Katrien Smets

2.5k citations

13 papers · 567 indexed · h-index 11

Impact in

Psychiatry and Mental health top 5%
- Epilepsy research and treatment
Cellular and Molecular Neuroscience top 10%
- Neuroscience and Neuropharmacology Research
- Genetic Neurodegenerative Diseases

Papers in

Cellular and Molecular Neuroscience 6
- Genetic Neurodegenerative Diseases 3
- Hereditary Neurological Disorders 2
Psychiatry and Mental health 5
- Epilepsy research and treatment 5

Co-authors: Peter De Jonghe Berten Ceulemans Tine Deconinck Lieve Claes Jonathan Baets Kristien Wouters Anouk Van de Vel Ann Löfgren
Journals: Human Mutation (2 papers)Neuroradiology (1 paper)Epilepsy & Behavior (1 paper)Orphanet Journal of Rare Diseases (1 paper)Brain (1 paper)
Partner nations: Belgium United States Germany

In The Last Decade

Katrien Smets

13 papers receiving 560 citations

Peers

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-authors

The 25 scholars most cited alongside Katrien Smets, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Katrien Smets Line = papers co-authored together Katrien Smets links everyone, so they are left out of the graph.

All Works

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13 of 13 papers shown

#	Work
1	Occupational airborne allergic contact dermatitis caused by N‐(4‐hydroxyphenyl)benzenesulfonamide Contact Dermatitis ·Olivier Aerts, Evelyne Mangodt, Katrien Smets, Michelle Mertens, L. Constandt, An Goossens	2018	3
2	STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations Orphanet Journal of Rare Diseases ·Stefanie N. Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Lüdger Schöls, Rebecca Schüle, Peter De Jonghe, Jonathan Baets, Matthis Synofzik	2017	45
3	Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48) Neurology Genetics ·Jennifer Hirst, Marianna Madeo, Katrien Smets, James R. Edgar, Lüdger Schöls, Jun Li, Anna Yarrow, Tine Deconinck, Jonathan Baets, Elisabeth Van Aken, Jan De Bleecker, Manuel B. Datiles, Ricardo H. Roda, Joachim Liepert, Stephan Züchner, Caterina Mariotti, Peter De Jonghe, Craig Blackstone, Michael C. Kruer	2016	24
4	Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions Brain ·Paola S. Denora, Katrien Smets, Federica Zolfanelli, Chantal Ceuterick-de Groote, Carlo Casali, Tine Deconinck, Anne Sieben, Michael Gonzales, Stephan Züchner, Frédéric Darios, D. Peeters, Alexis Brice, Alessandro Malandrini, Peter De Jonghe, Filippo M. Santorelli, Giovanni Stévanin, Jean‐Jacques Martin, Khalid Hamid El Hachimi	2016	49
5	Automated non-EEG based seizure detection: Do users have a say? Epilepsy & Behavior ·Anouk Van de Vel, Katrien Smets, Kristien Wouters, Berten Ceulemans	2016	55
6	The spectrum of epilepsy caused by POLG mutations Acta Neurologica Belgica ·Wouter Janssen, Annelies Quaegebeur, Gert Van Goethem, Ann Löfgren, Katrien Smets, Rik Vandenberghe, Wim Van Paesschen	2015	16
7	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 ·Katrien Smets, Anna Duarri, Tine Deconinck, Berten Ceulemans, Bart P.C. van de Warrenburg, Stephan Züchner, Michael Gonzalez, Rebecca Schüle, Matthis Synofzik, Nathalie Van der Aa, Peter De Jonghe, Dineke S. Verbeek, Jonathan Baets	2015	48
8	Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28 Neurology ·Katrien Smets, Tine Deconinck, Jonathan Baets, Anne Sieben, Jean‐Jacques Martin, Iris Smouts, Shuaiyu Wang, Franco Taroni, Daniela Di Bella, Wim Van Hecke, Paul M. Parizel, C. Jadoul, Robert De Potter, Francine Couvreur, Elena I. Rugarli, Peter De Jonghe	2014	21
9	First line management of prolonged convulsive seizures in children and adults: good practice points Acta Neurologica Belgica ·Liesbeth De Waele, Paul Boon, Berten Ceulemans, Bernard Dan, Anna Jansen, Benjamin Legros, Patricia Leroy, Françoise Delmelle, Michel Ossemann, Sylvie De Raedt, Katrien Smets, Patrick Van de Voorde, Hélène Verhelst, Lieven Lagae	2013	5
10	Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium: an update Acta Neurologica Belgica ·Paul Boon, Sebastiaan Engelborghs, Henri Hauman, Anna Jansen, Lieven Lagae, Benjamin Legros, Michel Ossemann, Bernard Sadzot, Katrien Smets, Etienne Urbain, Kenou van Rijckevorsel	2012	11
11	TheSCN1Avariant database: a novel research and diagnostic tool Human Mutation ·Lieve Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets, Tine Van Dyck, Tine Deconinck, Albena Jordanova, Peter De Jonghe	2009	103
12	Meningoencephalitis caused by Streptococcus pneumoniae: a diagnostic and therapeutic challenge Neuroradiology ·Philippe G. Jorens, Paul M. Parizel, Hendrik E. Demey, Katrien Smets, Kris Jadoul, Marcel M. Verbeek, Ron A. Wevers, Patrick Cras	2005	35
13	De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy Human Mutation ·Lieve Claes, Berten Ceulemans, Dominique Audenaert, Katrien Smets, Ann Löfgren, Jurgen Del‐Favero, Sirpa Ala‐Mello, Lina Basel‐Vanagaite, Barbara Plecko, Salmo Raskin, Paul Thiry, Nicole I. Wolf, Christine Van Broeckhoven, Peter De Jonghe	2003	152

About Katrien Smets

Katrien Smets is a scholar working on Cellular and Molecular Neuroscience, Psychiatry and Mental health, Neurology, Microbiology and Pediatrics, Perinatology and Child Health, having authored 13 papers that have together received 567 indexed citations. Recurring topics across this work include Epilepsy research and treatment (5 papers), Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (3 papers), Neurological diseases and metabolism (2 papers), Hereditary Neurological Disorders (2 papers), Pharmacological Effects and Toxicity Studies (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Ion channel regulation and function (1 paper). The work is most often cited by research in Psychiatry and Mental health (264 citations), Cellular and Molecular Neuroscience (239 citations), Neurology (49 citations), Microbiology (30 citations) and Genetics (126 citations). Katrien Smets has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Peter De Jonghe, Berten Ceulemans, Tine Deconinck, Lieve Claes, Jonathan Baets, Kristien Wouters, Anouk Van de Vel, Ann Löfgren, Salmo Raskin and Jurgen Del‐Favero. Their work appears in journals such as Human Mutation, Neuroradiology, Epilepsy & Behavior, Orphanet Journal of Rare Diseases and Brain.

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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