Nienke E. Verbeek

4.5k citations

23 papers · 777 indexed · h-index 18

Genetics top 5%
Psychiatry and Mental health top 5%
Molecular Biology
Cellular and Molecular Neuroscience top 10%
Pediatrics, Perinatology and Child Health top 10%

Co-authors: 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
Topics: Epilepsy research and treatment (11 papers)Genomics and Rare Diseases (9 papers)Genetics and Neurodevelopmental Disorders (9 papers)
Cited by: Psychiatry and Mental health Genetics Cellular and Molecular Neuroscience
Journals: PLoS ONE Neurology PEDIATRICS
Partner nations: Netherlands Germany United Kingdom

In The Last Decade

Nienke E. Verbeek

23 papers receiving 762 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome 2023 ·Epilepsia Open ·(unknown),Floor E. Jansen,Charlotte W. Ockeloen,Marjan J. A. van Kempen,(unknown),Marjolein H. Willemsen,Emanuela Scarano,(unknown),Evelien Zonneveld‐Huijssoon,Karen Low,Allan Bayat,Sanjay M. Sisodiya,Debopam Samanta,Gaëtan Lesca,Daniëlle de Jong,(unknown),Nienke E. Verbeek,Tjitske Kleefstra,Eva H. Brilstra,Danique R.M. Vlaskamp	7
2	Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield 2021 ·Genetics in Medicine ·(unknown),Jordi Corominas,(unknown),Maartje Pennings,Rowdy Meijer,Nienke E. Verbeek,Bart van de Warrenburg,Meyke Schouten,Helger G. Yntema,Lisenka E.L.M. Vissers,Erik‐Jan Kamsteeg,Christian Gilissen	22
3	A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene 2020 ·Parkinsonism & Related Disorders ·Karlien Mul,Meyke Schouten,(unknown),Dennis Dooijes,Frederic A. M. Hennekam,Nicolette C. Notermans,Peter Praamstra,Judith van Gaalen,Erik‐Jan Kamsteeg,Nienke E. Verbeek,Bart P.C. van de Warrenburg	6
4	Outcomes and comorbidities of SCN1A-related seizure disorders 2018 ·Epilepsy & Behavior ·Iris Lange,Boudewijn Gunning,Anja C. M. Sonsma,(unknown),Marjan van Kempen,Nienke E. Verbeek,(unknown),Joost Nicolai,Nine Knoers,Bobby P.C. Koeleman,Eva H. Brilstra	31
5	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 2018 ·Epilepsia ·Iris Lange,Boudewijn Gunning,Anja C. M. Sonsma,(unknown),Marjan van Kempen,Nienke E. Verbeek,Joost Nicolai,Nine Knoers,Bobby P.C. Koeleman,Eva H. Brilstra	97
6	Relationship of electrophysiological dysfunction and clinical severity inSCN2A-related epilepsies 2018 ·Human Mutation ·Stephan Lauxmann,Nienke E. Verbeek,Yuanyuan Liu,(unknown),Stephan A. Müller,Johannes R. Lemke,Marjan J. A. van Kempen,Holger Lerche,Ulrike B. S. Hedrich	25
7	Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells 2017 ·Genome Medicine ·Sjors Middelkamp,Sebastiaan van Heesch,A. Koen Braat,Joep de Ligt,Maarten van Iterson,Marieke Simonis,Markus J. van Roosmalen,Martijn J. E. Kelder,Evelien Kruisselbrink,Ron Hochstenbach,Nienke E. Verbeek,Elly F. Ippel,Youri Adolfs,R. Jeroen Pasterkamp,Wigard P. Kloosterman,Ewart Kuijk,Edwin Cuppen	25
8	Photosensitivity in Dravet syndrome is under-recognized and related to prognosis 2016 ·Clinical Neurophysiology ·Nienke E. Verbeek,Dorothée Kasteleijn‐Nolst Trenité,Merel Wassenaar,(unknown),Anja C. M. Sonsma,W. Boudewijn Gunning,Al de Weerd,Nine Knoers,(unknown),(unknown),Frans S. S. Leijten,Eva H. Brilstra	17
9	Seizure precipitants in Dravet syndrome: What events and activities are specifically provocative compared with other epilepsies? 2015 ·Epilepsy & Behavior ·Nienke E. Verbeek,Merel Wassenaar,Jolien S. van Campen,Anja C. M. Sonsma,Boudewijn Gunning,Nine Knoers,Dick Lindhout,Floor E. Jansen,Frans S. S. Leijten,Eva H. Brilstra,Dorothée Kasteleijn‐Nolst Trenité	29
10	Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome 2014 ·Human Genetics ·Katherina Walz,(unknown),Paul M. Neilsen,Joseph Foster,Francesco Brancati,Korcan Demir,Richard Fisher,(unknown),Nienke E. Verbeek,Kathrine Bjørgo,(unknown),Paolo Curatolo,Giuseppe Novelli,Clemer Abad,Lei Cao,Lily Zhang,Oscar Diaz‐Horta,Juan I. Young,David F. Callen,Mustafa Tekin	40
11	Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study 2013 ·PLoS ONE ·Nienke E. Verbeek,Nicoline van der Maas,Floor E. Jansen,Marjan J. A. van Kempen,Dick Lindhout,Eva H. Brilstra	40
12	PRRT2phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions 2012 ·Neurology ·(unknown),Guido J. Breedveld,(unknown),Eva H. Brilstra,Nienke E. Verbeek,Corien C. Verschuuren‐Bemelmans,Maartje Boon,Johnny P.A. Samijn,Karin E. M. Diderich,Ingrid M.B.H. van de Laar,Ben A. Oostra,Vincenzo Bonifati,Anneke Maat‐Kievit	65
13	Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome 2011 ·European Journal of Neuroscience ·Linda Volkers,Kristopher M. Kahlig,Nienke E. Verbeek,(unknown),Marjan J. A. van Kempen,Hans Stroink,Paul B. Augustijn,Onno van Nieuwenhuizen,Dick Lindhout,Alfred L. George,Bobby P.C. Koeleman,Martin B. Rook	46
14	Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism 2011 ·Neurogenetics ·Emma van Daalen,Chantal Kemner,Nienke E. Verbeek,Bert van der Zwaag,(unknown),Patrick Rump,(unknown),Ruben van ‘t Slot,Maretha Jonge,Wouter Staal,Frits A. Beemer,Jacob Vorstman,J. Peter H. Burbach,Hans Kristian Ploos van Amstel,Ron Hochstenbach,Eva H. Brilstra,Martin Poot	62
15	Adults with a history of possible Dravet syndrome: An illustration of the importance of analysis of the SCN1A gene 2011 ·Epilepsia ·Nienke E. Verbeek,Marjan van Kempen,W. Boudewijn Gunning,W.O. Renier,(unknown),Dick Lindhout,Eva H. Brilstra	16
16	Copy Number Variations in Patients With Electrical Status Epilepticus in Sleep 2011 ·Journal of Child Neurology ·Sietske H. Kevelam,Floor E. Jansen,Ellen van Binsbergen,Kees P. J. Braun,Nienke E. Verbeek,Dick Lindhout,Martin Poot,Eva H. Brilstra	26
17	Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome 2011 ·Human Mutation ·Willy M. Nillesen,Helger G. Yntema,(unknown),Nienke E. Verbeek,Louise C. Wilson,Frances M. Cowan,Marga Schepens,Annick Raas‐Rothschild,(unknown),Marcella Zollino,Raymon Vijzelaar,Giovanni Neri,Marcel Nelen,Hans van Bokhoven,Jacques C. Giltay,Tjitske Kleefstra	12
18	A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder 2009 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Bert van der Zwaag,Wouter Staal,Ron Hochstenbach,Martin Poot,Henk A. Spierenburg,Maretha Jonge,Nienke E. Verbeek,Ruben van ‘t Slot,Michael A. van Es,Frank J. T. Staal,Christine M. Freitag,Jacobine E. Buizer‐Voskamp,Marcel Nelen,Leonard H. van den Berg,Hans Kristian Ploos van Amstel,Hermán van Engeland,J. Peter H. Burbach	80
19	HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing 2009 ·European Journal of Human Genetics ·Wenke Seifert,(unknown),Katrin Hoffmann,Tom H. Lindner,C. Bassir,Fuat Aksu,Christoph Hübner,Nienke E. Verbeek,Stefan Mundlos,Denise Horn	22
20	Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions 2009 ·Neuroscience Letters ·Linda Volkers,Martin B. Rook,(unknown),Nienke E. Verbeek,W. Antoinette Groenewegen,Marjan J. A. van Kempen,Dick Lindhout,Bobby P.C. Koeleman	24

About Nienke E. Verbeek

Nienke E. Verbeek is a scholar working on Psychiatry and Mental health, Genetics and Microbiology, having authored 23 papers that have together received 777 indexed citations. Recurring topics across this work include Epilepsy research and treatment (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). The work is most often cited by research in Psychiatry and Mental health (351 citations), Genetics (392 citations) and Cellular and Molecular Neuroscience (152 citations). Nienke E. Verbeek has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent 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. Their work appears in journals such as PLoS ONE, Neurology and PEDIATRICS.

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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