Catherine McWilliam
Impact in
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- Genetic Neurodegenerative Diseases
-
- Parkinson's Disease Mechanisms and Treatments
Papers in
- Genetics 5
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Connective tissue disorders research 2
- Genomics and Rare Diseases 1
- Co-authors
- Cheryl Longman (3 shared papers)Yvonne Robb (3 shared papers)Mark Hamilton (3 shared papers)Maria Elena Farrugia (3 shared papers)Richard Petty (3 shared papers)Helen Gregory (3 shared papers)Berit Adam (2 shared papers)Anneli Cooper (2 shared papers)
- Journals
- European Journal of Paediatric Neurology (1 paper)Neuromuscular Disorders (1 paper)European Journal of Human Genetics (1 paper)PLoS ONE (1 paper)European Heart Journal (1 paper)
- Partner nations
- United KingdomSingaporeDenmark
In The Last Decade
Catherine McWilliam
9 papers receiving 144 citations
Peers
Comparison fields: 5 of 52
- Cellular and Molecular Neuroscience 69
- Neurology 21
- Genetics 35
- Molecular Biology 79
- Genetics 6
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 | 77 | |
| 2 | 2017 | 30 | |
| 3 | 2016 | 19 | |
| 4 | 2019 | 11 | |
| 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 Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Pulmonary and Respiratory Medicine and Surgery, having authored 9 papers that have together received 145 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Aortic Disease and Treatment Approaches (2 papers), Aortic aneurysm repair treatments (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Connective tissue disorders research (2 papers), Autism Spectrum Disorder Research (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (69 citations), Neurology (21 citations), Genetics (35 citations), Molecular Biology (79 citations) and Genetics (6 citations). Catherine McWilliam has collaborated with scholars based in United Kingdom, Singapore and Denmark. Frequent co-authors include Cheryl Longman, Yvonne Robb, Mark Hamilton, Maria Elena Farrugia, Richard Petty, Helen Gregory, Berit Adam, Anneli Cooper, Sarah A. Cumming and Darren G. Monckton. Their work appears in journals such as European Journal of Paediatric Neurology, Neuromuscular Disorders, European Journal of Human Genetics, PLoS ONE and European Heart Journal.
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.