Stephen Clayton
- Genetics top 2%
- Molecular Biology top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Cancer Research
- Plant Science
- Co-authors
- Diana RajanHelen V. FirthManuel CorpasA. Paul BevanNigel P. CarterYves MoreauShola M. RichardsSteven Van Vooren
- Topics
- Genomic variations and chromosomal abnormalities (5 papers)Genomics and Rare Diseases (3 papers)Chromosomal and Genetic Variations (2 papers)
- Partner nations
- United KingdomBelgiumEstonia
In The Last Decade
Stephen Clayton
7 papers receiving 1.4k citations
Hit Papers
Peers
Comparison fields: 5 of 87
- Genetics 1.1k
- Molecular Biology 751
- Pediatrics, Perinatology and Child Health 166
- Cancer Research 151
- Plant Science 107
Countries citing papers authored by Stephen Clayton
This map shows the geographic impact of Stephen Clayton'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 Stephen Clayton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen Clayton more than expected).
Fields of papers citing papers by Stephen Clayton
This network shows the impact of papers produced by Stephen Clayton. 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 Stephen Clayton. The network helps show where Stephen Clayton may publish in the future.
Co-authorship network of co-authors of Stephen Clayton
This figure shows the co-authorship network connecting the top 25 collaborators of Stephen Clayton. A scholar is included among the top collaborators of Stephen Clayton based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephen Clayton. Stephen Clayton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 193 | |
| 3 | 7 | |
| 4 | 10 | |
| 5 | 4 | |
| 6 | 29 | |
| 7 | DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resourcesbreakdown → | 1200 |
About Stephen Clayton
Stephen Clayton is a scholar working on Sensory Systems, Genetics and Cancer Research, having authored 7 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (751 citations) and Cancer Research (151 citations). Stephen Clayton has collaborated with scholars based in United Kingdom, Belgium and Estonia. Frequent co-authors include Diana Rajan, Helen V. Firth, Manuel Corpas, A. Paul Bevan, Nigel P. Carter, Yves Moreau, Shola M. Richards, Steven Van Vooren, Tomas Fitzgerald and Rosemary E. Kelsell. Their work appears in journals such as Bioinformatics, PLoS ONE and The American Journal of 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.