Matthew M. Hayward

3.4k total citations
24 papers, 1.4k citations indexed

About

Matthew M. Hayward is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Matthew M. Hayward has authored 24 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Organic Chemistry and 6 papers in Pharmacology. Recurrent topics in Matthew M. Hayward's work include Phytochemistry and Bioactivity Studies (5 papers), Chemical synthesis and alkaloids (5 papers) and Protein Degradation and Inhibitors (4 papers). Matthew M. Hayward is often cited by papers focused on Phytochemistry and Bioactivity Studies (5 papers), Chemical synthesis and alkaloids (5 papers) and Protein Degradation and Inhibitors (4 papers). Matthew M. Hayward collaborates with scholars based in United States, United Kingdom and Russia. Matthew M. Hayward's co-authors include Benjamin F. Cravatt, Melissa M. Dix, Kirk L. Stevens, Yoshito Kishi, Kevin J. Duffy, Peter I. Dalko, Jiasheng Guo, Taka-Aki Ichu, Radu M. Suciu and A. Gilbert and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Angewandte Chemie International Edition.

In The Last Decade

Matthew M. Hayward

22 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew M. Hayward United States 15 909 612 235 159 119 24 1.4k
Nigel J. Liverton United States 24 726 0.8× 711 1.2× 201 0.9× 69 0.4× 103 0.9× 61 1.8k
Kiyohiro Nishikawa Japan 21 767 0.8× 348 0.6× 397 1.7× 97 0.6× 210 1.8× 56 1.4k
Yoan Ferandin France 25 954 1.0× 904 1.5× 410 1.7× 103 0.6× 179 1.5× 34 2.0k
Aubry K. Miller Germany 23 817 0.9× 580 0.9× 203 0.9× 101 0.6× 146 1.2× 55 1.7k
Philip G. Kasprzyk United States 22 1.1k 1.2× 299 0.5× 638 2.7× 104 0.7× 85 0.7× 50 1.8k
Jason G. Kettle United Kingdom 24 853 0.9× 890 1.5× 298 1.3× 61 0.4× 98 0.8× 61 1.7k
Todd C. Somers United States 14 890 1.0× 707 1.2× 301 1.3× 74 0.5× 108 0.9× 18 1.6k
Naomi Robertson United Kingdom 18 1.2k 1.3× 392 0.6× 252 1.1× 48 0.3× 88 0.7× 33 1.5k
S. J. DESOLMS United States 23 1.5k 1.6× 627 1.0× 752 3.2× 77 0.5× 99 0.8× 39 2.2k
Butrus Atrash United Kingdom 18 767 0.8× 260 0.4× 323 1.4× 62 0.4× 41 0.3× 39 1.2k

Countries citing papers authored by Matthew M. Hayward

Since Specialization
Citations

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

Fields of papers citing papers by Matthew M. Hayward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew M. Hayward

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew M. Hayward. A scholar is included among the top collaborators of Matthew M. Hayward 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 Matthew M. Hayward. Matthew M. Hayward 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.
Liu, Zhonglin, Marscha Hirschi, Oleg Brodsky, et al.. (2024). An allosteric cyclin E-CDK2 site mapped by paralog hopping with covalent probes. Nature Chemical Biology. 21(3). 420–431. 7 indexed citations
2.
Farley, Kathleen A., Ye Che, Ricardo Lira, et al.. (2024). Cyclic Peptide C5aR1 Antagonist Design Using Solution Conformational Analysis Derived from Residual Dipolar Couplings. ACS Medicinal Chemistry Letters. 15(11). 2060–2066.
3.
Derheimer, Frederick A., Natalie Miller, Casey L. Quinlan, et al.. (2024). Abstract LB028: Discovery and characterization of selective heterobifunctional degraders of EP300 in hematopoietic malignancies. Cancer Research. 84(7_Supplement). LB028–LB028.
4.
Abbasov, Mikail E., Madeline E. Kavanagh, Taka-Aki Ichu, et al.. (2021). A proteome-wide atlas of lysine-reactive chemistry. Nature Chemistry. 13(11). 1081–1092. 156 indexed citations
5.
Schiemer, James, Reto Horst, Yilin Meng, et al.. (2020). Snapshots and ensembles of BTK and cIAP1 protein degrader ternary complexes. Nature Chemical Biology. 17(2). 152–160. 83 indexed citations
6.
Whitby, Landon R., R. Scott Obach, Gabriel M. Simon, Matthew M. Hayward, & Benjamin F. Cravatt. (2017). Quantitative Chemical Proteomic Profiling of thein VivoTargets of Reactive Drug Metabolites. ACS Chemical Biology. 12(8). 2040–2050. 27 indexed citations
7.
Bar‐Peled, Liron, Esther K. Kemper, Radu M. Suciu, et al.. (2017). Chemical Proteomics Identifies Druggable Vulnerabilities in a Genetically Defined Cancer. Cell. 171(3). 696–709.e23. 195 indexed citations
8.
Niessen, Sherry, Melissa M. Dix, Zachary E. Potter, et al.. (2017). Proteome-wide Map of Targets of T790M-EGFR-Directed Covalent Inhibitors. Cell chemical biology. 24(11). 1388–1400.e7. 77 indexed citations
9.
Wang, Qi, David M. Rubitski, Matthew M. Hayward, et al.. (2015). Identification of Phosphorylation Consensus Sequences and Endogenous Neuronal Substrates of the Psychiatric Risk Kinase TNIK. Journal of Pharmacology and Experimental Therapeutics. 356(2). 410–423. 29 indexed citations
10.
Henderson, Jaclyn L., Bethany L. Kormos, Matthew M. Hayward, et al.. (2014). Discovery and Preclinical Profiling of 3-[4-(Morpholin-4-yl)-7 H -pyrrolo[2,3- d ]pyrimidin-5-yl]benzonitrile (PF-06447475), a Highly Potent, Selective, Brain Penetrant, and in Vivo Active LRRK2 Kinase Inhibitor. Journal of Medicinal Chemistry. 58(1). 419–432. 140 indexed citations
11.
Lanning, Bryan, Landon R. Whitby, Melissa M. Dix, et al.. (2014). A road map to evaluate the proteome-wide selectivity of covalent kinase inhibitors. Nature Chemical Biology. 10(9). 760–767. 265 indexed citations
12.
Tu, Meihua, K. Brajesh, Alan M. Mathiowetz, et al.. (2012). Exploring Aromatic Chemical Space with NEAT: Novel and Electronically Equivalent Aromatic Template. Journal of Chemical Information and Modeling. 52(5). 1114–1123. 12 indexed citations
13.
Herbert, Paulo, et al.. (2005). In‐vitro evaluation of the PALL Leukotrap Affinity Prion Reduction Filter as a secondary device following primary leucoreduction. Vox Sanguinis. 89(4). 220–228. 12 indexed citations
14.
Guo, Jiasheng, Kevin J. Duffy, Kirk L. Stevens, et al.. (1998). Total Synthesis of Altohyrtin A (Spongistatin 1): Part 1. Angewandte Chemie International Edition. 37(1-2). 187–190. 105 indexed citations
15.
Guo, Jiasheng, Kevin J. Duffy, Kirk L. Stevens, et al.. (1998). Totalsynthese von Altohyrtin A (Spongistatin 1): Teil 1. Angewandte Chemie. 110(1-2). 198–202. 21 indexed citations
16.
Hayward, Matthew M., Kevin J. Duffy, Peter I. Dalko, et al.. (1998). Totalsynthese von Altohyrtin A (Spongistatin 1): Teil 2. Angewandte Chemie. 110(1-2). 202–206. 17 indexed citations
17.
Hayward, Matthew M., Kevin J. Duffy, Peter I. Dalko, et al.. (1998). Total Synthesis of Altohyrtin A (Spongistatin 1): Part 2. Angewandte Chemie International Edition. 37(1-2). 190–196. 89 indexed citations
18.
Cox, Julia, Matthew M. Hayward, Sarina van der Zee, et al.. (1997). Bidirectional binding of the TATA box binding protein to the TATA box. Proceedings of the National Academy of Sciences. 94(25). 13475–13480. 54 indexed citations
19.
Hayward, Matthew M., et al.. (1989). NAPHTHYL‐ AND QUINOLYLLUCIFERIN: GREEN AND RED LIGHT EMITTING FIREFLY LUCIFERIN ANALOGUES. Photochemistry and Photobiology. 49(5). 689–695. 55 indexed citations
20.
Napier, J. A. F., Paul Ashford, & Matthew M. Hayward. (1985). What is the ‘Optimum’ Optimal Additive Solution?. Vox Sanguinis. 49(5). 315–318. 4 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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