Arnaud Jacquier

1.0k total citations
28 papers, 703 citations indexed

About

Arnaud Jacquier is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Arnaud Jacquier has authored 28 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Arnaud Jacquier's work include Amyotrophic Lateral Sclerosis Research (10 papers), Hereditary Neurological Disorders (8 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Arnaud Jacquier is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (10 papers), Hereditary Neurological Disorders (8 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Arnaud Jacquier collaborates with scholars based in France, United States and Italy. Arnaud Jacquier's co-authors include Serge Przedborski, Diane B. Ré, Burcin Ikiz, Virginia Le Verche, Georg Haase, Emmanuelle Buhler, Dimitra Papadimitriou, Christopher E. Henderson, G Haase and Delphine Bohl and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Neuroscience.

In The Last Decade

Arnaud Jacquier

27 papers receiving 693 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arnaud Jacquier France	12	329	275	271	184	130	28	703
Alya R. Raphael United States	10	390 1.2×	203 0.7×	276 1.0×	173 0.9×	145 1.1×	10	676
Constantin d’Ydewalle Belgium	12	685 2.1×	351 1.3×	177 0.7×	176 1.0×	134 1.0×	16	997
Mito Shiote Japan	14	216 0.7×	198 0.7×	412 1.5×	276 1.5×	50 0.4×	21	643
Silvia Rathke‐Hartlieb Germany	9	554 1.7×	325 1.2×	317 1.2×	159 0.9×	119 0.9×	9	979
Sara K. Custer United States	9	444 1.3×	214 0.8×	276 1.0×	208 1.1×	120 0.9×	13	692
Hitoshi Osuga Canada	11	468 1.4×	232 0.8×	479 1.8×	305 1.7×	146 1.1×	13	1.0k
Jackson Sandoe United States	6	572 1.7×	221 0.8×	388 1.4×	259 1.4×	39 0.3×	6	933
Elizabeth C. Lopes Australia	13	251 0.8×	211 0.8×	432 1.6×	247 1.3×	35 0.3×	17	680
Kevin Drenner United States	9	514 1.6×	143 0.5×	528 1.9×	345 1.9×	70 0.5×	12	881
Young Bin Hong South Korea	18	442 1.3×	542 2.0×	177 0.7×	103 0.6×	161 1.2×	56	994

Countries citing papers authored by Arnaud Jacquier

Since Specialization

Citations

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

Fields of papers citing papers by Arnaud Jacquier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Jacquier

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

All Works

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20 of 20 papers shown

Risson, Valérie, et al.. (2025). Delivery of Prime editing in human stem cells using pseudoviral NanoScribes particles. Nature Communications. 16(1). 397–397. 3 indexed citations

Fontaine, Fanny, Audrey Labalme, Chloé Laurencin, et al.. (2025). Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia. European Journal of Human Genetics. 33(8). 997–1005.

Girard, Emmanuelle, Nathalie Streichenberger, Philippe Petiot, et al.. (2024). Mitochondrial disorders are associated with morphological neuromuscular junction defects. Neuromuscular Disorders. 45. 105235–105235. 1 indexed citations

Soendenbroe, Casper, Peter Schjerling, René B. Svensson, et al.. (2024). Muscle fibroblasts and stem cells stimulate motor neurons in an age and exercise‐dependent manner. Aging Cell. 24(3). e14413–e14413. 5 indexed citations

Zhao, Zehui, Charlène Magnani, Olivier Binda, et al.. (2023). Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments. Nature Communications. 14(1). 7384–7384. 7 indexed citations

Fernández‐Eulate, Gorka, Philippe Latour, Tanya Stojkovic, et al.. (2023). Genetic characterization of non-5q proximal spinal muscular atrophy in a French cohort: the place of whole exome sequencing. European Journal of Human Genetics. 32(1). 37–43. 2 indexed citations

Jacquier, Arnaud, Fanny Fontaine, Nicolas Lacoste, et al.. (2022). Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy. Brain. 146(8). 3470–3483. 11 indexed citations

Jacquier, Arnaud, Nicolas Lacoste, Valérie Risson, et al.. (2022). Expanding the phenotypic variability of MORC2 gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy. Human Mutation. 43(12). 1898–1908. 6 indexed citations

Pégat, Antoine, Nathalie Streichenberger, Nicolas Lacoste, et al.. (2022). Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report. Genes. 13(12). 2245–2245. 5 indexed citations

10.

Jacquier, Arnaud, et al.. (2022). Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies. Frontiers in Cellular Neuroscience. 16. 896854–896854. 8 indexed citations

11.

Pipis, Menelaos, Andrea Cortese, James M. Polke, et al.. (2021). Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype. Journal of Neurology Neurosurgery & Psychiatry. 93(1). 48–56. 11 indexed citations

12.

Jacquier, Arnaud, Valérie Risson, & Laurent Schaeffer. (2019). Modeling Charcot-Marie-Tooth Disease <em>In Vitro</em> by Transfecting Mouse Primary Motoneurons. Journal of Visualized Experiments. 3 indexed citations

13.

Jacquier, Arnaud, Cécile Delorme, Edwige Belotti, et al.. (2017). Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death. Acta Neuropathologica Communications. 5(1). 55–55. 18 indexed citations

14.

Delloye‐Bourgeois, Céline, Arnaud Jacquier, Florie Reynaud, et al.. (2014). PlexinA1 is a new Slit receptor and mediates axon guidance function of Slit C-terminal fragments. Nature Neuroscience. 18(1). 36–45. 84 indexed citations

15.

Delloye‐Bourgeois, Céline, Arnaud Jacquier, Julien Falk, & Valérie Castellani. (2014). Use of pHluorin to Assess the Dynamics of Axon Guidance Receptors in Cell Culture and in the Chick Embryo. Journal of Visualized Experiments. e50883–e50883. 9 indexed citations

16.

Kariya, Shingo, Diane B. Ré, Arnaud Jacquier, et al.. (2012). Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies. Human Molecular Genetics. 21(15). 3421–3434. 44 indexed citations

17.

Jacquier, Arnaud, et al.. (2009). Astrocytic protection of spinal motor neurons but not cortical neurons against loss of Als2/alsin function. Human Molecular Genetics. 18(12). 2127–2139. 15 indexed citations

18.

Papadimitriou, Dimitra, Virginia Le Verche, Arnaud Jacquier, et al.. (2009). Inflammation in ALS and SMA: Sorting out the good from the evil. Neurobiology of Disease. 37(3). 493–502. 105 indexed citations

19.

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. Neuromuscular Disorders. 17(9-10). 767–767. 3 indexed citations

20.

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H. The American Journal of Human Genetics. 81(1). 1–16. 117 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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