Suzanne Lesage

16.5k total citations · 1 hit paper
70 papers, 3.8k citations indexed

About

Suzanne Lesage is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Suzanne Lesage has authored 70 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Neurology, 23 papers in Neurology and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Suzanne Lesage's work include Parkinson's Disease Mechanisms and Treatments (55 papers), Neurological diseases and metabolism (23 papers) and Nuclear Receptors and Signaling (16 papers). Suzanne Lesage is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (55 papers), Neurological diseases and metabolism (23 papers) and Nuclear Receptors and Signaling (16 papers). Suzanne Lesage collaborates with scholars based in France, United States and United Kingdom. Suzanne Lesage's co-authors include Alexis Brice, Olga Corti, Alexandra Dürr, Mathieu Anheim, Ebba Lohmann, Aurélie Honoré, Pierre Pollak, Laura Pieri, Christophe Verny and Franck Letournel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Physiological Reviews and PLoS ONE.

In The Last Decade

Suzanne Lesage

70 papers receiving 3.7k citations

Hit Papers

align trajectories

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.

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome

2013 531 citations Suzanne Lesage, Mathieu Anheim et al. Annals of Neurology profile →

Peers

Suzanne Lesage

NEURO

CMN

PHYSI

NEURO

Christina Patrick United States

Hideki Shimura Japan

Olga Corti France

Julie van der Zee Belgium

Cornelis Blauwendraat United States

Sonja W. Scholz United States

Pavan K. Auluck United States

Marcie A. Glicksman United States

Ellen Gerhardt Germany

Zdenek Berger United States

Christina Patrick United States

Suzanne Lesage

2.8k ×1.1

NEURO

1.7k ×1.4

CMN

1.4k ×1.4

1.6k ×1.7

PHYSI

1.4k ×1.8

NEURO

Citations per year, relative to Suzanne Lesage Suzanne Lesage (= 1×) peers Christina Patrick

Countries citing papers authored by Suzanne Lesage

Since Specialization

Citations

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

Fields of papers citing papers by Suzanne Lesage

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Lesage

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne Lesage. A scholar is included among the top collaborators of Suzanne Lesage 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 Suzanne Lesage. Suzanne Lesage 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

Faouzi, Johann, Manuela Tan, Suzanne Lesage, et al.. (2024). Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores. npj Parkinson s Disease. 10(1). 8–8. 5 indexed citations

Tesson, Christelle, Thomas Courtin, Graziella Mangone, et al.. (2023). Differences in Survival across Monogenic Forms of Parkinson's Disease. Annals of Neurology. 94(1). 123–132. 6 indexed citations

Courtin, Thomas, Christelle Tesson, Justine Guégan, et al.. (2023). Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism. Movement Disorders Clinical Practice. 10(4). 664–669. 7 indexed citations

Real, Raquel, Alejandro Martínez-Carrasco, Regina H. Reynolds, et al.. (2022). Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia. Brain. 146(5). 1873–1887. 31 indexed citations

Emelyanov, Anton, Tatiana Usenko, Christelle Tesson, et al.. (2018). Mutation analysis of Parkinson's disease genes in a Russian data set. Neurobiology of Aging. 71. 267.e7–267.e10. 38 indexed citations

Lassot, Irina, Suzanne Lesage, Barbara A. Zieba, et al.. (2018). The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21. Cell Reports. 25(9). 2484–2496.e9. 30 indexed citations

Bouhouche, Ahmed, Christelle Tesson, Valérie Drouet, et al.. (2017). Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel. Frontiers in Neurology. 8. 567–567. 14 indexed citations

Nichols, Noah, José Brás, Dena G. Hernandez, et al.. (2015). EIF4G1 mutations do not cause Parkinson's disease. Neurobiology of Aging. 36(8). 2444.e1–2444.e4. 15 indexed citations

Anheim, Mathieu, Alexis Elbaz, Suzanne Lesage, et al.. (2012). Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology. 78(6). 417–420. 183 indexed citations

10.

Lohmann, Ebba, Suzanne Lesage, Haşmet Hanağası, et al.. (2012). Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population. European Journal of Neurology. 19(5). 769–775. 12 indexed citations

11.

Lesage, Suzanne & Alexis Brice. (2011). Role of Mendelian genes in “sporadic” Parkinson's disease. Parkinsonism & Related Disorders. 18. S66–S70. 97 indexed citations

12.

Mitsui, Jun, Yuji Takahashi, Jun Goto, et al.. (2010). Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines. The American Journal of Human Genetics. 87(1). 75–89. 73 indexed citations

13.

Vitte, Jérémie, Sabine Traver, A. Maues de Paula, et al.. (2010). Leucine-Rich Repeat Kinase 2 Is Associated With the Endoplasmic Reticulum in Dopaminergic Neurons and Accumulates in the Core of Lewy Bodies in Parkinson Disease. Journal of Neuropathology & Experimental Neurology. 69(9). 959–972. 61 indexed citations

14.

Bardien, Soraya, et al.. (2010). LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson’s disease patients. Journal of Neural Transmission. 117(7). 847–853. 27 indexed citations

15.

Ribeiro, Maria-João, Stéphane Thobois, Ebba Lohmann, et al.. (2009). A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations. Journal of Nuclear Medicine. 50(8). 1244–1250. 29 indexed citations

16.

Lohmann, Ebba, Laurence Leclere, Suzanne Lesage, et al.. (2008). A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism & Related Disorders. 15(4). 273–276. 21 indexed citations

17.

Lesage, Suzanne, Laurence Leclere, Ebba Lohmann, et al.. (2007). Frequency of the <i>LRRK2 </i>G2019S Mutation in Siblings with Parkinson’s Disease. Neurodegenerative Diseases. 4(2-3). 195–198. 10 indexed citations

18.

Ibáñez, Pablo, Suzanne Lesage, Ebba Lohmann, et al.. (2006). Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain. 129(3). 686–694. 123 indexed citations

19.

Pineda-Trujillo, Nicolás, Maria Apergi, Sonia Moreno, et al.. (2006). A genetic cluster of early onset Parkinson's disease in a Colombian population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(8). 885–889. 19 indexed citations

20.

Leutenegger, Anne‐Louise, Mustafa A. Salih, Pablo Ibáñez, et al.. (2006). Juvenile-Onset Parkinsonism as a Result of the First Mutation in the Adenosine Triphosphate Orientation Domain of PINK1. Archives of Neurology. 63(9). 1257–1257. 26 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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