Thomas Chaillou

1.2k total citations
36 papers, 889 citations indexed

About

Thomas Chaillou is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Thomas Chaillou has authored 36 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Physiology and 12 papers in Cell Biology. Recurrent topics in Thomas Chaillou's work include Muscle Physiology and Disorders (17 papers), Muscle metabolism and nutrition (12 papers) and Exercise and Physiological Responses (11 papers). Thomas Chaillou is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Muscle metabolism and nutrition (12 papers) and Exercise and Physiological Responses (11 papers). Thomas Chaillou collaborates with scholars based in Sweden, United States and Lithuania. Thomas Chaillou's co-authors include John J. McCarthy, Tyler J. Kirby, Johanna T. Lanner, Jonathan H. England, Karyn A. Esser, Jonah D. Lee, Arthur J. Cheng, Xavier Bigard, Nathalie Koulmann and Xiping Zhang and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Physiology and Analytical Biochemistry.

In The Last Decade

Thomas Chaillou

36 papers receiving 885 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Chaillou Sweden 16 540 298 227 175 135 36 889
Ivan J. Vechetti United States 21 953 1.8× 488 1.6× 226 1.0× 201 1.1× 117 0.9× 61 1.4k
Antonios Matsakas United Kingdom 24 1.0k 1.9× 598 2.0× 326 1.4× 207 1.2× 199 1.5× 60 1.6k
Stephan Klossner Switzerland 9 237 0.4× 165 0.6× 156 0.7× 121 0.7× 122 0.9× 10 531
Robert A. Seaborne United Kingdom 12 509 0.9× 413 1.4× 252 1.1× 75 0.4× 166 1.2× 20 798
Jessica Cannavino Italy 7 664 1.2× 341 1.1× 168 0.7× 81 0.5× 63 0.5× 9 852
Anne‐Cécile Durieux France 21 1.1k 2.0× 532 1.8× 502 2.2× 164 0.9× 165 1.2× 25 1.6k
Leticia Brotto United States 18 553 1.0× 214 0.7× 115 0.5× 72 0.4× 98 0.7× 37 853
Jae‐Sung You United States 18 955 1.8× 442 1.5× 583 2.6× 233 1.3× 81 0.6× 26 1.3k
Thomas J. McLoughlin United States 14 586 1.1× 278 0.9× 208 0.9× 231 1.3× 53 0.4× 22 896
Barbara Vernus France 20 1.1k 2.0× 579 1.9× 252 1.1× 165 0.9× 147 1.1× 28 1.4k

Countries citing papers authored by Thomas Chaillou

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Chaillou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Chaillou

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Chaillou. A scholar is included among the top collaborators of Thomas Chaillou 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 Chaillou. Thomas Chaillou 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.
Gustafsson, Johanna, et al.. (2025). Cold- and hot-water immersion are not more effective than placebo for the recovery of physical performance and training adaptations in national level soccer players. European Journal of Applied Physiology. 125(11). 3179–3194. 2 indexed citations
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Chaillou, Thomas, et al.. (2024). What are the potential mechanisms of fatigue-induced skeletal muscle hypertrophy with low-load resistance exercise training?. American Journal of Physiology-Cell Physiology. 328(3). C1001–C1014. 4 indexed citations
4.
Eimantas, Nerijus, et al.. (2023). Moderate muscle cooling induced by single and intermittent/prolonged cold-water immersions differently affects muscle contractile function in young males. Frontiers in Physiology. 14. 1172817–1172817. 4 indexed citations
5.
Chaillou, Thomas, et al.. (2023). Does the blunted stimulation of skeletal muscle protein synthesis by aging in response to mechanical load result from impaired ribosome biogenesis?. SHILAP Revista de lepidopterología. 4. 1171850–1171850. 4 indexed citations
6.
Youhanna, Sonia, Sabine U. Vorrink, Sara Henriksson, et al.. (2022). Enzymatically dissociated muscle fibers display rapid dedifferentiation and impaired mitochondrial calcium control. iScience. 25(12). 105654–105654. 5 indexed citations
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Kamandulis, Sigitas, Audrius Sniečkus, Vytautas Streckis, et al.. (2021). Increasing the resting time between drop jumps lessens delayed-onset muscle soreness and limits the extent of prolonged low-frequency force depression in human knee extensor muscles. European Journal of Applied Physiology. 122(1). 255–266. 4 indexed citations
10.
Chaillou, Thomas, et al.. (2020). Glutamine-stimulated in vitro hypertrophy is preserved in muscle cells from older women. Mechanisms of Ageing and Development. 187. 111228–111228. 2 indexed citations
11.
Vechetti, Ivan J., Yuan Wen, Thomas Chaillou, et al.. (2019). Life-long reduction in myomiR expression does not adversely affect skeletal muscle morphology. Scientific Reports. 9(1). 5483–5483. 28 indexed citations
12.
Ferreira, Duarte M. S., Arthur J. Cheng, Leandro Z. Agudelo, et al.. (2019). LIM and cysteine-rich domains 1 (LMCD1) regulates skeletal muscle hypertrophy, calcium handling, and force. Skeletal Muscle. 9(1). 26–26. 27 indexed citations
13.
Chaillou, Thomas. (2018). Skeletal Muscle Fiber Type in Hypoxia: Adaptation to High-Altitude Exposure and Under Conditions of Pathological Hypoxia. Frontiers in Physiology. 9. 1450–1450. 53 indexed citations
14.
Cheng, Arthur J., Sarah J. Willis, Christoph Zinner, et al.. (2017). Post‐exercise recovery of contractile function and endurance in humans and mice is accelerated by heating and slowed by cooling skeletal muscle. The Journal of Physiology. 595(24). 7413–7426. 60 indexed citations
15.
Chaillou, Thomas & Johanna T. Lanner. (2016). Regulation of myogenesis and skeletal muscle regeneration: effects of oxygen levels on satellite cell activity. The FASEB Journal. 30(12). 3929–3941. 63 indexed citations
16.
Kirby, Tyler J., Jonah D. Lee, Jonathan H. England, et al.. (2015). Blunted hypertrophic response in aged skeletal muscle is associated with decreased ribosome biogenesis. Journal of Applied Physiology. 119(4). 321–327. 63 indexed citations
17.
Chaillou, Thomas, Xiping Zhang, & John J. McCarthy. (2015). Expression of Muscle‐Specific Ribosomal Protein L3‐Like Impairs Myotube Growth. Journal of Cellular Physiology. 231(9). 1894–1902. 46 indexed citations
18.
Chaillou, Thomas, et al.. (2014). Effect of hypoxia exposure on the recovery of skeletal muscle phenotype during regeneration. Molecular and Cellular Biochemistry. 390(1-2). 31–40. 17 indexed citations
19.
Chaillou, Thomas, et al.. (2013). Ambient hypoxia enhances the loss of muscle mass after extensive injury. Pflügers Archiv - European Journal of Physiology. 466(3). 587–598. 42 indexed citations
20.
Banzet, Sébastien, et al.. (2011). Pitfalls of reverse transcription quantitative polymerase chain reaction standardization: Volume-related inhibitors of reverse transcription. Analytical Biochemistry. 415(2). 151–157. 11 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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