Ujjaldeep Jaggi

611 total citations
32 papers, 483 citations indexed

About

Ujjaldeep Jaggi is a scholar working on Epidemiology, Immunology and Ophthalmology. According to data from OpenAlex, Ujjaldeep Jaggi has authored 32 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Epidemiology, 23 papers in Immunology and 5 papers in Ophthalmology. Recurrent topics in Ujjaldeep Jaggi's work include Herpesvirus Infections and Treatments (23 papers), Immune Response and Inflammation (11 papers) and Cytomegalovirus and herpesvirus research (10 papers). Ujjaldeep Jaggi is often cited by papers focused on Herpesvirus Infections and Treatments (23 papers), Immune Response and Inflammation (11 papers) and Cytomegalovirus and herpesvirus research (10 papers). Ujjaldeep Jaggi collaborates with scholars based in United States and Austria. Ujjaldeep Jaggi's co-authors include Siva Karthik Varanasi, Homayon Ghiasi, Barry T. Rouse, Harry H. Matundan, Siddheshvar Bhela, Shaohui Wang, Satoshi Hirose, Fernanda Giménez, Naveen K. Rajasagi and Dallas R. Donohoe and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Journal of Virology.

In The Last Decade

Ujjaldeep Jaggi

29 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ujjaldeep Jaggi United States 14 272 226 120 70 56 32 483
Siva Karthik Varanasi United States 12 171 0.6× 119 0.5× 123 1.0× 43 0.6× 35 0.6× 14 365
Fernanda Giménez United States 10 170 0.6× 164 0.7× 165 1.4× 94 1.3× 75 1.3× 12 487
Kaska Wloka United Kingdom 5 237 0.9× 55 0.2× 59 0.5× 228 3.3× 35 0.6× 6 503
Marta Subías Spain 8 429 1.6× 48 0.2× 96 0.8× 31 0.4× 61 1.1× 10 552
Michelle Elvington United States 11 364 1.3× 55 0.2× 90 0.8× 22 0.3× 42 0.8× 14 526
Bruno Jorge de Andrade Silva Brazil 8 168 0.6× 149 0.7× 132 1.1× 19 0.3× 14 0.3× 14 440
Minjian Ni United States 10 275 1.0× 43 0.2× 132 1.1× 81 1.2× 102 1.8× 15 496
Pedro H. Papotto Portugal 9 407 1.5× 42 0.2× 83 0.7× 24 0.3× 17 0.3× 13 524
Maanasa Indaram United States 11 89 0.3× 117 0.5× 95 0.8× 160 2.3× 63 1.1× 24 420
Kumarkrishna Raychaudhuri United States 6 173 0.6× 42 0.2× 103 0.9× 119 1.7× 106 1.9× 11 405

Countries citing papers authored by Ujjaldeep Jaggi

Since Specialization
Citations

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

Fields of papers citing papers by Ujjaldeep Jaggi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ujjaldeep Jaggi

This figure shows the co-authorship network connecting the top 25 collaborators of Ujjaldeep Jaggi. A scholar is included among the top collaborators of Ujjaldeep Jaggi 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 Ujjaldeep Jaggi. Ujjaldeep Jaggi 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.
Jaggi, Ujjaldeep, et al.. (2024). Absence of CD80 reduces HSV-1 replication in the eye and delays reactivation but not latency levels. Journal of Virology. 98(3). e0201023–e0201023. 2 indexed citations
2.
Jaggi, Ujjaldeep, et al.. (2024). A novel GFP-based strategy to quantitate cellular spatial associations in HSV-1 viral pathogenesis. mBio. 15(10). e0145424–e0145424. 1 indexed citations
3.
Wang, Shaohui, Ujjaldeep Jaggi, Makoto Katsumata, & Homayon Ghiasi. (2024). The importance of IFNα2A (Roferon-A) in HSV-1 latency and T cell exhaustion in ocularly infected mice. PLoS Pathogens. 20(10). e1012612–e1012612. 3 indexed citations
4.
5.
Hirose, Satoshi, Shaohui Wang, Ujjaldeep Jaggi, et al.. (2023). IL-17A expression by both T cells and non-T cells contribute to HSV-IL-2-induced CNS demyelination. Frontiers in Immunology. 14. 1102486–1102486. 1 indexed citations
6.
Jaggi, Ujjaldeep, Shaohui Wang, Kevin R. Mott, & Homayon Ghiasi. (2023). Binding of herpesvirus entry mediator (HVEM) and HSV-1 gD affect reactivation but not latency levels. PLoS Pathogens. 19(9). e1011693–e1011693.
7.
Wang, Shaohui, Ujjaldeep Jaggi, & Homayon Ghiasi. (2022). Knockout of signal peptide peptidase in the eye reduces HSV-1 replication and eye disease in ocularly infected mice. PLoS Pathogens. 18(10). e1010898–e1010898. 2 indexed citations
8.
Wang, Shaohui, et al.. (2022). Absence of signal peptide peptidase in peripheral sensory neurons affects latency-reactivation in HSV-1 ocularly infected mice. PLoS Pathogens. 18(1). e1010281–e1010281. 5 indexed citations
9.
Matundan, Harry H., et al.. (2021). Absence of CD28-CTLA4-PD-L1 Costimulatory Molecules Reduces Herpes Simplex Virus 1 Reactivation. mBio. 12(4). e0117621–e0117621. 2 indexed citations
10.
11.
Jaggi, Ujjaldeep, Harry H. Matundan, Satoshi Hirose, et al.. (2021). Essential role of M1 macrophages in blocking cytokine storm and pathology associated with murine HSV-1 infection. PLoS Pathogens. 17(10). e1009999–e1009999. 20 indexed citations
12.
Wang, Shaohui, et al.. (2021). Blocking HSV-1 glycoprotein K binding to signal peptide peptidase reduces virus infectivity in vitro and in vivo. PLoS Pathogens. 17(8). e1009848–e1009848. 2 indexed citations
13.
Jaggi, Ujjaldeep, Mingjie Yang, Harry H. Matundan, et al.. (2020). Increased phagocytosis in the presence of enhanced M2-like macrophage responses correlates with increased primary and latent HSV-1 infection. PLoS Pathogens. 16(10). e1008971–e1008971. 61 indexed citations
14.
Hirose, Satoshi, Pedram Shafiei-Jahani, Shaohui Wang, et al.. (2020). Type 2 Innate Lymphoid Cells Induce CNS Demyelination in an HSV-IL-2 Mouse Model of Multiple Sclerosis. iScience. 23(10). 101549–101549. 21 indexed citations
15.
Lee, Der‐Horng, Ujjaldeep Jaggi, & Homayon Ghiasi. (2019). CCR2+ migratory macrophages with M1 status are the early-responders in the cornea of HSV-1 infected mice. PLoS ONE. 14(4). e0215727–e0215727. 17 indexed citations
16.
Jaggi, Ujjaldeep, et al.. (2018). Role of Herpes Simplex Virus Type 1 (HSV-1) Glycoprotein K (gK) Pathogenic CD8+ T Cells in Exacerbation of Eye Disease. Frontiers in Immunology. 9. 2895–2895. 28 indexed citations
17.
Varanasi, Siva Karthik, Ujjaldeep Jaggi, Nissim Hay, & Barry T. Rouse. (2018). Hexokinase II may be dispensable for CD4 T cell responses against a virus infection. PLoS ONE. 13(1). e0191533–e0191533. 13 indexed citations
18.
Jaggi, Ujjaldeep, Siva Karthik Varanasi, Siddheshvar Bhela, & Barry T. Rouse. (2018). On the role of retinoic acid in virus induced inflammatory response in cornea. Microbes and Infection. 20(6). 337–345. 23 indexed citations
19.
Varanasi, Siva Karthik, Naveen K. Rajasagi, Ujjaldeep Jaggi, & Barry T. Rouse. (2018). Role of IL-18 induced Amphiregulin expression on virus induced ocular lesions. Mucosal Immunology. 11(6). 1705–1715. 17 indexed citations
20.
Bhela, Siddheshvar, Sachin Mulik, Fernanda Giménez, et al.. (2015). Role of miR-155 in the Pathogenesis of Herpetic Stromal Keratitis. American Journal Of Pathology. 185(4). 1073–1084. 47 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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