Valeria Cavalli

6.3k total citations · 1 hit paper
66 papers, 4.5k citations indexed

About

Valeria Cavalli is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Valeria Cavalli has authored 66 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 35 papers in Cellular and Molecular Neuroscience and 18 papers in Cell Biology. Recurrent topics in Valeria Cavalli's work include Nerve injury and regeneration (27 papers), Neurogenesis and neuroplasticity mechanisms (14 papers) and Signaling Pathways in Disease (13 papers). Valeria Cavalli is often cited by papers focused on Nerve injury and regeneration (27 papers), Neurogenesis and neuroplasticity mechanisms (14 papers) and Signaling Pathways in Disease (13 papers). Valeria Cavalli collaborates with scholars based in United States, Italy and Switzerland. Valeria Cavalli's co-authors include Yongcheol Cho, Namiko Abe, Jean Grüenberg, Jung Eun Shin, Lawrence S.B. Goldstein, Vitaly A. Klyachko, Pan‐Yue Deng, Kristen M. Naegle, Roman Sloutsky and Judith Klumperman and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Valeria Cavalli

63 papers receiving 4.5k citations

Hit Papers

Intrinsic mechanisms of neuronal axon regeneration 2018 2026 2020 2023 2018 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valeria Cavalli United States 33 2.4k 2.0k 1.1k 828 558 66 4.5k
Sarah E. Newey United Kingdom 24 2.7k 1.1× 1.4k 0.7× 896 0.8× 391 0.5× 562 1.0× 32 4.0k
Markus Plomann Germany 31 2.2k 0.9× 1.3k 0.6× 1.1k 1.0× 427 0.5× 335 0.6× 49 3.7k
Jeffery L. Twiss United States 45 4.5k 1.8× 3.0k 1.5× 1.1k 1.0× 1.1k 1.3× 601 1.1× 98 6.9k
Feng‐Quan Zhou United States 30 1.9k 0.8× 1.9k 1.0× 838 0.8× 807 1.0× 451 0.8× 51 3.8k
Eyleen L. K. Goh Singapore 28 1.7k 0.7× 1.4k 0.7× 445 0.4× 883 1.1× 432 0.8× 70 4.3k
Toshio Ohshima Japan 43 3.2k 1.3× 2.6k 1.3× 1.8k 1.7× 1.7k 2.1× 1.2k 2.1× 168 6.9k
Hirotaka James Okano Japan 44 3.8k 1.5× 1.5k 0.8× 519 0.5× 991 1.2× 614 1.1× 156 7.5k
Akio Wanaka Japan 48 3.6k 1.5× 2.1k 1.0× 1.3k 1.2× 1.1k 1.3× 619 1.1× 169 7.0k
Bernard Rogister Belgium 40 2.2k 0.9× 1.7k 0.8× 534 0.5× 1.3k 1.6× 255 0.5× 138 5.3k
Nozomu Mori Japan 42 4.1k 1.7× 1.3k 0.6× 819 0.8× 393 0.5× 878 1.6× 214 6.8k

Countries citing papers authored by Valeria Cavalli

Since Specialization
Citations

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

Fields of papers citing papers by Valeria Cavalli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeria Cavalli

This figure shows the co-authorship network connecting the top 25 collaborators of Valeria Cavalli. A scholar is included among the top collaborators of Valeria Cavalli 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 Valeria Cavalli. Valeria Cavalli 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.
2.
Kuruvilla, Rejji, et al.. (2025). Satellite glial cells: Shaping peripheral input into the brain-body axis?. Neuron. 113(20). 3333–3351. 2 indexed citations
3.
Rosen, Sarah F., et al.. (2024). Endothelin B receptor inhibition rescues aging-dependent neuronal regenerative decline. eLife. 13. 2 indexed citations
4.
Deng, Pan‐Yue, Ajeet Kumar, Valeria Cavalli, & Vitaly A. Klyachko. (2024). Circuit-based intervention corrects excessive dentate gyrus output in the fragile X mouse model. eLife. 12. 2 indexed citations
5.
Mokalled, Mayssa H., et al.. (2023). Self-renewing macrophages in dorsal root ganglia contribute to promote nerve regeneration. Proceedings of the National Academy of Sciences. 120(7). e2215906120–e2215906120. 48 indexed citations
6.
Avraham, Oshri, Alexander Chamessian, Lite Yang, et al.. (2022). Profiling the molecular signature of satellite glial cells at the single cell level reveals high similarities between rodents and humans. Pain. 163(12). 2348–2364. 45 indexed citations
7.
Deng, Pan‐Yue, Ajeet Kumar, Valeria Cavalli, & Vitaly A. Klyachko. (2022). FMRP regulates GABAA receptor channel activity to control signal integration in hippocampal granule cells. Cell Reports. 39(7). 110820–110820. 9 indexed citations
8.
Ewan, Eric E., et al.. (2021). Ascending dorsal column sensory neurons respond to spinal cord injury and downregulate genes related to lipid metabolism. Scientific Reports. 11(1). 374–374. 19 indexed citations
10.
Deng, Pan‐Yue, Oshri Avraham, Valeria Cavalli, & Vitaly A. Klyachko. (2021). Hyperexcitability of Sensory Neurons in Fragile X Mouse Model. Frontiers in Molecular Neuroscience. 14. 796053–796053. 9 indexed citations
11.
Avraham, Oshri, Pan‐Yue Deng, Rejji Kuruvilla, et al.. (2020). Satellite glial cells promote regenerative growth in sensory neurons. Nature Communications. 11(1). 4891–4891. 153 indexed citations
12.
Pita‐Thomas, Wolfgang, et al.. (2019). HDAC5 promotes optic nerve regeneration by activating the mTOR pathway. Experimental Neurology. 317. 271–283. 32 indexed citations
13.
Carlin, Dan, Alexandra E. Halevi, Eric E. Ewan, Amy M. Moore, & Valeria Cavalli. (2019). Nociceptor Deletion of Tsc2 Enhances Axon Regeneration by Inducing a Conditioning Injury Response in Dorsal Root Ganglia. eNeuro. 6(3). ENEURO.0168–19.2019. 21 indexed citations
14.
Oh, Young Mi, et al.. (2018). Epigenetic regulator UHRF1 inactivates REST and growth suppressor gene expression via DNA methylation to promote axon regeneration. Proceedings of the National Academy of Sciences. 115(52). E12417–E12426. 55 indexed citations
15.
Deng, Pan‐Yue, Dan Carlin, Young Mi Oh, et al.. (2018). Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus ofFmr1Knock-Out Mice. Journal of Neuroscience. 39(1). 28–43. 44 indexed citations
16.
Cho, Yongcheol, Dongeun Park, & Valeria Cavalli. (2015). Filamin A Is Required in Injured Axons for HDAC5 Activity and Axon Regeneration. Journal of Biological Chemistry. 290(37). 22759–22770. 19 indexed citations
17.
Deng, Pan‐Yue, Ziv Rotman, Jay A. Blundon, et al.. (2013). FMRP Regulates Neurotransmitter Release and Synaptic Information Transmission by Modulating Action Potential Duration via BK Channels. Neuron. 77(4). 696–711. 265 indexed citations
18.
Abe, Namiko, et al.. (2010). Mammalian Target of Rapamycin (mTOR) Activation Increases Axonal Growth Capacity of Injured Peripheral Nerves. Journal of Biological Chemistry. 285(36). 28034–28043. 177 indexed citations
19.
Cavalli, Valeria, Sameer B. Shah, Kristina Schimmelpfeng, et al.. (2007). Dynactin Is Required for Coordinated Bidirectional Motility, but Not for Dynein Membrane Attachment. Molecular Biology of the Cell. 18(6). 2081–2089. 100 indexed citations
20.
Vallone, Beatrice, Paola Vecchini, Valeria Cavalli, & Maurizio Brunori. (1993). Site‐directed mutagenesis in hemoglobin. FEBS Letters. 324(2). 117–122. 10 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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