Matthew G. Stanton
- Molecular Biology top 10%
- Organic Chemistry top 10%
- Immunology
- Infectious Diseases top 10%
- Genetics
- Co-authors
- Michel R. GagnéIain J. McFadyenCosmin MihaiTatiana KetovaJoyce ChanStaci SabnisAlex BulychevJoseph J. Senn
- Topics
- RNA Interference and Gene Delivery (6 papers)Advanced biosensing and bioanalysis techniques (4 papers)Asymmetric Synthesis and Catalysis (4 papers)
- Partner nations
- United States
In The Last Decade
Matthew G. Stanton
19 papers receiving 1.4k citations
Hit Papers
Peers
Comparison fields: 5 of 100
- Molecular Biology 988
- Organic Chemistry 221
- Immunology 216
- Infectious Diseases 167
- Genetics 157
Countries citing papers authored by Matthew G. Stanton
This map shows the geographic impact of Matthew G. Stanton'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 G. Stanton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew G. Stanton more than expected).
Fields of papers citing papers by Matthew G. Stanton
This network shows the impact of papers produced by Matthew G. Stanton. 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 G. Stanton. The network helps show where Matthew G. Stanton may publish in the future.
Co-authorship network of co-authors of Matthew G. Stanton
This figure shows the co-authorship network connecting the top 25 collaborators of Matthew G. Stanton. A scholar is included among the top collaborators of Matthew G. Stanton 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 G. Stanton. Matthew G. Stanton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 33 | |
| 2 | 37 | |
| 3 | 21 | |
| 4 | 218 | |
| 5 | 2 | |
| 6 | A Novel Amino Lipid Series for mRNA Delivery: Improved Endosomal Escape and Sustained Pharmacology and Safety in Non-human Primatesbreakdown → | 603 |
| 7 | 20 | |
| 8 | 9 | |
| 9 | 8 | |
| 10 | 105 | |
| 11 | 53 | |
| 12 | 36 | |
| 13 | 7 | |
| 14 | 37 | |
| 15 | 21 | |
| 16 | 61 | |
| 17 | 45 | |
| 18 | 44 | |
| 19 | 43 |
About Matthew G. Stanton
Matthew G. Stanton is a scholar working on Organic Chemistry, Molecular Biology and Rehabilitation, having authored 19 papers that have together received 1.4k indexed citations. Recurring topics across this work include RNA Interference and Gene Delivery (6 papers), Advanced biosensing and bioanalysis techniques (4 papers) and Asymmetric Synthesis and Catalysis (4 papers). The work is most often cited by research in Molecular Biology (988 citations), Process Chemistry and Technology (32 citations) and Immunology (216 citations). Matthew G. Stanton has collaborated with scholars based in United States. Frequent co-authors include Michel R. Gagné, Iain J. McFadyen, Cosmin Mihai, Tatiana Ketova, Joyce Chan, Staci Sabnis, Alex Bulychev, Joseph J. Senn, Kerry E. Benenato and Timothy Salerno. Their work appears in journals such as Journal of the American Chemical Society, Neurology and Journal of Medicinal Chemistry.
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.