Catherine McWilliam
Impact in
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- Genetic Neurodegenerative Diseases
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- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Mitochondrial Function and Pathology 2
- Genetics 5
- Connective tissue disorders research 2
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Cheryl Longman (3 shared papers)Maria Elena Farrugia (3 shared papers)Helen Gregory (3 shared papers)Richard Petty (3 shared papers)Mark Hamilton (3 shared papers)Anneli Cooper (2 shared papers)Darren G. Monckton (2 shared papers)Sarah A. Cumming (2 shared papers)
- Journals
- Scientific Reports (1 paper)European Journal of Human Genetics (1 paper)European Heart Journal (1 paper)Human Molecular Genetics (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- United KingdomSingaporeNetherlands
In The Last Decade
Catherine McWilliam
9 papers receiving 134 citations
Peers
Comparison fields: 5 of 56
- Cellular and Molecular Neuroscience 66
- Neurology 27
- Genetics 37
- Molecular Biology 87
- Aging 1
Countries citing papers authored by Catherine McWilliam
This map shows the geographic impact of Catherine McWilliam'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 Catherine McWilliam with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine McWilliam more than expected).
Fields of papers citing papers by Catherine McWilliam
This network shows the impact of papers produced by Catherine McWilliam. 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 Catherine McWilliam. The network helps show where Catherine McWilliam may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine McWilliam, 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 | 69 | |
| 2 | 2017 | 29 | |
| 3 | 2016 | 19 | |
| 4 | 2019 | 10 | |
| 5 | 2022 | 3 | |
| 6 | 2022 | 2 | |
| 7 | 2019 | 1 | |
| 8 | 2009 | 1 | |
| 9 | 2019 | 1 |
About Catherine McWilliam
Catherine McWilliam is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Pulmonary and Respiratory Medicine, having authored 9 papers that have together received 135 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (3 papers), Connective tissue disorders research (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), Aortic Disease and Treatment Approaches (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Aortic aneurysm repair treatments (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (66 citations), Neurology (27 citations), Genetics (37 citations), Molecular Biology (87 citations) and Aging (1 citation). Catherine McWilliam has collaborated with scholars based in United Kingdom, Singapore and Netherlands. Frequent co-authors include Cheryl Longman, Maria Elena Farrugia, Helen Gregory, Richard Petty, Mark Hamilton, Anneli Cooper, Darren G. Monckton, Sarah A. Cumming, Berit Adam and Michael Tschannen. Their work appears in journals such as Scientific Reports, European Journal of Human Genetics, European Heart Journal, Human Molecular Genetics and Neuromuscular Disorders.
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.