Katrien Smets

2.5k total citations
13 papers, 567 citations indexed

About

Katrien Smets is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Katrien Smets has authored 13 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Katrien Smets's work include Epilepsy research and treatment (5 papers), Mitochondrial Function and Pathology (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Katrien Smets is often cited by papers focused on Epilepsy research and treatment (5 papers), Mitochondrial Function and Pathology (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Katrien Smets collaborates with scholars based in Belgium, United States and Germany. Katrien Smets's co-authors include Peter De Jonghe, Berten Ceulemans, Tine Deconinck, Lieve Claes, Jonathan Baets, Anouk Van de Vel, Kristien Wouters, Ann Löfgren, Salmo Raskin and Dominique Audenaert and has published in prestigious journals such as Brain, Neurology and Human Mutation.

In The Last Decade

Katrien Smets

13 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrien Smets Belgium 11 264 239 232 126 74 13 567
Noriyuki Akasaka Japan 14 214 0.8× 122 0.5× 175 0.8× 245 1.9× 122 1.6× 27 566
Elvio Della Giustina Italy 11 106 0.4× 151 0.6× 88 0.4× 87 0.7× 51 0.7× 21 373
Hisashi Kawawaki Japan 12 177 0.7× 96 0.4× 173 0.7× 116 0.9× 78 1.1× 63 541
Yoram Nevo Israel 14 186 0.7× 90 0.4× 241 1.0× 80 0.6× 148 2.0× 31 641
Paola Diadori Canada 10 179 0.7× 147 0.6× 86 0.4× 109 0.9× 114 1.5× 16 425
José Pedro Vieira Portugal 15 131 0.5× 108 0.5× 228 1.0× 250 2.0× 78 1.1× 48 702
D Fontan France 14 185 0.7× 149 0.6× 271 1.2× 152 1.2× 181 2.4× 43 719
Joshua B. Silverman United States 12 112 0.4× 130 0.5× 157 0.7× 45 0.4× 46 0.6× 25 549
Stephan Theiss Germany 16 90 0.3× 287 1.2× 435 1.9× 61 0.5× 18 0.2× 40 731
Nienke E. Verbeek Netherlands 18 351 1.3× 152 0.6× 308 1.3× 392 3.1× 136 1.8× 23 777

Countries citing papers authored by Katrien Smets

Since Specialization
Citations

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

Fields of papers citing papers by Katrien Smets

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrien Smets

This figure shows the co-authorship network connecting the top 25 collaborators of Katrien Smets. A scholar is included among the top collaborators of Katrien Smets 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 Katrien Smets. Katrien Smets is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Aerts, Olivier, et al.. (2018). Occupational airborne allergic contact dermatitis caused by N‐(4‐hydroxyphenyl)benzenesulfonamide. Contact Dermatitis. 80(1). 71–73. 3 indexed citations
2.
Hayer, Stefanie N., Tine Deconinck, Benjamin Bender, et al.. (2017). STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations. Orphanet Journal of Rare Diseases. 12(1). 31–31. 45 indexed citations
3.
Hirst, Jennifer, Marianna Madeo, Katrien Smets, et al.. (2016). Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurology Genetics. 2(5). e98–e98. 24 indexed citations
4.
Denora, Paola S., Katrien Smets, Carlo Casali, et al.. (2016). Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions. Brain. 139(Pt 6). aww061–aww061. 49 indexed citations
5.
Vel, Anouk Van de, Katrien Smets, Kristien Wouters, & Berten Ceulemans. (2016). Automated non-EEG based seizure detection: Do users have a say?. Epilepsy & Behavior. 62. 121–128. 55 indexed citations
6.
Quaegebeur, Annelies, Gert Van Goethem, Ann Löfgren, et al.. (2015). The spectrum of epilepsy caused by POLG mutations. Acta Neurologica Belgica. 116(1). 17–25. 16 indexed citations
7.
Smets, Katrien, Anna Duarri, Tine Deconinck, et al.. (2015). First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy. BMC Medical Genetics. 16(1). 51–51. 48 indexed citations
8.
Smets, Katrien, Tine Deconinck, Jonathan Baets, et al.. (2014). Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28. Neurology. 82(23). 2092–2100. 21 indexed citations
9.
Waele, Liesbeth De, Paul Boon, Berten Ceulemans, et al.. (2013). First line management of prolonged convulsive seizures in children and adults: good practice points. Acta Neurologica Belgica. 113(4). 375–380. 5 indexed citations
10.
Boon, Paul, Sebastiaan Engelborghs, Anna Jansen, et al.. (2012). Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium: an update. Acta Neurologica Belgica. 112(2). 119–131. 11 indexed citations
11.
Claes, Lieve, Liesbet Deprez, Arvid Suls, et al.. (2009). TheSCN1Avariant database: a novel research and diagnostic tool. Human Mutation. 30(10). E904–E920. 103 indexed citations
12.
Jorens, Philippe G., Paul M. Parizel, Hendrik E. Demey, et al.. (2005). Meningoencephalitis caused by Streptococcus pneumoniae: a diagnostic and therapeutic challenge. Neuroradiology. 47(10). 758–764. 35 indexed citations
13.
Claes, Lieve, Berten Ceulemans, Dominique Audenaert, et al.. (2003). De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy. Human Mutation. 21(6). 615–621. 152 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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