Charles M. Swanson

644 total citations
21 papers, 438 citations indexed

About

Charles M. Swanson is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Charles M. Swanson has authored 21 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Hematology and 8 papers in Genetics. Recurrent topics in Charles M. Swanson's work include Multiple Myeloma Research and Treatments (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Glycosylation and Glycoproteins Research (4 papers). Charles M. Swanson is often cited by papers focused on Multiple Myeloma Research and Treatments (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Glycosylation and Glycoproteins Research (4 papers). Charles M. Swanson collaborates with scholars based in United States and Ireland. Charles M. Swanson's co-authors include Jeffrey R. Sawyer, Janet L. Lukacs, Paula E. North, Regina Lichti Binz, Richard W. Nicholas, Bart Barlogie, Gael Sammartino, Christopher Cunniff, James R. Thomas and Edward L. Thomas and has published in prestigious journals such as Blood, Cancer and British Journal of Haematology.

In The Last Decade

Charles M. Swanson

20 papers receiving 409 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Charles M. Swanson United States 12 247 185 88 81 73 21 438
Beth A. Pitel United States 13 148 0.6× 170 0.9× 105 1.2× 53 0.7× 56 0.8× 37 442
Stéphanie Struski France 16 264 1.1× 171 0.9× 106 1.2× 76 0.9× 112 1.5× 30 596
Patrik Andreasson Sweden 9 141 0.6× 259 1.4× 58 0.7× 43 0.5× 59 0.8× 13 425
Gael Sammartino United States 9 203 0.8× 201 1.1× 37 0.4× 26 0.3× 70 1.0× 17 320
F Desangles France 9 339 1.4× 206 1.1× 83 0.9× 90 1.1× 77 1.1× 18 552
Françoise Brizard France 14 278 1.1× 343 1.9× 77 0.9× 61 0.8× 93 1.3× 33 680
Jeanne Dietz‐Band United States 8 117 0.5× 67 0.4× 63 0.7× 18 0.2× 142 1.9× 9 334
Sabine Naumann United States 9 105 0.4× 42 0.2× 29 0.3× 150 1.9× 50 0.7× 10 301
T.S.K. Wan China 13 269 1.1× 249 1.3× 99 1.1× 33 0.4× 174 2.4× 44 610
Lisbeth Haugom Norway 13 192 0.8× 35 0.2× 47 0.5× 206 2.5× 75 1.0× 19 486

Countries citing papers authored by Charles M. Swanson

Since Specialization
Citations

This map shows the geographic impact of Charles M. Swanson'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 Charles M. Swanson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles M. Swanson more than expected).

Fields of papers citing papers by Charles M. Swanson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles M. Swanson. 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 Charles M. Swanson. The network helps show where Charles M. Swanson may publish in the future.

Co-authorship network of co-authors of Charles M. Swanson

This figure shows the co-authorship network connecting the top 25 collaborators of Charles M. Swanson. A scholar is included among the top collaborators of Charles M. Swanson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Charles M. Swanson. Charles M. Swanson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sawyer, Jeffrey R., John D. Shaughnessy, Joshua Epstein, et al.. (2016). Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma. Leukemia. 31(3). 637–644. 21 indexed citations
2.
Sawyer, Jeffery R., Erming Tian, Brian A. Walker, et al.. (2016). Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC. Blood. 128(22). 3266–3266. 2 indexed citations
3.
Sawyer, Jeffrey R., Erming Tian, Christoph Heuck, et al.. (2015). Evidence of an epigenetic origin for high-risk 1q21 copy number aberrations in multiple myeloma. Blood. 125(24). 3756–3759. 39 indexed citations
4.
Sawyer, Jeffrey R., Christoph Heuck, Donald J. Johann, et al.. (2015). Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region. Clinical Lymphoma Myeloma & Leukemia. 15. e47–e47. 1 indexed citations
5.
Sawyer, Jeffrey R., Erming Tian, Christoph Heuck, et al.. (2014). Jumping translocations of 1q12 in multiple myeloma: a novel mechanism for deletion of 17p in cytogenetically defined high-risk disease. Blood. 123(16). 2504–2512. 39 indexed citations
6.
Sawyer, Jeffrey R., Erming Tian, Christoph Heuck, et al.. (2012). Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification. Blood. 120(21). 3983–3983. 1 indexed citations
7.
Sawyer, Jeffrey R., Erming Tian, John D. Shaughnessy, et al.. (2011). Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC). Blood. 118(21). 298–298. 1 indexed citations
8.
Sawyer, Jeffrey R., Erming Tian, Edward L. Thomas, et al.. (2009). Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon. British Journal of Haematology. 147(4). 484–494. 26 indexed citations
9.
Sawyer, Jeffrey R., Regina Lichti Binz, Charles M. Swanson, & Cynthia Lim. (2007). De novo proximal duplication of 1(q12q22) in a female infant with multiple congenital anomalies. American Journal of Medical Genetics Part A. 143A(4). 338–342. 15 indexed citations
10.
Sawyer, Jeffrey R., et al.. (2005). Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone. Cancer Genetics and Cytogenetics. 159(1). 32–36. 21 indexed citations
11.
Sawyer, Jeffrey R., Edward L. Thomas, Janet L. Lukacs, et al.. (2002). Recurring breakpoints of 1p13∼p22 in osteochondroma. Cancer Genetics and Cytogenetics. 138(2). 102–106. 9 indexed citations
12.
Sawyer, Jeffrey R., Janet L. Lukacs, Edward L. Thomas, et al.. (2001). Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma. British Journal of Haematology. 112(1). 167–174. 70 indexed citations
13.
Sawyer, Jeffrey R., Charles M. Swanson, Janet L. Lukacs, et al.. (1998). Evidence of an association between 6q13-21 chromosome aberrations and locally aggressive behavior in patients with cartilage tumors. Cancer. 82(3). 474–483. 56 indexed citations
14.
Sawyer, Jeffrey R., et al.. (1998). A new reciprocal translocation (12;22)(q24.3;q11.2–12) in a malignant rhabdoid tumor of the brain. Cancer Genetics and Cytogenetics. 101(1). 62–67. 19 indexed citations
15.
Sawyer, Jeffrey R., Charles M. Swanson, Janet L. Lukacs, et al.. (1997). Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome. American Journal of Medical Genetics. 69(4). 383–387. 10 indexed citations
16.
17.
Sawyer, Jeffrey R., et al.. (1995). Chromosome instability in ICF syndrome: Formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization. American Journal of Medical Genetics. 56(2). 203–209. 45 indexed citations
18.
Sawyer, Jeffrey R., Charles M. Swanson, Gary J. Roloson, Darryl C. Longee, & William M. Chadduck. (1992). Cytogenetic findings in a case of pediatric glioblastoma. Cancer Genetics and Cytogenetics. 64(1). 75–79. 11 indexed citations
19.
Sawyer, Jeffrey R., Charles M. Swanson, William M. Chadduck, & Gary J. Roloson. (1991). Evolution of tumor chromosome abnormalities after therapy in a pediatric astrocytoma. Cancer Genetics and Cytogenetics. 53(1). 119–123. 7 indexed citations
20.
Sawyer, Jeffrey R., Charles M. Swanson, Gary J. Roloson, et al.. (1991). Molecular cytogenetic analysis of a medulloblastoma with isochromosome 17 and double minutes. Cancer Genetics and Cytogenetics. 57(2). 181–186. 13 indexed citations

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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