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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Identifying antimalarial compounds targeting dihydrofolate reductase-thymidylate synthase (DHFR-TS) by chemogenomic profiling
Aiyada Aroonsri, Olugbenga Akinola, Navaporn Posayapisit, et al.
International Journal for Parasitology (2016) Vol. 46, Iss. 8, pp. 527-535
Closed Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond
Wesley C. Van Voorhis, John H. Adams, Roberto Adelfio, et al.
PLoS Pathogens (2016) Vol. 12, Iss. 7, pp. e1005763-e1005763
Open Access | Times Cited: 431
Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways
Erik L. Allman, Heather J. Painter, Jasmeet Samra, et al.
Antimicrobial Agents and Chemotherapy (2016) Vol. 60, Iss. 11, pp. 6635-6649
Open Access | Times Cited: 139
Metabolomics-Based Screening of the Malaria Box Reveals both Novel and Established Mechanisms of Action
Darren J. Creek, Hwa H. Chua, Simon A. Cobbold, et al.
Antimicrobial Agents and Chemotherapy (2016) Vol. 60, Iss. 11, pp. 6650-6663
Open Access | Times Cited: 99
Drug targets for resistant malaria: Historic to future perspectives
Sahil Kumar, Tulika Bhardwaj, D.N. Prasad, et al.
Biomedicine & Pharmacotherapy (2018) Vol. 104, pp. 8-27
Closed Access | Times Cited: 89
Synthesis and antiproliferative activity of a series of novel 6-substituted pyrido[3,2- d ]pyrimidines as potential nonclassical lipophilic antifolates targeting dihydrofolate reductase
Meng Wang, Jiajia Yang, Mengmeng Yuan, et al.
European Journal of Medicinal Chemistry (2017) Vol. 128, pp. 88-97
Closed Access | Times Cited: 45
Design, Syntheses and Biological Evaluation of 4-Aminoquinoline-Thiazolidinone Hybrids
Gul Naz Fatima, Sarvesh Paliwal, Shailendra K. Saraf
Chemistry Africa (2025)
Closed Access
A toolbox for conditional control of gene expression in apicomplexan parasites
Sylvie Briquet, Mathieu Gissot, Olivier Silvie
Molecular Microbiology (2021) Vol. 117, Iss. 3, pp. 618-631
Open Access | Times Cited: 20
Structure- and ligand-based drug design methods for the modeling of antimalarial agents: a review of updates from 2012 onwards
Vivek K. Vyas, Sapna Bhati, Shivani Patel, et al.
Journal of Biomolecular Structure and Dynamics (2021) Vol. 40, Iss. 20, pp. 10481-10506
Closed Access | Times Cited: 19
Diaminoquinazoline MMV675968 from Pathogen Box inhibits Acinetobacter baumannii growth through targeting of dihydrofolate reductase
Warangkhana Songsungthong, Suganya Yongkiettrakul, Louise E. Bohan, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 22
To kill a piroplasm: genetic technologies to advance drug discovery and target identification in Babesia
Caroline D. Keroack, Brendan Elsworth, Manoj T. Duraisingh
International Journal for Parasitology (2018) Vol. 49, Iss. 2, pp. 153-163
Closed Access | Times Cited: 19
Recent advances on patents of Plasmodium falciparum dihydroorotate dehydrogenase ( Pf DHODH) inhibitors as antimalarial agents
Pinky Gehlot, Vivek K. Vyas
Expert Opinion on Therapeutic Patents (2023) Vol. 33, Iss. 9, pp. 579-596
Closed Access | Times Cited: 6
The relative rate of kill of the MMV Malaria Box compounds provides links to the mode of antimalarial action and highlights scaffolds of medicinal chemistry interest
Imran Ullah, Raman Sharma, Antonio Mete, et al.
Journal of Antimicrobial Chemotherapy (2019) Vol. 75, Iss. 2, pp. 362-370
Open Access | Times Cited: 14
Validation ofPlasmodium falciparumdeoxyhypusine synthase as an antimalarial target
Aiyada Aroonsri, Navaporn Posayapisit, Jindaporn Kongsee, et al.
PeerJ (2019) Vol. 7, pp. e6713-e6713
Open Access | Times Cited: 11
Antimalarial target vulnerability of the putative Plasmodium falciparum methionine synthase
Nirut Leela, Parichat Prommana, Sumalee Kamchonwongpaisan, et al.
PeerJ (2024) Vol. 12, pp. e16595-e16595
Open Access | Times Cited: 1
A novel bicyclic 2,4-diaminopyrimidine inhibitor of Streptococcus suis dihydrofolate reductase
Warangkhana Songsungthong, Sunisa Prasopporn, Louise E. Bohan, et al.
PeerJ (2021) Vol. 9, pp. e10743-e10743
Open Access | Times Cited: 9
Overexpression of the HECT ubiquitin ligase PfUT prolongs the intraerythrocytic cycle and reduces invasion efficiency of Plasmodium falciparum
Monika Jankowska-Döllken, Cecília P. Sanchez, Marek Cyrklaff, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 9
Muddled mechanisms: recent progress towards antimalarial target identification
Rachel L. Edwards, Audrey R. Odom John
F1000Research (2016) Vol. 5, pp. 2514-2514
Open Access | Times Cited: 6
The PTEX Pore Component EXP2 Is Important for Intrahepatic Development during the Plasmodium Liver Stage
Tahir Hussain, Jose Linera-Gonzalez, John M. Beck, et al.
mBio (2022) Vol. 13, Iss. 6
Open Access | Times Cited: 5
A proteomic glimpse into the effect of antimalarial drugs onPlasmodium falciparumproteome towards highlighting possible therapeutic targets
Majid Dousti, Raúl Manzano-Román, Sajad Rashidi, et al.
Pathogens and Disease (2020) Vol. 79, Iss. 1
Closed Access | Times Cited: 6
Tools for attenuation of gene expression in malaria parasites
Philip J. Shaw, Aiyada Aroonsri
International Journal for Parasitology (2017) Vol. 47, Iss. 7, pp. 385-398
Closed Access | Times Cited: 4
Antimalarial mechanism of action of the natural product 9-methoxystrobilurin G
Philip J. Shaw, Parichat Prommana, Chawanee Thongpanchang, et al.
Molecular Omics (2024) Vol. 20, Iss. 9, pp. 584-594
Closed Access
Investigation of an Allosteric Deoxyhypusine Synthase Inhibitor in P. falciparum
Aiyada Aroonsri, Chayaphat Wongsombat, Philip J. Shaw, et al.
Molecules (2022) Vol. 27, Iss. 8, pp. 2463-2463
Open Access | Times Cited: 2
The PTEX pore component EXP2 is important for intrahepatic development during the Plasmodium liver stage
Tahir Hussain, Jose Linera-Gonzalez, John M. Beck, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Identification of mRNA 5′ cap-associated proteins in the human malaria parasite Plasmodium falciparum
Chayaphat Wongsombat, Yodying Yingchutrakul, Nattida Suwanakitti, et al.
Molecular and Biochemical Parasitology (2021) Vol. 247, pp. 111443-111443
Closed Access | Times Cited: 1
Susceptibility of Southeast Asian Plasmodium falciparum isolates to P218
Navaporn Posayapisit, Jutharat Pengon, Philip J. Shaw, et al.
International Journal of Antimicrobial Agents (2023) Vol. 62, Iss. 1, pp. 106838-106838
Closed Access
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