Chantal Sellier

3.7k total citations · 1 hit paper
24 papers, 2.2k citations indexed

About

Chantal Sellier is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Chantal Sellier has authored 24 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 9 papers in Genetics. Recurrent topics in Chantal Sellier's work include Genetic Neurodegenerative Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). Chantal Sellier is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). Chantal Sellier collaborates with scholars based in France, United States and Netherlands. Chantal Sellier's co-authors include Nicolas Charlet‐Berguerand, Frank Ruffenach, Flora Tassone, Peter K. Todd, Angéline Gaucherot, Rob Willemsen, Adeline Page, Sorana Ciura, Maria‐Letizia Campanari and Edor Kabashi and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Neuron.

In The Last Decade

Chantal Sellier

24 papers receiving 2.2k citations

Hit Papers

align trajectories sort by overperformance

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.

Loss of C9 ORF 72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death

2016 305 citations Chantal Sellier, Maria‐Letizia Campanari et al. The EMBO Journal profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chantal Sellier France	17	1.5k	767	707	577	417	24	2.2k
Tao Zu United States	17	2.0k 1.4×	1.0k 1.4×	394 0.6×	1.5k 2.5×	556 1.3×	23	2.8k
Jennifer Skaug Canada	10	1.1k 0.7×	407 0.5×	572 0.8×	200 0.3×	277 0.7×	11	1.8k
Adrian J. Waite United Kingdom	17	643 0.4×	725 0.9×	235 0.3×	324 0.6×	352 0.8×	20	1.3k
Caroline Rouaux France	17	935 0.6×	353 0.5×	184 0.3×	516 0.9×	178 0.4×	23	1.5k
Sílvia Porta United States	20	1.4k 0.9×	664 0.9×	124 0.2×	423 0.7×	191 0.5×	27	2.0k
Graciela K. Penchaszadeh United States	16	1.4k 0.9×	430 0.6×	530 0.7×	628 1.1×	793 1.9×	20	2.4k
Yubing Lu United States	14	1.0k 0.7×	1.1k 1.5×	123 0.2×	367 0.6×	687 1.6×	29	1.8k
Donato Goffredo Italy	12	2.0k 1.3×	543 0.7×	212 0.3×	1.8k 3.2×	78 0.2×	14	2.6k
Shibi Likhite United States	15	928 0.6×	1.0k 1.3×	272 0.4×	306 0.5×	778 1.9×	36	1.9k
Serena Lattante Italy	23	771 0.5×	1.2k 1.6×	215 0.3×	209 0.4×	764 1.8×	54	1.8k

Countries citing papers authored by Chantal Sellier

Since Specialization

Citations

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

Fields of papers citing papers by Chantal Sellier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chantal Sellier

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sellier, Chantal, Philippe Corcia, Patrick Vourc’h, & Luc Dupuis. (2024). C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?. Revue Neurologique. 180(5). 417–428. 7 indexed citations

Pfister, Véronique, Angéline Gaucherot, Frank Ruffenach, et al.. (2020). Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders. The EMBO Journal. 39(4). e100574–e100574. 102 indexed citations

Sellier, Chantal, Estefanía Cerro-Herreros, Markus Blatter, et al.. (2018). rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. Nature Communications. 9(1). 2009–2009. 57 indexed citations

Sellier, Chantal, et al.. (2018). Daunorubicin reduces MBNL1 titration by expanded CUG repeat RNA and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy. Disease Models & Mechanisms. 11(4). 13 indexed citations

Glineburg, M. Rebecca, Peter K. Todd, Nicolas Charlet‐Berguerand, & Chantal Sellier. (2018). Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome. Brain Research. 1693(Pt A). 43–54. 54 indexed citations

Frick, Petra, Chantal Sellier, Ian R. Mackenzie, et al.. (2018). Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers. Acta Neuropathologica Communications. 6(1). 72–72. 82 indexed citations

Willemsen, Rob, et al.. (2017). Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?. European Journal of Medical Genetics. 61(11). 674–679. 22 indexed citations

Ishiguro, Taro, Nozomu Sato, Morio Ueyama, et al.. (2017). Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31. Neuron. 94(1). 108–124.e7. 91 indexed citations

Sellier, Chantal, Maria‐Letizia Campanari, Angéline Gaucherot, et al.. (2016). Loss of C9 ORF 72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death. The EMBO Journal. 35(12). 1276–1297. 305 indexed citations breakdown →

10.

Sellier, Chantal, Karen Usdin, Chiara Pastori, et al.. (2014). The multiple molecular facets of fragile X-associated tremor/ataxia syndrome. Journal of Neurodevelopmental Disorders. 6(1). 23–23. 32 indexed citations

11.

Todd, Peter K., Seok Yoon Oh, Amy Krans, et al.. (2013). CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome. Neuron. 78(3). 440–455. 357 indexed citations

12.

Todd, Peter K., Seok Yoon Oh, Amy Krans, et al.. (2013). CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome. Neuron. 79(2). 402–402. 1 indexed citations

13.

Almeida, Sandra, Eduardo Gascon, Hélène Tran, et al.. (2013). Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons. Acta Neuropathologica. 126(3). 385–399. 251 indexed citations

14.

Sellier, Chantal, Fernande Freyermuth, Ricardos Tabet, et al.. (2013). Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome. Cell Reports. 3(3). 869–880. 189 indexed citations

15.

Sellier, Chantal, et al.. (2010). Calcium Dynamics During Physiological Acidification in Xenopus Oocyte. The Journal of Membrane Biology. 236(3). 233–245. 12 indexed citations

16.

Sellier, Chantal, Frédérique Rau, Yilei Liu, et al.. (2010). Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients. The EMBO Journal. 29(7). 1248–1261. 290 indexed citations

17.

Dehennaut, Vanessa, Tony Lefebvre, Chantal Sellier, et al.. (2007). O-Linked N-Acetylglucosaminyltransferase Inhibition Prevents G2/M Transition in Xenopus laevis Oocytes. Journal of Biological Chemistry. 282(17). 12527–12536. 60 indexed citations

18.

Sellier, Chantal, et al.. (2006). Intracellular acidification delays hormonal G2/M transition and inhibits G2/M transition triggered by thiophosphorylated MAPK in Xenopus oocytes. Journal of Cellular Biochemistry. 98(2). 287–300. 16 indexed citations

19.

Bodart, Jean‐François, et al.. (2005). Differential roles of p39Mos–Xp42Mpk1 cascade proteins on Raf1 phosphorylation and spindle morphogenesis in Xenopus oocytes. Developmental Biology. 283(2). 373–383. 16 indexed citations

20.

Sellier, Chantal, Sigurd Elz, Armin Buschauer, & Walter Schunack. (1992). Histamine analogues: imidazolylalkylguanidines, synthesis and in vitro pharmacology. European Journal of Medicinal Chemistry. 27(1). 27–32. 3 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.

Explore authors with similar magnitude of impact