Elizabeth Ormondroyd
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
-
- Cardiomyopathy and Myosin Studies
- Cardiac electrophysiology and arrhythmias
Papers in
- Genetics 18
- Genomics and Rare Diseases 12
- BRCA gene mutations in cancer 10
- Genomic variations and chromosomal abnormalities 3
-
- Cardiomyopathy and Myosin Studies 6
- Cardiovascular Effects of Exercise 2
- Co-authors
- Hugh Watkins (14 shared papers)Michael Parker (3 shared papers)Michael P. Mackley (6 shared papers)Edward Blair (6 shared papers)Maggie Watson (4 shared papers)Rosalind A. Eeles (4 shared papers)Clare Moynihan (4 shared papers)Benjamin Fletcher (1 shared paper)
- Journals
- European Journal of Human Genetics (9 papers)Genetics in Medicine (3 papers)Journal of Cardiovascular Magnetic Resonance (2 papers)Circulation Genomic and Precision Medicine (1 paper)Genomics (1 paper)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Elizabeth Ormondroyd
30 papers receiving 910 citations
Peers
Comparison fields: 5 of 80
- Genetics 407
- Cardiology and Cardiovascular Medicine 184
- Pediatrics, Perinatology and Child Health 111
- Reproductive Medicine 46
- Public Health, Environmental and Occupational Health 121
Countries citing papers authored by Elizabeth Ormondroyd
This map shows the geographic impact of Elizabeth Ormondroyd'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 Elizabeth Ormondroyd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elizabeth Ormondroyd more than expected).
Fields of papers citing papers by Elizabeth Ormondroyd
This network shows the impact of papers produced by Elizabeth Ormondroyd. 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 Elizabeth Ormondroyd. The network helps show where Elizabeth Ormondroyd may publish in the future.
Co-authors
The 25 scholars most cited alongside Elizabeth Ormondroyd, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 110 | |
| 2 | 1994 | 82 | |
| 3 | 2011 | 73 | |
| 4 | 2013 | 66 | |
| 5 | 2018 | 66 | |
| 6 | 2013 | 56 | |
| 7 | A new member of the DP family, DP-3, with distinct protein products suggests a regulatory role for alternative splicing in the cell cycle transcription factor DRTF1/E2F. | 1995 | 51 |
| 8 | 2016 | 49 | |
| 9 | 2017 | 47 | |
| 10 | 1991 | 42 | |
| 11 | 2007 | 37 | |
| 12 | 2021 | 30 | |
| 13 | 2018 | 26 | |
| 14 | 2019 | 23 | |
| 15 | 2017 | 23 | |
| 16 | 1994 | 23 | |
| 17 | 2008 | 15 | |
| 18 | 2020 | 15 | |
| 19 | 2017 | 15 | |
| 20 | 2022 | 15 |
About Elizabeth Ormondroyd
Elizabeth Ormondroyd is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Molecular Biology, Public Health, Environmental and Occupational Health and Cancer Research, having authored 31 papers that have together received 939 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (10 papers), Cancer Genomics and Diagnostics (6 papers), Cardiomyopathy and Myosin Studies (6 papers), Ethics in Clinical Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Cardiovascular Effects of Exercise (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (407 citations), Cardiology and Cardiovascular Medicine (184 citations), Pediatrics, Perinatology and Child Health (111 citations), Reproductive Medicine (46 citations) and Public Health, Environmental and Occupational Health (121 citations). Elizabeth Ormondroyd has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Hugh Watkins, Michael Parker, Michael P. Mackley, Edward Blair, Maggie Watson, Rosalind A. Eeles, Clare Moynihan, Benjamin Fletcher, Jenny C. Taylor and N B La Thangue. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Journal of Cardiovascular Magnetic Resonance, Circulation Genomic and Precision Medicine and Genomics.
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.