Arvid Suls

8.3k citations

44 papers · 2.4k indexed · h-index 22

Impact in

Psychiatry and Mental health top 1%
- Epilepsy research and treatment
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in

Clinical Biochemistry 12
- Metabolism and Genetic Disorders 12
Psychiatry and Mental health 13
- Epilepsy research and treatment 13

Co-authors: Peter De Jonghe Ingrid E. Scheffer Renzo Guerrini Liesbet Deprez Sarah Weckhuysen Samuel F. Berkovic Carla Marini Saul A. Mullen
Journals: Neurology (8 papers)Epilepsia (7 papers)Annals of Neurology (5 papers)Epilepsy Research (3 papers)Vaccine (2 papers)
Partner nations: Belgium Australia Germany

In The Last Decade

Arvid Suls

42 papers receiving 2.4k citations

Peers

Countries citing papers authored by Arvid Suls

Since Specialization

Citations

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

Fields of papers citing papers by Arvid Suls

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Arvid Suls, 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 Arvid Suls Line = papers co-authored together Arvid Suls links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genetic Landscape of a Cohort of Children With Varicella Zoster Virus Encephalitis, Cerebellitis, and Stroke The Journal of Infectious Diseases ·Zhao Hui-xiong, 和茂前田, Esther Bartholomeus, Nicolas Deconinck, Christophe Barrea, Kaitlyn Cimney, Anna Jansen, Hélène Verhelst, Akbarali Sattorov, Won-Chul Yang, My Kieu Ha, Arvid Suls, Renée M. van der Sluis, Benson Ogunjimi, Trine H. Mogensen	2025	0
2	IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assay British Journal of Cancer ·Е. Н. Ширяев, Stephen Reinhardt, M. Scalora, Joe Ibrahim, Arvid Suls, Dieter Peeters, F. Hartjes, Alexander Hoischen, Erik Fransén, Marc Peeters, Guy Van Camp, Ken Op de Beeck	2024	6
3	Preexisting memory CD4 T cells in naïve individuals confer robust immunity upon hepatitis B vaccination eLife ·George Elias, Pieter Meysman, Esther Bartholomeus, Nicolas De Neuter, Barbara Bigliardi, Arvid Suls, Hilde Jansens, Aisha Souquette, Hans De Reu, Marie‐Paule Emonds, Evelien Smits, Eva Lion, Paul G. Thomas, Geert Mortier, Pierre Van Damme, Philippe Beutels, Kris Laukens, Viggo Van Tendeloo, Benson Ogunjimi	2022	11
4	Memory CD4+ T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatus Genes and Immunity ·Nicolas De Neuter, Esther Bartholomeus, George Elias, Barbara Bigliardi, Arvid Suls, Hilde Jansens, Evelien Smits, Niel Hens, Philippe Beutels, Pierre Van Damme, Geert Mortier, Viggo Van Tendeloo, Kris Laukens, Pieter Meysman, Benson Ogunjimi	2018	13
5	On the feasibility of mining CD8+ T cell receptor patterns underlying immunogenic peptide recognition Immunogenetics ·Nicolas De Neuter, Wout Bittremieux, Charlie Beirnaert, Bart Cuypers, 明子寺坂, Pieter Moris, Arvid Suls, Viggo Van Tendeloo, Benson Ogunjimi, Kris Laukens, Pieter Meysman	2017	50
6	Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects American Journal of Medical Genetics Part A ·Carla Marini, Katia Hardies, Tiziana Pisano, Patrick May, Sarah Weckhuysen, Elena Cellini, Arvid Suls, Davide Mei, Rudi Balling, Peter De Jonghe, Ingo Helbig, Domenico Garozzo, Renzo Guerrini	2017	16
7	Early and effective treatment of KCNQ 2 encephalopathy Epilepsia ·Tiziana Pisano, Adam L. Numis, Sinéad B. Heavin, Sarah Weckhuysen, Marco Angriman, Arvid Suls, Barbara Podestà, Ronald L. Thibert, Kevin A. Shapiro, Renzo Guerrini, Ingrid E. Scheffer, Carla Marini, Maria Roberta Cilio	2015	186
8	The role of SLC2A1 in early onset and childhood absence epilepsies Epilepsy Research ·Hiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, Arvid Suls, Sarah von Spiczak, Laura L. Klitten, Hans A. Dahl, Klaus Brusgaard, Bernd A. Neubauer, Peter De Jonghe, Niels Tommerup, Ulrich Stephani, Helle Hjalgrim, Rikke S. Møller	2013	11
9	A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family Journal of the Peripheral Nervous System ·Fiore Manganelli, Chiara Pisciotta, Maria Nolano, Simona Capponi, Alessandro Geroldi, 快夫中西, Emilia Bellone, Arvid Suls, Paola Mandich, Lucio Santoro	2012	11
10	Do mutations in SCN1B cause Dravet syndrome? Epilepsy Research ·Young Ok Kim, Leanne M. Dibbens, Carla Marini, Arvid Suls, Nicole Chémaly, Davide Mei, Jacinta M. McMahon, Xenia Iona, Samuel F. Berkovic, Peter De Jonghe, Renzo Guerrini, Rima Nabbout, Ingrid E. Scheffer	2012	12
11	Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation European Journal of Paediatric Neurology ·Felicia Lyngmo Flordin, Arvid Suls, Tine Deconinck, Peter De Jonghe, Ilan Linder, Sara Kivity, Ron Dabby, Esther Leshinsky‐Silver, Dorit Lev, Tally Lerman‐Sagie	2011	19
12	Glucose Transporter 1 Deficiency as a Treatable Cause of Myoclonic Astatic Epilepsy Archives of Neurology ·Saul A. Mullen, Carla Marini, Arvid Suls, Davide Mei, Claude Valot, Daniela Buti, Todor Arsov, John A. Damiano, Kate Lawrence, Peter De Jonghe, Samuel F. Berkovic, Ingrid E. Scheffer, Renzo Guerrini	2011	91
13	Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency Neurology ·Saul A. Mullen, Arvid Suls, Peter De Jonghe, Samuel F. Berkovic, Ingrid E. Scheffer	2010	120
14	Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene Neurology ·Arvid Suls, Reana Velizarova, Iglika Yordanova, Liesbet Deprez, 友博黒川, Joost Wauters, Velina Guergueltcheva, U. Lindemann, Ivo Kremensky, Albena Jordanova, Peter De Jonghe	2010	43
15	Mild adolescent/adult onset epilepsy and paroxysmal exercise‐induced dyskinesia due to GLUT1 deficiency Epilepsia ·Zaid Afawi, Arvid Suls, Dana Ekstein, Sara Kivity, Miriam Y. Neufeld, Karen Oliver, Peter De Jonghe, Amos D. Korczyn, Samuel F. Berkovic	2010	18
16	Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1 Annals of Neurology ·Arvid Suls, Saul A. Mullen, Yvonne Weber, Kristien Verhaert, Berten Ceulemans, Renzo Guerrini, Thomas V. Wuttke, Sardar S. Fatah, Liesbet Deprez, Lieve Claes, Albena Jordanova, Samuel F. Berkovic, Holger Lerche, Peter De Jonghe, Ingrid E. Scheffer	2009	187
17	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
18	Epilepsy as part of the phenotype associated with ATP1A2 mutations Epilepsia ·Liesbet Deprez, Sarah Weckhuysen, 赵秀萍, Tine Deconinck, Kristl G. Claeys, Lieve Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs, Wim Van Paesschen, Peter De Jonghe	2007	80
19	Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients Human Mutation ·Arvid Suls, Kristl G. Claeys, D. Goossens, Gorbunova Elena A, Rob van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, А.И. Синани, Dhana Priya K, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barišić, Jean‐Paul Misson, J. Wauters, Jurgen Del‐Favero, Peter De Jonghe, Lieve Claes	2006	90
20	Mutation analysis of the LGI1/Epitempin gene in 48 patients with distinct epilepsy syndromes Epilepsia ·Arvid Suls, Hidayati Rina Setyawati, Dominique Audenaert, Liesbet Deprez, 友博黒川, Berten Ceulemans, Kristl G. Claeys, Christine Van Broeckhoven, Peter De Jonghe	2005	1

About Arvid Suls

Arvid Suls is a scholar working on Clinical Biochemistry, Psychiatry and Mental health, Biochemistry, Genetics and Cellular and Molecular Neuroscience, having authored 44 papers that have together received 2.4k indexed citations. Recurring topics across this work include Epilepsy research and treatment (13 papers), Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers), Glycogen Storage Diseases and Myoclonus (5 papers), Neuroscience and Neuropharmacology Research (5 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Psychiatry and Mental health (1.1k citations), Clinical Biochemistry (359 citations), Cellular and Molecular Neuroscience (627 citations), Genetics (866 citations) and Pediatrics, Perinatology and Child Health (341 citations). Arvid Suls has collaborated with scholars based in Belgium, Australia and Germany. Frequent co-authors include Peter De Jonghe, Ingrid E. Scheffer, Renzo Guerrini, Liesbet Deprez, Sarah Weckhuysen, Samuel F. Berkovic, Carla Marini, Saul A. Mullen, Tine Van Dyck and Albena Jordanova. Their work appears in journals such as Neurology, Epilepsia, Annals of Neurology, Epilepsy Research and Vaccine.

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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