Etienne Léveillé

616 total citations
26 papers, 246 citations indexed

About

Etienne Léveillé is a scholar working on Genetics, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Etienne Léveillé has authored 26 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in Etienne Léveillé's work include Neurological diseases and metabolism (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Hereditary Neurological Disorders (6 papers). Etienne Léveillé is often cited by papers focused on Neurological diseases and metabolism (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Hereditary Neurological Disorders (6 papers). Etienne Léveillé collaborates with scholars based in Canada, United States and France. Etienne Léveillé's co-authors include Ziv Gan‐Or, Owen A. Ross, Guy A. Rouleau, Dan Spiegelman, Nicolas Dupré, Mehrdad A. Estiar, Elena Guadagno, Jennifer A. Ruskey, Jean‐François Trempe and Nathalie A. Johnson and has published in prestigious journals such as Blood, Cancer Research and Scientific Reports.

In The Last Decade

Etienne Léveillé

23 papers receiving 242 citations

Peers

Etienne Léveillé
Etienne Léveillé
Citations per year, relative to Etienne Léveillé Etienne Léveillé (= 1×) peers Raquel Samões

Countries citing papers authored by Etienne Léveillé

Since Specialization
Citations

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

Fields of papers citing papers by Etienne Léveillé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Etienne Léveillé

This figure shows the co-authorship network connecting the top 25 collaborators of Etienne Léveillé. A scholar is included among the top collaborators of Etienne Léveillé 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 Etienne Léveillé. Etienne Léveillé 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.
Feng, Yanzhi, Etienne Léveillé, Jae H. Park, & Markus Müschen. (2025). Moving cellular therapies to the front line for Ph+ B cell acute lymphoblastic leukemia. Cell Reports Medicine. 6(7). 102184–102184. 1 indexed citations
2.
Léveillé, Etienne, Shalin Kothari, Kadriye Nehir Cosgun, Coraline Mlynarczyk, & Markus Müschen. (2024). Tuning Responses to Polatuzumab Vedotin in B-cell Lymphoma. Cancer Discovery. 14(9). 1577–1580.
3.
Lin, Derrick T., Anthos Christofides, Etienne Léveillé, et al.. (2024). Clonal hematopoiesis of indeterminate potential is associated with increased risk of immune checkpoint inhibitor myocarditis in a prospective study of a cardio-oncology cohort. Cardio-Oncology. 10(1). 84–84. 5 indexed citations
4.
Léveillé, Etienne, Mark E. Robinson, Thierry Bertomeu, et al.. (2024). Metabolic Determinants of Ferroptosis in B-Cell Lymphoma. Blood. 144(Supplement 1). 976–976. 1 indexed citations
5.
Léveillé, Etienne, Anthos Christofides, Derrick Lin, et al.. (2024). Clonal Hematopoiesis Is Associated With Cardiomyopathy During Solid Tumor Therapy. JACC CardioOncology. 6(4). 605–607. 5 indexed citations
6.
Estiar, Mehrdad A., Simon Veyron, Kheireddin Mufti, et al.. (2022). Genetic, structural and clinical analysis of spastic paraplegia 4. Parkinsonism & Related Disorders. 98. 62–69. 14 indexed citations
7.
Léveillé, Etienne, et al.. (2022). Determinants of hyponatremia following a traumatic brain injury. Neurological Sciences. 43(6). 3775–3782. 2 indexed citations
8.
Léveillé, Etienne, Lai N. Chan, Abu‐Sayeef Mirza, Kohei Kume, & Markus Müschen. (2022). SYK and ZAP70 kinases in autoimmunity and lymphoid malignancies. Cellular Signalling. 94. 110331–110331. 17 indexed citations
9.
Kume, Kohei, Zhengshan Chen, Lai N. Chan, et al.. (2022). Divergent MYC- and BCL6-Driven Metabolic Programs Enable Dynamic Regulation of Cell Biomass in B-Cell Malignancies. Blood. 140(Supplement 1). 5900–5901. 1 indexed citations
10.
Yoon, Grace, Mehrdad A. Estiar, Simon Veyron, et al.. (2021). GCH1 mutations in hereditary spastic paraplegia. Clinical Genetics. 100(1). 51–58. 5 indexed citations
11.
Estiar, Mehrdad A., Eric Yu, Jay P. Ross, et al.. (2021). Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders. 36(7). 1664–1675. 14 indexed citations
12.
Léveillé, Etienne, Owen A. Ross, & Ziv Gan‐Or. (2021). Tau and MAPT genetics in tauopathies and synucleinopathies. Parkinsonism & Related Disorders. 90. 142–154. 42 indexed citations
13.
Ruskey, Jennifer A., Kristina Martens, Mekale Kibreab, et al.. (2021). Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease. Frontiers in Neurology. 11. 587992–587992. 20 indexed citations
14.
Chan, Lai N., Christian Hurtz, Etienne Léveillé, et al.. (2021). Identification of BCL6 As Synthetic Lethality in RAS-Driven B-Cell Transformation. Blood. 138(Supplement 1). 792–792. 1 indexed citations
15.
Estiar, Mehrdad A., Etienne Léveillé, Dan Spiegelman, et al.. (2020). Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Molecular Genetics & Genomic Medicine. 8(3). e1052–e1052. 18 indexed citations
16.
Léveillé, Etienne, et al.. (2020). Clinical Characterization of Traumatic Acute Interhemispheric Subdural Hematoma. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 47(4). 504–510. 5 indexed citations
17.
Léveillé, Etienne, Mehrdad A. Estiar, Lynne Krohn, et al.. (2019). SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia. Journal of Human Genetics. 64(11). 1145–1151. 10 indexed citations
18.
Ross, Jay P., Etienne Léveillé, Lan Xiong, et al.. (2018). Association study of essential tremor genetic loci in Parkinson's disease. Neurobiology of Aging. 66. 178.e13–178.e15. 7 indexed citations
19.
Léveillé, Etienne, Hernán Gonorazky, Marie‐France Rioux, et al.. (2018). Triple A syndrome presenting as complicated hereditary spastic paraplegia. Molecular Genetics & Genomic Medicine. 6(6). 1134–1139. 8 indexed citations
20.
Bencheikh, Bouchra Ouled Amar, Etienne Léveillé, Jennifer A. Ruskey, et al.. (2018). Sequencing of the GBA coactivator, Saposin C, in Parkinson disease. Neurobiology of Aging. 72. 187.e1–187.e3. 14 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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