Lieve Claes

4.1k total citations · 1 hit paper
20 papers, 2.6k citations indexed

About

Lieve Claes is a scholar working on Psychiatry and Mental health, Molecular Biology and Genetics. According to data from OpenAlex, Lieve Claes has authored 20 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Psychiatry and Mental health, 10 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Lieve Claes's work include Epilepsy research and treatment (11 papers), Ion channel regulation and function (5 papers) and Neuroscience and Neuropharmacology Research (4 papers). Lieve Claes is often cited by papers focused on Epilepsy research and treatment (11 papers), Ion channel regulation and function (5 papers) and Neuroscience and Neuropharmacology Research (4 papers). Lieve Claes collaborates with scholars based in Belgium, United States and Germany. Lieve Claes's co-authors include Peter De Jonghe, Berten Ceulemans, Lieven Lagae, Jurgen Del‐Favero, Christine Van Broeckhoven, Liesbet Deprez, Arvid Suls, Albena Jordanova, Marc Cruts and Peter De Rijk and has published in prestigious journals such as Journal of Neuroscience, Brain and Annals of Neurology.

In The Last Decade

Lieve Claes

19 papers receiving 2.5k citations

Hit Papers

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause ... 2001 2026 2009 2017 2001 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
    2001 916 citations Lieve Claes, Jurgen Del‐Favero et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lieve Claes Belgium 16 1.5k 1.1k 890 865 436 20 2.6k
Yuwu Jiang China 30 842 0.5× 1.6k 1.5× 869 1.0× 905 1.0× 400 0.9× 227 3.2k
Andy Peiffer United States 15 575 0.4× 1.5k 1.3× 499 0.6× 806 0.9× 118 0.3× 19 2.6k
Nanda A. Singh United States 11 747 0.5× 1.8k 1.6× 553 0.6× 1.4k 1.6× 109 0.3× 12 2.4k
Marion Bankstahl Germany 27 929 0.6× 462 0.4× 79 0.1× 975 1.1× 669 1.5× 69 2.1k
Galila Agam Israel 25 388 0.3× 764 0.7× 420 0.5× 472 0.5× 117 0.3× 55 1.6k
T. Serikawa Japan 23 159 0.1× 942 0.8× 791 0.9× 397 0.5× 115 0.3× 62 2.0k
Fang He China 20 231 0.1× 623 0.6× 410 0.5× 191 0.2× 86 0.2× 59 1.3k
E. Roulet Switzerland 24 242 0.2× 777 0.7× 256 0.3× 365 0.4× 102 0.2× 39 1.5k
Jingmin Wang China 22 119 0.1× 757 0.7× 400 0.4× 203 0.2× 112 0.3× 117 1.5k
Robert A. Furlong United Kingdom 19 278 0.2× 679 0.6× 309 0.3× 529 0.6× 36 0.1× 32 1.5k

Countries citing papers authored by Lieve Claes

Since Specialization
Citations

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

Fields of papers citing papers by Lieve Claes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lieve Claes

This figure shows the co-authorship network connecting the top 25 collaborators of Lieve Claes. A scholar is included among the top collaborators of Lieve Claes 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 Lieve Claes. Lieve Claes 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.
Travassos, Ana Rita, et al.. (2011). Non-fragrance allergens in specific cosmetic products. Contact Dermatitis. 65(5). 276–285. 63 indexed citations
2.
Nardelli, Andrea, et al.. (2011). Fragrance allergens in ‘specific’ cosmetic products. Contact Dermatitis. 64(4). 212–219. 37 indexed citations
3.
Arts, Willem F., et al.. (2011). Vlaamse migranten in Wallonië : 1850-2000.. 1 indexed citations
4.
Liao, Yunxiang, Liesbet Deprez, Snezana Maljevic, et al.. (2010). Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy. Brain. 133(5). 1403–1414. 124 indexed citations
5.
Patiño, Gustavo A., Lieve Claes, Luis F. Lopez‐Santiago, et al.. (2009). A Functional Null Mutation ofSCN1Bin a Patient with Dravet Syndrome. Journal of Neuroscience. 29(34). 10764–10778. 203 indexed citations
6.
Suls, Arvid, Saul A. Mullen, Yvonne Weber, et al.. (2009). Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1. Annals of Neurology. 66(3). 415–419. 187 indexed citations
7.
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
8.
Singh, Nanda A., Chris Pappas, E. Jill Dahle, et al.. (2009). A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome. PLoS Genetics. 5(9). e1000649–e1000649. 203 indexed citations
9.
Claes, Lieve, et al.. (2009). Het Aartsbisdom Mechelen-Brussel : 450 jaar geschiedenis. 1 indexed citations
10.
Neuwirth, Magdolna, Péter Barsi, Veronika Karcagi, et al.. (2008). [Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].. PubMed. 61(11-12). 402–8. 1 indexed citations
11.
Deprez, Liesbet, Sarah Weckhuysen, Tine Deconinck, et al.. (2007). Epilepsy as part of the phenotype associated with ATP1A2 mutations. Epilepsia. 49(3). 500–508. 80 indexed citations
12.
Claeys, Kristl G., Lieve Claes, Johan Van Goethem, et al.. (2007). Epilepsy and migraine in a patient with Urbach–Wiethe disease. Seizure. 16(5). 465–468. 15 indexed citations
13.
Suls, Arvid, Kristl G. Claeys, D. Goossens, et al.. (2006). Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients. Human Mutation. 27(9). 914–920. 90 indexed citations
14.
Kearney, Jennifer A., Yan Yang, Barbara Beyer, et al.. (2006). Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. Human Molecular Genetics. 15(6). 1043–1048. 55 indexed citations
15.
Weckx, Stefan, Jurgen Del‐Favero, Rosa Rademakers, et al.. (2005). novoSNP, a novel computational tool for sequence variation discovery. Genome Research. 15(3). 436–442. 214 indexed citations
16.
Deprez, Liesbet, Lieve Claes, Kristl G. Claeys, et al.. (2005). Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation. Human Genetics. 118(5). 618–625. 16 indexed citations
17.
Ceulemans, Berten, Lieve Claes, & Lieven Lagae. (2004). Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy. Pediatric Neurology. 30(4). 236–243. 112 indexed citations
18.
Ceulemans, Berten, Marc Boel, Lieve Claes, et al.. (2004). Severe Myoclonic Epilepsy in Infancy: Toward an Optimal Treatment. Journal of Child Neurology. 19(7). 516–521. 45 indexed citations
19.
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
20.
Claes, Lieve, Jurgen Del‐Favero, Berten Ceulemans, et al.. (2001). De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy. The American Journal of Human Genetics. 68(6). 1327–1332. 916 indexed citations breakdown →

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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