Fouad H. Darras

458 total citations
11 papers, 401 citations indexed

About

Fouad H. Darras is a scholar working on Pharmacology, Molecular Biology and Computational Theory and Mathematics. According to data from OpenAlex, Fouad H. Darras has authored 11 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pharmacology, 6 papers in Molecular Biology and 5 papers in Computational Theory and Mathematics. Recurrent topics in Fouad H. Darras's work include Cholinesterase and Neurodegenerative Diseases (9 papers), Computational Drug Discovery Methods (5 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (3 papers). Fouad H. Darras is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (9 papers), Computational Drug Discovery Methods (5 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (3 papers). Fouad H. Darras collaborates with scholars based in Germany, United Arab Emirates and Jordan. Fouad H. Darras's co-authors include Michael Decker, Jörg Heilmann, Beata Kling, Guozheng Huang, Sarah Wehle, Christoph Sotriffer, Steffen Pockes, Bassem Sadek, Yuan‐Ping Pang and Hans‐Joachim Wittmann and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Behavioural Brain Research and Physiology & Behavior.

In The Last Decade

Fouad H. Darras

11 papers receiving 396 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fouad H. Darras Germany 9 212 199 159 141 54 11 401
Stefanie Hagenow Germany 14 123 0.6× 196 1.0× 125 0.8× 78 0.6× 93 1.7× 20 389
Paula Zaręba Poland 11 217 1.0× 143 0.7× 103 0.6× 162 1.1× 26 0.5× 31 390
Sarah Wehle Germany 8 204 1.0× 126 0.6× 161 1.0× 146 1.0× 16 0.3× 8 362
Annamaria Lubelska Poland 16 98 0.5× 265 1.3× 187 1.2× 60 0.4× 91 1.7× 25 511
Agnieszka Jankowska Poland 11 122 0.6× 217 1.1× 62 0.4× 39 0.3× 34 0.6× 25 354
Agnieszka Olejarz‐Maciej Poland 15 99 0.5× 257 1.3× 179 1.1× 56 0.4× 120 2.2× 34 515
Samuele Maramai Italy 13 196 0.9× 242 1.2× 116 0.7× 104 0.7× 8 0.1× 29 512
Barbara Mordyl Poland 14 80 0.4× 173 0.9× 169 1.1× 57 0.4× 15 0.3× 41 460
Hee-Jin Ha South Korea 13 60 0.3× 196 1.0× 114 0.7× 47 0.3× 45 0.8× 21 460
Shawn B. Jones United States 4 193 0.9× 164 0.8× 125 0.8× 121 0.9× 7 0.1× 8 447

Countries citing papers authored by Fouad H. Darras

Since Specialization
Citations

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

Fields of papers citing papers by Fouad H. Darras

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fouad H. Darras. 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 Fouad H. Darras. The network helps show where Fouad H. Darras may publish in the future.

Co-authorship network of co-authors of Fouad H. Darras

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

All Works

11 of 11 papers shown
1.
Zahra, Jalal A., et al.. (2023). Synthesis, biological evaluation, and computational studies of N -benzyl pyridinium–curcumin derivatives as potent AChE inhibitors with antioxidant activity. Journal of Enzyme Inhibition and Medicinal Chemistry. 38(1). 2281264–2281264. 3 indexed citations
2.
Darras, Fouad H. & Yuan‐Ping Pang. (2017). On the use of the experimentally determined enzyme inhibition constant as a measure of absolute binding affinity. Biochemical and Biophysical Research Communications. 489(4). 451–454. 19 indexed citations
5.
Darras, Fouad H., Sarah Wehle, Guozheng Huang, Christoph Sotriffer, & Michael Decker. (2014). Amine substitution of quinazolinones leads to selective nanomolar AChE inhibitors with ‘inverted’ binding mode. Bioorganic & Medicinal Chemistry. 22(17). 4867–4881. 52 indexed citations
6.
Darras, Fouad H., et al.. (2014). Synthesis and biological evaluation of bivalent cannabinoid receptor ligands based on hCB2R selective benzimidazoles reveal unexpected intrinsic properties. Bioorganic & Medicinal Chemistry. 22(15). 3938–3946. 21 indexed citations
7.
Darras, Fouad H., et al.. (2014). Cyclic acyl guanidines bearing carbamate moieties allow potent and dirigible cholinesterase inhibition of either acetyl- or butyrylcholinesterase. Bioorganic & Medicinal Chemistry. 22(17). 5020–5034. 14 indexed citations
8.
Huang, Guozheng, Beata Kling, Fouad H. Darras, Jörg Heilmann, & Michael Decker. (2014). Identification of a neuroprotective and selective butyrylcholinesterase inhibitor derived from the natural alkaloid evodiamine. European Journal of Medicinal Chemistry. 81. 15–21. 62 indexed citations
9.
Darras, Fouad H., Steffen Pockes, Guozheng Huang, et al.. (2014). Synthesis, Biological Evaluation, and Computational Studies of Tri- and Tetracyclic Nitrogen-Bridgehead Compounds as Potent Dual-Acting AChE Inhibitors andhH3Receptor Antagonists. ACS Chemical Neuroscience. 5(3). 225–242. 72 indexed citations
10.
Darras, Fouad H., Beata Kling, Jörg Heilmann, & Michael Decker. (2012). Neuroprotective Tri- and Tetracyclic BChE Inhibitors Releasing Reversible Inhibitors upon Carbamate Transfer. ACS Medicinal Chemistry Letters. 3(11). 914–919. 81 indexed citations
11.
Voelter, Wolfgang, et al.. (2007). Synthesis of 8-Substituted 12-Methyl-12H-imidazo[4’,5’: 2,3][1,4]diazepino[6,7,1-jk]carbazoles. Heterocycles. 71(12). 2681–2681. 6 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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