Sreeja Parameswaran

1.5k total citations
29 papers, 397 citations indexed

About

Sreeja Parameswaran is a scholar working on Molecular Biology, Immunology and Rheumatology. According to data from OpenAlex, Sreeja Parameswaran has authored 29 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Immunology and 8 papers in Rheumatology. Recurrent topics in Sreeja Parameswaran's work include RNA modifications and cancer (5 papers), Eosinophilic Esophagitis (4 papers) and IL-33, ST2, and ILC Pathways (4 papers). Sreeja Parameswaran is often cited by papers focused on RNA modifications and cancer (5 papers), Eosinophilic Esophagitis (4 papers) and IL-33, ST2, and ILC Pathways (4 papers). Sreeja Parameswaran collaborates with scholars based in United States, Japan and United Kingdom. Sreeja Parameswaran's co-authors include Matthew T. Weirauch, Leah C. Kottyan, Marc E. Rothenberg, Lisa J. Martin, Ted Hong, Artem Barski, Ivan Marazzi, Xing Liu, Juan I. Fuxman Bass and Carmy Forney and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Sreeja Parameswaran

27 papers receiving 395 citations

Peers

Sreeja Parameswaran
Huw B. Thomas United Kingdom
Irina R. Sagalovskiy United States
Stephanie L Schell United States
Esther Zumaquero United States
Ayako Ito Japan
Olga Mamaeva United States
Huw B. Thomas United Kingdom
Sreeja Parameswaran
Citations per year, relative to Sreeja Parameswaran Sreeja Parameswaran (= 1×) peers Huw B. Thomas

Countries citing papers authored by Sreeja Parameswaran

Since Specialization
Citations

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

Fields of papers citing papers by Sreeja Parameswaran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sreeja Parameswaran

This figure shows the co-authorship network connecting the top 25 collaborators of Sreeja Parameswaran. A scholar is included among the top collaborators of Sreeja Parameswaran 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 Sreeja Parameswaran. Sreeja Parameswaran 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.
Lawson, Lucinda P., Sreeja Parameswaran, Ronald Allan M. Panganiban, et al.. (2025). Update on the genetics of allergic diseases. Journal of Allergy and Clinical Immunology. 155(6). 1738–1752. 3 indexed citations
2.
Yoneyama, Yosuke, Ranran Zhang, Mari Maezawa, et al.. (2025). Intercellular mRNA transfer alters the human pluripotent stem cell state. Proceedings of the National Academy of Sciences. 122(4). e2413351122–e2413351122.
3.
Schnell, Dan, Sreeja Parameswaran, Nathan Salomonis, et al.. (2025). A survey of pathogenic involvement in non-communicable human diseases. Communications Medicine. 5(1). 242–242. 1 indexed citations
4.
Parameswaran, Sreeja, Carmy Forney, Charles A. Moore, et al.. (2024). Genome-wide epigenetic profiling and transcriptome analysis in pediatric Obstructive Sleep Apnea: A focus on Black female children. Heliyon. 10(23). e40830–e40830. 1 indexed citations
5.
Parameswaran, Sreeja, Lee Edsall, Andrew VonHandorf, et al.. (2024). Human cytomegalovirus infection coopts chromatin organization to diminish TEAD1 transcription factor activity. eLife. 13.
6.
Yu, Meng, Sreeja Parameswaran, Wei Wei, et al.. (2024). The unique functions of Runx1 in skeletal muscle maintenance and regeneration are facilitated by an ETS interaction domain. Development. 151(24). 1 indexed citations
7.
Lu, Xiaoming, Xiaoting Chen, Sreeja Parameswaran, et al.. (2024). Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis. The American Journal of Human Genetics. 111(2). 280–294. 5 indexed citations
8.
Sun, Chengyi, Casey O. Swoboda, Michael J. Petrany, et al.. (2024). Lineage tracing of nuclei in skeletal myofibers uncovers distinct transcripts and interplay between myonuclear populations. Nature Communications. 15(1). 9372–9372. 7 indexed citations
9.
Chen, Xiaoting, Benjamin Wronowski, Sreeja Parameswaran, et al.. (2023). maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks. PLoS Computational Biology. 19(1). e1010863–e1010863. 16 indexed citations
10.
Bray, David A., Xiaoting Chen, Sreeja Parameswaran, et al.. (2022). CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants. Cell Genomics. 2(2). 100098–100098. 8 indexed citations
11.
Song, Ran, Yajing Gao, Igor Dozmorov, et al.. (2021). IRF1 governs the differential interferon-stimulated gene responses in human monocytes and macrophages by regulating chromatin accessibility. Cell Reports. 34(12). 108891–108891. 50 indexed citations
12.
Parameswaran, Sreeja, et al.. (2021). Runx Transcription Factors in T Cells—What Is Beyond Thymic Development?. Frontiers in Immunology. 12. 701924–701924. 27 indexed citations
13.
Hong, Ted, Sreeja Parameswaran, Daniel Miller, et al.. (2021). Epstein–Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci. Genome Research. 31(12). 2185–2198. 33 indexed citations
14.
Hass, Matthew R., Sreeja Parameswaran, Mario Pujato, et al.. (2021). Runx1 shapes the chromatin landscape via a cascade of direct and indirect targets. PLoS Genetics. 17(6). e1009574–e1009574. 15 indexed citations
15.
Kottyan, Leah C., Michael P. Trimarchi, Xiaoming Lu, et al.. (2020). Replication and meta-analyses nominate numerous eosinophilic esophagitis risk genes. Journal of Allergy and Clinical Immunology. 147(1). 255–266. 34 indexed citations
16.
Parameswaran, Sreeja, Xiaoting Chen, John B. Harley, et al.. (2020). Comprehensive Review of Steroid-Sensitive Nephrotic Syndrome Genetic Risk Loci and Transcriptional Regulation as a Possible Mechanistic Link to Disease Risk. Kidney International Reports. 6(1). 187–195. 4 indexed citations
17.
Kottyan, Leah C., Sreeja Parameswaran, Matthew T. Weirauch, Marc E. Rothenberg, & Lisa J. Martin. (2020). The genetic etiology of eosinophilic esophagitis. Journal of Allergy and Clinical Immunology. 145(1). 9–15. 54 indexed citations
18.
Parameswaran, Sreeja, et al.. (2019). Small molecule allosteric uncoupling of microtubule depolymerase activity from motility in human Kinesin-5 during mitotic spindle assembly. Scientific Reports. 9(1). 19900–19900. 11 indexed citations
19.
Parameswaran, Sreeja, et al.. (2019). New role of Epstein-Barr virus in pathogenesis of acute and chronic lymphocytic leukemia. The Journal of Immunology. 202(1_Supplement). 197.11–197.11. 1 indexed citations
20.
Parameswaran, Sreeja, et al.. (2010). Loop 5-directed Compounds Inhibit Chimeric Kinesin-5 Motors. Journal of Biological Chemistry. 286(8). 6201–6210. 18 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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