Inès Mademan
Impact in
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
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- Neurological diseases and metabolism
Papers in
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- Hereditary Neurological Disorders 3
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- RNA and protein synthesis mechanisms 2
- RNA Research and Splicing 2
- Co-authors
- Peter De Jonghe (4 shared papers)Jonathan Baets (4 shared papers)Laurie B. Griffin (2 shared papers)Anthony Antonellis (2 shared papers)Tine Deconinck (2 shared papers)William W. Motley (1 shared paper)Steven S. Scherer (1 shared paper)Els De Vriendt (1 shared paper)
- Partner nations
- BelgiumUnited StatesSpain
In The Last Decade
Inès Mademan
4 papers receiving 108 citations
Peers
Comparison fields: 5 of 29
- Cellular and Molecular Neuroscience 49
- Neurology 15
- Cell Biology 19
- Nephrology 7
- Molecular Biology 67
Countries citing papers authored by Inès Mademan
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
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-authors
The 25 scholars most cited alongside Inès Mademan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 34 | |
| 2 | 2013 | 28 | |
| 3 | 2017 | 26 | |
| 4 | 2018 | 21 |
About Inès Mademan
Inès Mademan is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Nephrology and Cell Biology, having authored 4 papers that have together received 109 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (3 papers), Neurological diseases and metabolism (2 papers), RNA and protein synthesis mechanisms (2 papers), RNA Research and Splicing (2 papers), Renal Diseases and Glomerulopathies (1 paper), Lysosomal Storage Disorders Research (1 paper) and Cellular transport and secretion (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (49 citations), Neurology (15 citations), Cell Biology (19 citations), Nephrology (7 citations) and Molecular Biology (67 citations). Inès Mademan has collaborated with scholars based in Belgium, United States and Spain. Frequent co-authors include Peter De Jonghe, Jonathan Baets, Laurie B. Griffin, Anthony Antonellis, Tine Deconinck, William W. Motley, Steven S. Scherer, Els De Vriendt, Albena Jordanova and Thomas Voït. Their work appears in journals such as Neurology, Neurology Genetics and Human Mutation.
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.