Stéphanie Guey

1.3k total citations
32 papers, 599 citations indexed

About

Stéphanie Guey is a scholar working on Neurology, Rheumatology and Genetics. According to data from OpenAlex, Stéphanie Guey has authored 32 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Neurology, 18 papers in Rheumatology and 7 papers in Genetics. Recurrent topics in Stéphanie Guey's work include Cerebrovascular and genetic disorders (19 papers), Moyamoya disease diagnosis and treatment (17 papers) and Intracerebral and Subarachnoid Hemorrhage Research (6 papers). Stéphanie Guey is often cited by papers focused on Cerebrovascular and genetic disorders (19 papers), Moyamoya disease diagnosis and treatment (17 papers) and Intracerebral and Subarachnoid Hemorrhage Research (6 papers). Stéphanie Guey collaborates with scholars based in France, Germany and United States. Stéphanie Guey's co-authors include Dominique Hervé, Elisabeth Tournier‐Lasserve, Manoëlle Kossorotoff, Hugues Chabriat, Françoise Bergametti, Markus Kraemer, Jan Claudius Schwitalla, Éric Jouvent, Saskia A.J. Lesnik Oberstein and Emmanuelle Génin and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Stéphanie Guey

28 papers receiving 590 citations

Peers

Stéphanie Guey

NEURO

RHEUM

PMH

PRM

GENET

Poneh Adib‐Samii United Kingdom

Thorsten Rosenbaum Germany

Saara Tikka Finland

Julie W. Rutten Netherlands

Miyuki Kanematsu Japan

Gido Gravesteijn Netherlands

P Mennonna Italy

Sietske H. Kevelam Netherlands

F. Andreux France

Mourad Majidi United States

Poneh Adib‐Samii United Kingdom

Stéphanie Guey

274 ×0.7

NEURO

153 ×0.4

RHEUM

32 ×0.2

PMH

70 ×0.6

PRM

78 ×0.8

GENET

Citations per year, relative to Stéphanie Guey Stéphanie Guey (= 1×) peers Poneh Adib‐Samii

Countries citing papers authored by Stéphanie Guey

Since Specialization

Citations

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

Fields of papers citing papers by Stéphanie Guey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Guey

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

Siguret, Virginie, et al.. (2025). Cerebral Venous Thrombosis and Nitrous Oxide Intoxication: Report of Two Cases and Review of the Literature. Brain and Behavior. 15(3). e70394–e70394. 1 indexed citations

Nataf, F., Nathaniel Scher, Marc A. Bollet, et al.. (2025). Improving methodology of radiosurgery for posterior fossa cavernomas: higher volume, lower dose. Acta Neurochirurgica. 167(1). 29–29.

Hervé, Dominique, Sonia Reyes, Stéphanie Guey, et al.. (2024). Determining Clinical Disease Progression in Symptomatic Patients With CADASIL. Neurology. 104(1). e210193–e210193.

Houillier, Caroline, Rénata Ursu, Carole Soussain, et al.. (2024). Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System: A Multicentric Cohort Study. Annals of Neurology. 97(3). 435–448. 2 indexed citations

Reyes, Sonia, Stéphanie Guey, Dominique Hervé, et al.. (2024). CADA-PRO: A Patient Questionnaire Measuring Key Cognitive, Motor, Emotional, and Behavioral Outcomes in CADASIL. Stroke. 55(10). 2439–2448. 2 indexed citations

Guey, Stéphanie & Hugues Chabriat. (2024). Monogenic causes of cerebral small vessel disease and stroke. Handbook of clinical neurology. 204. 273–287. 2 indexed citations

Guey, Stéphanie, Dominique Hervé, Manoëlle Kossorotoff, et al.. (2023). Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathy. Human Genomics. 17(1). 24–24. 5 indexed citations

Zhang, Ruiting, Jessica Lebenberg, Stéphanie Guey, et al.. (2022). Elderly CADASIL patients with intact neurological status. Journal of Stroke. 24(3). 352–362. 12 indexed citations

Guey, Stéphanie & Dominique Hervé. (2022). Main features of COL4A1-COL4A2 related cerebral microangiopathies. SHILAP Revista de lepidopterología. 3. 100140–100140. 19 indexed citations

10.

Yang, David Dawei, Marlène Rio, Caroline Michot, et al.. (2022). Natural history of Myhre syndrome. Orphanet Journal of Rare Diseases. 17(1). 304–304. 13 indexed citations

11.

Aloui, Chaker, Stéphanie Guey, Eva Pipiras, et al.. (2020). Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome. Journal of Medical Genetics. 57(5). 339–346. 9 indexed citations

12.

Pinard, Amélie, Stéphanie Guey, Dongchuan Guo, et al.. (2019). The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. Genetics in Medicine. 22(2). 427–431. 34 indexed citations

13.

Sène, D., Marc Polivka, Natalia Shor, et al.. (2019). Cerebral Amyloid Angiopathy Related Inflammation With Prominent Meningeal Involvement. A Report of 2 Cases. Frontiers in Neurology. 10. 984–984. 12 indexed citations

14.

Grangeon, Lou, Stéphanie Guey, Jan Claudius Schwitalla, et al.. (2019). Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy. Stroke. 50(4). 789–796. 30 indexed citations

15.

Guey, Stéphanie, Markus Kraemer, Dominique Hervé, et al.. (2017). Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians. European Journal of Human Genetics. 25(8). 995–1003. 84 indexed citations

16.

Guey, Stéphanie, Lou Grangeon, Françis Brunelle, et al.. (2017). De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy. Journal of Medical Genetics. 54(8). 550–557. 31 indexed citations

17.

Kossorotoff, Manoëlle, Elisabeth Tournier‐Lasserve, Dominique Hervé, & Stéphanie Guey. (2015). Moyamoya disease and syndromes: from genetics to clinical management. The Application of Clinical Genetics. 8. 49–49. 136 indexed citations

18.

Gazal, Steven, Edgard Verdura, Françoise Bergametti, et al.. (2015). Can whole-exome sequencing data be used for linkage analysis?. European Journal of Human Genetics. 24(4). 581–586. 8 indexed citations

19.

Guey, Stéphanie, Jérôme Mawet, Dominique Hervé, et al.. (2015). Prevalence and characteristics of migraine in CADASIL. Cephalalgia. 36(11). 1038–1047. 56 indexed citations

20.

Roux, Charles, Stéphanie Guey, Isabelle Crassard, et al.. (2011). A rare cause of gait ataxia. The Lancet. 378(9798). 1274–1274. 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.

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