Peter D. Stenson
Impact in
- Genetics top 0.2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Molecular Biology top 1%
- RNA and protein synthesis mechanisms
- Genomics and Phylogenetic Studies
- RNA modifications and cancer
- Bioinformatics and Genomic Networks
Papers in
- Genetics 46
- Genomics and Rare Diseases 39
- Genomic variations and chromosomal abnormalities 19
- Genetic Associations and Epidemiology 7
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- RNA and protein synthesis mechanisms 12
- RNA modifications and cancer 10
- Genomics and Phylogenetic Studies 8
- RNA Research and Splicing 6
- Co-authors
- D.N. Cooper (63 shared papers)Edward V. Ball (14 shared papers)Matthew Mort (17 shared papers)Andrew D. Phillips (7 shared papers)Nick Thomas (4 shared papers)Michael Krawczak (6 shared papers)Katy Shaw (3 shared papers)Shaun S. Abeysinghe (4 shared papers)
- Journals
- Human Mutation (17 papers)Human Genetics (10 papers)The American Journal of Human Genetics (5 papers)Proceedings of the National Academy of Sciences (4 papers)Genome Medicine (4 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Peter D. Stenson
61 papers receiving 8.8k citations
Peter D. Stenson's Hit Papers
Peers
Comparison fields: 5 of 158
- Genetics 4.0k
- Molecular Biology 5.7k
- Cancer Research 1.1k
- Clinical Biochemistry 287
- Genetics 366
Countries citing papers authored by Peter D. Stenson
This map shows the geographic impact of Peter D. Stenson'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 Peter D. Stenson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter D. Stenson more than expected).
Fields of papers citing papers by Peter D. Stenson
This network shows the impact of papers produced by Peter D. Stenson. 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 Peter D. Stenson. The network helps show where Peter D. Stenson may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter D. Stenson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human Gene Mutation Database (HGMD®): 2003 update Hit paper breakdown → | 2003 | 1356 |
| 2 | The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine Hit paper breakdown → | 2013 | 955 |
| 3 | 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 | 921 |
| 4 | Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models Hit paper breakdown → | 2012 | 899 |
| 5 | The Human Gene Mutation Database: 2008 update Hit paper breakdown → | 2009 | 630 |
| 6 | M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity Hit paper breakdown → | 2016 | 512 |
| 7 | The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting Hit paper breakdown → | 2020 | 410 |
| 8 | 2013 | 376 | |
| 9 | 2015 | 242 | |
| 10 | 2000 | 212 | |
| 11 | 2012 | 188 | |
| 12 | 2012 | 177 | |
| 13 | 2005 | 174 | |
| 14 | 2005 | 121 | |
| 15 | 2005 | 116 | |
| 16 | 2013 | 112 | |
| 17 | 2004 | 104 | |
| 18 | 2010 | 103 | |
| 19 | 2015 | 88 | |
| 20 | 2008 | 78 |
About Peter D. Stenson
Peter D. Stenson is a scholar working on Genetics, Molecular Biology, Cancer Research, Plant Science and Cellular and Molecular Neuroscience, having authored 63 papers that have together received 8.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (39 papers), Genomic variations and chromosomal abnormalities (19 papers), Cancer Genomics and Diagnostics (14 papers), RNA and protein synthesis mechanisms (12 papers), RNA modifications and cancer (10 papers), Genomics and Phylogenetic Studies (8 papers), Genetic Associations and Epidemiology (7 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Genetics (4.0k citations), Molecular Biology (5.7k citations), Cancer Research (1.1k citations), Clinical Biochemistry (287 citations) and Genetics (366 citations). Peter D. Stenson has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include D.N. Cooper, Edward V. Ball, Matthew Mort, Andrew D. Phillips, Nick Thomas, Michael Krawczak, Katy Shaw, Shaun S. Abeysinghe, Matthew Hayden and Sally Heywood. Their work appears in journals such as Human Mutation, Human Genetics, The American Journal of Human Genetics, Proceedings of the National Academy of Sciences and Genome Medicine.
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.