Parithi Balachandran

485 total citations
7 papers, 122 citations indexed

About

Parithi Balachandran is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Parithi Balachandran has authored 7 papers receiving a total of 122 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Plant Science and 2 papers in Genetics. Recurrent topics in Parithi Balachandran's work include Genomics and Phylogenetic Studies (5 papers), Chromosomal and Genetic Variations (3 papers) and Nanopore and Nanochannel Transport Studies (2 papers). Parithi Balachandran is often cited by papers focused on Genomics and Phylogenetic Studies (5 papers), Chromosomal and Genetic Variations (3 papers) and Nanopore and Nanochannel Transport Studies (2 papers). Parithi Balachandran collaborates with scholars based in United States, Austria and United Kingdom. Parithi Balachandran's co-authors include Christine R. Beck, Peter A. Audano, Nicholas Brookhouser, Xiao Wang, Kylie Standage-Beier, David A. Brafman, Evan E. Eichler, Laura G. Reinholdt, David Gordon and Anne Czechanski and has published in prestigious journals such as Nature Communications, Genome Medicine and Chromosome Research.

In The Last Decade

Parithi Balachandran

7 papers receiving 121 citations

Peers

Parithi Balachandran
Avery Davis Bell United States
Wan Kin Au Yeung Japan
Izabela Harabula Germany
Xiuling Fu China
Corinne Simonti United States
Luis Enrique Cabrera-Quio Austria
Hironori Abe United States
Rachel Waymack United States
Jennifer A. Urban United States
Avery Davis Bell United States
Parithi Balachandran
Citations per year, relative to Parithi Balachandran Parithi Balachandran (= 1×) peers Avery Davis Bell

Countries citing papers authored by Parithi Balachandran

Since Specialization
Citations

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

Fields of papers citing papers by Parithi Balachandran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Parithi Balachandran

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

All Works

7 of 7 papers shown
1.
Audano, Peter A., Parithi Balachandran, Anne Czechanski, et al.. (2023). Resolution of structural variation in diverse mouse genomes reveals chromatin remodeling due to transposable elements. Cell Genomics. 3(5). 100291–100291. 27 indexed citations
2.
Balachandran, Parithi, et al.. (2022). Transposable element-mediated rearrangements are prevalent in human genomes. Nature Communications. 13(1). 7115–7115. 39 indexed citations
3.
Daniš, Daniel, Julius O.B. Jacobsen, Parithi Balachandran, et al.. (2022). SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing. Genome Medicine. 14(1). 44–44. 16 indexed citations
4.
Balachandran, Parithi & Christine R. Beck. (2020). Structural variant identification and characterization. Chromosome Research. 28(1). 31–47. 18 indexed citations
5.
Standage-Beier, Kylie, et al.. (2019). RNA-Guided Recombinase-Cas9 Fusion Targets Genomic DNA Deletion and Integration. The CRISPR Journal. 2(4). 209–222. 17 indexed citations
6.
Balachandran, Parithi, et al.. (2017). SNaReSim: Synthetic Nanopore Read Simulator. 14. 338–344. 4 indexed citations
7.
Treviño, Robert P., et al.. (2017). High Accuracy Base Calls in Nanopore Sequencing. 12–16. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Avery Davis Bell Breakdown of academic impact, for papers by Wan Kin Au Yeung Breakdown of academic impact, for papers by Izabela Harabula Breakdown of academic impact, for papers by Xiuling Fu Breakdown of academic impact, for papers by Corinne Simonti Breakdown of academic impact, for papers by Luis Enrique Cabrera-Quio Breakdown of academic impact, for papers by Hironori Abe Breakdown of academic impact, for papers by Rachel Waymack Breakdown of academic impact, for papers by Jennifer A. Urban
Rankless by CCL
2026