Katy Evans
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- Genomics and Phylogenetic Studies
- RNA Research and Splicing
Papers in
- Genetics 2
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 1
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- Cancer Genomics and Diagnostics 2
- Co-authors
- Andrew D. Phillips (2 shared papers)Edward V. Ball (2 shared papers)D.N. Cooper (2 shared papers)Matthew Hayden (2 shared papers)Sally Heywood (2 shared papers)Matthew Mort (2 shared papers)Peter D. Stenson (2 shared papers)Michelle Hussain (1 shared paper)
- Journals
- Human Genetics (2 papers)
- Partner nations
- United KingdomPortugal
In The Last Decade
Katy Evans
2 papers receiving 1.4k citations
Katy Evans's Hit Papers
Peers
Comparison fields: 5 of 86
- Genetics 454
- Molecular Biology 695
- Sensory Systems 40
- Clinical Biochemistry 47
- Genetics 68
Countries citing papers authored by Katy Evans
This map shows the geographic impact of Katy Evans'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 Katy Evans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katy Evans more than expected).
Fields of papers citing papers by Katy Evans
This network shows the impact of papers produced by Katy Evans. 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 Katy Evans. The network helps show where Katy Evans may publish in the future.
Co-authors
The 10 scholars most cited alongside Katy Evans, 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 | The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies Hit paper breakdown → | 2017 | 934 |
| 2 | The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting Hit paper breakdown → | 2020 | 435 |
About Katy Evans
Katy Evans is a scholar working on Genetics, Cancer Research, Molecular Biology, Infectious Diseases and Organic Chemistry, having authored 2 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Cancer Genomics and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (454 citations), Molecular Biology (695 citations), Sensory Systems (40 citations), Clinical Biochemistry (47 citations) and Genetics (68 citations). Katy Evans has collaborated with scholars based in United Kingdom and Portugal. Frequent co-authors include Andrew D. Phillips, Edward V. Ball, D.N. Cooper, Matthew Hayden, Sally Heywood, Matthew Mort, Peter D. Stenson, Michelle Hussain, Luı́sa Azevedo and David Millar. Their work appears in journals such as Human 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.