Benoît Renvoisé

1.0k total citations
16 papers, 727 citations indexed

About

Benoît Renvoisé is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Benoît Renvoisé has authored 16 papers receiving a total of 727 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 7 papers in Cell Biology and 5 papers in Molecular Biology. Recurrent topics in Benoît Renvoisé's work include Hereditary Neurological Disorders (9 papers), Cellular transport and secretion (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Benoît Renvoisé is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Cellular transport and secretion (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Benoît Renvoisé collaborates with scholars based in United States, France and United Kingdom. Benoît Renvoisé's co-authors include Craig Blackstone, James H. Hurley, Neggy Rismanchi, Jennifer Lippincott‐Schwartz, Dong Yang, Joanna C. Bakowska, Julia T. Stadler, Jaerak Chang, Rajat Singh and Suzie Lefebvre and has published in prestigious journals such as PLoS ONE, The FASEB Journal and Journal of Cell Science.

In The Last Decade

Benoît Renvoisé

16 papers receiving 722 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Benoît Renvoisé United States	14	391	354	227	134	118	16	727
Rachel Allison United Kingdom	12	363 0.9×	544 1.5×	371 1.6×	79 0.6×	69 0.6×	13	870
Mirko Koppen Germany	8	206 0.5×	1.1k 3.2×	247 1.1×	87 0.6×	135 1.1×	9	1.3k
Ryota Kunita Japan	13	171 0.4×	240 0.7×	100 0.4×	84 0.6×	66 0.6×	14	612
Michael S. Fernandopulle United States	8	134 0.3×	496 1.4×	99 0.4×	78 0.6×	39 0.3×	9	693
Noemí Cabrera-Poch Spain	10	707 1.8×	680 1.9×	264 1.2×	54 0.4×	46 0.4×	10	1.1k
Cecilia Zuliani Germany	11	133 0.3×	506 1.4×	191 0.8×	78 0.6×	56 0.5×	11	797
Marco Henneke Germany	19	120 0.3×	834 2.4×	109 0.5×	80 0.6×	115 1.0×	35	1.1k
Brett J Winborn United States	7	182 0.5×	890 2.5×	323 1.4×	85 0.6×	67 0.6×	8	1.2k
Anny Devoy United Kingdom	14	206 0.5×	824 2.3×	230 1.0×	171 1.3×	110 0.9×	16	1.3k
Mathilde Chaineau Canada	14	397 1.0×	421 1.2×	92 0.4×	103 0.8×	43 0.4×	19	747

Countries citing papers authored by Benoît Renvoisé

Since Specialization

Citations

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

Fields of papers citing papers by Benoît Renvoisé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benoît Renvoisé

This figure shows the co-authorship network connecting the top 25 collaborators of Benoît Renvoisé. A scholar is included among the top collaborators of Benoît Renvoisé 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 Benoît Renvoisé. Benoît Renvoisé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Zhu, Peng‐Peng, Jonathon Nixon‐Abell, James Henderson, et al.. (2022). Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons. Human Molecular Genetics. 31(16). 2779–2795. 16 indexed citations

Renvoisé, Benoît, Mélanie Falgairolle, Jeeva Munasinghe, et al.. (2016). Reep1null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation. Human Molecular Genetics. 25(23). ddw315–ddw315. 70 indexed citations

Renvoisé, Benoît, et al.. (2016). Could low-dose naltrexone be an effective treatment for Hailey-Hailey Disease?. 1(1). 3 indexed citations

Zhao, Guohua, Peng‐Peng Zhu, Benoît Renvoisé, et al.. (2016). Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology. Experimental Cell Research. 349(1). 32–44. 39 indexed citations

Renvoisé, Benoît, Johnny Habchi, Emma V. Yates, et al.. (2015). Neuronal Cx3cr1 Deficiency Protects against Amyloid β-Induced Neurotoxicity. PLoS ONE. 10(6). e0127730–e0127730. 26 indexed citations

Renvoisé, Benoît, et al.. (2014). Spastin-Interacting Protein NA14/SSNA1 Functions in Cytokinesis and Axon Development. PLoS ONE. 9(11). e112428–e112428. 20 indexed citations

Renvoisé, Benoît, Jaerak Chang, Rajat Singh, et al.. (2014). Lysosomal abnormalities in hereditary spastic paraplegia types SPG 15 and SPG 11. Annals of Clinical and Translational Neurology. 1(6). 379–389. 82 indexed citations

Renvoisé, Benoît, Julia T. Stadler, Rajat Singh, Joanna C. Bakowska, & Craig Blackstone. (2012). Spg20−/− mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling. Human Molecular Genetics. 21(16). 3604–3618. 45 indexed citations

Renvoisé, Benoît, et al.. (2012). A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies. Journal of Cell Science. 125(Pt 12). 2862–74. 22 indexed citations

10.

Lee, Seongju, et al.. (2012). MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis. Molecular Biology of the Cell. 23(22). 4347–4361. 36 indexed citations

11.

Renvoisé, Benoît & Craig Blackstone. (2010). Emerging themes of ER organization in the development and maintenance of axons. Current Opinion in Neurobiology. 20(5). 531–537. 48 indexed citations

12.

Renvoisé, Benoît, et al.. (2010). SPG20 Protein Spartin Is Recruited to Midbodies by ESCRT-III Protein Ist1 and Participates in Cytokinesis. Molecular Biology of the Cell. 21(19). 3293–3303. 67 indexed citations

13.

Renvoisé, Benoît, Sabrina Colasse, P Burlet, et al.. (2009). The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy. Human Molecular Genetics. 18(7). 1181–1189. 22 indexed citations

14.

Yang, Dong, Neggy Rismanchi, Benoît Renvoisé, et al.. (2009). Structural basis for midbody targeting of spastin by the ESCRT‐III protein CHMP1B. The FASEB Journal. 23(S1). 3 indexed citations

15.

Yang, Dong, Neggy Rismanchi, Benoît Renvoisé, et al.. (2008). Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B. Nature Structural & Molecular Biology. 15(12). 1278–1286. 200 indexed citations

16.

Renvoisé, Benoît, et al.. (2006). Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells. Journal of Cell Science. 119(4). 680–692. 28 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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