Rohit Reja

3.2k total citations
19 papers, 1.2k citations indexed

About

Rohit Reja is a scholar working on Molecular Biology, Immunology and Nephrology. According to data from OpenAlex, Rohit Reja has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 5 papers in Immunology and 2 papers in Nephrology. Recurrent topics in Rohit Reja's work include RNA Research and Splicing (5 papers), Immune Response and Inflammation (4 papers) and Inflammasome and immune disorders (3 papers). Rohit Reja is often cited by papers focused on RNA Research and Splicing (5 papers), Immune Response and Inflammation (4 papers) and Inflammasome and immune disorders (3 papers). Rohit Reja collaborates with scholars based in United States, France and Australia. Rohit Reja's co-authors include Vishva M. Dixit, Kim Newton, Joshua D. Webster, Zora Modrušan, B. Franklin Pugh, Merone Roose‐Girma, Vinesh Vinayachandran, Debra L. Dugger, Allie Maltzman and Katherine E. Wickliffe and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Rohit Reja

16 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rohit Reja United States 14 981 312 93 90 83 19 1.2k
Allie Maltzman France 8 1.0k 1.0× 588 1.9× 133 1.4× 164 1.8× 50 0.6× 9 1.2k
Insa Buers Germany 18 666 0.7× 267 0.9× 101 1.1× 87 1.0× 58 0.7× 28 1.2k
Melanie R. Shakespear Australia 7 794 0.8× 362 1.2× 153 1.6× 85 0.9× 37 0.4× 7 1.0k
Inge Bruggeman Belgium 7 1.1k 1.1× 531 1.7× 139 1.5× 187 2.1× 21 0.3× 10 1.3k
R. G. Ebb United States 7 743 0.8× 173 0.6× 175 1.9× 78 0.9× 49 0.6× 7 933
Joanne M. Hildebrand Australia 22 1.5k 1.6× 845 2.7× 278 3.0× 244 2.7× 39 0.5× 38 2.0k
Il‐Young Hwang United States 20 572 0.6× 539 1.7× 144 1.5× 137 1.5× 28 0.3× 40 1.2k
Pin Ling Taiwan 19 628 0.6× 270 0.9× 214 2.3× 151 1.7× 12 0.1× 39 1.2k
Matija Zelic United States 11 1.0k 1.1× 788 2.5× 133 1.4× 156 1.7× 22 0.3× 13 1.4k
Jonilson Berlink Lima Brazil 13 603 0.6× 355 1.1× 60 0.6× 165 1.8× 19 0.2× 22 962

Countries citing papers authored by Rohit Reja

Since Specialization
Citations

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

Fields of papers citing papers by Rohit Reja

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rohit Reja

This figure shows the co-authorship network connecting the top 25 collaborators of Rohit Reja. A scholar is included among the top collaborators of Rohit Reja 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 Rohit Reja. Rohit Reja 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.
Newton, Kim, Katherine E. Wickliffe, Allie Maltzman, et al.. (2025). cFLIP suppresses caspase-1- and MLKL-independent perinatal lethality driven by auto-processing impaired caspase-8 D387A. Cell Death and Differentiation.
2.
Ndoja, Ada, Christopher M. Rose, Eva Lin, et al.. (2025). COP1 Deficiency in BRAFV600E Melanomas Confers Resistance to Inhibitors of the MAPK Pathway. Cells. 14(13). 975–975.
3.
Gitlin, Alexander D., Allie Maltzman, Klaus Heger, et al.. (2024). N4BP1 coordinates ubiquitin-dependent crosstalk within the IκB kinase family to limit Toll-like receptor signaling and inflammation. Immunity. 57(5). 973–986.e7. 13 indexed citations
4.
Rohatgi, Neha, et al.. (2024). Seed sequences mediate off-target activity in the CRISPR-interference system. Cell Genomics. 4(11). 100693–100693. 4 indexed citations
5.
Solon, Margaret, Nianfeng Ge, Susan Haller, et al.. (2024). ZBP1 and TRIF trigger lethal necroptosis in mice lacking caspase-8 and TNFR1. Cell Death and Differentiation. 31(5). 672–682. 21 indexed citations
6.
Luchetti, Giovanni, Justin L. Roncaioli, Roberto A. Chavez, et al.. (2021). Shigella ubiquitin ligase IpaH7.8 targets gasdermin D for degradation to prevent pyroptosis and enable infection. Cell Host & Microbe. 29(10). 1521–1530.e10. 121 indexed citations
7.
Ndoja, Ada, Rohit Reja, Seung-Hye Lee, et al.. (2020). Ubiquitin Ligase COP1 Suppresses Neuroinflammation by Degrading c/EBPβ in Microglia. Cell. 182(5). 1156–1169.e12. 107 indexed citations
8.
Kayagaki, Nobuhiko, Bettina L. Lee, Irma B. Stowe, et al.. (2019). IRF2 transcriptionally induces GSDMD expression for pyroptosis. Science Signaling. 12(582). 131 indexed citations
9.
He, Meng, Mira S. Chaurushiya, Joshua D. Webster, et al.. (2019). Intrinsic apoptosis shapes the tumor spectrum linked to inactivation of the deubiquitinase BAP1. Science. 364(6437). 283–285. 71 indexed citations
10.
Newton, Kim, Katherine E. Wickliffe, Allie Maltzman, et al.. (2019). Activity of caspase-8 determines plasticity between cell death pathways. Nature. 575(7784). 679–682. 289 indexed citations
11.
Pham, Victoria C., Joshua D. Webster, Rohit Reja, et al.. (2019). The RIPK4–IRF6 signalling axis safeguards epidermal differentiation and barrier function. Nature. 574(7777). 249–253. 54 indexed citations
12.
Abed, Mona, Erik Verschueren, Hanna G. Budayeva, et al.. (2019). The Gag protein PEG10 binds to RNA and regulates trophoblast stem cell lineage specification. PLoS ONE. 14(4). e0214110–e0214110. 49 indexed citations
13.
García‐Martínez, José, Rohit Reja, Pedro Furió‐Tarí, et al.. (2018). The SAGA/TREX-2 subunit Sus1 binds widely to transcribed genes and affects mRNA turnover globally. Epigenetics & Chromatin. 11(1). 13–13. 15 indexed citations
14.
Vinayachandran, Vinesh, Rohit Reja, Matthew J. Rossi, et al.. (2018). Widespread and precise reprogramming of yeast protein–genome interactions in response to heat shock. Genome Research. 28(3). 357–366. 51 indexed citations
15.
Aguilar‐Gurrieri, Carmen, Amédé Larabi, Vinesh Vinayachandran, et al.. (2016). Structural evidence for Nap1‐dependent H2A–H2B deposition and nucleosome assembly. The EMBO Journal. 35(13). 1465–1482. 58 indexed citations
16.
Reja, Rohit, Vinesh Vinayachandran, Sujana Ghosh, & B. Franklin Pugh. (2015). Molecular mechanisms of ribosomal protein gene coregulation. Genes & Development. 29(18). 1942–1954. 80 indexed citations
17.
Schneider, Maren, Doris Hellerschmied, Tobias Schubert, et al.. (2015). The Nuclear Pore-Associated TREX-2 Complex Employs Mediator to Regulate Gene Expression. Cell. 162(5). 1016–1028. 91 indexed citations
18.
Reja, Rohit, AJ Venkatakrishnan, Byoung-Chul Kim, et al.. (2009). MitoInteractome: Mitochondrial protein interactome database, and its application in 'aging network' analysis. BMC Genomics. 10(S3). S20–S20. 27 indexed citations
19.
Bhak, Jong, Ho Ghang, Rohit Reja, & Sangsoo Kim. (2008). Personal Genomics, Bioinformatics, and Variomics. Genomics & Informatics. 6(4). 161–165.

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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