Carmen Espinós
- Neurology top 2%
- Neurological diseases and metabolism 25
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- Hereditary Neurological Disorders 36
- Genetic Neurodegenerative Diseases 25
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics 7
- Neurology top 5%
- Neurological diseases and metabolism 25
- Molecular Biology top 10%
- Mitochondrial Function and Pathology 11
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- Metabolism and Genetic Disorders 6
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- Platelet Disorders and Treatments 6
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- Trace Elements in Health 6
- Co-authors
- Francesc PalauTeresa SevillaVincenzo LupoDolores Martínez‐RubioJuan J. VílchezJosé M. MillánRafael SiveraMaría José Chumillas
- Partner nations
- SpainCzechiaUnited States
In The Last Decade
Carmen Espinós
93 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 93
- Neurology 426
- Cellular and Molecular Neuroscience 831
- Sensory Systems 203
- Neurology 249
- Molecular Biology 1.1k
Countries citing papers authored by Carmen Espinós
This map shows the geographic impact of Carmen Espinós'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 Carmen Espinós with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carmen Espinós more than expected).
Fields of papers citing papers by Carmen Espinós
This network shows the impact of papers produced by Carmen Espinós. 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 Carmen Espinós. The network helps show where Carmen Espinós may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Carmen Espinós, 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 | 2024 | 2 | |
| 2 | 2023 | 6 | |
| 3 | 2023 | 3 | |
| 4 | 2021 | 12 | |
| 5 | 2021 | 10 | |
| 6 | 2020 | 19 | |
| 7 | 2018 | 15 | |
| 8 | 2018 | 17 | |
| 9 | 2017 | 8 | |
| 10 | 2017 | 13 | |
| 11 | 2017 | 14 | |
| 12 | 2013 | 36 | |
| 13 | 2012 | 25 | |
| 14 | 2009 | 47 | |
| 15 | Gene symbol: SH3TC2. Disease: Charcot-Marie-Tooth type 4C. | 2008 | 1 |
| 16 | 2006 | 74 | |
| 17 | 2005 | 17 | |
| 18 | 2004 | 14 | |
| 19 | 2001 | 25 | |
| 20 | 2000 | 8 |
About Carmen Espinós
Carmen Espinós is a scholar working on Neurology, Cellular and Molecular Neuroscience and Sensory Systems, having authored 95 papers that have together received 1.9k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (36 papers), Neurological diseases and metabolism (25 papers), Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (11 papers), Hearing, Cochlea, Tinnitus, Genetics (7 papers), Metabolism and Genetic Disorders (6 papers), Platelet Disorders and Treatments (6 papers) and Trace Elements in Health (6 papers). The work is most often cited by research in Neurology (426 citations), Cellular and Molecular Neuroscience (831 citations) and Sensory Systems (203 citations). Carmen Espinós has collaborated with scholars based in Spain, Czechia and United States. Frequent co-authors include Francesc Palau, Teresa Sevilla, Vincenzo Lupo, Dolores Martínez‐Rubio, Juan J. Vílchez, José M. Millán, Rafael Sivera, María José Chumillas, Nuria Muelas and Carmén Nájera. Their work appears in journals such as PLoS ONE, Brain and Neurology.
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.