Omnia E. Hussein

2.1k total citations
25 papers, 1.7k citations indexed

About

Omnia E. Hussein is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Pharmacology. According to data from OpenAlex, Omnia E. Hussein has authored 25 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Pathology and Forensic Medicine and 11 papers in Pharmacology. Recurrent topics in Omnia E. Hussein's work include Chemotherapy-induced organ toxicity mitigation (9 papers), Genomics, phytochemicals, and oxidative stress (7 papers) and Drug-Induced Hepatotoxicity and Protection (7 papers). Omnia E. Hussein is often cited by papers focused on Chemotherapy-induced organ toxicity mitigation (9 papers), Genomics, phytochemicals, and oxidative stress (7 papers) and Drug-Induced Hepatotoxicity and Protection (7 papers). Omnia E. Hussein collaborates with scholars based in Egypt, Saudi Arabia and Jordan. Omnia E. Hussein's co-authors include Ayman M. Mahmoud, Sanaa M. Abd El-Twab, Walaa G. Hozayen, Mousa O. Germoush, Mansur Abdullah Sandhu, May Bin‐Jumah, René Hernández-Bautista, Emad H. M. Hassanein, Ahmed M. Sayed and Mohammad H. Abukhalil and has published in prestigious journals such as Life Sciences, Environmental Science and Pollution Research and Oxidative Medicine and Cellular Longevity.

In The Last Decade

Omnia E. Hussein

24 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Omnia E. Hussein Egypt 19 684 413 403 237 182 25 1.7k
Sana Nafees India 23 534 0.8× 415 1.0× 466 1.2× 217 0.9× 128 0.7× 47 1.7k
El‐Shaimaa A. Arafa Egypt 25 789 1.2× 303 0.7× 275 0.7× 261 1.1× 172 0.9× 63 2.1k
Bidya Dhar Sahu India 26 745 1.1× 462 1.1× 291 0.7× 215 0.9× 90 0.5× 58 2.1k
Mehdi Goudarzi Iran 27 372 0.5× 378 0.9× 375 0.9× 354 1.5× 96 0.5× 94 1.8k
Ghada M. Suddеk Egypt 28 546 0.8× 238 0.6× 268 0.7× 185 0.8× 100 0.5× 77 1.8k
Robert Domitrović Croatia 28 748 1.1× 479 1.2× 686 1.7× 370 1.6× 250 1.4× 54 2.5k
Mir Tahir India 22 553 0.8× 328 0.8× 399 1.0× 241 1.0× 164 0.9× 26 1.6k
Mohammad H. Abukhalil Jordan 21 454 0.7× 313 0.8× 217 0.5× 207 0.9× 125 0.7× 37 1.5k
Emad H. M. Hassanein Egypt 26 566 0.8× 416 1.0× 289 0.7× 131 0.6× 61 0.3× 71 1.6k
Mohamed M. Sayed‐Ahmed Saudi Arabia 29 784 1.1× 372 0.9× 334 0.8× 144 0.6× 80 0.4× 48 2.3k

Countries citing papers authored by Omnia E. Hussein

Since Specialization
Citations

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

Fields of papers citing papers by Omnia E. Hussein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Omnia E. Hussein. 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 Omnia E. Hussein. The network helps show where Omnia E. Hussein may publish in the future.

Co-authorship network of co-authors of Omnia E. Hussein

This figure shows the co-authorship network connecting the top 25 collaborators of Omnia E. Hussein. A scholar is included among the top collaborators of Omnia E. Hussein 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 Omnia E. Hussein. Omnia E. Hussein 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.
Alruhaimi, Reem S., Ahmad Ahmeda, Omnia E. Hussein, et al.. (2024). Galangin attenuates chlorpyrifos-induced kidney injury by mitigating oxidative stress and inflammation and upregulating Nrf2 and farnesoid-X-receptor in rats. Environmental Toxicology and Pharmacology. 110. 104542–104542. 4 indexed citations
2.
Alruhaimi, Reem S., Omnia E. Hussein, Sulaiman Mohammed Alnasser, et al.. (2024). Haloxylon salicornicum Phytochemicals Suppress NF‐κB, iNOS and Pro‐Inflammatory Cytokines in Lipopolysaccharide‐Induced Macrophages. Chemistry & Biodiversity. 22(2). e202401623–e202401623.
3.
Alruhaimi, Reem S., Omnia E. Hussein, Sulaiman Mohammed Alnasser, et al.. (2024). Oxidative Stress, Inflammation, and Altered Lymphocyte E-NTPDase Are Implicated in Acute Dyslipidemia in Rats: Protective Role of Arbutin. Pharmaceuticals. 17(10). 1343–1343. 2 indexed citations
4.
Abduh, Maisa Siddiq, Reem S. Alruhaimi, Haifa A. Alqhtani, et al.. (2022). Rosmarinic acid mitigates chlorpyrifos-induced oxidative stress, inflammation, and kidney injury in rats by modulating SIRT1 and Nrf2/HO-1 signaling. Life Sciences. 313. 121281–121281. 34 indexed citations
5.
Abukhalil, Mohammad H., Omnia E. Hussein, Saleem H. Aladaileh, et al.. (2021). Visnagin prevents isoproterenol‐induced myocardial injury by attenuating oxidative stress and inflammation and upregulating Nrf2 signaling in rats. Journal of Biochemical and Molecular Toxicology. 35(11). e22906–e22906. 32 indexed citations
6.
Abukhalil, Mohammad H., Osama Y. Althunibat, Saleem H. Aladaileh, et al.. (2021). Galangin attenuates diabetic cardiomyopathy through modulating oxidative stress, inflammation and apoptosis in rats. Biomedicine & Pharmacotherapy. 138. 111410–111410. 94 indexed citations
7.
Sayed, Ahmed M., et al.. (2020). Flavonoids-mediated SIRT1 signaling activation in hepatic disorders. Life Sciences. 259. 118173–118173. 52 indexed citations
8.
Hussein, Omnia E., Walaa G. Hozayen, May Bin‐Jumah, et al.. (2020). Chicoric acid prevents methotrexate hepatotoxicity via attenuation of oxidative stress and inflammation and up-regulation of PPARγ and Nrf2/HO-1 signaling. Environmental Science and Pollution Research. 27(17). 20725–20735. 33 indexed citations
9.
Elgebaly, Hassan A., Mousa O. Germoush, Ahmed Soffar, et al.. (2020). Adenium obesum Flowers Extract Mitigates Testicular Injury and Oxidative Stress in Streptozotocin-induced Diabetic Rats. International Journal of Pharmacology. 16(4). 310–318. 2 indexed citations
10.
Abukhalil, Mohammad H., Omnia E. Hussein, May Bin‐Jumah, et al.. (2020). Farnesol attenuates oxidative stress and liver injury and modulates fatty acid synthase and acetyl-CoA carboxylase in high cholesterol-fed rats. Environmental Science and Pollution Research. 27(24). 30118–30132. 33 indexed citations
11.
Mahmoud, Ayman M., Omnia E. Hussein, Sanaa M. Abd El-Twab, & Walaa G. Hozayen. (2019). Ferulic acid protects against methotrexate nephrotoxicityviaactivation of Nrf2/ARE/HO-1 signaling and PPARγ, and suppression of NF-κB/NLRP3 inflammasome axis. Food & Function. 10(8). 4593–4607. 127 indexed citations
12.
El-Twab, Sanaa M. Abd, Omnia E. Hussein, Walaa G. Hozayen, May Bin‐Jumah, & Ayman M. Mahmoud. (2019). Chicoric acid prevents methotrexate-induced kidney injury by suppressing NF-κB/NLRP3 inflammasome activation and up-regulating Nrf2/ARE/HO-1 signaling. Inflammation Research. 68(6). 511–523. 85 indexed citations
13.
Hroob, Amir M. Al, Mohammad H. Abukhalil, Omnia E. Hussein, & Ayman M. Mahmoud. (2018). Pathophysiological mechanisms of diabetic cardiomyopathy and the therapeutic potential of epigallocatechin-3-gallate. Biomedicine & Pharmacotherapy. 109. 2155–2172. 75 indexed citations
14.
Germoush, Mousa O., Sarah I. Othman, Omnia E. Hussein, et al.. (2018). Umbelliferone prevents oxidative stress, inflammation and hematological alterations, and modulates glutamate-nitric oxide-cGMP signaling in hyperammonemic rats. Biomedicine & Pharmacotherapy. 102. 392–402. 47 indexed citations
15.
Mahmoud, Ayman M., Sarah I. Othman, Mousa O. Germoush, et al.. (2017). Commiphora molmol Modulates Glutamate‐Nitric Oxide‐cGMP and Nrf2/ARE/HO‐1 Pathways and Attenuates Oxidative Stress and Hematological Alterations in Hyperammonemic Rats. Oxidative Medicine and Cellular Longevity. 2017(1). 7369671–7369671. 20 indexed citations
16.
Mahmoud, Ayman M., Omnia E. Hussein, Walaa G. Hozayen, & Sanaa M. Abd El-Twab. (2017). Methotrexate hepatotoxicity is associated with oxidative stress, and down-regulation of PPARγ and Nrf2: Protective effect of 18β-Glycyrrhetinic acid. Chemico-Biological Interactions. 270. 59–72. 132 indexed citations
17.
Mahmoud, Ayman M., Omnia E. Hussein, & Mousa O. Germoush. (2016). Ruta graveolens Protects Against Isoniazid/Rifampicin-Induced Nephrotoxicity through Modulation of Oxidative Stress and Inflammation. 2(1). 8–13. 9 indexed citations
18.
Mahmoud, Ayman M., Omnia E. Hussein, & Ommega Internationals. (2016). Hesperidin as a Promising Anti-Diabetic Flavonoid: the Underlying Molecular Mechanism. 3(2). 0–0. 5 indexed citations
19.
El-Twab, Sanaa M. Abd, Walaa G. Hozayen, Omnia E. Hussein, & Ayman M. Mahmoud. (2016). 18β-Glycyrrhetinic acid protects against methotrexate-induced kidney injury by up-regulating the Nrf2/ARE/HO-1 pathway and endogenous antioxidants. Renal Failure. 38(9). 1516–1527. 81 indexed citations
20.
Mahmoud, Ayman M., Mousa O. Germoush, Mohammed Alotaibi, & Omnia E. Hussein. (2016). Possible involvement of Nrf2 and PPARγ up-regulation in the protective effect of umbelliferone against cyclophosphamide-induced hepatotoxicity. Biomedicine & Pharmacotherapy. 86. 297–306. 142 indexed citations

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