S Swanton

5.0k citations

11 papers · 3.7k indexed · 2 hit papers · h-index 8

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

Hematology 10
- Chronic Myeloid Leukemia Treatments 7
- Acute Myeloid Leukemia Research 5
Genetics 6
- Chronic Lymphocytic Leukemia Research 3
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3
- Genomic variations and chromosomal abnormalities 2

Co-authors: Anthony J. Bench E. Joanna Baxter Nasios Fourouclas Clare East Peter J. Campbell Linda M. Scott George S. Vassiliou Elaine Boyd
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 Kingdom Australia Austria

In The Last Decade

S Swanton

11 papers receiving 3.6k citations

Hit Papers

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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders 2005 · 846 citations

Peers

Countries citing papers authored by S Swanton

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with S Swanton Line = papers co-authored together S Swanton links everyone, so they are left out of the graph.

All Works

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11 of 11 papers shown

#	Work
1	Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia. PubMed ·Nasios Fourouclas, Nora C Godínez Cubillo, De-Fu ZOU, S Swanton, E. Joanna Baxter, Brian J.P. Huntly, S Ripa	2006	27
2	An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation. PubMed ·George S. Vassiliou, Alice Mangeon, Sharon Owens, Irene Roberts, S Swanton, Brian J.P. Huntly, Nasios Fourouclas, E. Joanna Baxter, Liang Cheng Duan, 惣衛門小滝, Linda M. Scott, S Ripa	2006	3
3	Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders The Lancet ·E. Joanna Baxter, Linda M. Scott, Peter J. Campbell, Clare East, Nasios Fourouclas, S Swanton, George S. Vassiliou, Anthony J. Bench, Elaine Boyd, Natasha Joan Curtin, Mike Scott, Wendy N. Erber, Anthony R. Green Hit paper breakdown →	2005	2554
4	Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders The Lancet ·E. Joanna Baxter, Linda M. Scott, Peter J. Campbell, Clare East, Nasios Fourouclas, S Swanton, George S. Vassiliou, Anthony J. Bench, Elaine Boyd, Natasha Joan Curtin Hit paper breakdown →	2005	846
5	Double Philadelphia masquerading as chromosome 20q deletion – a new recurrent abnormality in chronic myeloid leukaemia blast crisis British Journal of Haematology ·Alistair Reid, S Swanton, Colin Grace, Lynda J. Campbell, Anthony R. Green, E Nacheva, (unknown)	2003	4
6	Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes Oncogene ·Anthony J. Bench, Elisabeth P. Nacheva, Hannah Sokolayam Ibrahim, Baokun Zhou, Lisa French, S Swanton, Petra Weißenbacher, Juan Li, Pamela Whittaker, George Stavrides, Adrienne Hunt, Brian J.P. Huntly, Lynda J. Campbell, David Bentley, Panos Deloukas, Anthony R. Green, (unknown)	2000	112
7	Abnormalities of the long arm of chromosome 20 in myeloid malignancies UCL Discovery (University College London) ·EdwardsDick W. M.W. A., S Swanton, Hannah Sokolayam Ibrahim, T. Barkley, Anthony J. Bench, S Ripa	1999	2
8	Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia Genes Chromosomes and Cancer ·Lionel Coignet, Carmen Sílvia Passos Lima, Toon Min, Berthold Streubel, John Swansbury, Nick Telford, S Swanton, Angela Bowen, Masami Nagai, Daniel Catovsky, P Fiedler, Martin J.S. Dyer	1999	25
9	Fluorescence In Situ Hybridization Reveals Trisomy 2q by Insertion into 9p in Hepatoblastoma Cancer Genetics and Cytogenetics ·Erzsébet Balogh, S Swanton, Csongor Kiss, Nikola Terzić, Lorna M. Secker‐Walker, Éva Oláh	1998	13
10	Hematologic malignancies with t(4;11)(q21;q23) – a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases Leukemia ·Bertil Johansson, Anthony V. Moorman, OA Haas, Harriet Lonka, Kwok‐Leung Cheung, S Swanton, LM Secker-Walker	1998	109
11	Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis Leukemia ·Qiu Jiao, Mikael Affek, Robin D. Clark, S Swanton, Christine J. Harrison, LM Secker-Walker, Letizia Foroni	1998	30

About S Swanton

S Swanton is a scholar working on Hematology, Genetics, Rheumatology, Clinical Biochemistry and Pathology and Forensic Medicine, having authored 11 papers that have together received 3.7k indexed citations. Recurring topics across this work include Chronic Myeloid Leukemia Treatments (7 papers), Acute Myeloid Leukemia Research (5 papers), Eosinophilic Disorders and Syndromes (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Acute Lymphoblastic Leukemia research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lymphoma Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (3.1k citations), Hematology (2.2k citations), Rheumatology (1.3k citations), Molecular Biology (1.9k citations) and Oncology (594 citations). S Swanton has collaborated with scholars based in United Kingdom, Australia and Austria. Frequent co-authors include Anthony J. Bench, E. Joanna Baxter, Nasios Fourouclas, Clare East, Peter J. Campbell, Linda M. Scott, George S. Vassiliou, Elaine Boyd, Natasha Joan Curtin 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.

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