Erin O’Ferrall

601 total citations
27 papers, 274 citations indexed

About

Erin O’Ferrall is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Erin O’Ferrall has authored 27 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Erin O’Ferrall's work include Muscle Physiology and Disorders (8 papers), Inflammatory Myopathies and Dermatomyositis (6 papers) and Cardiomyopathy and Myosin Studies (6 papers). Erin O’Ferrall is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Inflammatory Myopathies and Dermatomyositis (6 papers) and Cardiomyopathy and Myosin Studies (6 papers). Erin O’Ferrall collaborates with scholars based in Canada, Australia and Japan. Erin O’Ferrall's co-authors include George Karpati, Rima Rozen, Sahar Sibani, David S. Rosenblatt, Benedicte Christensen, Irfan Saadi, Michael Sinnreich, Walter E. Mushynski, Ilan Weisberg and Daniel Leclerc and has published in prestigious journals such as Neurology, Annals of Neurology and Journal of Neurochemistry.

In The Last Decade

Erin O’Ferrall

22 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erin O’Ferrall Canada 11 108 86 57 41 41 27 274
Maja Djordjevic Serbia 11 68 0.6× 118 1.4× 60 1.1× 20 0.5× 13 0.3× 40 360
Francesco Canonico Italy 10 32 0.3× 109 1.3× 35 0.6× 49 1.2× 16 0.4× 51 301
Athina Xaidara Greece 10 23 0.2× 121 1.4× 30 0.5× 55 1.3× 16 0.4× 21 355
Jessica Connor United States 9 34 0.3× 80 0.9× 37 0.6× 34 0.8× 24 0.6× 13 293
M. Biegstraaten Netherlands 9 107 1.0× 85 1.0× 146 2.6× 39 1.0× 6 0.1× 12 523
Halûk Yavuz Türkiye 8 29 0.3× 88 1.0× 15 0.3× 27 0.7× 21 0.5× 14 245
Stephanie DeArmey United States 14 319 3.0× 99 1.2× 128 2.2× 10 0.2× 12 0.3× 19 573
Kouichi Utsumi Japan 11 66 0.6× 54 0.6× 78 1.4× 21 0.5× 29 0.7× 20 336
Jessica R. Chang United States 10 35 0.3× 189 2.2× 86 1.5× 54 1.3× 51 1.2× 39 475
Joanne Mackey United States 12 439 4.1× 133 1.5× 186 3.3× 80 2.0× 8 0.2× 16 781

Countries citing papers authored by Erin O’Ferrall

Since Specialization
Citations

This map shows the geographic impact of Erin O’Ferrall'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 Erin O’Ferrall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erin O’Ferrall more than expected).

Fields of papers citing papers by Erin O’Ferrall

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erin O’Ferrall. 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 Erin O’Ferrall. The network helps show where Erin O’Ferrall may publish in the future.

Co-authorship network of co-authors of Erin O’Ferrall

This figure shows the co-authorship network connecting the top 25 collaborators of Erin O’Ferrall. A scholar is included among the top collaborators of Erin O’Ferrall 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 Erin O’Ferrall. Erin O’Ferrall 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.
O’Connell, Colleen, Victoria Hodgkinson, Dick Drost, et al.. (2025). Thinking outside the box: A re-evaluation of Canadian recommended outcome measures in adult spinal muscular atrophy – report of a national consensus workshop. Journal of Neuromuscular Diseases. 12(5). 699–710.
2.
Martin, Florence, Eric Bareke, Annie Laplante, et al.. (2022). Novel homozygous nonsense mutation of MLIP and compensatory alternative splicing. npj Genomic Medicine. 7(1). 36–36. 2 indexed citations
3.
Karamchandani, Jason, Bruno‐Pierre Dubé, Océane Landon‐Cardinal, et al.. (2022). Myositis with prominent B-cell aggregates causing shrinking lung syndrome in systemic lupus erythematosus: a case report. BMC Rheumatology. 6(1). 11–11. 1 indexed citations
4.
Hodgkinson, Victoria, Bernard Brais, Kristine Chapman, et al.. (2021). A Canadian Adult Spinal Muscular Atrophy Outcome Measures Toolkit: Results of a National Consensus using a Modified Delphi Method. Journal of Neuromuscular Diseases. 8(4). 579–588. 14 indexed citations
5.
Brais, Bernard, et al.. (2021). AUTOIMMUNE & INFLAMMATORY NMD. Neuromuscular Disorders. 31. S55–S55.
6.
Brais, Bernard, et al.. (2021). DISTAL MYOPATHIES. Neuromuscular Disorders. 31. S71–S71.
7.
Hodgkinson, Victoria, Kristine Chapman, Aaron Izenberg, et al.. (2020). Response to Provincial Governments’ Decisions Regarding Monitoring for Adults with Spinal Muscular Atrophy. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(2). 201–203. 3 indexed citations
8.
Nicolau, Stefan, Karine Choquet, Eric Bareke, et al.. (2020). A Molecular Diagnosis of LGMDR1 Established by RNA Sequencing. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(2). 293–296. 2 indexed citations
9.
Robertson, Rebecca, Vladimir V. Rymar, Abbas F. Sadikot, et al.. (2020). BAG3P215L/KO Mice as a Model of BAG3P209L Myofibrillar Myopathy. American Journal Of Pathology. 190(3). 554–562. 1 indexed citations
10.
Statland, Jeffrey, Anthony A. Amato, Elena Bravver, et al.. (2018). Preliminary Results from a Phase 2 Study to Evaluate ACE-083, a Local Muscle Therapeutic, in Patients with Facioscapulohumeral Muscular Dystrophy (S38.001). Neurology. 90(15_supplement). 4 indexed citations
11.
McCormick, Anna, Alex MacKenzie, Erin O’Ferrall, et al.. (2017). The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities. Paediatrics & Child Health. 23(1). 20–26. 11 indexed citations
12.
Gentil, Benoît J., Erin O’Ferrall, Colin Chalk, et al.. (2017). A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade. Journal of Neuropathology & Experimental Neurology. 76(9). 789–799. 12 indexed citations
13.
Robertson, Rebecca, Robert J. Bryson‐Richardson, Jessie R. Lavoie, et al.. (2017). Mouse model of BAG3 myofibrillar myopathy. Neuromuscular Disorders. 27. S121–S121. 1 indexed citations
14.
Srour, Myriam, Jeremy Schwartzentruber, Véronique Bolduc, et al.. (2014). Mutations in riboflavin transporter present with severe sensory loss and deafness in childhood. Muscle & Nerve. 50(5). 775–779. 20 indexed citations
15.
Tétreault, Martine, Sylvie Provost, Benjamin Béland, et al.. (2014). G.P.197. Neuromuscular Disorders. 24(9-10). 875–876.
16.
O’Ferrall, Erin, et al.. (2010). Demyelinating symmetric motor polyneuropathy with high titers of anti‐GM1 antibodies. Muscle & Nerve. 42(4). 604–608. 5 indexed citations
17.
Karpati, George & Erin O’Ferrall. (2009). Sporadic inclusion body myositis: Pathogenic considerations. Annals of Neurology. 65(1). 7–11. 31 indexed citations
18.
Sibani, Sahar, Daniel Leclerc, Ilan Weisberg, et al.. (2003). Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation. Human Mutation. 21(5). 509–520. 41 indexed citations
19.
O’Ferrall, Erin, Janice Robertson, & Walter E. Mushynski. (2000). Inhibition of Aberrant and Constitutive Phosphorylation of the High‐Molecular‐Mass Neurofilament Subunit by CEP‐1347 (KT7515), an Inhibitor of the Stress‐Activated Protein Kinase Signaling Pathway. Journal of Neurochemistry. 75(6). 2358–2367. 14 indexed citations
20.
Sibani, Sahar, Benedicte Christensen, Erin O’Ferrall, et al.. (2000). Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria. Human Mutation. 15(3). 280–287. 66 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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