Jonathan Baets

8.9k citations

82 papers · 2.3k · h-index 27

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 50
- Hereditary Neurological Disorders 36
- Genetic Neurodegenerative Diseases 20
Molecular Biology 31
- Ion channel regulation and function 7
- Mitochondrial Function and Pathology 6
- RNA Research and Splicing 5

Co-authors: Peter De Jonghe (46 shared papers)Vincent Timmerman (22 shared papers)Annelies Rotthier (5 shared papers)Tine Deconinck (22 shared papers)Albena Jordanova (10 shared papers)Katrien Janssens (3 shared papers)Michaela Auer‐Grumbach (5 shared papers)Els De Vriendt (7 shared papers)
Journals: Neuromuscular Disorders (9 papers)Brain (7 papers)Neurology (6 papers)European Journal of Neurology (6 papers)European Journal of Human Genetics (3 papers)
Partner nations: Belgium Germany United States

In The Last Decade

Jonathan Baets

76 papers receiving 2.3k citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 82 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy Nature Genetics ·Ingo Kurth, Torsten Pamminger, J. Christopher Hennings, Désirée Soehendra, Antje K. Huebner, Annelies Rotthier, Jonathan Baets, Jan Senderek, Haluk Topaloğlu, Sandra A. Farrell, Gudrun Nürnberg, Peter Nürnberg, Peter De Jonghe, Andreas Gal, Christoph Kaether, Vincent Timmerman, Christian A. Hübner	2009	195
2	Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I The American Journal of Human Genetics ·Annelies Rotthier, Michaela Auer‐Grumbach, Katrien Janssens, Jonathan Baets, Anke Penno, Leonardo Almeida-Souza, Kim van Hoof, An Jacobs, Els De Vriendt, Beate Schlotter‐Weigel, Wolfgang N. Löscher, Petr Vondráček, Pavel Seeman, Peter De Jonghe, Patrick Van Dijck, Albena Jordanova, Thorsten Hornemann, Vincent Timmerman	2010	140
3	Mechanisms of disease in hereditary sensory and autonomic neuropathies Nature Reviews Neurology ·Annelies Rotthier, Jonathan Baets, Vincent Timmerman, Katrien Janssens	2012	125
4	Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation Brain ·Annelies Rotthier, Jonathan Baets, Els De Vriendt, Alice K. Jacobs, Michaela Auer‐Grumbach, Nicolas Lévy, Nathalie Bonello‐Palot, (unknown), Joachim Weis, A. Nascimento, Mariëlle E.M. Swinkels, Moyo C. Kruyt, Albena Jordanova, Peter De Jonghe, Vincent Timmerman	2009	125
5	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	105
6	Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I The American Journal of Human Genetics ·Christian Guelly, Peng-Peng Zhu, Lea Leonardis, Lea Papić, Janez Zidar, Maria Schabhüttl, Heimo Strohmaier, Joachim Weis, Tim M. Strom, Jonathan Baets, Jan C. Willems, Peter De Jonghe, Mary M. Reilly, Eleonore Fröhlich, Martina Hatz, Slave Trajanoski, Thomas R. Pieber, Andreas Janecke, Craig Blackstone, Michaela Auer‐Grumbach	2010	99
7	Mutations in SACS cause atypical and late-onset forms of ARSACS Neurology ·Jonathan Baets, Tine Deconinck, Kaat Smets, D. Goossens, Peter Van den Bergh, Karine Dahan, Eric Schmedding, Patrick Santens, V. Milić Rašić, Philip Van Damme, Wim Robberecht, Linda De Meırleır, B. Michielsens, Jurgen Del‐Favero, Albena Jordanova, Peter De Jonghe	2010	90
8	Unrestrained poly-ADP-ribosylation provides insights into chromatin regulation and human disease Molecular Cell ·Evgeniia Prokhorova, Thomas Agnew, Anne R. Wondisford, Michael Tellier, Nicole Kaminski, Danique Beijer, James Holder, Joséphine Groslambert, Marcin J. Suskiewicz, Kang Zhu, Julia M. Reber, Sarah C. Krassnig, Luca Palazzo, Shona Murphy, Michael L. Nielsen, Aswin Mangerich, Dragana Ahel, Jonathan Baets, Roderick J. O’Sullivan, Ivan Ahel	2021	76
9	Dominant GDAP1 mutations cause predominantly mild CMT phenotypes Neurology ·(unknown), Jonathan Baets, Gian Maria Fabrizi, E. Jaakkola, Dagmara Kabzińska, Jacek Pilch, Alice B. Schindler, David R. Cornblath, Kenneth H. Fischbeck, Michaela Auer‐Grumbach, Christian Guelly, Nina Huber, Els De Vriendt, Vincent Timmerman, Ueli Suter, I Hausmanowa-Pétrusewicz, Axel Niemann, Andrzej Kochański, Peter De Jonghe, Albena Jordanova	2011	66
10	Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy Brain ·Kristl G. Claeys, Stephan Züchner, Marina Kennerson, José Berciano, Abel Garcı́a Garcı́a, K. Verhoeven, Elsdon Storey, John Merory, H.M.E. Bienfait, Martin Lammens, Eva Nelis, Jonathan Baets, Els De Vriendt, Zwi Berneman, Ilse De Veuster, Jeffery M. Vance, Garth A. Nicholson, Vincent Timmerman, Peter De Jonghe	2009	64
11	Recent advances in Charcot–Marie–Tooth disease Current Opinion in Neurology ·Jonathan Baets, Peter De Jonghe, Vincent Timmerman	2014	60
12	Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges Journal of Neurology ·Maria Schabhüttl, Thomas Wieland, Jan Senderek, Jonathan Baets, Vincent Timmerman, Peter De Jonghe, Mary M. Reilly, Karl Stieglbauer, Eva Laich, Reinhard Windhager, Wolfgang Erwa, Slave Trajanoski, Tim M. Strom, Michaela Auer‐Grumbach	2014	56
13	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	54
14	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	47
15	EFNS guidelines on the molecular diagnosis of mitochondrial disorders European Journal of Neurology ·Josef Finsterer, Hanne F. Harbo, Jonathan Baets, Christine Van Broeckhoven, Stefano Di Donato, Bertrand Fontaine, Peter De Jonghe, Alexander Lossos, Timothy Lynch, Caterina Mariotti, Lüdger Schöls, Antonella Spinazzola, Zoltán Szolnoki, Sarah J. Tabrizi, Chantal Tallaksen, Massimo Zeviani, J‐M. Burgunder, Thomas Gasser	2009	46
16	Ascorbic acid for the treatment of Charcot-Marie-Tooth disease Cochrane Database of Systematic Reviews ·Burkhard Gess, Jonathan Baets, Peter De Jonghe, Mary M. Reilly, Davide Pareyson, Peter Young	2015	42
17	EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias European Journal of Neurology ·Thomas Gasser, Josef Finsterer, Jonathan Baets, Christine Van Broeckhoven, Stefano Di Donato, Bertrand Fontaine, Peter De Jonghe, Alexander Lossos, Timothy Lynch, Caterina Mariotti, Lüdger Schöls, Antonella Spinazzola, Zoltán Szolnoki, Sarah J. Tabrizi, Chantal Tallaksen, Massimo Zeviani, J‐M. Burgunder, H. F. Harbo	2009	41
18	EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington’s disease, Parkinson’s disease and dystonias European Journal of Neurology ·H. F. Harbo, Josef Finsterer, Jonathan Baets, Christine Van Broeckhoven, Stefano Di Donato, Bertrand Fontaine, Peter De Jonghe, Alexander Lossos, Timothy Lynch, Caterina Mariotti, Lüdger Schöls, Antonella Spinazzola, Zoltán Szolnoki, Sarah J. Tabrizi, Chantal Tallaksen, Massimo Zeviani, Jean‐Marc Burgunder, Thomas Gasser	2009	41
19	CMT disease severity correlates with mutation-induced open conformation of histidyl-tRNA synthetase, not aminoacylation loss, in patient cells Proceedings of the National Academy of Sciences ·David Blocquel, Litao Sun, Żaneta Matuszek, Sheng Li, Thomas G. Weber, Bernhard Kuhle, Grace Kooi, Na Wei, Jonathan Baets, Tao Pan, Paul Schimmel, Xiang‐Lei Yang	2019	34
20	A novel AARS mutation in a family with dominant myeloneuropathy Neurology ·William W. Motley, Laurie B. Griffin, Inès Mademan, Jonathan Baets, Els De Vriendt, Peter De Jonghe, Anthony Antonellis, Albena Jordanova, Steven S. Scherer	2015	34

About Jonathan Baets

Jonathan Baets is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Neurology and Physiology, having authored 82 papers that have together received 2.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (36 papers), Genetic Neurodegenerative Diseases (20 papers), Neurological diseases and metabolism (12 papers), Ion channel regulation and function (7 papers), Mitochondrial Function and Pathology (6 papers), Cellular transport and secretion (5 papers), RNA Research and Splicing (5 papers) and Endoplasmic Reticulum Stress and Disease (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (324 citations), Cell Biology (449 citations), Neurology (301 citations) and Molecular Biology (1.0k citations). Jonathan Baets has collaborated with scholars based in Belgium, Germany and United States. Frequent 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. Their work appears in journals such as Neuromuscular Disorders, Brain, Neurology, European Journal of Neurology and European Journal of Human Genetics.

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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Jonathan Baets

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Jonathan Baets

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