Inès Mademan

592 total citations
4 papers, 109 citations indexed

About

Inès Mademan is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Inès Mademan has authored 4 papers receiving a total of 109 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 2 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Inès Mademan's work include Hereditary Neurological Disorders (3 papers), Neurological diseases and metabolism (2 papers) and RNA and protein synthesis mechanisms (2 papers). Inès Mademan is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Neurological diseases and metabolism (2 papers) and RNA and protein synthesis mechanisms (2 papers). Inès Mademan collaborates with scholars based in Belgium, United States and Spain. Inès Mademan's co-authors include Jonathan Baets, Peter De Jonghe, Laurie B. Griffin, Anthony Antonellis, William W. Motley, Tine Deconinck, Albena Jordanova, Els De Vriendt, Steven S. Scherer and Argirios Dinopoulos and has published in prestigious journals such as Neurology, Human Mutation and Neurology Genetics.

In The Last Decade

Inès Mademan

4 papers receiving 108 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inès Mademan Belgium 4 67 49 19 15 13 4 109
Ieva Mičule Latvia 7 64 1.0× 33 0.7× 13 0.7× 6 0.4× 23 1.8× 19 125
Eugenia Borgione Italy 8 81 1.2× 27 0.6× 8 0.4× 13 0.9× 22 1.7× 19 125
Spencer Goodman United States 5 61 0.9× 21 0.4× 15 0.8× 8 0.5× 8 0.6× 7 105
Chiara Gemelli Italy 6 37 0.6× 63 1.3× 18 0.9× 12 0.8× 39 3.0× 20 101
Yong Suk Hur South Korea 5 53 0.8× 37 0.8× 35 1.8× 13 0.9× 13 1.0× 6 96
Xidi Yuan Germany 6 53 0.8× 47 1.0× 22 1.2× 27 1.8× 25 1.9× 9 127
Jonas Van Lent Belgium 5 52 0.8× 62 1.3× 20 1.1× 10 0.7× 17 1.3× 7 101
Matt Hurles United Kingdom 2 51 0.8× 32 0.7× 26 1.4× 12 0.8× 17 1.3× 3 107
Massimo Plumari Italy 5 107 1.6× 76 1.6× 16 0.8× 10 0.7× 27 2.1× 10 127
Suad Alyamani Saudi Arabia 4 67 1.0× 35 0.7× 12 0.6× 6 0.4× 10 0.8× 8 118

Countries citing papers authored by Inès Mademan

Since Specialization
Citations

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

Fields of papers citing papers by Inès Mademan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inès Mademan

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

All Works

4 of 4 papers shown
1.
Salter, Claire, Danique Beijer, Katy Barwick, et al.. (2018). Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies. Neurology Genetics. 4(2). e222–e222. 21 indexed citations
2.
Meyer‐Schuman, Rebecca, Vincenzo Lupo, Shawna Feely, et al.. (2017). Substrate interaction defects in histidyl-tRNA synthetase linked to dominant axonal peripheral neuropathy. Human Mutation. 39(3). 415–432. 26 indexed citations
3.
Motley, William W., Laurie B. Griffin, Inès Mademan, et al.. (2015). A novel AARS mutation in a family with dominant myeloneuropathy. Neurology. 84(20). 2040–2047. 34 indexed citations
4.
Mademan, Inès, Tine Deconinck, Argirios Dinopoulos, et al.. (2013). De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy. Neurology. 81(22). 1953–1958. 28 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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