Jonathan Baets

8.6k total citations
80 papers, 2.2k citations indexed

About

Jonathan Baets is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Jonathan Baets has authored 80 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Cellular and Molecular Neuroscience, 40 papers in Molecular Biology and 20 papers in Neurology. Recurrent topics in Jonathan Baets's work include Hereditary Neurological Disorders (37 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (20 papers). Jonathan Baets is often cited by papers focused on Hereditary Neurological Disorders (37 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (20 papers). Jonathan Baets collaborates with scholars based in Belgium, Germany and United States. Jonathan Baets's co-authors include Peter De Jonghe, Vincent Timmerman, Annelies Rotthier, Tine Deconinck, Albena Jordanova, Katrien Janssens, Michaela Auer‐Grumbach, Els De Vriendt, Katrien Smets and Danique Beijer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Jonathan Baets

75 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan Baets Belgium 26 1.1k 1.1k 470 384 324 80 2.2k
Mériem Tazir Algeria 21 948 0.9× 1.0k 1.0× 415 0.9× 437 1.1× 473 1.5× 47 2.1k
Albena Jordanova Belgium 32 1.7k 1.5× 1.9k 1.8× 570 1.2× 638 1.7× 518 1.6× 87 3.6k
Jun Mitsui Japan 24 480 0.4× 860 0.8× 212 0.5× 281 0.7× 582 1.8× 115 1.7k
Velina Guergueltcheva Bulgaria 23 561 0.5× 899 0.9× 308 0.7× 213 0.6× 408 1.3× 52 1.6k
Carmen Espinós Spain 26 831 0.8× 1.1k 1.0× 215 0.5× 426 1.1× 249 0.8× 95 1.9k
Bernd Rautenstrauß Germany 26 725 0.7× 747 0.7× 330 0.7× 330 0.9× 236 0.7× 90 1.8k
Hiroyuki Ishiura Japan 25 633 0.6× 844 0.8× 177 0.4× 383 1.0× 627 1.9× 146 1.8k
Ali Benomar Morocco 21 1.7k 1.5× 1.5k 1.4× 178 0.4× 346 0.9× 709 2.2× 69 2.3k
Benoît J. Gentil Canada 22 388 0.4× 1.1k 1.1× 274 0.6× 184 0.5× 257 0.8× 32 1.6k
R. H. M. King United Kingdom 31 1.3k 1.2× 742 0.7× 344 0.7× 370 1.0× 893 2.8× 79 2.4k

Countries citing papers authored by Jonathan Baets

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan Baets

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Baets

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Baets. A scholar is included among the top collaborators of Jonathan Baets 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 Jonathan Baets. Jonathan Baets 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.
Baets, Jonathan, et al.. (2025). Effects of virtual reality mindfulness on cognition and well-being in ALS: A randomized trial protocol. Contemporary Clinical Trials. 152. 107876–107876.
2.
Deconinck, Tine, Katrien Janssens, Alicia Alonso‐Jiménez, et al.. (2025). A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy. European Journal of Human Genetics. 34(1). 45–52.
3.
Ehnert, Sabrina, Stefan Hauser, Holger Hengel, et al.. (2024). Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis. Scientific Reports. 14(1). 7335–7335. 1 indexed citations
4.
5.
Lent, Jonas Van, Leen Vendredy, Elias Adriaenssens, et al.. (2022). Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A. Brain. 146(7). 2885–2896. 18 indexed citations
6.
Burnytė, Birutė, Els De Vriendt, Jonathan Baets, et al.. (2022). HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling. Orphanet Journal of Rare Diseases. 17(1). 374–374. 1 indexed citations
7.
Mazza, Davide, Franca Codazzi, Tyler Mark Pierson, et al.. (2019). Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation. Journal of Medical Genetics. 56(8). 499–511. 19 indexed citations
8.
Synofzik, Matthis, Katherine L. Helbig, Florian Harmuth, et al.. (2018). De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. European Journal of Human Genetics. 26(11). 1623–1634. 30 indexed citations
9.
Verbrugghe, Walter, et al.. (2017). Exertional rhabdomyolysis and heat stroke: Beware of volatile anesthetic sedation. World Journal of Critical Care Medicine. 6(1). 21–21. 8 indexed citations
10.
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
11.
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
12.
Berciano, José, Jonathan Baets, Elena Gallardo, et al.. (2011). Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation. Journal of Neurology. 258(8). 1413–1421. 18 indexed citations
13.
Guelly, Christian, Lea Leonardis, Lea Papić, et al.. (2010). Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I. The American Journal of Human Genetics. 88(1). 99–105. 95 indexed citations
14.
Burgunder, Jean‐Marc, Lüdger Schöls, Jonathan Baets, et al.. (2010). EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders. European Journal of Neurology. 18(2). 207–217. 31 indexed citations
15.
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
16.
Kurth, Ingo, J. Christopher Hennings, Antje K. Huebner, et al.. (2009). Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy. Nature Genetics. 41(11). 1179–1181. 184 indexed citations
17.
Gasser, Thomas, Josef Finsterer, Jonathan Baets, et al.. (2009). EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. European Journal of Neurology. 17(2). 179–188. 35 indexed citations
18.
Bergen, Jan van, et al.. (2009). An extensive spinal epidural abscess successfully treated conservatively. Journal of Neurology Neurosurgery & Psychiatry. 80(3). 351–353. 16 indexed citations
19.
Baets, Jonathan, Ines Dierick, Chantal Ceuterick‐de Groote, et al.. (2009). Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity. Neuromuscular Disorders. 19(2). 172–175. 8 indexed citations
20.
Kılıç, Sara Şebnem, et al.. (2008). Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis. Neurogenetics. 10(2). 161–165. 17 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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