Angela Davies
- Immunology top 2%
- Genetics top 5%
- Genetics top 1%
- Molecular Biology
- Hematology top 5%
- Co-authors
- Frances FlinterMartin BobrowLennart HammarströmChristine KinnonSmith RjhDavid VetrieIgor VořechovskýRoland J. Levinsky
- Topics
- Genomic variations and chromosomal abnormalities (19 papers)Chromosomal and Genetic Variations (9 papers)Prenatal Screening and Diagnostics (6 papers)
- Cited by
- GeneticsImmunology
- Partner nations
- United KingdomGermanyBelgium
In The Last Decade
Angela Davies
30 papers receiving 1.8k citations
Hit Papers
Peers
Comparison fields: 5 of 80
- Immunology 956
- Genetics 663
- Genetics 634
- Molecular Biology 632
- Hematology 229
Countries citing papers authored by Angela Davies
This map shows the geographic impact of Angela Davies'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 Angela Davies with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angela Davies more than expected).
Fields of papers citing papers by Angela Davies
This network shows the impact of papers produced by Angela Davies. 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 Angela Davies. The network helps show where Angela Davies may publish in the future.
Co-authorship network of co-authors of Angela Davies
This figure shows the co-authorship network connecting the top 25 collaborators of Angela Davies. A scholar is included among the top collaborators of Angela Davies 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 Angela Davies. Angela Davies is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 29 | |
| 3 | 2 | |
| 4 | 9 | |
| 5 | 0 | |
| 6 | 53 | |
| 7 | 28 | |
| 8 | 26 | |
| 9 | 1 | |
| 10 | 2 | |
| 11 | 5 | |
| 12 | 30 | |
| 13 | 0 | |
| 14 | 30 | |
| 15 | 100 | |
| 16 | 1 | |
| 17 | 26 | |
| 18 | 14 | |
| 19 | 3 | |
| 20 | The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinasesbreakdown → | 1134 |
About Angela Davies
Angela Davies is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 32 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (9 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Genetics (634 citations), Immunology (956 citations) and Genetics (663 citations). Angela Davies has collaborated with scholars based in United Kingdom, Germany and Belgium. Frequent co-authors include Frances Flinter, Martin Bobrow, Lennart Hammarström, Christine Kinnon, Smith Rjh, David Vetrie, Igor Vořechovský, Roland J. Levinsky, Jill Holland and David Bentley. Their work appears in journals such as Nature, Nucleic Acids Research and The Journal of Immunology.
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.