Mark Stefanelli
Impact in
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- Multiple Sclerosis Research Studies
- Neurology top 10%
- Neuroinflammation and Neurodegeneration Mechanisms
Papers in
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- Multiple Sclerosis Research Studies 13
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- Genetic Neurodegenerative Diseases 5
- Hereditary Neurological Disorders 3
- Co-authors
- J Scott Sloka (6 shared papers)Michelle Ploughman (13 shared papers)William Pryse‐Phillips (6 shared papers)Marshall Godwin (5 shared papers)Craig S. Moore (6 shared papers)Yanli Fan (1 shared paper)Nicholas Katsanis (1 shared paper)Jane S. Green (1 shared paper)
- Journals
- Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (6 papers)Multiple Sclerosis and Related Disorders (2 papers)Multiple Sclerosis Journal (2 papers)The American Journal of Human Genetics (2 papers)Neurology (2 papers)
- Partner nations
- CanadaUnited StatesItaly
In The Last Decade
Mark Stefanelli
33 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 102
- Pathology and Forensic Medicine 425
- Neurology 91
- Genetics 234
- Developmental Neuroscience 28
- Neurology 76
Countries citing papers authored by Mark Stefanelli
This map shows the geographic impact of Mark Stefanelli'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 Mark Stefanelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Stefanelli more than expected).
Fields of papers citing papers by Mark Stefanelli
This network shows the impact of papers produced by Mark Stefanelli. 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 Mark Stefanelli. The network helps show where Mark Stefanelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Stefanelli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 243 | |
| 2 | 2005 | 144 | |
| 3 | 2011 | 71 | |
| 4 | 2005 | 58 | |
| 5 | 2018 | 52 | |
| 6 | 2011 | 50 | |
| 7 | 2006 | 48 | |
| 8 | 2022 | 44 | |
| 9 | 2008 | 43 | |
| 10 | 2014 | 37 | |
| 11 | 2018 | 37 | |
| 12 | 2005 | 35 | |
| 13 | 2012 | 35 | |
| 14 | 2010 | 34 | |
| 15 | 2019 | 33 | |
| 16 | 2002 | 28 | |
| 17 | 2021 | 13 | |
| 18 | 2004 | 8 | |
| 19 | 2006 | 8 | |
| 20 | 2005 | 6 |
About Mark Stefanelli
Mark Stefanelli is a scholar working on Pathology and Forensic Medicine, Cellular and Molecular Neuroscience, Molecular Biology, Neurology and Neurology, having authored 38 papers that have together received 1.1k indexed citations. Recurring topics across this work include Multiple Sclerosis Research Studies (13 papers), Genetic Neurodegenerative Diseases (5 papers), Hereditary Neurological Disorders (3 papers), Neurological diseases and metabolism (2 papers), Mitochondrial Function and Pathology (2 papers), Peripheral Neuropathies and Disorders (2 papers), Neurogenesis and neuroplasticity mechanisms (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (425 citations), Neurology (91 citations), Genetics (234 citations), Developmental Neuroscience (28 citations) and Neurology (76 citations). Mark Stefanelli has collaborated with scholars based in Canada, United States and Italy. Frequent co-authors include J Scott Sloka, Michelle Ploughman, William Pryse‐Phillips, Marshall Godwin, Craig S. Moore, Yanli Fan, Nicholas Katsanis, Jane S. Green, Elizabeth Dicks and Bridget A. Fernandez. Their work appears in journals such as Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Multiple Sclerosis and Related Disorders, Multiple Sclerosis Journal, The American Journal of Human Genetics and Neurology.
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.