Mark Stefanelli

1.5k total citations
35 papers, 995 citations indexed

About

Mark Stefanelli is a scholar working on Pathology and Forensic Medicine, Neurology and Molecular Biology. According to data from OpenAlex, Mark Stefanelli has authored 35 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pathology and Forensic Medicine, 8 papers in Neurology and 6 papers in Molecular Biology. Recurrent topics in Mark Stefanelli's work include Multiple Sclerosis Research Studies (15 papers), Genetic Neurodegenerative Diseases (5 papers) and Peripheral Neuropathies and Disorders (4 papers). Mark Stefanelli is often cited by papers focused on Multiple Sclerosis Research Studies (15 papers), Genetic Neurodegenerative Diseases (5 papers) and Peripheral Neuropathies and Disorders (4 papers). Mark Stefanelli collaborates with scholars based in Canada, Italy and United States. Mark Stefanelli's co-authors include J Scott Sloka, Michelle Ploughman, William Pryse‐Phillips, Marshall Godwin, Craig S. Moore, Patrick S. Parfrey, Philip L. Beales, Susan Moore, Yanli Fan and Nicholas Katsanis and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Behavioural Brain Research.

In The Last Decade

Mark Stefanelli

30 papers receiving 965 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Stefanelli Canada 16 449 267 234 135 111 35 995
Steven C. Marks United States 20 186 0.4× 347 1.3× 421 1.8× 125 0.9× 48 0.4× 42 1.6k
Małgorzata Bilińska Poland 18 280 0.6× 99 0.4× 70 0.3× 275 2.0× 68 0.6× 78 792
Anna Pokryszko‐Dragan Poland 20 414 0.9× 153 0.6× 46 0.2× 229 1.7× 81 0.7× 78 1.0k
Federica Esposito Italy 17 373 0.8× 212 0.8× 40 0.2× 169 1.3× 52 0.5× 68 810
Jaspreet Pannu United States 15 370 0.8× 547 2.0× 75 0.3× 103 0.8× 27 0.2× 28 1.3k
Christopher Severson United States 10 176 0.4× 121 0.5× 122 0.5× 272 2.0× 30 0.3× 13 778
María Fernanda Mendes Brazil 15 323 0.7× 81 0.3× 166 0.7× 30 0.2× 64 0.6× 54 835
Mark Wardle United Kingdom 15 585 1.3× 177 0.7× 56 0.2× 85 0.6× 56 0.5× 35 972
Lara Kular Sweden 19 178 0.4× 608 2.3× 101 0.4× 255 1.9× 232 2.1× 35 1.1k
Mihir Gupta United States 17 92 0.2× 351 1.3× 80 0.3× 134 1.0× 50 0.5× 53 1.2k

Countries citing papers authored by Mark Stefanelli

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mark Stefanelli

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Stefanelli. A scholar is included among the top collaborators of Mark Stefanelli 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 Mark Stefanelli. Mark Stefanelli 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.
Fudge, Neva J., Sarah Anthony, Nicholas J. Snow, et al.. (2025). An Overview of Multiple Sclerosis Care in Rural and Urban Newfoundland and Labrador. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 52(6). 904–912.
2.
Yang, Joseph Yuan‐Mou, et al.. (2025). A case of anti-N-methyl-D-aspartate receptor encephalitis with associated ovarian teratoma in a 23-year-old female. Radiology Case Reports. 20(10). 5286–5291.
3.
Fudge, Neva J., et al.. (2025). Investigating T-cell-derived extracellular vesicles as biomarkers of disease activity, axonal injury, and disability in multiple sclerosis. Clinical & Experimental Immunology. 219(1). 2 indexed citations
4.
Morrow, Sarah A., et al.. (2022). Use of natalizumab in persons with multiple sclerosis: 2022 update. Multiple Sclerosis and Related Disorders. 65. 103995–103995. 41 indexed citations
5.
Galloway, Dylan A., John B. Williams, Janet E. Brown, et al.. (2021). Interleukin-1 receptor antagonist: An exploratory plasma biomarker that correlates with disability and provides pathophysiological insights in relapsing-remitting multiple sclerosis. Multiple Sclerosis and Related Disorders. 52. 103006–103006. 12 indexed citations
6.
Chaves, Arthur R., Liam Kelly, Craig S. Moore, Mark Stefanelli, & Michelle Ploughman. (2019). Prolonged cortical silent period is related to poor fitness and fatigue, but not tumor necrosis factor, in Multiple Sclerosis. Clinical Neurophysiology. 130(4). 474–483. 30 indexed citations
7.
Galloway, Dylan A., et al.. (2018). miR‐223 promotes regenerative myeloid cell phenotype and function in the demyelinated central nervous system. Glia. 67(5). 857–869. 51 indexed citations
8.
Chaves, Arthur R., Elizabeth M. Wallack, Liam Kelly, et al.. (2018). Asymmetry of Brain Excitability: A New Biomarker that Predicts Objective and Subjective Symptoms in Multiple Sclerosis. Behavioural Brain Research. 359. 281–291. 37 indexed citations
9.
Ploughman, Michelle, Serge Beaulieu, Nancy E. Mayo, et al.. (2015). Predictors of chronic cerebrospinal venous insufficiency procedure use among older people with multiple sclerosis: a national case–control study. BMC Health Services Research. 15(1). 161–161. 1 indexed citations
10.
Ploughman, Michelle, et al.. (2014). Navigating the “liberation procedure”: a qualitative study of motivating and hesitating factors among people with multiple sclerosis. Patient Preference and Adherence. 8. 1205–1205. 4 indexed citations
11.
Meijer, Inge A., Cynthia V. Bourassa, Nancy D. Merner, et al.. (2013). A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundland Families (S43.002). Neurology. 80(7_supplement).
12.
Pryse‐Phillips, William, et al.. (2013). An Observational Study of Venoplasty in Patients with Multiple Sclerosis. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 40(2). 203–209. 4 indexed citations
13.
Bourassa, Cynthia V., Inge A. Meijer, Nancy D. Merner, et al.. (2012). VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families. The American Journal of Human Genetics. 91(3). 548–552. 32 indexed citations
14.
Ploughman, Michelle, et al.. (2011). Factors influencing healthy aging with multiple sclerosis: a qualitative study. Disability and Rehabilitation. 34(1). 26–33. 69 indexed citations
15.
Ploughman, Michelle, et al.. (2010). Applying cognitive debriefing to pre-test patient-reported outcomes in older people with multiple sclerosis. Quality of Life Research. 19(4). 483–487. 32 indexed citations
16.
Sloka, J Scott, William Pryse‐Phillips, & Mark Stefanelli. (2005). Incidence and Prevalence of Multiple Sclerosis in Newfoundland and Labrador. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 32(1). 37–42. 34 indexed citations
17.
Sloka, J Scott, et al.. (2005). Co-occurrence of autoimmune thyroid disease in a multiple sclerosis cohort. PubMed. 2(1). 9–9. 56 indexed citations
18.
Sloka, J Scott, William Pryse‐Phillips, & Mark Stefanelli. (2005). Multiple Sclerosis in Newfoundland and Labrador - A Model for Disease Prevalence. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 32(1). 43–49. 6 indexed citations
19.
Stefanelli, Mark, et al.. (2004). A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy. American Journal of Medical Genetics Part A. 131A(3). 249–254. 6 indexed citations
20.
Meijer, Inge A., et al.. (2002). A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13. The American Journal of Human Genetics. 70(3). 763–769. 20 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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