R. Matthew Cross

792 total citations
16 papers, 412 citations indexed

About

R. Matthew Cross is a scholar working on Molecular Biology, Organic Chemistry and Public Health, Environmental and Occupational Health. According to data from OpenAlex, R. Matthew Cross has authored 16 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Organic Chemistry and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in R. Matthew Cross's work include Malaria Research and Control (5 papers), Research on Leishmaniasis Studies (4 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (4 papers). R. Matthew Cross is often cited by papers focused on Malaria Research and Control (5 papers), Research on Leishmaniasis Studies (4 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (4 papers). R. Matthew Cross collaborates with scholars based in United States, Switzerland and Australia. R. Matthew Cross's co-authors include Roman Manetsch, Dennis E. Kyle, Tina Mutka, Andrii Monastyrskyi, Jeremy N. Burrows, Kyung Woon Jung, Ralph Nicholas Salvatore, A. S. Nagle, Feixia Chu and Alexis N. LaCrue and has published in prestigious journals such as Journal of Medicinal Chemistry, Antimicrobial Agents and Chemotherapy and The Journal of Organic Chemistry.

In The Last Decade

R. Matthew Cross

15 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Matthew Cross United States 10 219 144 136 50 47 16 412
Mohammad Hassam India 11 455 2.1× 136 0.9× 75 0.6× 25 0.5× 71 1.5× 24 584
Scott Eagon United States 12 296 1.4× 43 0.3× 195 1.4× 15 0.3× 49 1.0× 26 459
Jacques Bompart France 11 243 1.1× 137 1.0× 141 1.0× 5 0.1× 51 1.1× 25 425
José M. Bueno Spain 11 205 0.9× 134 0.9× 118 0.9× 4 0.1× 86 1.8× 16 410
Parameshwar Makam India 12 459 2.1× 29 0.2× 126 0.9× 11 0.2× 56 1.2× 21 577
Kekeli Ekoue‐Kovi United States 9 772 3.5× 108 0.8× 322 2.4× 20 0.4× 49 1.0× 12 904
Yuanda Hua United States 13 271 1.2× 108 0.8× 57 0.4× 7 0.1× 17 0.4× 15 446
Amit Verma India 9 720 3.3× 25 0.2× 158 1.2× 12 0.2× 24 0.5× 15 867
Sophie Girault France 8 202 0.9× 149 1.0× 111 0.8× 3 0.1× 40 0.9× 8 337
Rishi Kumar India 16 398 1.8× 109 0.8× 212 1.6× 3 0.1× 34 0.7× 28 557

Countries citing papers authored by R. Matthew Cross

Since Specialization
Citations

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

Fields of papers citing papers by R. Matthew Cross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Matthew Cross

This figure shows the co-authorship network connecting the top 25 collaborators of R. Matthew Cross. A scholar is included among the top collaborators of R. Matthew Cross 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 R. Matthew Cross. R. Matthew Cross is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Lukesh, John C., Daniel W. Carney, Huijun Dong, et al.. (2017). Vinblastine 20′ Amides: Synthetic Analogues That Maintain or Improve Potency and Simultaneously Overcome Pgp-Derived Efflux and Resistance. Journal of Medicinal Chemistry. 60(17). 7591–7604. 15 indexed citations
2.
Allemann, Oliver, et al.. (2017). Key analogs of a uniquely potent synthetic vinblastine that contain modifications of the C20′ ethyl substituent. Bioorganic & Medicinal Chemistry Letters. 27(14). 3055–3059. 9 indexed citations
3.
Cross, R. Matthew, Andrii Monastyrskyi, Alexis N. LaCrue, et al.. (2014). Orally Bioavailable 6-Chloro-7-methoxy-4(1H)-quinolones Efficacious against Multiple Stages of Plasmodium. Journal of Medicinal Chemistry. 57(21). 8860–8879. 33 indexed citations
4.
Saénz, Fabián E., Alexis N. LaCrue, R. Matthew Cross, et al.. (2013). 4-(1 H )-Quinolones and 1,2,3,4-Tetrahydroacridin-9(10 H )-Ones Prevent the Transmission of Plasmodium falciparum to Anopheles freeborni. Antimicrobial Agents and Chemotherapy. 57(12). 6187–6195. 18 indexed citations
5.
Cross, R. Matthew, et al.. (2013). Utilizing wide area maritime domain awareness (MDA) data to cue a remote surveillance system. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 8899. 889915–889915. 2 indexed citations
6.
LaCrue, Alexis N., Fabián E. Saénz, R. Matthew Cross, et al.. (2012). 4(1H)-Quinolones with Liver Stage Activity against Plasmodium berghei. Antimicrobial Agents and Chemotherapy. 57(1). 417–424. 23 indexed citations
7.
Cross, R. Matthew, et al.. (2011). Optimization of 1,2,3,4-Tetrahydroacridin-9(10H)-ones as Antimalarials Utilizing Structure–Activity and Structure–Property Relationships. Journal of Medicinal Chemistry. 54(13). 4399–4426. 48 indexed citations
8.
Cross, R. Matthew, et al.. (2011). Synthesis, Antimalarial Activity, and Structure–Activity Relationship of 7-(2-Phenoxyethoxy)-4(1H)-quinolones. Journal of Medicinal Chemistry. 54(24). 8321–8327. 47 indexed citations
9.
Cross, R. Matthew & Roman Manetsch. (2010). Divergent Route to Access Structurally Diverse 4-Quinolones via Mono or Sequential Cross-Couplings. The Journal of Organic Chemistry. 75(24). 8654–8657. 47 indexed citations
10.
Cross, R. Matthew, Andrii Monastyrskyi, Tina Mutka, et al.. (2010). Endochin Optimization: Structure−Activity and Structure−Property Relationship Studies of 3-Substituted 2-Methyl-4(1H)-quinolones with Antimalarial Activity. Journal of Medicinal Chemistry. 53(19). 7076–7094. 88 indexed citations
11.
Haring, Robert E., Randy Pollock, R. Matthew Cross, & Brian M. Sutin. (2004). Field testing the wide-field-of-view imaging spectrometer(WFIS). Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 5543. 283–283.
12.
Nagle, A. S., et al.. (2003). Selective mono protection of diols, diamines, and amino alcohols using cesium bases. Tetrahedron Letters. 44(30). 5695–5698. 17 indexed citations
13.
Haring, Robert E., Randy Pollock, & R. Matthew Cross. (2003). Wide-field-of-view imaging spectrometer (WFIS) engineering model laboratory tests and field demonstrations. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 3 indexed citations
14.
Haring, Robert E., Randy Pollock, R. Matthew Cross, & David Crisp. (2002). Oxygen A-band spectrometer breadboard for the Orbiting Carbon Observatory. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 4818. 201–201. 2 indexed citations
15.
Salvatore, Ralph Nicholas, et al.. (2002). Efficient Cs2CO3-promoted solution and solid phase synthesis of carbonates and carbamates in the presence of TBAI. Tetrahedron. 58(17). 3329–3347. 58 indexed citations
16.
Haring, Robert E., et al.. (2002). <title>Wide-field-of-view imaging spectrometer (WFIS): from a laboratory demonstration to a fully functional engineering model</title>. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 4486. 403–410. 2 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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