Daniel Perrett
Impact in
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 3
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 2
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- Biomedical Text Mining and Ontologies 1
- Congenital heart defects research 1
- Co-authors
- Helen V. Firth (3 shared papers)Simon Brent (2 shared papers)A. Paul Bevan (2 shared papers)Matthew E. Hurles (2 shared papers)Sarah Hunt (2 shared papers)Julia Foreman (2 shared papers)Caroline F. Wright (1 shared paper)G. Jawahar Swaminathan (1 shared paper)
- Partner nations
- United KingdomRussia
In The Last Decade
Daniel Perrett
3 papers receiving 51 citations
Peers
Comparison fields: 5 of 22
- Genetics 46
- Health Informatics 2
- Cancer Research 16
- Aging 1
- Pediatrics, Perinatology and Child Health 5
Countries citing papers authored by Daniel Perrett
This map shows the geographic impact of Daniel Perrett'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 Daniel Perrett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Perrett more than expected).
Fields of papers citing papers by Daniel Perrett
This network shows the impact of papers produced by Daniel Perrett. 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 Daniel Perrett. The network helps show where Daniel Perrett may publish in the future.
Co-authors
The 11 scholars most cited alongside Daniel Perrett, 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 | 2015 | 38 | |
| 2 | 2023 | 14 | |
| 3 | 2022 | 13 |
About Daniel Perrett
Daniel Perrett is a scholar working on Genetics, Molecular Biology, Cancer Research, Infectious Diseases and Organic Chemistry, having authored 3 papers that have together received 65 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Cancer Genomics and Diagnostics (2 papers), Biomedical Text Mining and Ontologies (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (46 citations), Health Informatics (2 citations), Cancer Research (16 citations), Aging (1 citation) and Pediatrics, Perinatology and Child Health (5 citations). Daniel Perrett has collaborated with scholars based in United Kingdom and Russia. Frequent co-authors include Helen V. Firth, Simon Brent, A. Paul Bevan, Matthew E. Hurles, Sarah Hunt, Julia Foreman, Caroline F. Wright, G. Jawahar Swaminathan, Erica Mazaika and Fiona Cunningham. Their work appears in journals such as Human Mutation and Annual Review of Genomics and 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.