Chandrashekara Mallappa

776 total citations
12 papers, 634 citations indexed

About

Chandrashekara Mallappa is a scholar working on Molecular Biology, Plant Science and Pathology and Forensic Medicine. According to data from OpenAlex, Chandrashekara Mallappa has authored 12 papers receiving a total of 634 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Plant Science and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Chandrashekara Mallappa's work include Photosynthetic Processes and Mechanisms (4 papers), Light effects on plants (4 papers) and Genomics and Chromatin Dynamics (4 papers). Chandrashekara Mallappa is often cited by papers focused on Photosynthetic Processes and Mechanisms (4 papers), Light effects on plants (4 papers) and Genomics and Chromatin Dynamics (4 papers). Chandrashekara Mallappa collaborates with scholars based in United States, Japan and India. Chandrashekara Mallappa's co-authors include Sudip Chattopadhyay, Vandana Yadav, Sreeramaiah N. Gangappa, Anthony N. Imbalzano, Yasuyuki Ohkawa, J. Manuel Hernández‐Hernández, Aparna Singh, Hasthi Ram, Brian T. Nasipak and Saı̈d Sif and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and The Plant Cell.

In The Last Decade

Chandrashekara Mallappa

12 papers receiving 626 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chandrashekara Mallappa United States 11 469 396 67 26 24 12 634
Da‐Hai Yang China 13 340 0.7× 529 1.3× 106 1.6× 16 0.6× 42 1.8× 25 709
Hisae Kojima Japan 7 318 0.7× 246 0.6× 43 0.6× 9 0.3× 12 0.5× 9 482
Minsoo Kim United States 12 583 1.2× 615 1.6× 28 0.4× 23 0.9× 27 1.1× 19 879
Yanhua Xu China 13 635 1.4× 365 0.9× 37 0.6× 73 2.8× 33 1.4× 23 890
Florian Brioudes France 7 386 0.8× 447 1.1× 39 0.6× 18 0.7× 42 1.8× 9 577
Weifeng Huang China 11 332 0.7× 289 0.7× 18 0.3× 32 1.2× 8 0.3× 17 551
Jin Xia China 11 291 0.6× 240 0.6× 221 3.3× 17 0.7× 28 1.2× 19 478
Augustyn Bogucki Switzerland 9 694 1.5× 467 1.2× 16 0.2× 47 1.8× 10 0.4× 9 769
Xunyan Liu China 11 317 0.7× 432 1.1× 33 0.5× 35 1.3× 15 0.6× 25 569

Countries citing papers authored by Chandrashekara Mallappa

Since Specialization
Citations

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

Fields of papers citing papers by Chandrashekara Mallappa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chandrashekara Mallappa

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

All Works

12 of 12 papers shown
1.
Harada, Akihito, Chandrashekara Mallappa, Seiji Okada, et al.. (2015). Spatial re-organization of myogenic regulatory sequences temporally controls gene expression. Nucleic Acids Research. 43(4). 2008–2021. 31 indexed citations
2.
Cho, Ok Hyun, Chandrashekara Mallappa, J. Manuel Hernández‐Hernández, Jaime A. Rivera‐Pérez, & Anthony N. Imbalzano. (2014). Contrasting roles for MyoD in organizing myogenic promoter structures during embryonic skeletal muscle development. Developmental Dynamics. 244(1). 43–55. 26 indexed citations
3.
Wu, Cheng, Fengtang Yang, Kristina Smith, et al.. (2014). Genome-Wide Characterization of Light-Regulated Genes inNeurospora crassa. G3 Genes Genomes Genetics. 4(9). 1731–1745. 73 indexed citations
4.
Hernández‐Hernández, J. Manuel, et al.. (2013). The Scaffold attachment factor b1 (Safb1) regulates myogenic differentiation by facilitating the transition of myogenic gene chromatin from a repressed to an activated state. Nucleic Acids Research. 41(11). 5704–5716. 26 indexed citations
5.
Ohkawa, Yasuyuki, et al.. (2011). An Improved Restriction Enzyme Accessibility Assay for Analyzing Changes in Chromatin Structure in Samples of Limited Cell Number. Methods in molecular biology. 798. 531–542. 8 indexed citations
6.
Ohkawa, Yasuyuki, et al.. (2011). Isolation of Nuclei from Skeletal Muscle Satellite Cells and Myofibers for Use in Chromatin Immunoprecipitation Assays. Methods in molecular biology. 798. 517–530. 12 indexed citations
7.
Stewart, Kathleen M., Rajini Mudhasani, Ananthi J. Asirvatham, et al.. (2010). SWI/SNF chromatin remodeling enzyme ATPases promote cell proliferation in normal mammary epithelial cells. Journal of Cellular Physiology. 223(3). 667–678. 29 indexed citations
8.
Mallappa, Chandrashekara, et al.. (2010). The expression of myogenic microRNAs indirectly requires protein arginine methyltransferase (Prmt)5 but directly requires Prmt4. Nucleic Acids Research. 39(4). 1243–1255. 35 indexed citations
9.
Mallappa, Chandrashekara, Brian T. Nasipak, Elliot J. Androphy, et al.. (2010). Myogenic MicroRNA Expression Requires ATP-Dependent Chromatin Remodeling Enzyme Function. Molecular and Cellular Biology. 30(13). 3176–3186. 25 indexed citations
10.
Mallappa, Chandrashekara, Aparna Singh, Hasthi Ram, & Sudip Chattopadhyay. (2008). GBF1, a Transcription Factor of Blue Light Signaling in Arabidopsis, Is Degraded in the Dark by a Proteasome-mediated Pathway Independent of COP1 and SPA1. Journal of Biological Chemistry. 283(51). 35772–35782. 37 indexed citations
11.
Mallappa, Chandrashekara, et al.. (2006). A Basic Leucine Zipper Transcription Factor, G-box-binding Factor 1, Regulates Blue Light-mediated Photomorphogenic Growth in Arabidopsis. Journal of Biological Chemistry. 281(31). 22190–22199. 92 indexed citations
12.
Yadav, Vandana, et al.. (2005). A Basic Helix-Loop-Helix Transcription Factor in Arabidopsis, MYC2, Acts as a Repressor of Blue Light–Mediated Photomorphogenic Growth. The Plant Cell. 17(7). 1953–1966. 240 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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2026