Carole Mathis

2.5k total citations
55 papers, 1.8k citations indexed

About

Carole Mathis is a scholar working on Molecular Biology, Physiology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Carole Mathis has authored 55 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 12 papers in Physiology and 10 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Carole Mathis's work include Gastrointestinal motility and disorders (7 papers), Bioinformatics and Genomic Networks (7 papers) and Gene expression and cancer classification (6 papers). Carole Mathis is often cited by papers focused on Gastrointestinal motility and disorders (7 papers), Bioinformatics and Genomic Networks (7 papers) and Gene expression and cancer classification (6 papers). Carole Mathis collaborates with scholars based in Switzerland, United States and Germany. Carole Mathis's co-authors include Manuel C. Peitsch, Julia Hoeng, Bruce V. MacFadyen, Rosario Vecchio, Florian Martin, Charles‐Henri Malbert, Alain Sewer, Nikolai V. Ivanov, Walter K. Schlage and Stefan Frentzel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and Gastroenterology.

In The Last Decade

Carole Mathis

55 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carole Mathis Switzerland 27 565 486 383 374 361 55 1.8k
Masafumi Wasa Japan 23 289 0.5× 225 0.5× 226 0.6× 323 0.9× 100 0.3× 74 1.4k
David I. Soybel United States 24 653 1.2× 322 0.7× 200 0.5× 832 2.2× 137 0.4× 137 2.3k
Ivan Tancevski Austria 25 434 0.8× 230 0.5× 169 0.4× 371 1.0× 38 0.1× 81 1.9k
Jing Tang China 30 1.0k 1.8× 243 0.5× 167 0.4× 237 0.6× 98 0.3× 109 2.3k
Lin Cong China 22 590 1.0× 149 0.3× 186 0.5× 208 0.6× 32 0.1× 62 1.7k
Valentina Valenti Italy 20 508 0.9× 154 0.3× 392 1.0× 326 0.9× 188 0.5× 66 2.0k
Paweł Wołkow Poland 25 687 1.2× 208 0.4× 326 0.9× 288 0.8× 20 0.1× 106 2.0k
Anahita Ghorbani United States 21 495 0.9× 119 0.2× 481 1.3× 274 0.7× 51 0.1× 44 2.0k
Yu Koyama Japan 24 1.0k 1.8× 398 0.8× 237 0.6× 494 1.3× 22 0.1× 103 2.1k
Shaoxi Cai China 24 712 1.3× 490 1.0× 515 1.3× 136 0.4× 59 0.2× 110 1.9k

Countries citing papers authored by Carole Mathis

Since Specialization
Citations

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

Fields of papers citing papers by Carole Mathis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carole Mathis

This figure shows the co-authorship network connecting the top 25 collaborators of Carole Mathis. A scholar is included among the top collaborators of Carole Mathis 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 Carole Mathis. Carole Mathis 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.
Sewer, Alain, Filippo Zanetti, Anita R. Iskandar, et al.. (2020). A meta-analysis of microRNAs expressed in human aerodigestive epithelial cultures and their role as potential biomarkers of exposure response to nicotine-containing products. Toxicology Reports. 7. 1282–1295. 3 indexed citations
2.
Malińska, Dominika, Mariusz R. Wiȩckowski, Bernadeta Michalska, et al.. (2019). Mitochondria as a possible target for nicotine action. Journal of Bioenergetics and Biomembranes. 51(4). 259–276. 70 indexed citations
3.
Marescotti, Diego, Carole Mathis, Vincenzo Belcastro, et al.. (2019). Systems toxicology assessment of a representative e-liquid formulation using human primary bronchial epithelial cells. Toxicology Reports. 7. 67–80. 15 indexed citations
4.
Iskandar, Anita R., Florian Martin, Patrice Leroy, et al.. (2018). Comparative biological impacts of an aerosol from carbon-heated tobacco and smoke from cigarettes on human respiratory epithelial cultures: A systems toxicology assessment. Food and Chemical Toxicology. 115. 109–126. 27 indexed citations
5.
6.
Iskandar, Anita R., Florian Martin, Walter K. Schlage, et al.. (2017). Comparative effects of a candidate modified-risk tobacco product Aerosol and cigarette smoke on human organotypic small airway cultures: a systems toxicology approach. Toxicology Research. 6(6). 930–946. 20 indexed citations
7.
Zanetti, Filippo, Alain Sewer, Carole Mathis, et al.. (2016). Systems Toxicology Assessment of the Biological Impact of a Candidate Modified Risk Tobacco Product on Human Organotypic Oral Epithelial Cultures. Chemical Research in Toxicology. 29(8). 1252–1269. 47 indexed citations
8.
9.
Majeed, Shoaib, Emmanuel Guedj, Rémi Dulize, et al.. (2015). Impact Assessment of Repeated Exposure of Organotypic 3D Bronchial and Nasal Tissue Culture Models to Whole Cigarette Smoke. Journal of Visualized Experiments. 33 indexed citations
10.
Iskandar, Anita R., Yang Xiang, Stefan Frentzel, et al.. (2015). Impact Assessment of Cigarette Smoke Exposure on Organotypic Bronchial Epithelial Tissue Cultures: A Comparison of Mono-Culture and Coculture Model Containing Fibroblasts. Toxicological Sciences. 147(1). 207–221. 50 indexed citations
11.
Kogel, Ulrike, Yu‐Tao Xiang, Philippe A. Guy, et al.. (2015). Biological impact of cigarette smoke compared to an aerosol produced from a prototypic modified risk tobacco product on normal human bronchial epithelial cells. Toxicology in Vitro. 29(8). 2102–2115. 31 indexed citations
12.
Iskandar, Anita R., Florian Martin, Marja Talikka, et al.. (2013). Systems Approaches Evaluating the Perturbation of Xenobiotic Metabolism in Response to Cigarette Smoke Exposure in Nasal and Bronchial Tissues. BioMed Research International. 2013. 1–14. 46 indexed citations
13.
Martin, Florian, Ty M. Thomson, Alain Sewer, et al.. (2012). Assessment of network perturbation amplitudes by applying high-throughput data to causal biological networks. BMC Systems Biology. 6(1). 54–54. 76 indexed citations
14.
Schlage, Walter K., Jurjen W. Westra, Stephan Gebel, et al.. (2011). A computable cellular stress network model for non-diseased pulmonary and cardiovascular tissue. BMC Systems Biology. 5(1). 168–168. 51 indexed citations
15.
Westra, Jurjen W., Walter K. Schlage, Brian P. Frushour, et al.. (2011). Construction of a computable cell proliferation network focused on non-diseased lung cells. BMC Systems Biology. 5(1). 105–105. 45 indexed citations
16.
Bullinger, Monika, Matthias Morfeld, Thomas Kohlmann, et al.. (2003). Der SF-36 in der rehabilitationswissenschaftlichen Forschung - Ergebnisse aus dem Norddeutschen Verbund für Rehabilitationsforschung (NVRF) im Förderschwerpunkt Rehabilitationswissenschaften. Die Rehabilitation. 42(4). 218–225. 53 indexed citations
17.
Mathis, Carole, et al.. (2002). Influences of pelvic floor structures and sacral innervation on the response to distension of the cat rectum. Neurogastroenterology & Motility. 14(3). 265–270. 1 indexed citations
18.
MacFadyen, Bruce V., et al.. (1998). Bile duct injury after laparoscopic cholecystectomy. Surgical Endoscopy. 12(4). 315–321. 231 indexed citations
19.
Mathis, Carole, et al.. (1997). Influence of jejunal nutrients on transpyloric flow and pyloric resistance in pigs. annales de biologie animale biochimie biophysique. 37(4). 411–425. 4 indexed citations
20.
Malbert, Charles‐Henri, Carole Mathis, & J.P. Laplace. (1994). Vagal control of transpyloric flow and pyloric resistance. Digestive Diseases and Sciences. 39(S12). 24S–27S. 11 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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