Nikita Kolhatkar

2.3k total citations · 1 hit paper
18 papers, 1.8k citations indexed

About

Nikita Kolhatkar is a scholar working on Immunology, Epidemiology and Rheumatology. According to data from OpenAlex, Nikita Kolhatkar has authored 18 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Immunology, 4 papers in Epidemiology and 4 papers in Rheumatology. Recurrent topics in Nikita Kolhatkar's work include T-cell and B-cell Immunology (10 papers), Immune Cell Function and Interaction (9 papers) and Immunotherapy and Immune Responses (4 papers). Nikita Kolhatkar is often cited by papers focused on T-cell and B-cell Immunology (10 papers), Immune Cell Function and Interaction (9 papers) and Immunotherapy and Immune Responses (4 papers). Nikita Kolhatkar collaborates with scholars based in United States, United Kingdom and China. Nikita Kolhatkar's co-authors include Lisa M. Coussens, Jairo Barreto, David G. DeNardo, Pauline Andreu, David J. Rawlings, Shaun W. Jackson, Nicole E. Scharping, Holly M. Jacobs, Marc A. Schwartz and Socheath Khim and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Immunology and Cancer Cell.

In The Last Decade

Nikita Kolhatkar

16 papers receiving 1.8k citations

Hit Papers

CD4+ T Cells Regulate Pulmonary Metastasis of Mammary Car... 2009 2026 2014 2020 2009 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nikita Kolhatkar United States 13 1.2k 682 433 219 174 18 1.8k
Benjamin Joachim Schmiedel Germany 21 995 0.8× 488 0.7× 603 1.4× 131 0.6× 81 0.5× 44 1.7k
Marshall D. Behrens United States 21 1.0k 0.8× 1.0k 1.5× 646 1.5× 256 1.2× 182 1.0× 33 2.0k
Jonathan H. Esensten United States 16 1.4k 1.1× 678 1.0× 437 1.0× 151 0.7× 91 0.5× 21 2.3k
Ayako Arai Japan 28 578 0.5× 955 1.4× 539 1.2× 141 0.6× 178 1.0× 107 2.1k
Dass S. Vinay United States 24 1.7k 1.4× 797 1.2× 302 0.7× 114 0.5× 72 0.4× 44 2.3k
Omar Perbellini Italy 22 922 0.7× 427 0.6× 327 0.8× 112 0.5× 214 1.2× 50 1.9k
Eugene Y. Chiang United States 21 1.9k 1.5× 1.4k 2.0× 494 1.1× 134 0.6× 78 0.4× 27 2.7k
Karen Clise-Dwyer United States 23 1.1k 0.9× 781 1.1× 795 1.8× 359 1.6× 63 0.4× 54 2.2k
Helena Stabile Italy 24 1.0k 0.8× 369 0.5× 529 1.2× 176 0.8× 101 0.6× 47 1.8k
Naoko Nakano Japan 13 1.3k 1.0× 525 0.8× 408 0.9× 93 0.4× 94 0.5× 26 1.9k

Countries citing papers authored by Nikita Kolhatkar

Since Specialization
Citations

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

Fields of papers citing papers by Nikita Kolhatkar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nikita Kolhatkar

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

All Works

18 of 18 papers shown
1.
Omange, Robert W., Samuel Kim, Nikita Kolhatkar, et al.. (2025). AI discovery of TLR agonist-driven phenotypes reveals unique features of peripheral cells from healthy donors and ART-suppressed people living with HIV. Frontiers in Immunology. 16. 1541152–1541152. 1 indexed citations
2.
McIlwain, David R., Han Chen, Sizun Jiang, et al.. (2021). Human influenza virus challenge identifies cellular correlates of protection for oral vaccination. Cell Host & Microbe. 29(12). 1828–1837.e5. 23 indexed citations
3.
Liebowitz, David, Keith Gottlieb, Nikita Kolhatkar, et al.. (2020). Efficacy, immunogenicity, and safety of an oral influenza vaccine: a placebo-controlled and active-controlled phase 2 human challenge study. The Lancet Infectious Diseases. 20(4). 435–444. 87 indexed citations
4.
Mateo, Roberto, et al.. (2019). 78. Oral Norovirus Vaccination in Humans Induces Plasmablast B-Cell Expansion and Follicular T-Cell Activation Comparable to Natural Infection. Open Forum Infectious Diseases. 6(Supplement_2). S2–S2. 1 indexed citations
5.
Kolhatkar, Nikita, et al.. (2018). 1947. Influenza Vaccination via Oral Tablet is Protective and Induces a Unique Mucosal Immune Response. Open Forum Infectious Diseases. 5(suppl_1). S561–S562. 4 indexed citations
6.
Jacobs, Holly M., Christopher D. Thouvenel, Tanvi Arkatkar, et al.. (2016). Cutting Edge: BAFF Promotes Autoantibody Production via TACI-Dependent Activation of Transitional B Cells. The Journal of Immunology. 196(9). 3525–3531. 43 indexed citations
7.
Jackson, Shaun W., Holly M. Jacobs, Tanvi Arkatkar, et al.. (2016). AI-18 B cell IFN-γ receptor signalling promotes autoimmune germinal centresvia cell-intrinsic induction of BCL-6. A9.2–A10.
8.
Jackson, Shaun W., Holly M. Jacobs, Tanvi Arkatkar, et al.. (2016). B cell IFN-γ receptor signaling promotes autoimmune germinal centers via cell-intrinsic induction of BCL-6. The Journal of Experimental Medicine. 213(5). 733–750. 164 indexed citations
9.
Jackson, Shaun W., Nicole E. Scharping, Nikita Kolhatkar, et al.. (2016). B cell IFN-γ receptor signaling promotes autoimmune germinal centers via cell-intrinsic induction of BCL-6. The Journal of Immunology. 196(1_Supplement). 47.5–47.5. 1 indexed citations
10.
Metzler, Genita, Nikita Kolhatkar, & David J. Rawlings. (2015). BCR and co-receptor crosstalk facilitate the positive selection of self-reactive transitional B cells. Current Opinion in Immunology. 37. 46–53. 16 indexed citations
11.
Jackson, Shaun W., Nikita Kolhatkar, & David J. Rawlings. (2015). B cells take the front seat: dysregulated B cell signals orchestrate loss of tolerance and autoantibody production. Current Opinion in Immunology. 33. 70–77. 49 indexed citations
12.
Kolhatkar, Nikita, Nicole E. Scharping, Jenna M. Sullivan, et al.. (2015). B‐cell intrinsic TLR7 signals promote depletion of the marginal zone in a murine model of Wiskott–Aldrich syndrome. European Journal of Immunology. 45(10). 2773–2779. 17 indexed citations
13.
Kolhatkar, Nikita, Archana Brahmandam, Christopher D. Thouvenel, et al.. (2015). Altered BCR and TLR signals promote enhanced positive selection of autoreactive transitional B cells in Wiskott-Aldrich syndrome. The Journal of Experimental Medicine. 212(10). 1663–1677. 57 indexed citations
14.
Jackson, Shaun W., Nicole E. Scharping, Nikita Kolhatkar, et al.. (2014). Opposing Impact of B Cell–Intrinsic TLR7 and TLR9 Signals on Autoantibody Repertoire and Systemic Inflammation. The Journal of Immunology. 192(10). 4525–4532. 133 indexed citations
15.
Schwartz, Marc A., et al.. (2014). CD4+ T Cells and CD40 Participate in Selection and Homeostasis of Peripheral B Cells. The Journal of Immunology. 193(7). 3492–3502. 24 indexed citations
16.
Giltiay, Natalia V., Craig P. Chappell, Xizhang Sun, et al.. (2013). Overexpression of TLR7 promotes cell-intrinsic expansion and autoantibody production by transitional T1 B cells. The Journal of Experimental Medicine. 210(12). 2773–2789. 89 indexed citations
17.
Barbone, Dario, Jeremy Ryan, Nikita Kolhatkar, et al.. (2011). The Bcl-2 repertoire of mesothelioma spheroids underlies acquired apoptotic multicellular resistance. Cell Death and Disease. 2(6). e174–e174. 41 indexed citations
18.
DeNardo, David G., et al.. (2009). CD4+ T Cells Regulate Pulmonary Metastasis of Mammary Carcinomas by Enhancing Protumor Properties of Macrophages. Cancer Cell. 16(2). 91–102. 1054 indexed citations breakdown →

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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