Jon W. Teague
Impact in
- Cancer Research top 0.01%
- Cancer Genomics and Diagnostics
- Hematology top 0.05%
- Acute Myeloid Leukemia Research
Papers in
-
- Cancer Genomics and Diagnostics 64
- Genetics 41
- Genomics and Rare Diseases 17
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 9
- Co-authors
- Michael R. Stratton (13 shared papers)Simon Andrew Forbes (11 shared papers)Sally Bamford (9 shared papers)Chai Yin Kok (7 shared papers)Elisabeth Dawson (4 shared papers)Jody Clements (3 shared papers)Peter J. Campbell (8 shared papers)Charlotte G. Cole (6 shared papers)
- Journals
- Nature (22 papers)Nature Genetics (18 papers)Nature Communications (16 papers)The American Journal of Human Genetics (7 papers)Cell (6 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Jon W. Teague
118 papers receiving 67.1k citations
Jon W. Teague's Hit Papers
Peers
Comparison fields: 5 of 188
- Cancer Research 21.7k
- Hematology 8.1k
- Oncology 16.6k
- Genetics 5.7k
- Molecular Biology 37.1k
Countries citing papers authored by Jon W. Teague
This map shows the geographic impact of Jon W. Teague'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 Jon W. Teague with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jon W. Teague more than expected).
Fields of papers citing papers by Jon W. Teague
This network shows the impact of papers produced by Jon W. Teague. 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 Jon W. Teague. The network helps show where Jon W. Teague may publish in the future.
Co-authors
The 25 scholars most cited alongside Jon W. Teague, 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 120 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 | Signatures of mutational processes in human cancer Hit paper breakdown → | 2013 | 7583 |
| 3 | Genomic Classification and Prognosis in Acute Myeloid Leukemia Hit paper breakdown → | 2016 | 3337 |
| 4 | Patterns of somatic mutation in human cancer genomes Hit paper breakdown → | 2007 | 2484 |
| 5 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 6 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 7 | COSMIC: exploring the world's knowledge of somatic mutations in human cancer Hit paper breakdown → | 2014 | 1913 |
| 8 | Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development Hit paper breakdown → | 2011 | 1872 |
| 9 | International network of cancer genome projects Hit paper breakdown → | 2010 | 1836 |
| 10 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences Hit paper breakdown → | 2016 | 1649 |
| 11 | Clinical and biological implications of driver mutations in myelodysplastic syndromes Hit paper breakdown → | 2013 | 1540 |
| 12 | Mutational Processes Molding the Genomes of 21 Breast Cancers Hit paper breakdown → | 2012 | 1476 |
| 13 | Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2 Hit paper breakdown → | 2013 | 1461 |
| 14 | The landscape of cancer genes and mutational processes in breast cancer Hit paper breakdown → | 2012 | 1403 |
| 15 | A comprehensive catalogue of somatic mutations from a human cancer genome Hit paper breakdown → | 2009 | 1340 |
| 16 | The Life History of 21 Breast Cancers Hit paper breakdown → | 2012 | 1092 |
| 17 | The patterns and dynamics of genomic instability in metastatic pancreatic cancer Hit paper breakdown → | 2010 | 1086 |
| 18 | Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma Hit paper breakdown → | 2011 | 1055 |
| 19 | SomaticSF3B1Mutation in Myelodysplasia with Ring Sideroblasts Hit paper breakdown → | 2011 | 1036 |
| 20 | The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website Hit paper breakdown → | 2004 | 1025 |
About Jon W. Teague
Jon W. Teague is a scholar working on Cancer Research, Genetics, Pathology and Forensic Medicine, Molecular Biology and Pulmonary and Respiratory Medicine, having authored 120 papers that have together received 68.4k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (64 papers), Genetic factors in colorectal cancer (23 papers), Genomics and Rare Diseases (17 papers), Genomics and Phylogenetic Studies (16 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Genomics and Chromatin Dynamics (9 papers) and Lung Cancer Treatments and Mutations (8 papers). The work is most often cited by research in Cancer Research (21.7k citations), Hematology (8.1k citations), Oncology (16.6k citations), Genetics (5.7k citations) and Molecular Biology (37.1k citations). Jon W. Teague has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Michael R. Stratton, Simon Andrew Forbes, Sally Bamford, Chai Yin Kok, Elisabeth Dawson, Jody Clements, Peter J. Campbell, Charlotte G. Cole, Nidhi Bindal and Mingming Jia. 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.