S Bort
Impact in
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neurology top 10%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders
Papers in
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- Hereditary Neurological Disorders 7
- Genetic Neurodegenerative Diseases 3
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- Neurological diseases and metabolism 3
- Botulinum Toxin and Related Neurological Disorders 2
- Co-authors
- Francesc Palau (7 shared papers)Juan J. Vílchez (5 shared papers)Teresa Sevilla (5 shared papers)Félix Prieto (3 shared papers)Eva Nelis (2 shared papers)Christine Van Broeckhoven (2 shared papers)Javier Arpa (3 shared papers)A Cruz-Martı́nez (3 shared papers)
- Journals
- Genomics (1 paper)European Journal of Neurology (1 paper)Human Mutation (1 paper)Human Molecular Genetics (1 paper)Human Genetics (1 paper)
- Partner nations
- SpainBelgiumUnited States
In The Last Decade
S Bort
8 papers receiving 282 citations
Peers
Comparison fields: 5 of 29
- Cellular and Molecular Neuroscience 226
- Neurology 77
- Neurology 77
- Cell Biology 39
- Genetics 20
Countries citing papers authored by S Bort
This map shows the geographic impact of S Bort'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 S Bort with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S Bort more than expected).
Fields of papers citing papers by S Bort
This network shows the impact of papers produced by S Bort. 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 S Bort. The network helps show where S Bort may publish in the future.
Co-authors
The 25 scholars most cited alongside S Bort, 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 | 1997 | 122 | |
| 2 | 1993 | 110 | |
| 3 | 1999 | 25 | |
| 4 | 1997 | 16 | |
| 5 | 2008 | 8 | |
| 6 | 1998 | 8 | |
| 7 | [Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure]. | 1995 | 2 |
| 8 | [The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1]. | 1995 | 1 |
About S Bort
S Bort is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Molecular Biology and Genetics, having authored 8 papers that have together received 292 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (7 papers), Neurological diseases and metabolism (3 papers), Genetic Neurodegenerative Diseases (3 papers), Botulinum Toxin and Related Neurological Disorders (2 papers), Cancer-related gene regulation (1 paper), Endoplasmic Reticulum Stress and Disease (1 paper), Wnt/β-catenin signaling in development and cancer (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (226 citations), Neurology (77 citations), Neurology (77 citations), Cell Biology (39 citations) and Genetics (20 citations). S Bort has collaborated with scholars based in Spain, Belgium and United States. Frequent co-authors include Francesc Palau, Juan J. Vílchez, Teresa Sevilla, Félix Prieto, Eva Nelis, Christine Van Broeckhoven, Javier Arpa, A Cruz-Martı́nez, Peter De Jonghe and Ann Löfgren. Their work appears in journals such as Genomics, European Journal of Neurology, Human Mutation, Human Molecular Genetics and Human Genetics.
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.