John Pullinger
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- Genomics and Rare Diseases
Papers in
- Genetics 33
- Genomics and Rare Diseases 19
- Genetics and Neurodevelopmental Disorders 7
- Genetic and Kidney Cyst Diseases 6
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- Cancer Genomics and Diagnostics 9
- Journals
- Genetics in Medicine (11 papers)Nature Communications (6 papers)Scientific Reports (5 papers)Brain (5 papers)Nature (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
John Pullinger
58 papers receiving 2.7k citations
John Pullinger's Hit Papers
Peers
Comparison fields: 5 of 107
- Cancer Research 415
- Genetics 616
- Endocrinology 85
- Molecular Biology 1.1k
- Biotechnology 79
Countries citing papers authored by John Pullinger
This map shows the geographic impact of John Pullinger'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 John Pullinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Pullinger more than expected).
Fields of papers citing papers by John Pullinger
This network shows the impact of papers produced by John Pullinger. 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 John Pullinger. The network helps show where John Pullinger may publish in the future.
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All Works
Showing the 20 most-cited of 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli Hit paper breakdown → | 2020 | 926 |
| 2 | Substitution mutational signatures in whole-genome–sequenced cancers in the UK population Hit paper breakdown → | 2022 | 195 |
| 3 | Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme Hit paper breakdown → | 2024 | 117 |
| 4 | 2021 | 106 | |
| 5 | 2020 | 83 | |
| 6 | Origins and impact of extrachromosomal DNA Hit paper breakdown → | 2024 | 82 |
| 7 | 2020 | 81 | |
| 8 | 2021 | 55 | |
| 9 | 2022 | 54 | |
| 10 | 2023 | 51 | |
| 11 | 2022 | 48 | |
| 12 | 2022 | 47 | |
| 13 | 2021 | 44 | |
| 14 | 2023 | 44 | |
| 15 | 2020 | 38 | |
| 16 | 2020 | 38 | |
| 17 | 2022 | 38 | |
| 18 | 2020 | 37 | |
| 19 | 2022 | 35 | |
| 20 | 2022 | 32 |
About John Pullinger
John Pullinger is a scholar working on Genetics, Cancer Research, Cellular and Molecular Neuroscience, Nephrology and Molecular Biology, having authored 59 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (19 papers), Cancer Genomics and Diagnostics (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genetic and Kidney Cyst Diseases (6 papers), Genetic Neurodegenerative Diseases (4 papers), Renal Diseases and Glomerulopathies (4 papers), Hereditary Neurological Disorders (3 papers) and Retinal Development and Disorders (3 papers). The work is most often cited by research in Cancer Research (415 citations), Genetics (616 citations), Endocrinology (85 citations), Molecular Biology (1.1k citations) and Biotechnology (79 citations). John Pullinger has collaborated with scholars based in United Kingdom, United States and Germany. Their work appears in journals such as Genetics in Medicine, Nature Communications, Scientific Reports, Brain and Nature.
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.