Michael R. Stratton
Impact in
- Cancer Research top 0.01%
- Cancer Genomics and Diagnostics
- Genetics top 0.02%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
-
- DNA Repair Mechanisms 27
- Genomics and Phylogenetic Studies 11
- Genetics 88
- BRCA gene mutations in cancer 43
- Genomic variations and chromosomal abnormalities 24
- Genomics and Rare Diseases 13
- Co-authors
- P. Andrew Futreal (51 shared papers)Peter J. Campbell (44 shared papers)Nazneen Rahman (30 shared papers)Richard Wooster (29 shared papers)Ludmil B. Alexandrov (18 shared papers)Simon Forbes (18 shared papers)Sally Bamford (14 shared papers)Nidhi Bindal (11 shared papers)
- Journals
- Nature Genetics (20 papers)Cancer Research (11 papers)Nature (11 papers)British Journal of Cancer (10 papers)Journal of Clinical Oncology (7 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Michael R. Stratton
211 papers receiving 39.3k citations
Michael R. Stratton's Hit Papers
Peers
Comparison fields: 5 of 189
- Cancer Research 12.2k
- Genetics 9.6k
- Oncology 8.7k
- Molecular Biology 20.8k
- Pathology and Forensic Medicine 5.0k
Countries citing papers authored by Michael R. Stratton
This map shows the geographic impact of Michael R. Stratton'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 Michael R. Stratton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael R. Stratton more than expected).
Fields of papers citing papers by Michael R. Stratton
This network shows the impact of papers produced by Michael R. Stratton. 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 Michael R. Stratton. The network helps show where Michael R. Stratton may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael R. Stratton, 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 221 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells Hit paper breakdown → | 2012 | 2692 |
| 2 | The cancer genome Hit paper breakdown → | 2009 | 2371 |
| 3 | A census of human cancer genes Hit paper breakdown → | 2004 | 2220 |
| 4 | COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer Hit paper breakdown → | 2010 | 1722 |
| 5 | COSMIC: exploring the world's knowledge of somatic mutations in human cancer Hit paper breakdown → | 2014 | 1703 |
| 6 | High burden and pervasive positive selection of somatic mutations in normal human skin Hit paper breakdown → | 2015 | 1151 |
| 7 | The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website Hit paper breakdown → | 2004 | 939 |
| 8 | JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis Hit paper breakdown → | 2007 | 905 |
| 9 | BRAF and RAS mutations in human lung cancer and melanoma. Hit paper breakdown → | 2002 | 843 |
| 10 | Universal Patterns of Selection in Cancer and Somatic Tissues Hit paper breakdown → | 2017 | 828 |
| 11 | Deciphering Signatures of Mutational Processes Operative in Human Cancer Hit paper breakdown → | 2013 | 742 |
| 12 | Mutational signatures associated with tobacco smoking in human cancer Hit paper breakdown → | 2016 | 696 |
| 13 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Hit paper breakdown → | 2006 | 691 |
| 14 | Somatic mutant clones colonize the human esophagus with age Hit paper breakdown → | 2018 | 672 |
| 15 | Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast Cancer Hit paper breakdown → | 1999 | 664 |
| 16 | The Catalogue of Somatic Mutations in Cancer (COSMIC) Hit paper breakdown → | 2008 | 660 |
| 17 | Tumor Exome Analysis Reveals Neoantigen-Specific T-Cell Reactivity in an Ipilimumab-Responsive Melanoma Hit paper breakdown → | 2013 | 627 |
| 18 | Clock-like mutational processes in human somatic cells Hit paper breakdown → | 2015 | 582 |
| 19 | High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma Hit paper breakdown → | 2014 | 528 |
| 20 | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 515 |
About Michael R. Stratton
Michael R. Stratton is a scholar working on Molecular Biology, Genetics, Cancer Research, Pathology and Forensic Medicine and Oncology, having authored 221 papers that have together received 40.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (71 papers), BRCA gene mutations in cancer (43 papers), Genetic factors in colorectal cancer (39 papers), DNA Repair Mechanisms (27 papers), Genomic variations and chromosomal abnormalities (24 papers), Genomics and Rare Diseases (13 papers), Genomics and Phylogenetic Studies (11 papers) and Cancer-related Molecular Pathways (10 papers). The work is most often cited by research in Cancer Research (12.2k citations), Genetics (9.6k citations), Oncology (8.7k citations), Molecular Biology (20.8k citations) and Pathology and Forensic Medicine (5.0k citations). Michael R. Stratton has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include P. Andrew Futreal, Peter J. Campbell, Nazneen Rahman, Richard Wooster, Ludmil B. Alexandrov, Simon Forbes, Sally Bamford, Nidhi Bindal, Serena Nik‐Zainal and Douglas F. Easton. Their work appears in journals such as Nature Genetics, Cancer Research, Nature, British Journal of Cancer and Journal of Clinical Oncology.
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.