Maurice S. Swanson
- Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 52
- Molecular Biology top 0.2%
- RNA Research and Splicing 72
- Muscle Physiology and Disorders 32
- RNA and protein synthesis mechanisms 31
- RNA modifications and cancer 31
- Mitochondrial Function and Pathology 20
- Photosynthetic Processes and Mechanisms 7
- Aging top 2%
- Genetics top 1%
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- Cardiomyopathy and Myosin Studies 16
- Co-authors
- Gideon DreyfussCharles A. ThorntonMarina M. ScottiAmi MankodiT NakagawaRahul KanadiaRichard T. MoxleySerafı́n Piñol-Roma
- Journals
- Proceedings of the National Academy of Sciences (11 papers)Molecular and Cellular Biology (10 papers)Nucleic Acids Research (6 papers)
- Partner nations
- United StatesPolandTaiwan
In The Last Decade
Maurice S. Swanson
124 papers receiving 13.6k citations
Hit Papers
Peers
Comparison fields: 5 of 141
- Cellular and Molecular Neuroscience 4.4k
- Molecular Biology 12.5k
- Aging 147
- Genetics 784
- Cardiology and Cardiovascular Medicine 1.6k
Countries citing papers authored by Maurice S. Swanson
This map shows the geographic impact of Maurice S. Swanson'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 Maurice S. Swanson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maurice S. Swanson more than expected).
Fields of papers citing papers by Maurice S. Swanson
This network shows the impact of papers produced by Maurice S. Swanson. 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 Maurice S. Swanson. The network helps show where Maurice S. Swanson may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Maurice S. Swanson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 3 | |
| 2 | 2024 | 6 | |
| 3 | 2024 | 3 | |
| 4 | 2024 | 2 | |
| 5 | 2024 | 2 | |
| 6 | 2023 | 12 | |
| 7 | 2020 | 7 | |
| 8 | 2018 | 83 | |
| 9 | 2017 | 191 | |
| 10 | 2014 | 45 | |
| 11 | 2013 | 39 | |
| 12 | 2009 | 15 | |
| 13 | 2006 | 274 | |
| 14 | 2006 | 40 | |
| 15 | A Muscleblind Knockout Model for Myotonic Dystrophybreakdown → | 2003 | 576 |
| 16 | 1999 | 112 | |
| 17 | 1993 | 39 | |
| 18 | RNA-binding proteins as developmental regulators.breakdown → | 1989 | 603 |
| 19 | 1988 | 118 | |
| 20 | 1986 | 195 |
About Maurice S. Swanson
Maurice S. Swanson is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cardiology and Cardiovascular Medicine, Biophysics and Genetics, having authored 126 papers that have together received 13.8k indexed citations. Recurring topics across this work include RNA Research and Splicing (72 papers), Genetic Neurodegenerative Diseases (52 papers), Muscle Physiology and Disorders (32 papers), RNA and protein synthesis mechanisms (31 papers), RNA modifications and cancer (31 papers), Mitochondrial Function and Pathology (20 papers), Cardiomyopathy and Myosin Studies (16 papers) and Photosynthetic Processes and Mechanisms (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.4k citations), Molecular Biology (12.5k citations), Aging (147 citations), Genetics (784 citations) and Cardiology and Cardiovascular Medicine (1.6k citations). Maurice S. Swanson has collaborated with scholars based in United States, Poland and Taiwan. Frequent co-authors include Gideon Dreyfuss, Charles A. Thornton, Marina M. Scotti, Ami Mankodi, T Nakagawa, Rahul Kanadia, Richard T. Moxley, Serafı́n Piñol-Roma, Yuan Yuan and Stephen A. Adam. Their work appears in journals such as Proceedings of the National Academy of Sciences, Molecular and Cellular Biology, Nucleic Acids Research, Genes & Development and Human Molecular Genetics.
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.