Thomas Bourinaris
Impact in
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- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
- Amyotrophic Lateral Sclerosis Research
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Papers in
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- Hereditary Neurological Disorders 3
- Genetic Neurodegenerative Diseases 3
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- Neurological diseases and metabolism 4
- Amyotrophic Lateral Sclerosis Research 3
- Parkinson's Disease Mechanisms and Treatments 2
- Neurological disorders and treatments 2
- Co-authors
- Henry Houlden (9 shared papers)Stéphanie Efthymiou (5 shared papers)Vincenzo Salpietro (5 shared papers)Ghazala Kaukab Raja (2 shared papers)Georgia Xiromerisiou (4 shared papers)Gerome Breen (1 shared paper)Asmat Ullah (1 shared paper)Sadia Saeed (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (1 paper)Neurological Sciences (1 paper)Orphanet Journal of Rare Diseases (1 paper)Annals of Clinical and Translational Neurology (1 paper)
- Partner nations
- United KingdomGreeceCyprus
In The Last Decade
Thomas Bourinaris
10 papers receiving 85 citations
Peers
Comparison fields: 5 of 29
- Neurology 30
- Neurology 37
- Cellular and Molecular Neuroscience 35
- Genetics 16
- Physiology 19
Countries citing papers authored by Thomas Bourinaris
This map shows the geographic impact of Thomas Bourinaris'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 Thomas Bourinaris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Bourinaris more than expected).
Fields of papers citing papers by Thomas Bourinaris
This network shows the impact of papers produced by Thomas Bourinaris. 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 Thomas Bourinaris. The network helps show where Thomas Bourinaris may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Bourinaris, 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 | 2018 | 29 | |
| 2 | 2017 | 12 | |
| 3 | 2020 | 11 | |
| 4 | 2020 | 10 | |
| 5 | 2021 | 7 | |
| 6 | 2021 | 4 | |
| 7 | 2019 | 4 | |
| 8 | 2021 | 3 | |
| 9 | 2020 | 3 | |
| 10 | 2020 | 3 |
About Thomas Bourinaris
Thomas Bourinaris is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Molecular Biology and Genetics, having authored 10 papers that have together received 86 indexed citations. Recurring topics across this work include Neurological diseases and metabolism (4 papers), Hereditary Neurological Disorders (3 papers), Amyotrophic Lateral Sclerosis Research (3 papers), Genetic Neurodegenerative Diseases (3 papers), Parkinson's Disease Mechanisms and Treatments (2 papers), Neurological disorders and treatments (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Ion channel regulation and function (1 paper). The work is most often cited by research in Neurology (30 citations), Neurology (37 citations), Cellular and Molecular Neuroscience (35 citations), Genetics (16 citations) and Physiology (19 citations). Thomas Bourinaris has collaborated with scholars based in United Kingdom, Greece and Cyprus. Frequent co-authors include Henry Houlden, Stéphanie Efthymiou, Vincenzo Salpietro, Ghazala Kaukab Raja, Georgia Xiromerisiou, Gerome Breen, Asmat Ullah, Sadia Saeed, Deborah Hughes and Evan Reid. Their work appears in journals such as European Journal of Human Genetics, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Neurological Sciences, Orphanet Journal of Rare Diseases and Annals of Clinical and Translational 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.