Michael R. Stratton
Impact in
- Cancer Research top 0.01%
- Cancer Genomics and Diagnostics
- Genetics top 0.01%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
Papers in
- Cancer Research 164
- Cancer Genomics and Diagnostics 154
- Genetics 158
- BRCA gene mutations in cancer 65
- Genomic variations and chromosomal abnormalities 37
- Genomics and Rare Diseases 24
- Co-authors
- P. Andrew Futreal (45 shared papers)Peter J. Campbell (39 shared papers)Nazneen Rahman (30 shared papers)Ludmil B. Alexandrov (18 shared papers)Richard Wooster (28 shared papers)Simon Andrew Forbes (14 shared papers)Sally Bamford (12 shared papers)Serena Nik-Zainal (12 shared papers)
- Journals
- Nature (60 papers)Nature Genetics (56 papers)Nature Communications (28 papers)The American Journal of Human Genetics (19 papers)Cell (12 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Michael R. Stratton
397 papers receiving 140.1k citations
Michael R. Stratton's Hit Papers
Peers
Comparison fields: 5 of 216
- Cancer Research 41.2k
- Genetics 35.5k
- Oncology 31.9k
- Molecular Biology 70.7k
- Pathology and Forensic Medicine 16.8k
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 406 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations of the BRAF gene in human cancer Hit paper breakdown → | 2002 | 8778 |
| 2 | Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls Hit paper breakdown → | 2007 | 7865 |
| 3 | Signatures of mutational processes in human cancer Hit paper breakdown → | 2013 | 7583 |
| 4 | Identification of the breast cancer susceptibility gene BRCA2 Hit paper breakdown → | 1995 | 2921 |
| 5 | Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells Hit paper breakdown → | 2012 | 2903 |
| 6 | The cancer genome Hit paper breakdown → | 2009 | 2645 |
| 7 | Patterns of somatic mutation in human cancer genomes Hit paper breakdown → | 2007 | 2484 |
| 8 | A census of human cancer genes Hit paper breakdown → | 2004 | 2481 |
| 9 | Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families Hit paper breakdown → | 1998 | 2460 |
| 10 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 11 | Systematic identification of genomic markers of drug sensitivity in cancer cells Hit paper breakdown → | 2012 | 1947 |
| 12 | Prospective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients Hit paper breakdown → | 2015 | 1939 |
| 13 | COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer Hit paper breakdown → | 2010 | 1919 |
| 14 | Genome-wide association study identifies novel breast cancer susceptibility loci Hit paper breakdown → | 2007 | 1916 |
| 15 | COSMIC: exploring the world's knowledge of somatic mutations in human cancer Hit paper breakdown → | 2014 | 1913 |
| 16 | Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development Hit paper breakdown → | 2011 | 1872 |
| 17 | International network of cancer genome projects Hit paper breakdown → | 2010 | 1836 |
| 18 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences Hit paper breakdown → | 2016 | 1649 |
| 19 | Clinical and biological implications of driver mutations in myelodysplastic syndromes Hit paper breakdown → | 2013 | 1540 |
| 20 | Localization of a Breast Cancer Susceptibility Gene, BRCA2 , to Chromosome 13q12-13 Hit paper breakdown → | 1994 | 1528 |
About Michael R. Stratton
Michael R. Stratton is a scholar working on Cancer Research, Genetics, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 406 papers that have together received 143.8k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (154 papers), Genetic factors in colorectal cancer (72 papers), BRCA gene mutations in cancer (65 papers), DNA Repair Mechanisms (47 papers), Genomic variations and chromosomal abnormalities (37 papers), Genomics and Chromatin Dynamics (26 papers), Genomics and Rare Diseases (24 papers) and Epigenetics and DNA Methylation (24 papers). The work is most often cited by research in Cancer Research (41.2k citations), Genetics (35.5k citations), Oncology (31.9k citations), Molecular Biology (70.7k citations) and Pathology and Forensic Medicine (16.8k 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, Ludmil B. Alexandrov, Richard Wooster, Simon Andrew Forbes, Sally Bamford, Serena Nik-Zainal, Nidhi Bindal and Douglas F. Easton. Their work appears in journals such as Nature, Nature Genetics, Nature Communications, The American Journal of Human Genetics and Cell.
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.