Vikas Anathy

2.9k total citations
66 papers, 2.1k citations indexed

About

Vikas Anathy is a scholar working on Molecular Biology, Immunology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Vikas Anathy has authored 66 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 24 papers in Immunology and 17 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Vikas Anathy's work include Redox biology and oxidative stress (18 papers), Endoplasmic Reticulum Stress and Disease (14 papers) and Asthma and respiratory diseases (11 papers). Vikas Anathy is often cited by papers focused on Redox biology and oxidative stress (18 papers), Endoplasmic Reticulum Stress and Disease (14 papers) and Asthma and respiratory diseases (11 papers). Vikas Anathy collaborates with scholars based in United States, Netherlands and India. Vikas Anathy's co-authors include Yvonne Janssen‐Heininger, Albert van der Vliet, Amy S. Guala, Matthew E. Poynter, Niki L. Reynaert, Scott W. Aesif, Sidra M. Hoffman, Jos van der Velden, Nicholas H. Heintz and Charles G. Irvin and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Vikas Anathy

66 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vikas Anathy United States	29	1.1k	455	441	377	294	66	2.1k
Ida Chiara Guerrera France	26	981 0.9×	196 0.4×	174 0.4×	257 0.7×	206 0.7×	96	1.8k
Levente József Canada	24	861 0.8×	947 2.1×	233 0.5×	320 0.8×	126 0.4×	32	2.3k
Suresh Mishra Canada	29	1.3k 1.2×	316 0.7×	413 0.9×	450 1.2×	74 0.3×	84	2.8k
Kei Yamamoto Japan	25	1.2k 1.1×	379 0.8×	304 0.7×	88 0.2×	288 1.0×	41	2.4k
Yoshimi Miki Japan	22	888 0.8×	325 0.7×	219 0.5×	94 0.2×	279 0.9×	41	1.8k
Young Do Yoo South Korea	25	1.6k 1.5×	301 0.7×	230 0.5×	209 0.6×	121 0.4×	54	2.6k
Jennifer L. Johnson United States	28	1.3k 1.2×	1.1k 2.4×	483 1.1×	95 0.3×	125 0.4×	52	2.6k
Margaret M. Allaman United States	23	967 0.9×	353 0.8×	175 0.4×	111 0.3×	135 0.5×	48	1.9k
Leopoldo Aguilera-Aguirre United States	22	907 0.8×	345 0.8×	348 0.8×	190 0.5×	56 0.2×	41	1.7k
Suk‐Hwan Baek South Korea	33	1.6k 1.5×	836 1.8×	447 1.0×	163 0.4×	92 0.3×	92	3.0k

Countries citing papers authored by Vikas Anathy

Since Specialization

Citations

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

Fields of papers citing papers by Vikas Anathy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vikas Anathy

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

All Works

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20 of 20 papers shown

Druso, Joseph E., Maximilian B. MacPherson, Shi Biao Chia, et al.. (2024). Endoplasmic Reticulum Oxidative Stress Promotes Glutathione-Dependent Oxidation of Collagen-1A1 and Promotes Lung Fibroblast Activation. American Journal of Respiratory Cell and Molecular Biology. 71(5). 589–602. 2 indexed citations

Chamberlain, Nicolas, R Chandrasekaran, Nirav Daphtary, et al.. (2024). The protein disulfide isomerase A3 and osteopontin axis promotes influenza‐induced lung remodelling. British Journal of Pharmacology. 181(22). 4610–4627. 1 indexed citations

Daphtary, Nirav, Minara Aliyeva, Kelly J. Butnor, et al.. (2023). Deletion of Miro1 in airway club cells potentiates allergic asthma phenotypes. SHILAP Revista de lepidopterología. 4. 1187945–1187945. 1 indexed citations

Ather, Jennifer L., et al.. (2023). Bariatric surgery decreases the capacity of plasma from obese asthmatic subjects to augment airway epithelial cell proinflammatory cytokine production. American Journal of Physiology-Lung Cellular and Molecular Physiology. 326(1). L71–L82. 3 indexed citations

Habibovic, Aida, Milena Hristova, Miao-chong J. Lin, et al.. (2023). Diet-induced obesity worsens allergen-induced type 2/type 17 inflammation in airways by enhancing DUOX1 activation. American Journal of Physiology-Lung Cellular and Molecular Physiology. 324(2). L228–L242. 4 indexed citations

Hondal, Robert J., Maximilian B. MacPherson, Sheryl L. White, et al.. (2023). Structural and functional fine mapping of cysteines in mammalian glutaredoxin reveal their differential oxidation susceptibility. Nature Communications. 14(1). 4550–4550. 9 indexed citations

Chandrasekaran, R, Nicolas Chamberlain, Nirav Daphtary, et al.. (2022). Mitoquinone mesylate attenuates pathological features of lean and obese allergic asthma in mice. American Journal of Physiology-Lung Cellular and Molecular Physiology. 324(2). L141–L153. 13 indexed citations

Anathy, Vikas, et al.. (2021). Lung epithelial endoplasmic reticulum and mitochondrial 3D ultrastructure: a new frontier in lung diseases. Histochemistry and Cell Biology. 155(2). 291–300. 8 indexed citations

Manuel, Allison M., Cheryl van de Wetering, Maximilian B. MacPherson, et al.. (2021). Dysregulation of Pyruvate Kinase M2 Promotes Inflammation in a Mouse Model of Obese Allergic Asthma. American Journal of Respiratory Cell and Molecular Biology. 64(6). 709–721. 13 indexed citations

10.

Nakada, Emily M., Nirav R. Bhakta, Nicolas Chamberlain, et al.. (2019). Conjugated bile acids attenuate allergen-induced airway inflammation and hyperresposiveness by inhibiting UPR transducers. JCI Insight. 4(9). 49 indexed citations

11.

Vliet, Albert van der, Yvonne Janssen‐Heininger, & Vikas Anathy. (2018). Oxidative stress in chronic lung disease: From mitochondrial dysfunction to dysregulated redox signaling. Molecular Aspects of Medicine. 63. 59–69. 124 indexed citations

12.

Ather, Jennifer L., Oliver Dienz, Jonathan E. Boyson, et al.. (2018). Serum Amyloid A3 is required for normal lung development and survival following influenza infection. Scientific Reports. 8(1). 16571–16571. 22 indexed citations

13.

Pociask, Derek, Keven M. Robinson, Kong Chen, et al.. (2017). Epigenetic and Transcriptomic Regulation of Lung Repair during Recovery from Influenza Infection. American Journal Of Pathology. 187(4). 851–863. 51 indexed citations

14.

Hoffman, Sidra M., James D. Nolin, Jane T. Jones, et al.. (2016). Ablation of the Thiol Transferase Glutaredoxin-1 Augments Protein S -Glutathionylation and Modulates Type 2 Inflammatory Responses and IL-17 in a House Dust Mite Model of Allergic Airway Disease in Mice. Annals of the American Thoracic Society. 13(Supplement_1). S97–S97. 7 indexed citations

15.

Anathy, Vikas, Scott W. Aesif, Sidra M. Hoffman, et al.. (2014). Glutaredoxin-1 Attenuates S -Glutathionylation of the Death Receptor Fas and Decreases Resolution of Pseudomonas aeruginosa Pneumonia. American Journal of Respiratory and Critical Care Medicine. 189(4). 463–474. 21 indexed citations

16.

Nolin, James D., Jane E. Tully, Sidra M. Hoffman, et al.. (2014). The glutaredoxin/S-glutathionylation axis regulates interleukin-17A-induced proinflammatory responses in lung epithelial cells in association with S-glutathionylation of nuclear factor κB family proteins. Free Radical Biology and Medicine. 73. 143–153. 20 indexed citations

17.

Janssen‐Heininger, Yvonne, James D. Nolin, Sidra M. Hoffman, et al.. (2013). Emerging mechanisms of glutathione‐dependent chemistry in biology and disease. Journal of Cellular Biochemistry. 114(9). 1962–1968. 36 indexed citations

18.

Tully, Jane E., James D. Nolin, Amy S. Guala, et al.. (2012). Cooperation between Classical and Alternative NF-κB Pathways Regulates Proinflammatory Responses in Epithelial Cells. American Journal of Respiratory Cell and Molecular Biology. 47(4). 497–508. 27 indexed citations

19.

Roberson, Elle C., Jane E. Tully, Amy S. Guala, et al.. (2011). Influenza Induces Endoplasmic Reticulum Stress, Caspase-12–Dependent Apoptosis, and c-Jun N-Terminal Kinase–Mediated Transforming Growth Factor–β Release in Lung Epithelial Cells. American Journal of Respiratory Cell and Molecular Biology. 46(5). 573–581. 109 indexed citations

20.

Anathy, Vikas, Kirankumar Santhakumar, & T. J. Pandian. (2003). Enhanced expression of β-thymosin mRNA in the ovary of GnRH analog or estradiol-17β-treated paradise fish, Macropodus opercularis. Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology. 134(3). 639–645. 4 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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