Daniel Perrett
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 11
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 1
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- Cancer Genomics and Diagnostics 2
- Co-authors
- Helen Firth (3 shared papers)A. Paul Bevan (2 shared papers)Simon Brent (2 shared papers)Matthew E. Hurles (2 shared papers)Julia Foreman (2 shared papers)Sarah E Hunt (2 shared papers)Caroline Fiona Wright (1 shared paper)Ganesh Jawahar Swaminathan (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Human Mutation (2 papers)Neurology (1 paper)Genetics in Medicine (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Daniel Perrett
12 papers receiving 749 citations
Daniel Perrett's Hit Papers
Peers
Comparison fields: 5 of 79
- Genetics 445
- Psychiatry and Mental health 91
- Molecular Biology 339
- Cancer Research 60
- Cellular and Molecular Neuroscience 54
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 | 2017 | 207 | |
| 2 | Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland Hit paper breakdown → | 2023 | 121 |
| 3 | 2017 | 111 | |
| 4 | 2018 | 91 | |
| 5 | 2019 | 62 | |
| 6 | 2019 | 50 | |
| 7 | 2015 | 48 | |
| 8 | 2018 | 33 | |
| 9 | 2023 | 24 | |
| 10 | 2022 | 20 | |
| 11 | 2023 | 12 | |
| 12 | Minimise transmission risk of CJD and vCJD in healthcare settings. Report on the Prevention of CJD and vCJD by Advisory Committee on Dangerous Pathogens' Transmission Spongiform Encephalopathy (ACDP TSE) Subgroup. | 2015 | 6 |
About Daniel Perrett
Daniel Perrett is a scholar working on Genetics, Cancer Research, Molecular Biology, Psychiatry and Mental health and Neurology, having authored 12 papers that have together received 785 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (2 papers), Biomedical Text Mining and Ontologies (1 paper), Neurological disorders and treatments (1 paper), Chromatin Remodeling and Cancer (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (445 citations), Psychiatry and Mental health (91 citations), Molecular Biology (339 citations), Cancer Research (60 citations) and Cellular and Molecular Neuroscience (54 citations). Daniel Perrett has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Helen Firth, A. Paul Bevan, Simon Brent, Matthew E. Hurles, Julia Foreman, Sarah E Hunt, Caroline Fiona Wright, Ganesh Jawahar Swaminathan, Erica Mazaika and James S. Ware. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, Neurology, Genetics in Medicine and European 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.