Stéphane Rousseau

2.8k total citations
10 papers, 334 citations indexed

About

Stéphane Rousseau is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stéphane Rousseau has authored 10 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Physiology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stéphane Rousseau's work include Alzheimer's disease research and treatments (6 papers), Genetic Neurodegenerative Diseases (2 papers) and Genomics and Rare Diseases (2 papers). Stéphane Rousseau is often cited by papers focused on Alzheimer's disease research and treatments (6 papers), Genetic Neurodegenerative Diseases (2 papers) and Genomics and Rare Diseases (2 papers). Stéphane Rousseau collaborates with scholars based in France, United States and Morocco. Stéphane Rousseau's co-authors include Dominique Campion, Thierry Frébourg, Anne Rovelet‐Lecrux, David Wallon, Didier Hannequin, Cyril Pottier, Anne‐Claire Richard, Adeline Rollin‐Sillaire, Barbara Jung and Claudia Caradec and has published in prestigious journals such as Journal of Neuroscience, Neurobiology of Disease and Journal of Alzheimer s Disease.

In The Last Decade

Stéphane Rousseau

10 papers receiving 329 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stéphane Rousseau France 8 131 127 101 70 53 10 334
Yingxue Ren United States 11 182 1.4× 164 1.3× 160 1.6× 63 0.9× 66 1.2× 30 481
Maria Khrestian United States 9 171 1.3× 121 1.0× 123 1.2× 77 1.1× 22 0.4× 16 369
Susana Carmona Portugal 7 133 1.0× 172 1.4× 146 1.4× 58 0.8× 69 1.3× 18 387
Doortje Dekens Netherlands 8 98 0.7× 90 0.7× 128 1.3× 83 1.2× 30 0.6× 10 358
Zhijun Lin China 9 108 0.8× 72 0.6× 43 0.4× 24 0.3× 43 0.8× 27 349
Aviva Rotter-Maskowitz Israel 2 138 1.1× 74 0.6× 40 0.4× 93 1.3× 36 0.7× 2 320
Sayuri Higaki Japan 8 272 2.1× 134 1.1× 63 0.6× 40 0.6× 22 0.4× 10 448
Christina B. Schroeter Germany 13 118 0.9× 43 0.3× 52 0.5× 46 0.7× 38 0.7× 29 307
Teng Wan China 11 206 1.6× 55 0.4× 42 0.4× 27 0.4× 25 0.5× 34 413
Baoshi Yuan China 11 94 0.7× 66 0.5× 77 0.8× 53 0.8× 53 1.0× 14 424

Countries citing papers authored by Stéphane Rousseau

Since Specialization
Citations

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

Fields of papers citing papers by Stéphane Rousseau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphane Rousseau

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

All Works

10 of 10 papers shown
1.
Grangeon, Lou, Camille Charbonnier, Stéphane Rousseau, et al.. (2024). Input of exome sequencing in early‐onset cerebral amyloid angiopathy. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 16(4). e70027–e70027. 1 indexed citations
2.
Miguel, Laëtitia, Anne Rovelet‐Lecrux, Pascal Chambon, et al.. (2022). Generation of 17q21.31 duplication iPSC-derived neurons as a model for primary tauopathies. Stem Cell Research. 61. 102762–102762. 1 indexed citations
3.
Rovelet‐Lecrux, Anne, Sébastien Feuillette, Laëtitia Miguel, et al.. (2021). Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathologica Communications. 9(1). 196–196. 16 indexed citations
4.
Grangeon, Lou, Kévin Cassinari, Stéphane Rousseau, et al.. (2021). Early-Onset Cerebral Amyloid Angiopathy and Alzheimer Disease Related to an APP Locus Triplication. Neurology Genetics. 7(5). e609–e609. 20 indexed citations
5.
Guennec, Kilan Le, Hélène Tubeuf, Didier Hannequin, et al.. (2018). Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer’s Disease Patient. Journal of Alzheimer s Disease. 62(2). 821–831. 11 indexed citations
6.
Guennec, Kilan Le, Sarah Veugelen, Olivier Quenez, et al.. (2017). Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds. Neurobiology of Disease. 104. 97–103. 16 indexed citations
7.
Nicolas, Gaël, Agnès Jacquin, Christel Thauvin‐Robinet, et al.. (2014). A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia. European Journal of Human Genetics. 22(10). 1236–1238. 37 indexed citations
8.
Pottier, Cyril, David Wallon, Stéphane Rousseau, et al.. (2013). TREM2 R47H Variant as a Risk Factor for Early-Onset Alzheimer's Disease. Journal of Alzheimer s Disease. 35(1). 45–49. 120 indexed citations
9.
Champy, Marie‐France, Mohammed Selloum, Claudia Caradec, et al.. (2008). Genetic background determines metabolic phenotypes in the mouse. Mammalian Genome. 19(5). 318–331. 82 indexed citations
10.
Helmlinger, Dominique, Gaël Yvert, Stéphane Rousseau, et al.. (2004). Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model. Journal of Neuroscience. 24(8). 1881–1887. 30 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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