Richard Chesworth

6.7k total citations · 2 hit papers
32 papers, 2.4k citations indexed

About

Richard Chesworth is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Richard Chesworth has authored 32 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 5 papers in Organic Chemistry and 4 papers in Pharmacology. Recurrent topics in Richard Chesworth's work include Cancer-related gene regulation (17 papers), Epigenetics and DNA Methylation (16 papers) and Acute Myeloid Leukemia Research (3 papers). Richard Chesworth is often cited by papers focused on Cancer-related gene regulation (17 papers), Epigenetics and DNA Methylation (16 papers) and Acute Myeloid Leukemia Research (3 papers). Richard Chesworth collaborates with scholars based in United States, United Kingdom and Japan. Richard Chesworth's co-authors include Robert A. Copeland, Mikel P. Moyer, Roy M. Pollock, Margaret Porter Scott, Victoria M. Richon, Christina J. Allain, Alejandra Raimondi, Christine R. Klaus, Tim J. Wigle and Kevin W. Kuntz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Blood.

In The Last Decade

Richard Chesworth

30 papers receiving 2.3k citations

Hit Papers

Durable tumor regression in genetically altered malignant... 2013 2026 2017 2021 2013 2013 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard Chesworth United States 17 2.1k 227 223 192 191 32 2.4k
Sandra E. Wilkinson United Kingdom 20 1.6k 0.8× 287 1.3× 110 0.5× 180 0.9× 368 1.9× 34 2.7k
Jeffrey J. Hale United States 24 2.0k 1.0× 650 2.9× 174 0.8× 256 1.3× 261 1.4× 52 3.0k
Lourdes Toral‐Barza United States 28 1.9k 0.9× 514 2.3× 78 0.3× 205 1.1× 301 1.6× 41 2.6k
Deborah Card United States 17 1.6k 0.8× 275 1.2× 136 0.6× 174 0.9× 283 1.5× 21 2.3k
Xiaoshan Min United States 22 1.3k 0.6× 206 0.9× 57 0.3× 76 0.4× 199 1.0× 34 2.0k
Shawn G. Payne United States 20 2.6k 1.3× 107 0.5× 145 0.7× 213 1.1× 254 1.3× 24 2.9k
Tjeerd Barf Netherlands 19 724 0.4× 360 1.6× 165 0.7× 286 1.5× 229 1.2× 33 1.7k
Haile Tecle United States 14 1.1k 0.6× 423 1.9× 58 0.3× 168 0.9× 403 2.1× 27 1.7k
Christine Huselton United States 18 1.6k 0.8× 429 1.9× 230 1.0× 79 0.4× 162 0.8× 37 2.3k
Péter Ács United States 26 969 0.5× 70 0.3× 524 2.3× 105 0.5× 451 2.4× 42 2.1k

Countries citing papers authored by Richard Chesworth

Since Specialization
Citations

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

Fields of papers citing papers by Richard Chesworth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard Chesworth

This figure shows the co-authorship network connecting the top 25 collaborators of Richard Chesworth. A scholar is included among the top collaborators of Richard Chesworth 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 Richard Chesworth. Richard Chesworth 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.
Alford, Joshua S., John W. Lampe, Richard Chesworth, et al.. (2022). Conformational-Design-Driven Discovery of EZM0414: A Selective, Potent SETD2 Inhibitor for Clinical Studies. ACS Medicinal Chemistry Letters. 13(7). 1137–1143. 16 indexed citations
2.
Morrison, Michael J., P. Ann Boriack‐Sjodin, Kerren K. Swinger, et al.. (2018). Identification of a peptide inhibitor for the histone methyltransferase WHSC1. PLoS ONE. 13(5). e0197082–e0197082. 22 indexed citations
3.
Chan-Penebre, Elayne, Kelli Armstrong, Allison E. Drew, et al.. (2017). Selective Killing of SMARCA2- and SMARCA4-deficient Small Cell Carcinoma of the Ovary, Hypercalcemic Type Cells by Inhibition of EZH2: In Vitro and In Vivo Preclinical Models. Molecular Cancer Therapeutics. 16(5). 850–860. 127 indexed citations
4.
Drew, Allison E., John E. Campbell, Cuyue Tang, et al.. (2017). Abstract 5060: Activity of the EZH2 inhibitor tazemetostat as a monotherapy and in combination with multiple myeloma therapies in preclinical models. Cancer Research. 77(13_Supplement). 5060–5060. 3 indexed citations
5.
Waters, Nigel J., Sherri Smith, Edward J. Olhava, et al.. (2015). Metabolism and disposition of the DOT1L inhibitor, pinometostat (EPZ-5676), in rat, dog and human. Cancer Chemotherapy and Pharmacology. 77(1). 43–62. 23 indexed citations
6.
Mitchell, Lorna H., Allison E. Drew, Scott Ribich, et al.. (2015). Aryl Pyrazoles as Potent Inhibitors of Arginine Methyltransferases: Identification of the First PRMT6 Tool Compound. ACS Medicinal Chemistry Letters. 6(6). 655–659. 95 indexed citations
7.
Campbell, John E., Kevin W. Kuntz, Sarah K. Knutson, et al.. (2015). EPZ011989, A Potent, Orally-Available EZH2 Inhibitor with Robust in Vivo Activity. ACS Medicinal Chemistry Letters. 6(5). 491–495. 94 indexed citations
8.
Duncan, Kenneth W., Nathalie Rioux, P. Ann Boriack‐Sjodin, et al.. (2015). Structure and Property Guided Design in the Identification of PRMT5 Tool Compound EPZ015666. ACS Medicinal Chemistry Letters. 7(2). 162–166. 103 indexed citations
9.
Wigle, Tim J., Kerren K. Swinger, John E. Campbell, et al.. (2015). A High-Throughput Mass Spectrometry Assay Coupled with Redox Activity Testing Reduces Artifacts and False Positives in Lysine Demethylase Screening. SLAS DISCOVERY. 20(6). 810–820. 31 indexed citations
10.
Rioux, Nathalie, Kenneth W. Duncan, Xiu‐Sheng Miao, et al.. (2015). Species differences in metabolism of EPZ015666, an oxetane-containing protein arginine methyltransferase-5 (PRMT5) inhibitor. Xenobiotica. 46(3). 268–277. 16 indexed citations
11.
Rioux, Nathalie, Lorna H. Mitchell, Philip R. Tiller, et al.. (2015). Structural and Kinetic Characterization of a Novel N-acetylated Aliphatic Amine Metabolite of the PRMT Inhibitor, EPZ011652. Drug Metabolism and Disposition. 43(7). 936–943. 5 indexed citations
12.
Rioux, Nathalie, Heike Keilhack, Blythe Thomson, et al.. (2015). Abstract A135: Physiologically-based pharmacokinetic modeling to support clinical investigation of the EZH2 inhibitor, tazemetostat (EPZ-6438) in INI1-deficient pediatric tumors. Molecular Cancer Therapeutics. 14(12_Supplement_2). A135–A135. 2 indexed citations
13.
Basavapathruni, Aravind, Edward J. Olhava, Scott R. Daigle, et al.. (2014). Nonclinical pharmacokinetics and metabolism of EPZ‐5676, a novel DOT1L histone methyltransferase inhibitor. Biopharmaceutics & Drug Disposition. 35(4). 237–252. 64 indexed citations
14.
Daigle, Scott R., Edward J. Olhava, Aravind Basavapathruni, et al.. (2013). Potent inhibition of DOT1L as treatment of MLL-fusion leukemia. Blood. 122(6). 1017–1025. 546 indexed citations breakdown →
15.
Basavapathruni, Aravind, Lei Jin, Scott R. Daigle, et al.. (2012). Conformational Adaptation Drives Potent, Selective and Durable Inhibition of the Human Protein Methyltransferase DOT1L. Chemical Biology & Drug Design. 80(6). 971–980. 114 indexed citations
16.
Prickaerts, Jos, Nick P. van Goethem, Richard Chesworth, et al.. (2011). EVP-6124, a novel and selective α7 nicotinic acetylcholine receptor partial agonist, improves memory performance by potentiating the acetylcholine response of α7 nicotinic acetylcholine receptors. Neuropharmacology. 62(2). 1099–1110. 174 indexed citations
17.
Wu, Jun, V. A. Vigont, Lori Hrdlicka, et al.. (2011). Neuronal Store-Operated Calcium Entry Pathway as a Novel Therapeutic Target for Huntington's Disease Treatment. Chemistry & Biology. 18(6). 777–793. 127 indexed citations
18.
Felsenstein, Kevin M., Zhiyong Yang, Scott Nolan, et al.. (2010). P3‐295: Pharmacokinetic and pharmacodynamic analysis of the gamma‐secretase modulator (GSM) EVP‐0015962. Alzheimer s & Dementia. 6(4S_Part_17). 4 indexed citations
19.
Patzke, Holger, Richard Chesworth, Jessica Smith, et al.. (2008). Discovery and Development of Novel HDAC Inhibitors for Huntington’s Disease. Neurotherapeutics. 5(2). 371–371. 1 indexed citations
20.
Chesworth, Richard, Michael P. Zawistoski, Bruce A. Lefker, et al.. (2004). Tetrahydroisoquinolines as subtype selective estrogen agonists/antagonists. Bioorganic & Medicinal Chemistry Letters. 14(11). 2729–2733. 32 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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