Thomas Voït

12.0k total citations · 1 hit paper
136 papers, 5.3k citations indexed

About

Thomas Voït is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Physiology. According to data from OpenAlex, Thomas Voït has authored 136 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 25 papers in Cardiology and Cardiovascular Medicine and 25 papers in Physiology. Recurrent topics in Thomas Voït's work include Muscle Physiology and Disorders (61 papers), Cardiomyopathy and Myosin Studies (21 papers) and Neurogenetic and Muscular Disorders Research (18 papers). Thomas Voït is often cited by papers focused on Muscle Physiology and Disorders (61 papers), Cardiomyopathy and Myosin Studies (21 papers) and Neurogenetic and Muscular Disorders Research (18 papers). Thomas Voït collaborates with scholars based in Germany, France and United States. Thomas Voït's co-authors include Uwe Mellies, R. Ragette, Helmut Teschler, Jörg Klepper, Christian Dohna‐Schwake, Alice Steinbrecher, William B. Dobyns, Luis Garcı́a, Hans van Bokhoven and Han G. Brunner and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Medicine.

In The Last Decade

Thomas Voït

130 papers receiving 5.2k citations

Hit Papers

Mutations in the O-Mannosyltransferase Gene POMT1 Give Ri... 2002 2026 2010 2018 2002 100 200 300 400 500
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. Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome
    2002 519 citations Alice Steinbrecher, Thomas Voït et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Voït Germany 40 3.5k 1.1k 1.0k 982 698 136 5.3k
Anneke J. van der Kooi Netherlands 45 3.2k 0.9× 1.4k 1.3× 688 0.7× 1.3k 1.3× 358 0.5× 151 6.4k
Paula R. Clemens United States 38 5.9k 1.7× 1.4k 1.3× 1.3k 1.3× 1.2k 1.2× 1.7k 2.5× 116 7.8k
Lucía Morandi Italy 43 3.7k 1.1× 786 0.7× 744 0.7× 835 0.9× 359 0.5× 143 5.2k
Kevin M. Flanigan United States 45 5.6k 1.6× 1.3k 1.3× 844 0.8× 1.1k 1.1× 1.2k 1.7× 189 7.3k
Serenella Servidei Italy 51 6.8k 2.0× 980 0.9× 791 0.8× 745 0.8× 716 1.0× 224 9.4k
Thomas Voit Germany 50 5.8k 1.7× 1.3k 1.2× 1.3k 1.3× 884 0.9× 780 1.1× 137 7.9k
Pascal Laforêt France 47 3.8k 1.1× 1.3k 1.2× 2.0k 1.9× 637 0.6× 514 0.7× 270 7.4k
Brenda Wong United States 36 2.9k 0.8× 914 0.9× 558 0.5× 1.1k 1.1× 299 0.4× 142 4.2k
Elena Pegoraro Italy 41 3.8k 1.1× 969 0.9× 592 0.6× 1.1k 1.1× 476 0.7× 196 5.6k
Paul Gregorevic Australia 50 5.8k 1.7× 1.4k 1.3× 1.5k 1.4× 534 0.5× 1.8k 2.6× 137 7.7k

Countries citing papers authored by Thomas Voït

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Voït

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Voït

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Voït. A scholar is included among the top collaborators of Thomas Voït 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 Thomas Voït. Thomas Voït 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
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Gresham, David, Velina Guergueltcheva, Teodora Chamova, et al.. (2024). Phenotypic Variability of LGMD 2C/R5 in a Genetically Homogenous Group of Bulgarian Muslim Roma. Genes. 15(9). 1144–1144.
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Voït, Thomas, et al.. (2024). Athlete Monitoring Systems in Elite Men’s Basketball: Challenges, Recommendations, and Future Perspectives. Translational Sports Medicine. 2024(1). 6326566–6326566. 3 indexed citations
5.
Weiß, Johannes, Paul Zimmermann, Sandra Haupt, et al.. (2024). Effects of Different Types of Intermittent Fasting Interventions on Metabolic Health in Healthy Individuals (EDIF): A Randomised Trial with a Controlled-Run in Phase. Nutrients. 16(8). 1114–1114. 11 indexed citations
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Schierbauer, Janis, Sandra Haupt, Thomas Voït, et al.. (2023). Acute Fluid Intake Impacts Assessment of Body Composition via Bioelectrical Impedance Analysis. A Randomized, Controlled Crossover Pilot Trial. Metabolites. 13(4). 473–473. 13 indexed citations
8.
Haupt, Sandra, Nadine Wachsmuth, Janis Schierbauer, et al.. (2023). Efficacy of Fasting in Type 1 and Type 2 Diabetes Mellitus: A Narrative Review. Nutrients. 15(16). 3525–3525. 20 indexed citations
9.
Massouridès, Emmanuelle, Nathalie Bourg, Laurence Suel, et al.. (2020). miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy. Scientific Reports. 10(1). 9139–9139. 20 indexed citations
10.
Buyse, Gunnar, Thomas Voït, Ulrike Schara, et al.. (2016). Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy. Pediatric Pulmonology. 52(4). 508–515. 33 indexed citations
11.
Goyenvalle, Aurélie, Graziella Griffith, Arran Babbs, et al.. (2015). Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers. Nature Medicine. 21(3). 270–275. 240 indexed citations
12.
Bemelmans, Alexis‐Pierre, Sandra Duqué, Christel Rivière, et al.. (2013). A Single Intravenous AAV9 Injection Mediates Bilateral Gene Transfer to the Adult Mouse Retina. PLoS ONE. 8(4). e61618–e61618. 12 indexed citations
13.
Gentil, Christel, France Leturcq, Rabah Ben Yaou, et al.. (2012). Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation. Human Molecular Genetics. 21(15). 3449–3460. 39 indexed citations
14.
Wanschitz, Julia, O. Dubourg, Emmanuelle Lacène, et al.. (2012). Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis. Neuromuscular Disorders. 23(1). 75–83. 31 indexed citations
15.
Çırak, Sebahattin, Florian von Deimling, Shrikesh Sachdev, et al.. (2010). Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy. Brain. 133(7). 2123–2135. 51 indexed citations
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Mellies, Uwe, Christian Dohna‐Schwake, Florian Stehling, & Thomas Voït. (2004). Sleep disordered breathing in spinal muscular atrophy. Neuromuscular Disorders. 14(12). 797–803. 88 indexed citations
18.
Klepper, Jörg, Anne Flörcken, Jorge Fischbarg, & Thomas Voït. (2003). Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro. European Journal of Pediatrics. 162(2). 84–89. 36 indexed citations
19.
Moolenaar, Sytske H., Udo F. H. Engelke, Manfred Spraul, et al.. (2001). β‐Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine. Magnetic Resonance in Medicine. 46(5). 1014–1017. 43 indexed citations
20.
Klepper, Joerg, Bernard Dan, Marc Abramowicz, et al.. (1999). Isolated hypoglycorrhachia in a female newborn: an additional case of GLUT-1 deficiency. Journal of Inherited Metabolic Disease. 22(1). 129. 1 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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