Catherine Roughley
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Ophthalmology top 5%
- Retinal Diseases and Treatments
Papers in
- Genetics 6
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
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- Medical Imaging and Pathology Studies 2
- Pulmonary Hypertension Research and Treatments 2
- Co-authors
- Nauman M. Butt (1 shared paper)Tim C. P. Somervaille (1 shared paper)Ciro Roberto Rinaldi (1 shared paper)Mamta Krishnan Garg (1 shared paper)Adam J. Mead (1 shared paper)David L. Tucker (1 shared paper)Sam Ackroyd (1 shared paper)John R. Murphy (1 shared paper)
- Journals
- The American Journal of Human Genetics (5 papers)Nature (2 papers)Blood (1 paper)Scientific Reports (1 paper)Circulation Genomic and Precision Medicine (1 paper)
- Partner nations
- United KingdomBelgiumUnited States
In The Last Decade
Catherine Roughley
14 papers receiving 1.5k citations
Catherine Roughley's Hit Papers
Peers
Comparison fields: 5 of 93
- Genetics 494
- Ophthalmology 101
- Clinical Biochemistry 75
- Molecular Biology 711
- Hematology 95
Countries citing papers authored by Catherine Roughley
This map shows the geographic impact of Catherine Roughley'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 Roughley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine Roughley more than expected).
Fields of papers citing papers by Catherine Roughley
This network shows the impact of papers produced by Catherine Roughley. 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 Roughley. The network helps show where Catherine Roughley may publish in the future.
Co-authors
The 10 scholars most cited alongside Catherine Roughley, 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 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 395 |
| 2 | 2016 | 379 | |
| 3 | 2020 | 174 | |
| 4 | 2019 | 172 | |
| 5 | 2017 | 112 | |
| 6 | 2018 | 53 | |
| 7 | 2019 | 50 | |
| 8 | 2018 | 50 | |
| 9 | 2016 | 46 | |
| 10 | 2020 | 34 | |
| 11 | 2018 | 31 | |
| 12 | 2022 | 28 | |
| 13 | 2017 | 24 | |
| 14 | 2022 | 5 |
About Catherine Roughley
Catherine Roughley is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Molecular Biology, Pathology and Forensic Medicine and Immunology and Allergy, having authored 14 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (2 papers), Genetic factors in colorectal cancer (2 papers), Medical Imaging and Pathology Studies (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Pulmonary Hypertension Research and Treatments (2 papers), Cancer Genomics and Diagnostics (1 paper) and Genomics and Phylogenetic Studies (1 paper). The work is most often cited by research in Genetics (494 citations), Ophthalmology (101 citations), Clinical Biochemistry (75 citations), Molecular Biology (711 citations) and Hematology (95 citations). Catherine Roughley has collaborated with scholars based in United Kingdom, Belgium and United States. Frequent co-authors include Nauman M. Butt, Tim C. P. Somervaille, Ciro Roberto Rinaldi, Mamta Krishnan Garg, Adam J. Mead, David L. Tucker, Sam Ackroyd, John R. Murphy, Claire Harrison and Joanne C Ewing. Their work appears in journals such as The American Journal of Human Genetics, Nature, Blood, Scientific Reports and Circulation Genomic and Precision Medicine.
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.