Shresh Pathak

2.4k total citations
28 papers, 1.6k citations indexed

About

Shresh Pathak is a scholar working on Molecular Biology, Neurology and Sensory Systems. According to data from OpenAlex, Shresh Pathak has authored 28 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Neurology and 9 papers in Sensory Systems. Recurrent topics in Shresh Pathak's work include Vestibular and auditory disorders (13 papers), Hearing, Cochlea, Tinnitus, Genetics (8 papers) and Inflammasome and immune disorders (6 papers). Shresh Pathak is often cited by papers focused on Vestibular and auditory disorders (13 papers), Hearing, Cochlea, Tinnitus, Genetics (8 papers) and Inflammasome and immune disorders (6 papers). Shresh Pathak collaborates with scholars based in United States, India and Australia. Shresh Pathak's co-authors include Manikuntala Kundu, Asima Bhattacharyya, Joyoti Basu, Sushil Kumar Pathak, Andrea Vambutas, Sanchita Basu, Anirban Banerjee, Debabrata Mandal, Tsuneyasu Kaisho and Elliot Goldofsky and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Immunology.

In The Last Decade

Shresh Pathak

28 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shresh Pathak United States	19	587	513	500	396	258	28	1.6k
Donghong Yan United States	19	562 1.0×	822 1.6×	126 0.3×	352 0.9×	93 0.4×	29	1.9k
Chandran Ramakrishna United States	21	834 1.4×	545 1.1×	566 1.1×	299 0.8×	205 0.8×	34	1.7k
J L Madara United States	16	687 1.2×	777 1.5×	159 0.3×	137 0.3×	302 1.2×	18	2.0k
Laurence Martin France	12	476 0.8×	420 0.8×	89 0.2×	145 0.4×	38 0.1×	13	1.2k
Sydney Lavoie United States	8	682 1.2×	571 1.1×	159 0.3×	105 0.3×	29 0.1×	9	1.6k
Pascale Alard United States	26	1.4k 2.4×	541 1.1×	112 0.2×	178 0.4×	98 0.4×	65	2.3k
Mercedes Monteleone Australia	14	866 1.5×	1.7k 3.3×	393 0.8×	349 0.9×	53 0.2×	20	2.2k
Katherine J. D. A. Excoffon United States	21	244 0.4×	542 1.1×	240 0.5×	173 0.4×	39 0.2×	45	1.4k
Tatsuya Kozaki Japan	13	997 1.7×	1.0k 2.0×	170 0.3×	245 0.6×	71 0.3×	19	1.9k
Zbigniew Mikulski United States	24	1.1k 1.9×	950 1.9×	219 0.4×	225 0.6×	122 0.5×	53	2.3k

Countries citing papers authored by Shresh Pathak

Since Specialization

Citations

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

Fields of papers citing papers by Shresh Pathak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shresh Pathak

This figure shows the co-authorship network connecting the top 25 collaborators of Shresh Pathak. A scholar is included among the top collaborators of Shresh Pathak 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 Shresh Pathak. Shresh Pathak 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

Pathak, Shresh, Natalie WH Tan, & Andrea Vambutas. (2025). A pilot study on the effect of SARS-CoV-2 spike protein on IL-1β-mediated inflammation in peripheral blood immune cells from AIED patients. Molecular Medicine. 31(1). 174–174. 1 indexed citations

Pathak, Shresh, et al.. (2024). Effect of betahistine on pro‐inflammatory cytokine expression in autoimmune inner ear disease and Meniere's disease patients. Laryngoscope Investigative Otolaryngology. 9(6). 1 indexed citations

Pathak, Shresh & Andrea Vambutas. (2022). NaCl exposure results in increased expression and processing of IL-1β in Meniere’s disease patients. Scientific Reports. 12(1). 4957–4957. 7 indexed citations

Pathak, Shresh & Andrea Vambutas. (2020). Autoimmune inner ear disease patient–associated 28-kDa proinflammatory IL-1β fragment results from caspase-7–mediated cleavage in vitro. JCI Insight. 5(3). 12 indexed citations

Vambutas, Andrea & Shresh Pathak. (2018). Monocytes, Macrophages, and Microglia and the Role of IL-1 in Autoimmune Inner Ear Disease (AIED). Current Otorhinolaryngology Reports. 6(2). 203–208. 5 indexed citations

Vambutas, Andrea, et al.. (2017). The Balance of Tissue Inhibitor of Metalloproteinase-1 and Matrix Metalloproteinase-9 in the Autoimmune Inner Ear Disease Patients. Journal of Interferon & Cytokine Research. 37(8). 354–361. 7 indexed citations

Pathak, Shresh, et al.. (2015). N-Acetylcysteine attenuates tumor necrosis factor alpha levels in autoimmune inner ear disease patients. Immunologic Research. 63(1-3). 236–245. 20 indexed citations

Vambutas, Andrea, Martin Lesser, Virginia Mullooly, et al.. (2014). Early efficacy trial of anakinra in corticosteroid-resistant autoimmune inner ear disease. Journal of Clinical Investigation. 124(9). 4115–4122. 59 indexed citations

Pathak, Shresh, Lynda Hatam, Vincent R. Bonagura, & Andrea Vambutas. (2013). Innate Immune Recognition of Molds and Homology to the Inner Ear Protein, Cochlin, in Patients with Autoimmune Inner Ear Disease. Journal of Clinical Immunology. 33(7). 1204–1215. 27 indexed citations

10.

Rai, Partab, Dileep Kumar, Shresh Pathak, et al.. (2012). Rapamycin-induced modulation of HIV gene transcription attenuates progression of HIVAN. Experimental and Molecular Pathology. 94(1). 255–261. 18 indexed citations

11.

Arora, Shitij, Mohammad Husain, Dileep Kumar, et al.. (2009). Human immunodeficiency virus downregulates podocyteapoEexpression. American Journal of Physiology-Renal Physiology. 297(3). F653–F661. 13 indexed citations

12.

Basu, Sanchita, Sushil Kumar Pathak, Gargi Chatterjee, et al.. (2008). Helicobacter pylori Protein HP0175 Transactivates Epidermal Growth Factor Receptor through TLR4 in Gastric Epithelial Cells. Journal of Biological Chemistry. 283(47). 32369–32376. 47 indexed citations

13.

Basu, Sanchita, Sushil Kumar Pathak, Anirban Banerjee, et al.. (2006). Execution of Macrophage Apoptosis by PE_PGRS33 of Mycobacterium tuberculosis Is Mediated by Toll-like Receptor 2-dependent Release of Tumor Necrosis Factor-α. Journal of Biological Chemistry. 282(2). 1039–1050. 182 indexed citations

14.

Pathak, Sushil Kumar, et al.. (2005). The Secreted Peptidyl Prolyl cis,trans -Isomerase HP0175 of Helicobacter pylori Induces Apoptosis of Gastric Epithelial Cells in a TLR4- and Apoptosis Signal-Regulating Kinase 1-Dependent Manner. The Journal of Immunology. 174(9). 5672–5680. 69 indexed citations

15.

Pathak, Sushil Kumar, Sanchita Basu, Asima Bhattacharyya, et al.. (2005). Mycobacterium tuberculosis Lipoarabinomannan-mediated IRAK-M Induction Negatively Regulates Toll-like Receptor-dependent Interleukin-12 p40 Production in Macrophages. Journal of Biological Chemistry. 280(52). 42794–42800. 90 indexed citations

16.

Pathak, Sushil Kumar, et al.. (2004). NF-κB- and C/EBPβ-driven Interleukin-1β Gene Expression and PAK1-mediated Caspase-1 Activation Play Essential Roles in Interleukin-1β Release from Helicobacter pylori Lipopolysaccharide-stimulated Macrophages. Journal of Biological Chemistry. 280(6). 4279–4288. 128 indexed citations

17.

Pathak, Sushil Kumar, Asima Bhattacharyya, Shresh Pathak, et al.. (2004). Toll-like Receptor 2 and Mitogen- and Stress-activated Kinase 1 Are Effectors of Mycobacterium avium-induced Cyclooxygenase-2 Expression in Macrophages. Journal of Biological Chemistry. 279(53). 55127–55136. 56 indexed citations

18.

Mandal, Debabrata, Véronique Baudin‐Creuza, Asima Bhattacharyya, et al.. (2003). Caspase 3-mediated Proteolysis of the N-terminal Cytoplasmic Domain of the Human Erythroid Anion Exchanger 1 (Band 3). Journal of Biological Chemistry. 278(52). 52551–52558. 109 indexed citations

19.

Bhattacharyya, Asima, et al.. (2003). Execution of Macrophage Apoptosis by Mycobacterium avium through Apoptosis Signal-regulating Kinase 1/p38 Mitogen-activated Protein Kinase Signaling and Caspase 8 Activation. Journal of Biological Chemistry. 278(29). 26517–26525. 54 indexed citations

20.

Bhattacharyya, Asima, Shresh Pathak, Simanti Datta, et al.. (2002). Mitogen-activated protein kinases and nuclear factor-κB regulate Helicobacter pylori-mediated interleukin-8 release from macrophages. Biochemical Journal. 368(1). 121–129. 94 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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