D.E. Wilcox
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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- Muscle Physiology and Disorders 5
- RNA modifications and cancer 2
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- Genetic Neurodegenerative Diseases 5
- Hereditary Neurological Disorders 1
- Co-authors
- Gerardo Del Valle (1 shared paper)Darren G. Monckton (1 shared paper)Catherine F. Higham (1 shared paper)Tetsuo Ashizawa (1 shared paper)M.A. Ferguson‐Smith (3 shared papers)Jillian M. Couto (1 shared paper)Fernando Morales (1 shared paper)Alison Wilcox (1 shared paper)
- Journals
- Neuromuscular Disorders (3 papers)Journal of Medical Genetics (2 papers)Human Genetics (2 papers)Clinical Genetics (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomHungaryNetherlands
In The Last Decade
D.E. Wilcox
10 papers receiving 282 citations
Peers
Comparison fields: 5 of 40
- Cellular and Molecular Neuroscience 165
- Neurology 60
- Molecular Biology 250
- Genetics 26
- Cardiology and Cardiovascular Medicine 48
Countries citing papers authored by D.E. Wilcox
This map shows the geographic impact of D.E. Wilcox'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 D.E. Wilcox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D.E. Wilcox more than expected).
Fields of papers citing papers by D.E. Wilcox
This network shows the impact of papers produced by D.E. Wilcox. 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 D.E. Wilcox. The network helps show where D.E. Wilcox may publish in the future.
Co-authors
The 25 scholars most cited alongside D.E. Wilcox, 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 | 128 | |
| 2 | 1986 | 34 | |
| 3 | 2007 | 33 | |
| 4 | 2012 | 25 | |
| 5 | 1985 | 20 | |
| 6 | 2005 | 15 | |
| 7 | 1990 | 12 | |
| 8 | 1991 | 8 | |
| 9 | 2012 | 6 | |
| 10 | 1988 | 5 |
About D.E. Wilcox
D.E. Wilcox is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Surgery and Genetics, having authored 10 papers that have together received 286 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (5 papers), Muscle Physiology and Disorders (5 papers), RNA modifications and cancer (2 papers), Cardiomyopathy and Myosin Studies (2 papers), Neurological diseases and metabolism (1 paper), Hereditary Neurological Disorders (1 paper), Autopsy Techniques and Outcomes (1 paper) and Cardiovascular Effects of Exercise (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (165 citations), Neurology (60 citations), Molecular Biology (250 citations), Genetics (26 citations) and Cardiology and Cardiovascular Medicine (48 citations). D.E. Wilcox has collaborated with scholars based in United Kingdom, Hungary and Netherlands. Frequent co-authors include Gerardo Del Valle, Darren G. Monckton, Catherine F. Higham, Tetsuo Ashizawa, M.A. Ferguson‐Smith, Jillian M. Couto, Fernando Morales, Alison Wilcox, Grant Hogg and Richard H. Wilson. Their work appears in journals such as Neuromuscular Disorders, Journal of Medical Genetics, Human Genetics, Clinical Genetics and Human Molecular 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.