Sagar Gaikwad

1.3k total citations
19 papers, 956 citations indexed

About

Sagar Gaikwad is a scholar working on Neurology, Physiology and Immunology. According to data from OpenAlex, Sagar Gaikwad has authored 19 papers receiving a total of 956 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 8 papers in Physiology and 6 papers in Immunology. Recurrent topics in Sagar Gaikwad's work include Neuroinflammation and Neurodegeneration Mechanisms (9 papers), Alzheimer's disease research and treatments (7 papers) and Immune Response and Inflammation (4 papers). Sagar Gaikwad is often cited by papers focused on Neuroinflammation and Neurodegeneration Mechanisms (9 papers), Alzheimer's disease research and treatments (7 papers) and Immune Response and Inflammation (4 papers). Sagar Gaikwad collaborates with scholars based in India, United States and Italy. Sagar Gaikwad's co-authors include Reena Agrawal-Rajput, Rakez Kayed, Mahendra Rai, Avinash P. Ingle, Stefania Galdiero, Annarita Falanga, L. Russo, Aniket Gade, Massimiliano Galdiero and Mauro Montalbano and has published in prestigious journals such as Journal of Biological Chemistry, Science Translational Medicine and Cell Reports.

In The Last Decade

Sagar Gaikwad

18 papers receiving 948 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sagar Gaikwad India 13 241 233 219 177 124 19 956
Ching‐Wen Chen United States 22 115 0.5× 399 1.7× 66 0.3× 186 1.1× 112 0.9× 50 1.3k
Qinqin Bai China 13 71 0.3× 399 1.7× 93 0.4× 340 1.9× 45 0.4× 42 1.0k
Haixia Ma China 18 123 0.5× 403 1.7× 45 0.2× 131 0.7× 63 0.5× 32 1.3k
Л. І. Остапченко Ukraine 21 164 0.7× 459 2.0× 190 0.9× 25 0.1× 52 0.4× 179 1.3k
Barnaby C. H. May United States 23 310 1.3× 1.1k 4.7× 63 0.3× 331 1.9× 95 0.8× 54 2.1k
Annie Hiniker United States 18 279 1.2× 638 2.7× 98 0.4× 99 0.6× 32 0.3× 41 1.4k
Tingting Chen China 18 62 0.3× 671 2.9× 111 0.5× 47 0.3× 24 0.2× 60 957
Xiaoyu Yu China 18 39 0.2× 395 1.7× 63 0.3× 59 0.3× 51 0.4× 60 882
Mohammad G. Mohammad United Arab Emirates 15 218 0.9× 202 0.9× 42 0.2× 63 0.4× 38 0.3× 33 804
J. C. K. Lai United States 15 220 0.9× 473 2.0× 38 0.2× 38 0.2× 90 0.7× 34 1.3k

Countries citing papers authored by Sagar Gaikwad

Since Specialization
Citations

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

Fields of papers citing papers by Sagar Gaikwad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sagar Gaikwad

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

All Works

19 of 19 papers shown
1.
Gaikwad, Sagar, Nicha Puangmalai, Mauro Montalbano, et al.. (2024). Nasal tau immunotherapy clears intracellular tau pathology and improves cognitive functions in aged tauopathy mice. Science Translational Medicine. 16(754). eadj5958–eadj5958. 16 indexed citations
2.
3.
Gaikwad, Sagar, Sudipta Senapati, Md. Anzarul Haque, & Rakez Kayed. (2023). Senescence, brain inflammation, and oligomeric tau drive cognitive decline in Alzheimer's disease: Evidence from clinical and preclinical studies. Alzheimer s & Dementia. 20(1). 709–727. 48 indexed citations
4.
Puangmalai, Nicha, Urmi Sengupta, Nemil Bhatt, et al.. (2022). Lysine 63-linked ubiquitination of tau oligomers contributes to the pathogenesis of Alzheimer’s disease. Journal of Biological Chemistry. 298(4). 101766–101766. 45 indexed citations
5.
Gaikwad, Sagar & Rakez Kayed. (2022). HMGB1‐Mediated Senescence and Brain Inflammation Contributes to Cognitive Dysfunctions. Alzheimer s & Dementia. 18(S4). 5 indexed citations
6.
Gaikwad, Sagar, Nicha Puangmalai, Alice Bittar, et al.. (2021). Tau oligomer induced HMGB1 release contributes to cellular senescence and neuropathology linked to Alzheimer’s disease and frontotemporal dementia. Cell Reports. 36(3). 109419–109419. 153 indexed citations
7.
Puangmalai, Nicha, Nemil Bhatt, Mauro Montalbano, et al.. (2020). Internalization mechanisms of brain-derived tau oligomers from patients with Alzheimer’s disease, progressive supranuclear palsy and dementia with Lewy bodies. Cell Death and Disease. 11(5). 314–314. 75 indexed citations
8.
Gaikwad, Sagar, et al.. (2020). Evaluation of clinical outcome of cementless ceramic on ceramic primary total hip replacement in young patients of avascular necrosis of femoral head. Journal of Arthroscopy and Joint Surgery. 8(4). 366–371. 2 indexed citations
9.
Gaikwad, Sagar, Nicha Puangmalai, Alice Bittar, et al.. (2020). Tau Oligomer Induced HMGB1 Release Contributes to Cellular Senescence and Neuropathology Linked to Alzheimer's Disease and Frontotemporal Dementia. SSRN Electronic Journal. 6 indexed citations
10.
Patro, A. Raj Kumar, Diwakar Singh, Sagar Gaikwad, et al.. (2019). Cytokine Signature Associated with Disease Severity in Dengue. Viruses. 11(1). 34–34. 76 indexed citations
11.
Gaikwad, Sagar, et al.. (2017). Spleen tyrosine kinase inhibition ameliorates airway inflammation through modulation of NLRP3 inflammosome and Th17/Treg axis. International Immunopharmacology. 54. 375–384. 37 indexed citations
12.
Agrawal-Rajput, Reena, et al.. (2016). Toll-like receptor-4 antagonism mediates benefits during neuroinflammation. Neural Regeneration Research. 11(4). 552–552. 13 indexed citations
13.
14.
Gaikwad, Sagar, et al.. (2016). CD40 Negatively Regulates ATP-TLR4-Activated Inflammasome in Microglia. Cellular and Molecular Neurobiology. 37(2). 351–359. 35 indexed citations
15.
Gaikwad, Sagar, et al.. (2015). The critical role of JNK and p38 MAPKs for TLR4 induced microglia-mediated neurotoxicity. European Journal of Experimental Biology. 5(8). 2 indexed citations
16.
Gaikwad, Sagar & Reena Agrawal-Rajput. (2015). Lipopolysaccharide fromRhodobacter sphaeroidesAttenuates Microglia-Mediated Inflammation and Phagocytosis and Directs Regulatory T Cell Response. International Journal of Inflammation. 2015. 1–13. 34 indexed citations
17.
Galdiero, Stefania, Mahendra Rai, Aniket Gade, et al.. (2013). Antiviral activity of mycosynthesized silver nanoparticles against herpes simplex virus and human parainfluenza virus type 3. International Journal of Nanomedicine. 8. 4303–4303. 277 indexed citations
18.
Gaikwad, Sagar, et al.. (2012). Green Synthesis of Silver Nanoparticles Using Aspergillus niger and Its Efficacy Against Human Pathogens. European Journal of Experimental Biology. 2(5). 51 indexed citations
19.
Mathur, M, et al.. (2012). Laboratory and clinical profile of dengue: A study from Mumbai. Annals of Tropical Medicine and Public Health. 5(1). 20–20. 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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