Muhammad Taha

12.8k total citations · 1 hit paper
393 papers, 11.1k citations indexed

About

Muhammad Taha is a scholar working on Organic Chemistry, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Muhammad Taha has authored 393 papers receiving a total of 11.1k indexed citations (citations by other indexed papers that have themselves been cited), including 289 papers in Organic Chemistry, 107 papers in Molecular Biology and 87 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Muhammad Taha's work include Synthesis and biological activity (211 papers), Natural Antidiabetic Agents Studies (86 papers) and Computational Drug Discovery Methods (54 papers). Muhammad Taha is often cited by papers focused on Synthesis and biological activity (211 papers), Natural Antidiabetic Agents Studies (86 papers) and Computational Drug Discovery Methods (54 papers). Muhammad Taha collaborates with scholars based in Pakistan, Saudi Arabia and Malaysia. Muhammad Taha's co-authors include Fazal Rahim, Khalid Mohammed Khan, Abdul Wadood, Nor Hadiani Ismail, Syahrul Imran, Shahnaz Perveen, Hayat Ullah, M. Iqbal Choudhary, Uzma Salar and Muhammad Ali and has published in prestigious journals such as Journal of Clinical Investigation, Scientific Reports and Chemical Engineering Journal.

In The Last Decade

Muhammad Taha

380 papers receiving 10.9k citations

Hit Papers

The mechanism underlying acetaminophen-induced hepatotoxi... 2012 2026 2016 2021 2012 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. The mechanism underlying acetaminophen-induced hepatotoxicity in humans and mice involves mitochondrial damage and nuclear DNA fragmentation
    2012 569 citations Muhammad Taha et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muhammad Taha Pakistan 55 7.7k 2.8k 2.4k 1.8k 1.5k 393 11.1k
Abdul Wadood Pakistan 49 4.9k 0.6× 2.6k 0.9× 1.6k 0.7× 1.4k 0.8× 1.1k 0.8× 365 8.9k
Fazal Rahim Pakistan 51 5.4k 0.7× 1.9k 0.7× 1.7k 0.7× 1.4k 0.8× 1.2k 0.8× 248 7.1k
Nor Hadiani Ismail Malaysia 46 2.9k 0.4× 1.5k 0.5× 1.0k 0.4× 540 0.3× 498 0.3× 221 5.2k
Syed Adnan Alı Shah Pakistan 42 3.1k 0.4× 1.6k 0.6× 578 0.2× 763 0.4× 850 0.6× 439 7.0k
Ajmal Khan Pakistan 35 2.0k 0.3× 1.6k 0.6× 617 0.3× 500 0.3× 794 0.5× 331 5.1k
Zaheer Ul‐Haq Pakistan 34 2.0k 0.3× 1.6k 0.6× 361 0.1× 923 0.5× 716 0.5× 303 4.7k
Umer Rashid Pakistan 35 1.6k 0.2× 1.0k 0.4× 369 0.2× 602 0.3× 772 0.5× 218 4.1k
Vladimir Poroikov Russia 43 3.0k 0.4× 3.4k 1.2× 277 0.1× 3.4k 1.9× 1.3k 0.9× 276 8.9k
Massoud Amanlou Iran 38 1.1k 0.1× 1.8k 0.6× 221 0.1× 661 0.4× 441 0.3× 283 5.1k
Guixia Liu China 39 1.4k 0.2× 3.4k 1.2× 231 0.1× 4.0k 2.3× 842 0.6× 199 7.8k

Countries citing papers authored by Muhammad Taha

Since Specialization
Citations

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

Fields of papers citing papers by Muhammad Taha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhammad Taha

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Taha. A scholar is included among the top collaborators of Muhammad Taha 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 Muhammad Taha. Muhammad Taha 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.
Taha, Muhammad, et al.. (2025). Tailoring Peptide Coacervates for Advanced Biotechnological Applications: Enhancing Control, Encapsulation, and Antioxidant Properties. ACS Applied Materials & Interfaces. 17(21). 31561–31574. 2 indexed citations
2.
Taha, Muhammad, Fazal Rahim, Javed Khan, et al.. (2025). Design and synthesis of benzimidazole analogs as a potent inhibitor of acetylcholinesterase and butyrylcholinesterase and their docking and MD simulation analysis. Journal of Molecular Structure. 1348. 143407–143407. 1 indexed citations
3.
Nawaz, Muhammad, et al.. (2024). Impact of Ag and Se on the Physiochemical, anti-bacterial, and cytotoxic activities of LaPO4 nanoparticles. Inorganic Chemistry Communications. 173. 113822–113822. 1 indexed citations
4.
Ali, Muhammad, Shahbaz Shamim, Uzma Salar, et al.. (2024). 2-amino-6-ethoxy-4-arylpyridine-3,5-dicarbonitrile Scaffolds as potential acetylcholinesterase and butyrylcholinesterase inhibitors. Journal of Molecular Structure. 1321. 139863–139863. 8 indexed citations
5.
Taha, Muhammad, Fazal Rahim, Imad Uddin, et al.. (2024). Exploring diabetics II inhibitors based on benzodioxin derivatives, structure activity relationship, molecular docking and ADME property study. Journal of Molecular Structure. 1306. 137797–137797. 2 indexed citations
6.
Ambreen, Nida, Faiza Saleem, Muhammad Arif Lodhi, et al.. (2024). Nicotinonitriles as potential inhibitors of α-glucosidase, tyrosinase, and urease enzymes: Synthesis, characterization, in vitro, and in silico studies. Journal of Molecular Structure. 1305. 137742–137742. 4 indexed citations
7.
Othman, Mohamed S., Shawkat Hayat, Fazal Rahim, et al.. (2024). New benzimidazole based Schiff bases as potent anti-alzheimer agents: Synthesis, bio-evaluation and molecular docking study. Journal of Molecular Structure. 1309. 138058–138058. 11 indexed citations
8.
Aleid, Ghada Mohamed, Muhammad Imran, Hayat Ullah, et al.. (2024). Design, synthesis, in vitro bio-evaluation and in silico molecular docking study of benzohydrazide based thiourea analogues. Results in Chemistry. 11. 101756–101756. 1 indexed citations
9.
Khan, Khalid Mohammed, Sridevi Chigurupati, Uzma Salar, et al.. (2024). Rhodanine-benzamides as potential hits for α-amylase enzyme inhibitors and radical (DPPH and ABTS) scavengers. Molecular Diversity. 29(5). 3857–3875.
10.
Othman, Mohamed S., Fazal Rahim, Hayat Ullah, et al.. (2024). New Cholinesterase inhibitors based on 1,2,4-triazole bearing benzenesulfonohydrazide skeleton: Synthesis, in vitro and in silico studies. Results in Chemistry. 10. 101717–101717. 4 indexed citations
11.
Taha, Muhammad, Fazal Rahim, Khalid Zaman, et al.. (2024). Identification of new structure of indol-3-acetyl-arylsulfonohydrazide as potent α-glucosidase and α-amylase inhibitors and molecular docking. Journal of Molecular Structure. 1323. 140719–140719. 1 indexed citations
12.
Aleid, Ghada Mohamed, Hayat Ullah, Reda Abdel‐Hameed, et al.. (2024). Design, synthesis, biological evaluation and molecular docking study of thiadiazole-isatin hybrid analogues as potential anti-diabetic and anti-bacterial agents. Results in Chemistry. 11. 101805–101805. 1 indexed citations
13.
Taha, Muhammad, Fazal Rahim, Sridevi Chigurupati, et al.. (2024). Synthesis of novel indazole derivatives as inhibitors of diabetics II along with molecular docking and simulation study. Journal of Molecular Structure. 1322. 140394–140394. 4 indexed citations
14.
Taha, Muhammad, et al.. (2024). Self-Assembly of a Dipeptide with a Reduced Amount of Copper into Antifungal and Antibacterial Particles. Biomacromolecules. 25(2). 1018–1026. 3 indexed citations
15.
Rehman, Wajid, Fakher Rahim, Rafaqat Hussain, et al.. (2024). Molecular modeling and synthesis of novel benzimidazole-derived thiazolidinone bearing chalcone derivatives: a promising approach to develop potential anti-diabetic agents. Zeitschrift für Naturforschung C. 80(7-8). 375–390. 3 indexed citations
16.
Taha, Muhammad, Aftab Ahmad Khan, Fazal Rahim, et al.. (2023). Synthesis, in vitro evaluation and molecular docking studies of hybrid 4-quinolinyl bearing 1,3,4-thiadiazole-2-amine as a new inhibitor of α-amylase and α-glucosidase. Journal of Molecular Structure. 1282. 135173–135173. 10 indexed citations
17.
Taha, Muhammad, Shawkat Hayat, Fazal Rahim, et al.. (2023). Exploring thiazole-based Schiff base analogs as potent α-glucosidase and α-amylase inhibitor: their synthesis and in-silico study. Journal of Molecular Structure. 1287. 135672–135672. 16 indexed citations
18.
Saleem, Faiza, Khalid Mohammed Khan, Musa Özil, et al.. (2023). Regioselective syntheses of 2-oxopyridine carbonitrile derivatives and evaluation for antihyperglycemic and antioxidant potential. International Journal of Biological Macromolecules. 241. 124589–124589. 13 indexed citations
19.
Khan, Aftab Ahmad, Hayat Ullah, Fazal Rahim, et al.. (2023). Synthesis, in vitro α-glucosidase and α-amylase activities, and an in silico molecular docking study of triazinoindole-thiazolidinone hybrid derivatives. Chemical Data Collections. 45. 101035–101035. 12 indexed citations
20.
Taha, Muhammad, Mohammed Salahuddin, Noor B. Almandil, et al.. (2022). In Vitro and in Vivo Anti diabetics Study of New Oxadiazole Derivatives Along with Molecular Docking Study. Polycyclic aromatic compounds. 43(8). 6911–6926. 3 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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