Katy Barwick
Impact in
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- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research
- Genetic Neurodegenerative Diseases
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- Metabolism and Genetic Disorders
Papers in
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- Hereditary Neurological Disorders 4
- Genetic Neurodegenerative Diseases 2
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- Cellular transport and secretion 2
- Co-authors
- Manju A. Kurian (10 shared papers)Andrew H. Crosby (5 shared papers)Barry A. Chioza (4 shared papers)Dora Steel (4 shared papers)Arianna Ferrini (2 shared papers)Saeed Al-Turki (2 shared papers)Matt Hurles (2 shared papers)Randy Blakely (2 shared papers)
- Journals
- Brain (2 papers)The American Journal of Human Genetics (2 papers)iScience (1 paper)Neurology (1 paper)Epigenomics (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Katy Barwick
13 papers receiving 239 citations
Peers
Comparison fields: 5 of 52
- Cellular and Molecular Neuroscience 81
- Clinical Biochemistry 20
- Neurology 41
- Cell Biology 40
- Neurology 18
Countries citing papers authored by Katy Barwick
This map shows the geographic impact of Katy Barwick'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 Katy Barwick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katy Barwick more than expected).
Fields of papers citing papers by Katy Barwick
This network shows the impact of papers produced by Katy Barwick. 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 Katy Barwick. The network helps show where Katy Barwick may publish in the future.
Co-authors
The 25 scholars most cited alongside Katy Barwick, 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 | 2012 | 72 | |
| 2 | 2021 | 36 | |
| 3 | 2013 | 36 | |
| 4 | 2018 | 22 | |
| 5 | 2021 | 21 | |
| 6 | 2016 | 14 | |
| 7 | 2022 | 13 | |
| 8 | 2024 | 8 | |
| 9 | 2020 | 6 | |
| 10 | 2016 | 6 | |
| 11 | 2023 | 5 | |
| 12 | 2022 | 3 | |
| 13 | 2023 | 2 | |
| 14 | 2025 | 0 | |
| 15 | 2025 | 0 |
About Katy Barwick
Katy Barwick is a scholar working on Cellular and Molecular Neuroscience, Cell Biology, Genetics, Molecular Biology and Neurology, having authored 15 papers that have together received 244 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Neurological disorders and treatments (3 papers), Genomics and Rare Diseases (2 papers), Genetic Neurodegenerative Diseases (2 papers), Cellular transport and secretion (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (81 citations), Clinical Biochemistry (20 citations), Neurology (41 citations), Cell Biology (40 citations) and Neurology (18 citations). Katy Barwick has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Manju A. Kurian, Andrew H. Crosby, Barry A. Chioza, Dora Steel, Arianna Ferrini, Saeed Al-Turki, Matt Hurles, Randy Blakely, Alicia M. Ruggiero and Jane Wright. Their work appears in journals such as Brain, The American Journal of Human Genetics, iScience, Neurology and Epigenomics.
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.