S Swanton
Impact in
- Genetics top 0.1%
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Chronic Lymphocytic Leukemia Research
- Hematology top 0.2%
- Chronic Myeloid Leukemia Treatments
- Acute Myeloid Leukemia Research
Papers in
-
- Chronic Myeloid Leukemia Treatments 6
- Acute Myeloid Leukemia Research 5
- Genetics 6
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3
- Chronic Lymphocytic Leukemia Research 3
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Anthony J. Bench (4 shared papers)Nasios Fourouclas (4 shared papers)E. Joanna Baxter (4 shared papers)Natasha Joan Curtin (2 shared papers)Linda M. Scott (3 shared papers)George S. Vassiliou (3 shared papers)Elaine Boyd (2 shared papers)Peter J. Campbell (2 shared papers)
- Journals
- The Lancet (2 papers)Leukemia (2 papers)British Journal of Haematology (1 paper)Oncogene (1 paper)Genes Chromosomes and Cancer (1 paper)
- Partner nations
- United KingdomAustriaAustralia
In The Last Decade
S Swanton
11 papers receiving 3.8k citations
S Swanton's Hit Papers
Peers
Comparison fields: 5 of 63
- Genetics 3.2k
- Hematology 2.1k
- Rheumatology 1.1k
- Molecular Biology 1.6k
- Oncology 564
Countries citing papers authored by S Swanton
This map shows the geographic impact of S Swanton'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 S Swanton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S Swanton more than expected).
Fields of papers citing papers by S Swanton
This network shows the impact of papers produced by S Swanton. 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 S Swanton. The network helps show where S Swanton may publish in the future.
Co-authors
The 25 scholars most cited alongside S Swanton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders Hit paper breakdown → | 2005 | 2663 |
| 2 | Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders Hit paper breakdown → | 2005 | 907 |
| 3 | 1998 | 120 | |
| 4 | 2000 | 117 | |
| 5 | 1998 | 30 | |
| 6 | Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia. | 2006 | 27 |
| 7 | 1999 | 26 | |
| 8 | 1998 | 16 | |
| 9 | 2003 | 4 | |
| 10 | An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation. | 2006 | 3 |
| 11 | Abnormalities of the long arm of chromosome 20 in myeloid malignancies | 1999 | 1 |
About S Swanton
S Swanton is a scholar working on Hematology, Genetics, Molecular Biology, Pathology and Forensic Medicine and Rheumatology, having authored 11 papers that have together received 3.9k indexed citations. Recurring topics across this work include Chronic Myeloid Leukemia Treatments (6 papers), Acute Myeloid Leukemia Research (5 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), Acute Lymphoblastic Leukemia research (2 papers), Lymphoma Diagnosis and Treatment (2 papers), Eosinophilic Disorders and Syndromes (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (3.2k citations), Hematology (2.1k citations), Rheumatology (1.1k citations), Molecular Biology (1.6k citations) and Oncology (564 citations). S Swanton has collaborated with scholars based in United Kingdom, Austria and Australia. Frequent co-authors include Anthony J. Bench, Nasios Fourouclas, E. Joanna Baxter, Natasha Joan Curtin, Linda M. Scott, George S. Vassiliou, Elaine Boyd, Peter J. Campbell, Clare East and Anthony R. Green. Their work appears in journals such as The Lancet, Leukemia, British Journal of Haematology, Oncogene and Genes Chromosomes and Cancer.
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.