A Multicentre Cohort Study. CNS Drugs. 39(3). 321–331. 6 indexed citations
7.
Harper, Alexander James, et al.. (2025). Nonseizure Outcomes in Dravet Syndrome: Potential Impact of Pharmacotherapy. CNS Drugs. 39(10). 995–1009.
8.
Strzelczyk, Adam, et al.. (2024). Cost-of-illness review of status epilepticus in Europe. Epilepsy & Behavior. 161. 110105–110105. 1 indexed citations
9.
Bhattarai, Nisha, Ludovica Montanucci, Eduardo Pérez‐Palma, et al.. (2024). Molecular dynamics simulations reveal molecular mechanisms for the gain and loss of function effects of four SCN2A variants. Biophysical Journal. 123(3). 109a–110a. 1 indexed citations
10.
Hendry, Kirsty, et al.. (2024). Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study. European Journal of Paediatric Neurology. 53. 138–143. 3 indexed citations
11.
Strzelczyk, Adam, Lieven Lagae, Jo M. Wilmshurst, et al.. (2023). Dravet syndrome: A systematic literature review of the illness burden. Epilepsia Open. 8(4). 1256–1270. 32 indexed citations
12.
Brunklaus, Andreas, et al.. (2023). Prophecy or empiricism? Clinical value of predicting versus determining genetic variant functions. Epilepsia. 64(11). 2909–2913. 2 indexed citations
13.
McTague, Amy, Andreas Brunklaus, Giulia Barcia, et al.. (2022). Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologists. European Journal of Medical Genetics. 65(7). 104531–104531. 3 indexed citations
14.
Brunklaus, Andreas, S. Robb, Rosaline C. M. Quinlivan, et al.. (2016). Vitamin D in corticosteroid-naïve and corticosteroid-treated Duchenne muscular dystrophy: what dose achieves optimal 25(OH) vitamin D levels?. Archives of Disease in Childhood. 101(10). 957–961. 11 indexed citations
15.
Brunklaus, Andreas, Rachael Ellis, Helen Stewart, et al.. (2015). Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families. European Journal of Paediatric Neurology. 19(4). 484–488. 20 indexed citations
16.
Brunklaus, Andreas, et al.. (2012). Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome. Brain. 135(8). 2329–2336. 254 indexed citations
17.
Brunklaus, Andreas, Liam Dorris, Rachael Ellis, et al.. (2012). The clinical utility of an SCN1A genetic diagnosis in infantile‐onset epilepsy. Developmental Medicine & Child Neurology. 55(2). 154–161. 54 indexed citations
18.
Zuberi, Sameer M., et al.. (2011). Genotype–phenotype associations in SCN1A -related epilepsies. Neurology. 76(7). 594–600. 191 indexed citations
19.
Brunklaus, Andreas, Keith Pohl, Sameer M. Zuberi, & Carlos de Sousa. (2011). Investigating neuroblastoma in childhood opsoclonus-myoclonus syndrome. Archives of Disease in Childhood. 97(5). 461–463. 48 indexed citations
20.
Michel, Tanja Maria, Sophia Frangou, Julia Jecel, et al.. (2007). Evidence for oxidative stress in the frontal cortex in patients with recurrent depressive disorder—a postmortem study. Psychiatry Research. 151(1-2). 145–150. 176 indexed citations

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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