Ellen Cottenie

583 total citations
3 papers, 71 citations indexed

About

Ellen Cottenie is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Ellen Cottenie has authored 3 papers receiving a total of 71 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 2 papers in Neurology and 1 paper in Molecular Biology. Recurrent topics in Ellen Cottenie's work include Hereditary Neurological Disorders (2 papers), Peripheral Neuropathies and Disorders (2 papers) and Genetics and Neurodevelopmental Disorders (1 paper). Ellen Cottenie is often cited by papers focused on Hereditary Neurological Disorders (2 papers), Peripheral Neuropathies and Disorders (2 papers) and Genetics and Neurodevelopmental Disorders (1 paper). Ellen Cottenie collaborates with scholars based in Australia, United Kingdom and Ireland. Ellen Cottenie's co-authors include Henry Houlden, Manoj P. Menezes, Sebastian Brandner, Janice R. Anderson, D J Dick, Alexander M. Rossor, Julian Blake, Mary M. Reilly, Tarek Yousry and Jasper M. Morrow and has published in prestigious journals such as Annals of Neurology and Neuromuscular Disorders.

In The Last Decade

Ellen Cottenie

3 papers receiving 70 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ellen Cottenie Australia 2 31 17 16 15 13 3 71
Liena E. O. Elsayed Sudan 6 53 1.7× 14 0.8× 40 2.5× 31 2.1× 9 0.7× 14 108
Suad Alyamani Saudi Arabia 4 35 1.1× 10 0.6× 67 4.2× 6 0.4× 23 1.8× 8 118
Corinna Hartmann Germany 5 27 0.9× 45 2.6× 36 2.3× 10 0.7× 14 1.1× 7 106
Chelsea Chambers United States 6 12 0.4× 26 1.5× 40 2.5× 6 0.4× 16 1.2× 10 98
Lance H. Rodan United States 5 31 1.0× 19 1.1× 72 4.5× 5 0.3× 6 0.5× 8 127
Rauan Kaiyrzhanov United Kingdom 7 16 0.5× 30 1.8× 19 1.2× 15 1.0× 4 0.3× 13 80
Thomas Bourinaris United Kingdom 5 35 1.1× 37 2.2× 23 1.4× 30 2.0× 5 0.4× 10 86
Marialuisa Valente Italy 6 13 0.4× 12 0.7× 40 2.5× 14 0.9× 24 1.8× 9 112
Vasiliki Nakou United Kingdom 5 31 1.0× 72 4.2× 27 1.7× 9 0.6× 16 1.2× 6 113
Gopinath M. Subramanian Australia 6 35 1.1× 35 2.1× 23 1.4× 9 0.6× 4 0.3× 8 89

Countries citing papers authored by Ellen Cottenie

Since Specialization
Citations

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

Fields of papers citing papers by Ellen Cottenie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ellen Cottenie. 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 Ellen Cottenie. The network helps show where Ellen Cottenie may publish in the future.

Co-authorship network of co-authors of Ellen Cottenie

This figure shows the co-authorship network connecting the top 25 collaborators of Ellen Cottenie. A scholar is included among the top collaborators of Ellen Cottenie 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 Ellen Cottenie. Ellen Cottenie is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

3 of 3 papers shown
1.
Cottenie, Ellen, Manoj P. Menezes, Alexander M. Rossor, et al.. (2013). Rapidly progressive asymmetrical weakness in Charcot–Marie–Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy. Neuromuscular Disorders. 23(5). 399–403. 34 indexed citations
2.
Kruer, Michael C., Sudeshna Dutta, Robert D. Steiner, et al.. (2013). Mutations in gamma adducin are associated with inherited cerebral palsy. Annals of Neurology. 74(6). 805–814. 36 indexed citations
3.
Pitceathly, Robert D. S., Sinéad M. Murphy, Ellen Cottenie, et al.. (2012). P50 Genetic dysfunction of MT-ATP6 can cause axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders. 22. S20–S20. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Liena E. O. Elsayed Breakdown of academic impact, for papers by Suad Alyamani Breakdown of academic impact, for papers by Corinna Hartmann Breakdown of academic impact, for papers by Chelsea Chambers Breakdown of academic impact, for papers by Lance H. Rodan Breakdown of academic impact, for papers by Rauan Kaiyrzhanov Breakdown of academic impact, for papers by Thomas Bourinaris Breakdown of academic impact, for papers by Marialuisa Valente Breakdown of academic impact, for papers by Vasiliki Nakou Breakdown of academic impact, for papers by Gopinath M. Subramanian
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2026