Elsa Rossignol

3.2k total citations
40 papers, 1.4k citations indexed

About

Elsa Rossignol is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Elsa Rossignol has authored 40 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Elsa Rossignol's work include Neuroscience and Neuropharmacology Research (13 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Elsa Rossignol is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Elsa Rossignol collaborates with scholars based in Canada, United States and France. Elsa Rossignol's co-authors include Gord Fishell, Mathieu Lachance, Anne Lortie, Renata Batista‐Brito, Xiao Jiang, Bernardo Rudy, Alexis Lupien‐Meilleur, Luis H. Ospina, Lionel Carmant and Vassilis Pachnis and has published in prestigious journals such as Nature Communications, Neuron and Journal of Neuroscience.

In The Last Decade

Elsa Rossignol

38 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elsa Rossignol Canada 19 684 655 393 288 248 40 1.4k
Robert F. Hunt United States 16 602 0.9× 551 0.8× 164 0.4× 182 0.6× 248 1.0× 24 1.3k
Vostrikov Vm Russia 15 482 0.7× 584 0.9× 366 0.9× 517 1.8× 341 1.4× 40 1.9k
Kerstin Ure United States 11 589 0.9× 799 1.2× 629 1.6× 346 1.2× 127 0.5× 13 1.6k
Thomas K. Creson United States 13 511 0.7× 634 1.0× 470 1.2× 263 0.9× 174 0.7× 18 1.2k
Ute Häussler Germany 20 1.0k 1.5× 625 1.0× 200 0.5× 307 1.1× 316 1.3× 33 1.7k
Kanehiro Hayashi Japan 19 505 0.7× 549 0.8× 194 0.5× 92 0.3× 248 1.0× 31 1.4k
Beatrice Paradiso Italy 17 394 0.6× 321 0.5× 157 0.4× 111 0.4× 165 0.7× 36 966
V.I. Rachmanova Russia 8 376 0.5× 354 0.5× 140 0.4× 364 1.3× 266 1.1× 12 1.3k
Dong‐Min Yin China 21 1.0k 1.5× 954 1.5× 194 0.5× 255 0.9× 72 0.3× 40 2.0k
Biljana Djukic United States 13 840 1.2× 785 1.2× 168 0.4× 203 0.7× 136 0.5× 15 1.5k

Countries citing papers authored by Elsa Rossignol

Since Specialization
Citations

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

Fields of papers citing papers by Elsa Rossignol

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elsa Rossignol

This figure shows the co-authorship network connecting the top 25 collaborators of Elsa Rossignol. A scholar is included among the top collaborators of Elsa Rossignol 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 Elsa Rossignol. Elsa Rossignol 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.
Marcoux, Danielle, et al.. (2025). Neuroichthyosis With a De Novo Variant c.494C>T in ELOVL1 and Severe Pruritus Relieved by Dupilumab. Pediatric Dermatology. 42(4). 844–848.
2.
Flamini, Robert, Andrea Rossi, Enrico Bertini, et al.. (2024). Stress and Quality of Life of Parents of Children With POLR3-Related Leukodystrophy: A Cross-Sectional Pilot Study. Journal of Child Neurology. 40(1). 26–38.
3.
Rousseau, Justine, Thi Tuyet Mai Nguyen, Norbert Fonya Ajeawung, et al.. (2023). The ATP6V1B2 DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice. Genes. 14(8). 1538–1538. 2 indexed citations
4.
Vannasing, Phetsamone, Julie Tremblay, Anne Lortie, et al.. (2023). Brain language networks and cognitive outcomes in children with frontotemporal lobe epilepsy. Frontiers in Human Neuroscience. 17. 1253529–1253529. 2 indexed citations
5.
Rossignol, Elsa, et al.. (2023). Interneuron odyssey: molecular mechanisms of tangential migration. Frontiers in Neural Circuits. 17. 1256455–1256455. 11 indexed citations
6.
Jouvet, Philippe, et al.. (2023). Pediatric Delirium: An Overlooked Diagnosis?. Pediatric Neurology. 145. 48–53. 1 indexed citations
7.
Lupien‐Meilleur, Alexis, Xiao Jiang, Mathieu Lachance, et al.. (2021). Reversing frontal disinhibition rescues behavioural deficits in models of CACNA1A-associated neurodevelopment disorders. Molecular Psychiatry. 26(12). 7225–7246. 14 indexed citations
8.
Jiang, Xiao, Nazzareno D’Avanzo, Mathieu Lachance, et al.. (2019). Both gain‐of‐function and loss‐of‐function de novo CACNA 1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome. Epilepsia. 60(9). 1881–1894. 62 indexed citations
9.
Eid, Lara, Mathieu Lachance, Gilles R.X. Hickson, & Elsa Rossignol. (2018). <em>Ex Utero</em> Electroporation and Organotypic Slice Cultures of Embryonic Mouse Brains for Live-Imaging of Migrating GABAergic Interneurons. Journal of Visualized Experiments. 3 indexed citations
10.
Rossignol, Elsa, et al.. (2015). Bilateral congenital corneal anesthesia in a patient with SCN9A mutation, confirmed primary erythromelalgia, and paroxysmal extreme pain disorder. Journal of American Association for Pediatric Ophthalmology and Strabismus. 19(5). 478–479. 12 indexed citations
11.
Meijer, Inge A., Florin Sasarman, Elsa Rossignol, et al.. (2015). LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy. SHILAP Revista de lepidopterología. 5. 85–88. 19 indexed citations
12.
Camuzeaux, Stéphane, Anne‐Marie Laberge, Pierre Allard, et al.. (2015). Normal Cerebrospinal Fluid Pyridoxal 5′-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy. JIMD Reports. 22. 67–75. 17 indexed citations
13.
Robinson, Marie‐Eve, et al.. (2014). Vanishing White Matter Disease in French-Canadian Patients From Quebec. Pediatric Neurology. 51(2). 225–232. 6 indexed citations
14.
Michaud, Jacques L., Mathieu Lachance, Fadi F. Hamdan, et al.. (2014). The genetic landscape of infantile spasms. Human Molecular Genetics. 23(18). 4846–4858. 140 indexed citations
15.
Perrault, Isabelle, Fadi F. Hamdan, Marlène Rio, et al.. (2014). Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness. The American Journal of Human Genetics. 94(6). 891–897. 35 indexed citations
16.
Close, Jennie, Han Xu, Renata Batista‐Brito, et al.. (2012). Satb1 Is an Activity-Modulated Transcription Factor Required for the Terminal Differentiation and Connectivity of Medial Ganglionic Eminence-Derived Cortical Interneurons. Journal of Neuroscience. 32(49). 17690–17705. 100 indexed citations
17.
Batista‐Brito, Renata, Elsa Rossignol, Jens Hjerling‐Leffler, et al.. (2009). The Cell-Intrinsic Requirement of Sox6 for Cortical Interneuron Development. Neuron. 63(4). 466–481. 166 indexed citations
18.
Rossignol, Elsa, Anne Lortie, Tammy Thomas, et al.. (2008). Vagus nerve stimulation in pediatric epileptic syndromes. Seizure. 18(1). 34–37. 71 indexed citations
19.
Dupré, Nicolas, Nicolas Chrestian, Jean‐Pierre Bouchard, et al.. (2008). Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians. Neuromuscular Disorders. 19(5). 330–334. 40 indexed citations
20.
Rossignol, Elsa, Guy D’Anjou, Normand Lapointe, Élie Haddad, & Michel Vanasse. (2007). Evolution and Treatment of Childhood Chronic Inflammatory Polyneuropathy. Pediatric Neurology. 36(2). 88–94. 31 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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