Srinivas Somarowthu

1.6k total citations
23 papers, 835 citations indexed

About

Srinivas Somarowthu is a scholar working on Molecular Biology, Cancer Research and Materials Chemistry. According to data from OpenAlex, Srinivas Somarowthu has authored 23 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Cancer Research and 5 papers in Materials Chemistry. Recurrent topics in Srinivas Somarowthu's work include RNA modifications and cancer (9 papers), Cancer-related molecular mechanisms research (9 papers) and RNA and protein synthesis mechanisms (9 papers). Srinivas Somarowthu is often cited by papers focused on RNA modifications and cancer (9 papers), Cancer-related molecular mechanisms research (9 papers) and RNA and protein synthesis mechanisms (9 papers). Srinivas Somarowthu collaborates with scholars based in United States, France and Italy. Srinivas Somarowthu's co-authors include Anna Marie Pyle, Fei Liu, Marco Marcia, Isabel Chillón, Michał Łęgiewicz, Mary Jo Ondrechen, David G. C. Hildebrand, Penny J. Beuning, Dagmar Ringe and Jacopo Manigrasso and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Srinivas Somarowthu

23 papers receiving 825 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Srinivas Somarowthu United States 16 735 368 75 42 39 23 835
Nathalie Ulryck France 17 946 1.3× 233 0.6× 70 0.9× 13 0.3× 38 1.0× 22 1.1k
Jainab Khatun United States 8 472 0.6× 263 0.7× 41 0.5× 19 0.5× 17 0.4× 12 547
Tracey E. Barrett United Kingdom 14 571 0.8× 116 0.3× 68 0.9× 9 0.2× 120 3.1× 15 691
Viswanath Bandaru United States 13 796 1.1× 92 0.3× 42 0.6× 17 0.4× 122 3.1× 15 871
Irina Tuszyńska Poland 14 595 0.8× 55 0.1× 50 0.7× 7 0.2× 47 1.2× 18 657
Mikael Holm United States 13 528 0.7× 96 0.3× 22 0.3× 6 0.1× 97 2.5× 20 625
Niroshika Keppetipola United States 14 392 0.5× 86 0.2× 23 0.3× 8 0.2× 44 1.1× 19 484
Peter Savory United Kingdom 12 620 0.8× 75 0.2× 27 0.4× 7 0.2× 42 1.1× 14 746
Simone Mörtl Germany 14 382 0.5× 69 0.2× 178 2.4× 14 0.3× 16 0.4× 15 528
Christine Lazennec France 13 500 0.7× 74 0.2× 67 0.9× 6 0.1× 74 1.9× 15 664

Countries citing papers authored by Srinivas Somarowthu

Since Specialization
Citations

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

Fields of papers citing papers by Srinivas Somarowthu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srinivas Somarowthu

This figure shows the co-authorship network connecting the top 25 collaborators of Srinivas Somarowthu. A scholar is included among the top collaborators of Srinivas Somarowthu 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 Srinivas Somarowthu. Srinivas Somarowthu 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.
Somarowthu, Srinivas, et al.. (2025). LncRNA SChLAP1 Promotes Cancer Cell Proliferation and Invasion Via Its Distinct Structural Domains and Conserved Regions. Journal of Molecular Biology. 437(19). 169350–169350. 1 indexed citations
2.
Somarowthu, Srinivas, et al.. (2024). A novel partnership between lncTCF7 and SND1 regulates the expression of the TCF7 gene via recruitment of the SWI/SNF complex. Scientific Reports. 14(1). 19384–19384. 2 indexed citations
3.
Somarowthu, Srinivas, et al.. (2022). The interplay of long noncoding RNAs and hepatitis B virus. Journal of Medical Virology. 95(1). 14 indexed citations
4.
Clark, Sean C., et al.. (2021). Purification and Structural Characterization of the Long Noncoding RNAs. Methods in molecular biology. 2372. 93–110. 5 indexed citations
5.
Mazina, Olga M., Srinivas Somarowthu, Lyudmila Y. Kadyrova, et al.. (2020). Replication protein A binds RNA and promotes R-loop formation. Journal of Biological Chemistry. 295(41). 14203–14213. 32 indexed citations
6.
Shenoda, Botros, Richa Gupta, Yuzhen Tian, et al.. (2020). Xist attenuates acute inflammatory response by female cells. Cellular and Molecular Life Sciences. 78(1). 299–316. 30 indexed citations
7.
Manigrasso, Jacopo, Isabel Chillón, Vito Genna, et al.. (2020). Visualizing group II intron dynamics between the first and second steps of splicing. Nature Communications. 11(1). 2837–2837. 48 indexed citations
8.
Owens, Michael C., et al.. (2019). Identifying Structural Domains and Conserved Regions in the Long Non-Coding RNA lncTCF7. International Journal of Molecular Sciences. 20(19). 4770–4770. 12 indexed citations
9.
Pyle, Anna Marie, et al.. (2019). Phylogenetic Analysis with Improved Parameters Reveals Conservation in lncRNA Structures. Journal of Molecular Biology. 431(8). 1592–1603. 40 indexed citations
10.
Liu, Fei, Srinivas Somarowthu, & Anna Marie Pyle. (2017). Visualizing the secondary and tertiary architectural domains of lncRNA RepA. Nature Chemical Biology. 13(3). 282–289. 96 indexed citations
11.
Somarowthu, Srinivas. (2015). Progress and Current Challenges in Modeling Large RNAs. Journal of Molecular Biology. 428(5). 736–747. 19 indexed citations
12.
Somarowthu, Srinivas, et al.. (2015). Prediction of distal residue participation in enzyme catalysis. Protein Science. 24(5). 762–778. 21 indexed citations
13.
Somarowthu, Srinivas, Michał Łęgiewicz, Isabel Chillón, et al.. (2015). HOTAIR Forms an Intricate and Modular Secondary Structure. Molecular Cell. 58(2). 353–361. 256 indexed citations
14.
Marcia, Marco, Elisabeth Narayanan, Kevin S. Keating, et al.. (2013). Solving nucleic acid structures by molecular replacement: examples from group II intron studies. Acta Crystallographica Section D Biological Crystallography. 69(11). 2174–2185. 17 indexed citations
15.
Marcia, Marco, Srinivas Somarowthu, & Anna Marie Pyle. (2013). Now on display: a gallery of group II intron structures at different stages of catalysis. Mobile DNA. 4(1). 14–14. 34 indexed citations
16.
Wang, Zhouxi, et al.. (2013). Protein function annotation with Structurally Aligned Local Sites of Activity (SALSAs). BMC Bioinformatics. 14(S3). S13–S13. 15 indexed citations
17.
Somarowthu, Srinivas, Michał Łęgiewicz, Kevin S. Keating, & Anna Marie Pyle. (2013). Visualizing the ai5γ group IIB intron. Nucleic Acids Research. 42(3). 1947–1958. 13 indexed citations
18.
Somarowthu, Srinivas, et al.. (2011). High‐performance prediction of functional residues in proteins with machine learning and computed input features. Biopolymers. 95(6). 390–400. 39 indexed citations
19.
Han, Gye Won, Jaeju Ko, Carol L. Farr, et al.. (2011). Crystal structure of a metal‐dependent phosphoesterase (YP_910028.1) from Bifidobacterium adolescentis: Computational prediction and experimental validation of phosphoesterase activity. Proteins Structure Function and Bioinformatics. 79(7). 2146–2160. 13 indexed citations
20.
Somarowthu, Srinivas, et al.. (2011). A Tale of Two Isomerases: Compact versus Extended Active Sites in Ketosteroid Isomerase and Phosphoglucose Isomerase. Biochemistry. 50(43). 9283–9295. 29 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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