S. Pinson

1.8k total citations
39 papers, 1.1k citations indexed

About

S. Pinson is a scholar working on Neurology, Surgery and Pathology and Forensic Medicine. According to data from OpenAlex, S. Pinson has authored 39 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Neurology, 10 papers in Surgery and 9 papers in Pathology and Forensic Medicine. Recurrent topics in S. Pinson's work include Neurofibromatosis and Schwannoma Cases (19 papers), Genetic factors in colorectal cancer (6 papers) and Meningioma and schwannoma management (5 papers). S. Pinson is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (19 papers), Genetic factors in colorectal cancer (6 papers) and Meningioma and schwannoma management (5 papers). S. Pinson collaborates with scholars based in France, United States and Spain. S. Pinson's co-authors include P. Wolkenstein, P. Combemale, Thomas Mognetti, Rodante E. Tabien, J. W. Stansel, Andrew H. Paterson, Zhongyi Li, М. Marchetti, Alain Calender and B. Guillot and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer Research.

In The Last Decade

S. Pinson

37 papers receiving 1.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
S. Pinson 399 254 242 216 205 39 1.1k
Heyoung L. McBride 222 0.6× 113 0.4× 216 0.9× 151 0.7× 196 1.0× 18 731
John C. Broome 254 0.6× 147 0.6× 240 1.0× 474 2.2× 342 1.7× 32 1.2k
F Resche 322 0.8× 178 0.7× 269 1.1× 110 0.5× 288 1.4× 42 1.0k
John‐Paul Kilday 313 0.8× 138 0.5× 108 0.4× 424 2.0× 344 1.7× 34 855
Indro Chakrabarti 115 0.3× 170 0.7× 273 1.1× 317 1.5× 87 0.4× 21 796
Woo‐Youl Jang 209 0.5× 175 0.7× 210 0.9× 286 1.3× 115 0.6× 60 797
P. Merel 656 1.6× 120 0.5× 84 0.3× 142 0.7× 210 1.0× 9 901
Pablo Sousa 257 0.6× 156 0.6× 176 0.7× 227 1.1× 177 0.9× 27 778
Agadha Wickremesekera 106 0.3× 113 0.4× 172 0.7× 139 0.6× 329 1.6× 42 795
James S. Waldron 205 0.5× 271 1.1× 102 0.4× 328 1.5× 252 1.2× 16 1.6k

Countries citing papers authored by S. Pinson

Since Specialization
Citations

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

Fields of papers citing papers by S. Pinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Pinson

This figure shows the co-authorship network connecting the top 25 collaborators of S. Pinson. A scholar is included among the top collaborators of S. Pinson 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 S. Pinson. S. Pinson 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.
Combemale, P., Laurène Sonzogni, Clément Devic, et al.. (2021). Individual Response to Radiation of Individuals with Neurofibromatosis Type I: Role of the ATM Protein and Influence of Statins and Bisphosphonates. Molecular Neurobiology. 59(1). 556–573. 18 indexed citations
2.
Pégat, Antoine, et al.. (2019). Charcot-Marie-Tooth (CMT)-like polyneuropathy revealing neurofibromatosis type 2: A case report and review of the literature. Revue Neurologique. 175(7-8). 486–489. 3 indexed citations
3.
Petronio, Marco, S. Pinson, Thomas Walter, et al.. (2015). Type 1 serrated polyposis represents a predominantly female disease with a high prevalence of dysplastic serrated adenomas, without germline mutation in MUTYH, APC, and PTEN genes. United European Gastroenterology Journal. 4(2). 305–313. 3 indexed citations
4.
Brahmi, Mehdi, Philippe Thiesse, Dominique Ranchère, et al.. (2015). Diagnostic Accuracy of PET/CT-Guided Percutaneous Biopsies for Malignant Peripheral Nerve Sheath Tumors in Neurofibromatosis Type 1 Patients. PLoS ONE. 10(10). e0138386–e0138386. 29 indexed citations
5.
Drouet, A., et al.. (2014). Neurofibromatose de type 2 : différence inter-générationnelle d’expression génétique et clinique. Archives de Pédiatrie. 21(11). 1233–1240. 2 indexed citations
6.
Combemale, P., L. Valeyrie‐Allanore, Francesco Giammarile, et al.. (2014). Utility of 18F-FDG PET with a Semi-Quantitative Index in the Detection of Sarcomatous Transformation in Patients with Neurofibromatosis Type 1. PLoS ONE. 9(2). e85954–e85954. 39 indexed citations
7.
Giraud, Sophie, et al.. (2013). Development of multidisciplinary committees for decision making and care management in hereditary colon cancer: the French state of the art. Journal of Community Genetics. 5(2). 185–189. 3 indexed citations
8.
Blanchard, G., S. Pinson, Christophe Rousselle, et al.. (2009). La réalisation systématique de l’imagerie par résonance magnétique cérébrale a-t-elle un intérêt chez l’enfant atteint de neurofibromatose de type 1 ?. Archives de Pédiatrie. 16(12). 1527–1532. 1 indexed citations
9.
Cardot‐Bauters, C., Emmanuelle Leteurtre, L Leclerc, et al.. (2008). Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?. Clinical Endocrinology. 69(3). 506–510. 20 indexed citations
10.
Gelsi‐Boyer, Véronique, Virginie Trouplin, José Adélaı̈de, et al.. (2008). Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1genes. BMC Cancer. 8(1). 299–299. 87 indexed citations
11.
Leroux, Dominique, Françoise Desseigne, Christine Lasset, et al.. (2007). Novel biallelic mutations inMSH6 andPMS2 genes: gene conversion as a likely cause ofPMS2 gene inactivation. Human Mutation. 28(11). 1084–1090. 51 indexed citations
12.
Giammarile, Francesco, et al.. (2007). Intérêt de la tomographie par émission de positons au fluorodéoxyglucose 18 dans la détection des neurofibrosarcomes au cours de la neurofibromatose de type 1. Annales de Dermatologie et de Vénéréologie. 134(10). 735–741. 17 indexed citations
13.
14.
Lesca, Gaëtan, Nelly Burnichon, Grégory Raux, et al.. (2006). Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients. Human Mutation. 27(6). 598–598. 74 indexed citations
15.
Köhler, R., et al.. (2005). Pseudarthrose congénitale de l’avant-bras associée à la neurofibromatose: À propos d’un cas et revue de la littérature. 91(8). 773–781. 1 indexed citations
16.
Köhler, R., et al.. (2005). Pseudarthrose congénitale de l’avant-bras associée à la neurofibromatose. Revue de Chirurgie Orthopédique et Réparatrice de l Appareil Moteur. 91(8). 773–781. 9 indexed citations
17.
Lesca, Gaëtan, Henri Plauchu, Florence Coulet, et al.. (2004). Molecular screening ofALK1/ACVRL1andENGgenes in hereditary hemorrhagic telangiectasia in France. Human Mutation. 23(4). 289–299. 91 indexed citations
18.
Pinson, S. & P. Wolkenstein. (2004). La neurofibromatose 1 (NF1) ou maladie de Von Recklinghausen. La Revue de Médecine Interne. 26(3). 196–215. 34 indexed citations
19.
Pinson, S., Alain Créange, S. Barbarot, et al.. (2002). Neurofibromatose 1 : recommandations de prise en charge. Archives de Pédiatrie. 9(1). 49–60. 34 indexed citations
20.
Chabre, Olivier, Patricia Niccoli‐Sire, S. Pinson, & Sophie Giraud. (2000). Phéochromocytomes : que nous apportent les gènes RET, VHL et NF1 ?. 2(4). 323–334. 1 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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