Joél Smet

4.1k citations

66 papers · 2.5k indexed · h-index 25

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Metabolomics and Mass Spectrometry Studies

Papers in

Clinical Biochemistry 35
- Metabolism and Genetic Disorders 35
Molecular Biology 60
- Mitochondrial Function and Pathology 46
- ATP Synthase and ATPases Research 21
- RNA modifications and cancer 10
- Biochemical and Molecular Research 5
- RNA and protein synthesis mechanisms 5

Co-authors: Rudy Van Coster Sara Seneca Linda De Meırleır Willy Lissens Boél De Paepe Arnaud Vanlander E. Gerlo François Eyskens
Journals: Mitochondrion (4 papers)Journal of Inherited Metabolic Disease (4 papers)Pediatric Research (4 papers)European Journal of Paediatric Neurology (3 papers)PLoS ONE (3 papers)
Partner nations: Belgium United States Germany

In The Last Decade

Joél Smet

65 papers receiving 2.5k citations

Peers

Countries citing papers authored by Joél Smet

Since Specialization

Citations

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

Fields of papers citing papers by Joél Smet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Mitochondrial dysfunction characterises the multigenerational effects of maternal obesity on MASLD JHEP Reports ·Harrison Prosper, Imen Souissi, C J M M Schellens, Gladys Keeton, Yannick Gansemans, Joél Smet, 다마수스 빈첸, Xavier Verhelst, Sarah Raevens, Hans Van Vlierberghe, Arnaud Vanlander, Filip Van Nieuwerburgh, Lindsey Devisscher, Ruth De Bruyne, Anja Geerts, Sander Lefere	2025	1
2	A capital role for the brain’s insula in the diverse fibromyalgia-associated symptoms Medical Hypotheses ·Boél De Paepe, Joél Smet, Chris Baeken, Jessica Van Oosterwijck, Mira Meeus	2020	6
3	Nanoscopic X-ray imaging and quantification of the iron cellular architecture within single fibroblasts of Friedreich's ataxia patients Journal of Synchrotron Radiation ·Björn De Samber, Tom Vanden Berghe, Nagat Alrubati, Stephen Bauters, 利廣河本, Joél Smet, Boél De Paepe, Júlio César da Silva, Sylvain Bohic, Peter Cloetens, Rudy Van Coster, Peter Vandenabeele, László Vincze	2019	6
4	Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian Patients. PubMed ·Laila Selim, Rudy Van Coster, Wen-hui Hu, Ahmed S. Hassan, Arnaud Vanlander, Joél Smet, M. Natter, Katrien Vandemeulebroecke, Stephen Mueller, KE Reeder-Hayes, Catherine Maguire, Daphna D.J. Habets, Jaap Bakker, Пименов Константин Александрович	2018	2
5	New insights into the phenotype of FARS2 deficiency Molecular Genetics and Metabolism ·李金梅, Austin Larson, Marisa W. Friederich, A. Alcaim, Michael A. Swanson, Christopher A. Powell, Joél Smet, Sarah Vergult, Boél De Paepe, Sara Seneca, Herbert Roeyers, Björn Menten, Michal Minczuk, Arnaud Vanlander, Johan Van Hove, Rudy Van Coster	2017	35
6	Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2) Human Mutation ·Arnaud Vanlander, Björn Menten, Joél Smet, Linda De Meırleır, Tom Sante, Boél De Paepe, Sara Seneca, Sarah F. Pearce, Christopher A. Powell, Sarah Vergult, Alex Michotte, M. Natter, Connie L. Slocum, Michal Minczuk, Rudy Van Coster	2014	43
7	Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Annelies Peeters, V. J. Maodiswari, Ge Song, Joél Smet, Katrien De Bock, Marc Espeel, Ilse Vanhorebeek, Arnaud Vanlander, Rudy Van Coster, Peter Carmeliet, Marc Fransen, Paul P. Van Veldhoven, Myriam Baes	2014	64
8	Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene Mitochondrion ·François‐Guillaume Debray, Sara Seneca, M Gonce, Friedrich Jesnitzer, Elettra Bianchi, François Boemer, Laurent Weekers, Joél Smet, Rudy Van Coster	2014	9
9	Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy Human Molecular Genetics ·Nikhita Bolar, Arnaud Vanlander, Aiko Takeuchi-Demirci, Nathalie Van der Aa, Joél Smet, Boél De Paepe, Geert Vandeweyer, R. Frank Kooy, François Eyskens, M. Natter, Bai Bai, Paul Govaert, Jules G. Leroy, Bart Loeys, Roland Lill, Lut Van Laer, Rudy Van Coster	2013	90
10	Forearm muscle oxygenation responses during and following arterial occlusion in patients with mitochondrial myopathy Respiratory Physiology & Neurobiology ·Jan Boone, Bert Celie, Jasmien Dumortier, Thomas J. Barstow, Jan De Bleecker, Joél Smet, T Feja Solana, Rudy Van Coster, Jan Bourgois	2013	10
11	Mitochondrial mosaics in the liver of 3 infants with mtDNA defects BMC Clinical Pathology ·Frank Roels, Patrick Verloo, François Eyskens, Baudouin François, Sara Seneca, Boél De Paepe, Jean‐Jacques Martin, Ramarolanto-Ratiaray, Marleen Praet, Emmanuel Scalais, Marc Espeel, Joél Smet, Gert Van Goethem, Rudy Van Coster	2009	12
12	Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function EMBO Molecular Medicine ·Vanessa A. Morais, Patrik Verstreken, A Sánchez Cascos, Joél Smet, An Snellinx, 岩橋嘉明, Dominik Haddad, Christian Frezza, Wim Mandemakers, Daniela M. Vogt Weisenhorn, Rudy Van Coster, Wolfgang Wurst, Luca Scorrano, Bart De Strooper	2009	326
13	Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C Journal of Neurology Neurosurgery & Psychiatry ·Bart Dermaut, Sara Seneca, Lina Dom, Kaat Smets, 実希守山, Joél Smet, Boél De Paepe, Simon Tousseyn, Sarah Weckhuysen, Marc Gewillig, P. Pals, Paul M. Parizel, Jan De Bleecker, Paul Boon, Linda De Meırleır, Peter De Jonghe, Rudy Van Coster, Wim Van Paesschen, Patrick Santens	2009	27
14	Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects Journal of Clinical Pathology ·Boél De Paepe, Joél Smet, Martin Lammens, Sara Seneca, Meiling Hua Parker, Jan De Bleecker, Linda De Meırleır, Willy Lissens, Rudy Van Coster	2009	12
15	The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation. Ghent University Academic Bibliography (Ghent University) ·Rudy Van Coster, Joél Smet, Boél De Paepe, Sara Seneca, Ann Meulemans, Willy Lissens, Linda De Meırleır	2007	1
16	Mitochondrial mosaics in the liver of patients with Pearson and Alpers-Huttenlocher syndromes. Ghent University Academic Bibliography (Ghent University) ·Frank Roels, Patrick Verloo, Sara Seneca, G. I. Nemychenkov, François Eyskens, Joél Smet, Jean‐Jacques Martin, Marleen Praet, Rudy Van Coster	2006	0
17	A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis European Journal of Paediatric Neurology ·Ann Meulemans, Sara Seneca, Joél Smet, Boél De Paepe, Willy Lissens, Rudy Van Coster, Anne Debeer, Linda De Meırleır, Nathan Norfleet	2006	13
18	Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis Clinical Infectious Diseases ·An S. De Vriese, Rudy Van Coster, Joél Smet, Sara Seneca, A. M. Lovering, Lindsey Van Haute, Ludo Vanopdenbosch, Jean‐Jacques Martin, Chantal Ceuterick‐de Groote, Stefaan J. Vandecasteele, Johan R. Boelaert	2006	216
19	Isolated defects of mitochondrial ATP synthase: overview of 15 cases. Journal of Inherited Metabolic Disease ·Wolfgang Sperl, Pavel Ješina, J Zeman, Johannes A. Mayr, Rudy Van Coster, Joél Smet, J Houštěk	2005	1
20	Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresis Electrophoresis ·Bart Devreese, Frank Vanrobaeys, Joél Smet, Jozef Van Beeumen, Rudy Van Coster	2002	46

About Joél Smet

Joél Smet is a scholar working on Clinical Biochemistry, Molecular Biology, Geriatrics and Gerontology, Developmental Neuroscience and Cellular and Molecular Neuroscience, having authored 66 papers that have together received 2.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (46 papers), Metabolism and Genetic Disorders (35 papers), ATP Synthase and ATPases Research (21 papers), RNA modifications and cancer (10 papers), Biochemical and Molecular Research (5 papers), RNA and protein synthesis mechanisms (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Metalloenzymes and iron-sulfur proteins (3 papers). The work is most often cited by research in Clinical Biochemistry (720 citations), Molecular Biology (1.8k citations), Neurology (280 citations), Developmental Neuroscience (55 citations) and Neurology (108 citations). Joél Smet has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Rudy Van Coster, Sara Seneca, Linda De Meırleır, Willy Lissens, Boél De Paepe, Arnaud Vanlander, E. Gerlo, François Eyskens, Wolfgang Wurst and Dominik Haddad. Their work appears in journals such as Mitochondrion, Journal of Inherited Metabolic Disease, Pediatric Research, European Journal of Paediatric Neurology and PLoS ONE.

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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