Matthew C. Madison
- Physiology top 10%
- Pulmonary and Respiratory Medicine
- Molecular Biology
- Immunology
- Health, Toxicology and Mutagenesis top 10%
- Co-authors
- Farrah KheradmandDavid B. CorryCameron LandersHui-Ying TungBrian E. GilbertM J HongRan YouPaul Porter
- Topics
- IL-33, ST2, and ILC Pathways (5 papers)Extracellular vesicles in disease (4 papers)Chronic Obstructive Pulmonary Disease (COPD) Research (4 papers)
- Partner nations
- United StatesNetherlandsFrance
In The Last Decade
Matthew C. Madison
14 papers receiving 526 citations
Hit Papers
Peers
Comparison fields: 5 of 89
- Physiology 215
- Pulmonary and Respiratory Medicine 179
- Molecular Biology 119
- Immunology 86
- Health, Toxicology and Mutagenesis 71
Countries citing papers authored by Matthew C. Madison
This map shows the geographic impact of Matthew C. Madison'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 Matthew C. Madison with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew C. Madison more than expected).
Fields of papers citing papers by Matthew C. Madison
This network shows the impact of papers produced by Matthew C. Madison. 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 Matthew C. Madison. The network helps show where Matthew C. Madison may publish in the future.
Co-authorship network of co-authors of Matthew C. Madison
This figure shows the co-authorship network connecting the top 25 collaborators of Matthew C. Madison. A scholar is included among the top collaborators of Matthew C. Madison 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 Matthew C. Madison. Matthew C. Madison is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 7 | |
| 3 | 6 | |
| 4 | 3 | |
| 5 | 24 | |
| 6 | 30 | |
| 7 | 0 | |
| 8 | 6 | |
| 9 | 30 | |
| 10 | Electronic cigarettes disrupt lung lipid homeostasis and innate immunity independent of nicotinebreakdown → | 254 |
| 11 | 30 | |
| 12 | 31 | |
| 13 | 14 | |
| 14 | 22 | |
| 15 | 37 | |
| 16 | 35 |
About Matthew C. Madison
Matthew C. Madison is a scholar working on Immunology, Otorhinolaryngology and Pulmonary and Respiratory Medicine, having authored 16 papers that have together received 529 indexed citations. Recurring topics across this work include IL-33, ST2, and ILC Pathways (5 papers), Extracellular vesicles in disease (4 papers) and Chronic Obstructive Pulmonary Disease (COPD) Research (4 papers). The work is most often cited by research in Physiology (215 citations), Pulmonary and Respiratory Medicine (179 citations) and Health, Toxicology and Mutagenesis (71 citations). Matthew C. Madison has collaborated with scholars based in United States, Netherlands and France. Frequent co-authors include Farrah Kheradmand, David B. Corry, Cameron Landers, Hui-Ying Tung, Brian E. Gilbert, M J Hong, Ran You, Paul Porter, Cheng‐Yen Chang and Matthew J. Campen. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The Journal of Immunology.
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.