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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:

In vitro activity of aryl-thiazole derivatives against Schistosoma mansoni schistosomula and adult worms
Adriana S. A. Pereira, Gilbert O. Silveira, Murilo Sena Amaral, et al.
PLoS ONE (2019) Vol. 14, Iss. 11, pp. e0225425-e0225425
Open Access | Times Cited: 19

Showing 19 citing articles:

Thiazole Ring—A Biologically Active Scaffold
Anthi Petrou, Maria Fesatidou, Athina Geronikaki
Molecules (2021) Vol. 26, Iss. 11, pp. 3166-3166
Open Access | Times Cited: 212
Alkyl 2-(2-(arylidene)alkylhydrazinyl)thiazole-4-carboxylates: Synthesis, acetyl cholinesterase inhibition and docking studies
Muhammad Haroon, Muhammad Khalid, Kiran Shahzadi, et al.
Journal of Molecular Structure (2021) Vol. 1245, pp. 131063-131063
Closed Access | Times Cited: 28
Long non-coding RNAs are essential for Schistosoma mansoni pairing-dependent adult worm homeostasis and fertility
Gilbert O. Silveira, Helena S. Coelho, Adriana S. A. Pereira, et al.
PLoS Pathogens (2023) Vol. 19, Iss. 5, pp. e1011369-e1011369
Open Access | Times Cited: 11
Long non-coding RNA levels can be modulated by 5-azacytidine in Schistosoma mansoni
Murilo Sena Amaral, Lucas F. Maciel, Gilbert O. Silveira, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 20
Thiazole, Isatin and Phthalimide Derivatives Tested in vivo against Cancer Models: A Literature Review of the Last Six Years
Aline Ferreira Pinto, Janine Siqueira Nunes, José Eduardo Severino Martins, et al.
Current Medicinal Chemistry (2023) Vol. 31, Iss. 20, pp. 2991-3032
Closed Access | Times Cited: 4
In vitro evaluation of alkaline lignins as antiparasitic agents and their use as an excipient in the release of benznidazole
Iranildo José da Cruz Filho, Denise Duarte, Douglas da Conceição Alves de Lima, et al.
International Journal of Biological Macromolecules (2023) Vol. 231, pp. 123339-123339
Open Access | Times Cited: 3
In vitro activity, ultrastructural analysis and in silico pharmacokinetic properties (ADMET) of thiazole compounds against adult worms of Schistosoma mansoni
Débora Verônica Sarmento Pereira da Silva, Pedro Henrique do Bomfim Nascimento, João Victor Ritinto da Rocha, et al.
Acta Tropica (2023) Vol. 245, pp. 106965-106965
Closed Access | Times Cited: 3
In vitro and in silico evaluation of the schistosomicidal activity of eugenol derivatives using biochemical, molecular, and morphological tools
Isabella Maria Monteiro de Souza, Rômulo Dias Novaes, Reggiani Vilela Gonçalves, et al.
˜The œJournal of venomous animals and toxins including tropical diseases (2022) Vol. 28
Open Access | Times Cited: 4
Therapeutic potential of hydantoin and thiohydantoin compounds against Schistosoma mansoni: An integrated in vitro, DNA, ultrastructural, and ADMET in silico approach
Antônio Sérgio de Almeida Júnior, Mayse Manuele Freitas Viana Leal, Diego Santa Clara Marques, et al.
Molecular and Biochemical Parasitology (2024) Vol. 260, pp. 111646-111646
Closed Access
Octopus vulgaris ink chemical profiling and validation of its potential as antioxidant, antimicrobial, anti-cancer as well as anti-Schistosomal drug in vitro
S.A.H. Hamdi, Maha A.M. El-Shazly, Mona Fol, et al.
Arquivo Brasileiro de Medicina Veterinária e Zootecnia (2024) Vol. 76, Iss. 5
Open Access
Radicicol, a Novel Lead Compound against the Migratory-Stage Schistosomula of Schistosoma japonicum
Liangxiong Xu, Qiuli Liu, Qingren Zeng, et al.
Antimicrobial Agents and Chemotherapy (2021) Vol. 65, Iss. 3
Open Access | Times Cited: 3
Three Small Molecule Entities (MPK18, MPK334 and YAK308) with Activity against Haemonchus contortus In Vitro
Aya C. Taki, Abdul Jabbar, Thomas Kurz, et al.
Molecules (2021) Vol. 26, Iss. 9, pp. 2819-2819
Open Access | Times Cited: 3
Current synthesis routes of thiazole and its derivatives and their broad spectrum therapeutic activity: A Review
Nadeem Alam, Sarika Arora, Asiya Ibrahim, et al.
Journal of Basic and Applied Research in Biomedicine (2022) Vol. 8, Iss. 1, pp. 35-40
Open Access | Times Cited: 2
Antitrichomonal activity and docking analysis of thiazole derivatives as TvMP50 protease inhibitors
Gonzalo J. Mena‐Rejón, Yussel Pérez‐Navarro, Julio César Torres‐Romero, et al.
Parasitology Research (2020) Vol. 120, Iss. 1, pp. 233-241
Closed Access | Times Cited: 2
The use of heterocyclic-based azo compounds bearing pyrrolidine, imidazole, triazole, and thiazole moieties for the treatment of neglected tropical disease caused by Schistosoma mansoni
Cauê Benito Scarim, Chung Man Chin
European Journal of Medicinal Chemistry Reports (2021) Vol. 1, pp. 100001-100001
Open Access | Times Cited: 2
Therapeutic efficacy of a newly synthesized benzimidazole compound BTP-OH against murine schistosomiasis mansoni
Amira Taman, Basem Mansour, Mona Youssef, et al.
Journal of Helminthology (2020) Vol. 94
Closed Access | Times Cited: 1
Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part III: Helminths
Sherif Abaza
Parasitologists United Journal (2022) Vol. 15, Iss. 2, pp. 126-143
Open Access | Times Cited: 1
Functional characterization of long non-coding RNAs in >i<Schistosoma mansoni>/i<
Gilbert O. Silveira
(2022)
Open Access
Effects of multiple doses of simvastatin and artesunate monotherapy on SCHISTOSOMA MANSONI adult worms during infection in hyperlidemic mice
Alba Cristina Miranda de Barros Alencar, Thais Silva dos Santos, Luciana Brandão-Bezerra, et al.
Revista de Patologia Tropical / Journal of Tropical Pathology (2021) Vol. 50, Iss. 1, pp. 21-39
Open Access
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