Lesley Mathews

2.2k total citations
21 papers, 1.4k citations indexed

About

Lesley Mathews is a scholar working on Oncology, Molecular Biology and Cancer Research. According to data from OpenAlex, Lesley Mathews has authored 21 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Oncology, 12 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Lesley Mathews's work include Cancer Cells and Metastasis (11 papers), Epigenetics and DNA Methylation (6 papers) and Cancer Genomics and Diagnostics (3 papers). Lesley Mathews is often cited by papers focused on Cancer Cells and Metastasis (11 papers), Epigenetics and DNA Methylation (6 papers) and Cancer Genomics and Diagnostics (3 papers). Lesley Mathews collaborates with scholars based in United States, Italy and Australia. Lesley Mathews's co-authors include William L. Farrar, Stephanie Cabarcas‐Petroski, Elaine M. Hurt, Francesco Crea, Xiaohu Zhang, Lei Sun, Marı́a Ana Duhagon, George J. Klarmann, Suneetha B. Thomas and Romano Danesi and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer Cell.

In The Last Decade

Lesley Mathews

20 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lesley Mathews United States 15 862 604 374 253 159 21 1.4k
Steven Pirie‐Shepherd United States 19 815 0.9× 356 0.6× 398 1.1× 148 0.6× 190 1.2× 36 1.4k
Nicole E. Willmarth United States 17 671 0.8× 496 0.8× 390 1.0× 139 0.5× 164 1.0× 23 1.2k
Mei Dong China 18 1.2k 1.4× 539 0.9× 332 0.9× 159 0.6× 119 0.7× 36 1.7k
Nino Keshelava United States 19 914 1.1× 454 0.8× 293 0.8× 120 0.5× 134 0.8× 33 1.4k
Nathan G. Dolloff United States 19 877 1.0× 515 0.9× 296 0.8× 148 0.6× 201 1.3× 41 1.4k
Charlotte Kopitz Germany 19 981 1.1× 639 1.1× 787 2.1× 361 1.4× 141 0.9× 40 1.7k
Magdalena Koziczak Switzerland 8 786 0.9× 703 1.2× 311 0.8× 156 0.6× 91 0.6× 9 1.4k
Katharine Ellwood‐Yen United States 8 787 0.9× 336 0.6× 287 0.8× 531 2.1× 152 1.0× 10 1.3k
Laura G.M. Daenen Netherlands 14 612 0.7× 679 1.1× 424 1.1× 192 0.8× 216 1.4× 30 1.3k
Derya Duranyıldız Türkiye 22 603 0.7× 662 1.1× 294 0.8× 234 0.9× 282 1.8× 85 1.4k

Countries citing papers authored by Lesley Mathews

Since Specialization
Citations

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

Fields of papers citing papers by Lesley Mathews

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lesley Mathews. 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 Lesley Mathews. The network helps show where Lesley Mathews may publish in the future.

Co-authorship network of co-authors of Lesley Mathews

This figure shows the co-authorship network connecting the top 25 collaborators of Lesley Mathews. A scholar is included among the top collaborators of Lesley Mathews 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 Lesley Mathews. Lesley Mathews 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.
Zhang, Ying, Stephanie Cabarcas‐Petroski, Lei Sun, et al.. (2016). Cryptotanshinone targets tumor-initiating cells through down-regulation of stemness genes expression. Oncology Letters. 11(6). 3803–3812. 12 indexed citations
2.
Rhyasen, Garrett W., Lyndsey Bolanos, Jing Fang, et al.. (2013). Targeting IRAK1 as a Therapeutic Approach for Myelodysplastic Syndrome. Cancer Cell. 24(1). 90–104. 155 indexed citations
3.
Mathews, Lesley. (2013). Genomic Analysis of Invasive Human Bone Marrow Derived Mesenchymal Stem Cells. PubMed. 1(3). 122–122. 3 indexed citations
4.
Casson, Lavona, Lauren A. Howell, Lesley Mathews, et al.. (2013). Inhibition of Ceramide Metabolism Sensitizes Human Leukemia Cells to Inhibition of BCL2-Like Proteins. PLoS ONE. 8(1). e54525–e54525. 39 indexed citations
6.
Sun, Lei, Lesley Mathews, Stephanie Cabarcas‐Petroski, et al.. (2013). Epigenetic Regulation of SOX9 by the NF-κB Signaling Pathway in Pancreatic Cancer Stem Cells. Stem Cells. 31(8). 1454–1466. 100 indexed citations
7.
Mathews, Lesley, Jonathan M. Keller, Bonnie L. Goodwin, et al.. (2012). A 1536-Well Quantitative High-Throughput Screen to Identify Compounds Targeting Cancer Stem Cells. SLAS DISCOVERY. 17(9). 1231–1242. 27 indexed citations
8.
Crea, Francesco, Elaine M. Hurt, Lesley Mathews, et al.. (2011). Pharmacologic disruption of Polycomb Repressive Complex 2 inhibits tumorigenicity and tumor progression in prostate cancer. Molecular Cancer. 10(1). 40–40. 143 indexed citations
9.
Mathews, Lesley, Stephanie Cabarcas‐Petroski, & William L. Farrar. (2011). DNA repair: the culprit for tumor-initiating cell survival?. Cancer and Metastasis Reviews. 30(2). 185–197. 27 indexed citations
10.
Mathews, Lesley, Stephanie Cabarcas‐Petroski, Elaine M. Hurt, et al.. (2011). Increased Expression of DNA Repair Genes in Invasive Human Pancreatic Cancer Cells. Pancreas. 40(5). 730–739. 53 indexed citations
11.
Cabarcas‐Petroski, Stephanie, Lesley Mathews, & William L. Farrar. (2011). The cancer stem cell niche—there goes the neighborhood?. International Journal of Cancer. 129(10). 2315–2327. 206 indexed citations
12.
Mathews, Lesley & William L. Farrar. (2011). CD200 (CD200 molecule). Atlas of Genetics and Cytogenetics in Oncology and Haematology.
13.
Mathews, Lesley, Elaine M. Hurt, Xiaohu Zhang, & William L. Farrar. (2010). Epigenetic regulation of CpG promoter methylation in invasive prostate cancer cells. Molecular Cancer. 9(1). 267–267. 32 indexed citations
14.
Crea, Francesco, Lesley Mathews, William L. Farrar, & Elaine M. Hurt. (2009). Targeting Prostate Cancer Stem Cells. Anti-Cancer Agents in Medicinal Chemistry. 9(10). 1105–1113. 18 indexed citations
15.
Mathews, Lesley, Francesco Crea, & William L. Farrar. (2009). Epigenetic gene regulation in stem cells and correlation to cancer. Differentiation. 78(1). 1–17. 58 indexed citations
16.
Klarmann, George J., Elaine M. Hurt, Lesley Mathews, et al.. (2009). Invasive prostate cancer cells are tumor initiating cells that have a stem cell-like genomic signature. Clinical & Experimental Metastasis. 26(5). 433–446. 181 indexed citations
17.
Mita, Monica, Alain C. Mita, Quincy S. Chu, et al.. (2008). Phase I Trial of the Novel Mammalian Target of Rapamycin Inhibitor Deforolimus (AP23573; MK-8669) Administered Intravenously Daily for 5 Days Every 2 Weeks to Patients With Advanced Malignancies. Journal of Clinical Oncology. 26(3). 361–367. 227 indexed citations
18.
Mathews, Lesley & Sallie S. Schneider. (2008). Insulin-like growth factor-I inhibits growth regulatory responses engaged by estrogen and progesterone in the mouse mammary gland. European Journal of Cancer Prevention. 17(4). 297–305. 4 indexed citations
19.
Lu, Shaolei, Karsten Becker, Haoheng Yan, et al.. (2008). Transcriptional Responses to Estrogen and Progesterone in Mammary Gland Identify Networks Regulating p53 Activity. Endocrinology. 149(10). 4809–4820. 24 indexed citations
20.
Becker, Karsten, Shaolei Lu, Ellen S. Dickinson, et al.. (2005). Estrogen and progesterone regulate radiation-induced p53 activity in mammary epithelium through TGF-β-dependent pathways. Oncogene. 24(42). 6345–6353. 33 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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