Nienke E. Verbeek

4.5k total citations
23 papers, 777 citations indexed

About

Nienke E. Verbeek is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Nienke E. Verbeek has authored 23 papers receiving a total of 777 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Psychiatry and Mental health and 7 papers in Molecular Biology. Recurrent topics in Nienke E. Verbeek's work include Epilepsy research and treatment (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Nienke E. Verbeek is often cited by papers focused on Epilepsy research and treatment (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Nienke E. Verbeek collaborates with scholars based in Netherlands, Germany and United Kingdom. Nienke E. Verbeek's co-authors include Eva H. Brilstra, Dick Lindhout, Nine Knoers, Marjan J. A. van Kempen, Bobby P.C. Koeleman, Anja C. M. Sonsma, Boudewijn Gunning, Floor E. Jansen, Iris Lange and Marjan van Kempen and has published in prestigious journals such as PLoS ONE, Neurology and PEDIATRICS.

In The Last Decade

Nienke E. Verbeek

23 papers receiving 762 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nienke E. Verbeek Netherlands 18 392 351 308 152 136 23 777
Amy Schneider Australia 13 275 0.7× 474 1.4× 199 0.6× 153 1.0× 251 1.8× 21 758
Marilena Vecchi Italy 15 367 0.9× 285 0.8× 255 0.8× 99 0.7× 164 1.2× 32 735
Katrien Smets Belgium 11 126 0.3× 264 0.8× 232 0.8× 239 1.6× 74 0.5× 13 567
Sawa Yasumoto Japan 17 345 0.9× 569 1.6× 344 1.1× 253 1.7× 190 1.4× 44 947
Xenia Iona Australia 12 268 0.7× 414 1.2× 257 0.8× 212 1.4× 132 1.0× 13 795
Tommy Stödberg Sweden 14 162 0.4× 174 0.5× 169 0.5× 67 0.4× 69 0.5× 22 625
Noriyuki Akasaka Japan 14 245 0.6× 214 0.6× 175 0.6× 122 0.8× 122 0.9× 27 566
R. Anne Howell Australia 9 408 1.0× 699 2.0× 241 0.8× 315 2.1× 233 1.7× 9 916
Hisashi Kawawaki Japan 12 116 0.3× 177 0.5× 173 0.6× 96 0.6× 78 0.6× 63 541
Bernardo Dalla Bernardina Italy 16 573 1.5× 255 0.7× 486 1.6× 176 1.2× 135 1.0× 31 972

Countries citing papers authored by Nienke E. Verbeek

Since Specialization
Citations

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

Fields of papers citing papers by Nienke E. Verbeek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nienke E. Verbeek. 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 Nienke E. Verbeek. The network helps show where Nienke E. Verbeek may publish in the future.

Co-authorship network of co-authors of Nienke E. Verbeek

This figure shows the co-authorship network connecting the top 25 collaborators of Nienke E. Verbeek. A scholar is included among the top collaborators of Nienke E. Verbeek 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 Nienke E. Verbeek. Nienke E. Verbeek 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.
Jansen, Floor E., Charlotte W. Ockeloen, Marjan J. A. van Kempen, et al.. (2023). Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome. Epilepsia Open. 8(4). 1300–1313. 7 indexed citations
2.
Corominas, Jordi, Maartje Pennings, Rowdy Meijer, et al.. (2021). Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield. Genetics in Medicine. 23(8). 1569–1573. 22 indexed citations
3.
Mul, Karlien, Meyke Schouten, Dennis Dooijes, et al.. (2020). A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene. Parkinsonism & Related Disorders. 80. 98–101. 6 indexed citations
4.
Lange, Iris, Boudewijn Gunning, Anja C. M. Sonsma, et al.. (2018). Outcomes and comorbidities of SCN1A-related seizure disorders. Epilepsy & Behavior. 90. 252–259. 31 indexed citations
5.
Lange, Iris, Boudewijn Gunning, Anja C. M. Sonsma, et al.. (2018). Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in SCN1A‐related seizure phenotypes. Epilepsia. 59(6). 1154–1165. 97 indexed citations
6.
Lauxmann, Stephan, Nienke E. Verbeek, Yuanyuan Liu, et al.. (2018). Relationship of electrophysiological dysfunction and clinical severity inSCN2A-related epilepsies. Human Mutation. 39(12). 1942–1956. 25 indexed citations
7.
Middelkamp, Sjors, Sebastiaan van Heesch, A. Koen Braat, et al.. (2017). Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells. Genome Medicine. 9(1). 9–9. 25 indexed citations
8.
Verbeek, Nienke E., Dorothée Kasteleijn‐Nolst Trenité, Merel Wassenaar, et al.. (2016). Photosensitivity in Dravet syndrome is under-recognized and related to prognosis. Clinical Neurophysiology. 128(2). 323–330. 17 indexed citations
9.
Verbeek, Nienke E., Merel Wassenaar, Jolien S. van Campen, et al.. (2015). Seizure precipitants in Dravet syndrome: What events and activities are specifically provocative compared with other epilepsies?. Epilepsy & Behavior. 47. 39–44. 29 indexed citations
10.
Walz, Katherina, Paul M. Neilsen, Joseph Foster, et al.. (2014). Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome. Human Genetics. 134(2). 181–190. 40 indexed citations
11.
Verbeek, Nienke E., Nicoline van der Maas, Floor E. Jansen, et al.. (2013). Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study. PLoS ONE. 8(6). e65758–e65758. 40 indexed citations
12.
Breedveld, Guido J., Eva H. Brilstra, Nienke E. Verbeek, et al.. (2012). PRRT2phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions. Neurology. 79(8). 777–784. 65 indexed citations
13.
Volkers, Linda, Kristopher M. Kahlig, Nienke E. Verbeek, et al.. (2011). Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome. European Journal of Neuroscience. 34(8). 1268–1275. 46 indexed citations
14.
Daalen, Emma van, Chantal Kemner, Nienke E. Verbeek, et al.. (2011). Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism. Neurogenetics. 12(4). 315–323. 62 indexed citations
15.
Verbeek, Nienke E., Marjan van Kempen, W. Boudewijn Gunning, et al.. (2011). Adults with a history of possible Dravet syndrome: An illustration of the importance of analysis of the SCN1A gene. Epilepsia. 52(4). e23–5. 16 indexed citations
16.
Kevelam, Sietske H., Floor E. Jansen, Ellen van Binsbergen, et al.. (2011). Copy Number Variations in Patients With Electrical Status Epilepticus in Sleep. Journal of Child Neurology. 27(2). 178–182. 26 indexed citations
17.
Nillesen, Willy M., Helger G. Yntema, Nienke E. Verbeek, et al.. (2011). Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome. Human Mutation. 32(7). 853–859. 12 indexed citations
18.
Zwaag, Bert van der, Wouter Staal, Ron Hochstenbach, et al.. (2009). A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(4). 960–966. 80 indexed citations
19.
Seifert, Wenke, Katrin Hoffmann, Tom H. Lindner, et al.. (2009). HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing. European Journal of Human Genetics. 17(12). 1570–1576. 22 indexed citations
20.
Volkers, Linda, Martin B. Rook, Nienke E. Verbeek, et al.. (2009). Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions. Neuroscience Letters. 462(1). 24–29. 24 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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