Baskar Bakthavachalu

905 total citations
16 papers, 544 citations indexed

About

Baskar Bakthavachalu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Baskar Bakthavachalu has authored 16 papers receiving a total of 544 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Baskar Bakthavachalu's work include RNA Research and Splicing (7 papers), Genetic Neurodegenerative Diseases (4 papers) and RNA regulation and disease (3 papers). Baskar Bakthavachalu is often cited by papers focused on RNA Research and Splicing (7 papers), Genetic Neurodegenerative Diseases (4 papers) and RNA regulation and disease (3 papers). Baskar Bakthavachalu collaborates with scholars based in India, United States and Ireland. Baskar Bakthavachalu's co-authors include Daniel R. Schoenberg, Murugesan V. S. Rajaram, Tracy Carlson, Jordi B. Torrelles, Bin Ni, Larry S. Schlesinger, Chandrama Mukherjee, Deepak P. Patil, Vasudevan Seshadri and Bhavana Muralidharan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Neuron.

In The Last Decade

Baskar Bakthavachalu

16 papers receiving 540 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Baskar Bakthavachalu India 10 402 171 87 80 76 16 544
Juliana Blin France 7 610 1.5× 343 2.0× 27 0.3× 81 1.0× 156 2.1× 7 778
Fengyu Wang China 10 228 0.6× 74 0.4× 56 0.6× 67 0.8× 62 0.8× 36 416
Kianoush Khaleghpour Canada 8 827 2.1× 51 0.3× 46 0.5× 43 0.5× 45 0.6× 8 957
Wonkyung Oh United States 14 438 1.1× 77 0.5× 92 1.1× 44 0.6× 107 1.4× 20 682
Kartik Soni India 7 369 0.9× 248 1.5× 45 0.5× 22 0.3× 71 0.9× 16 508
Denis Tempé France 10 647 1.6× 140 0.8× 121 1.4× 60 0.8× 102 1.3× 11 803
Christina Begon‐Pescia France 10 558 1.4× 86 0.5× 45 0.5× 62 0.8× 74 1.0× 14 780
Tina Solvik United States 4 335 0.8× 122 0.7× 23 0.3× 203 2.5× 48 0.6× 5 493
Francisco J. Sánchez‐Luque Spain 12 659 1.6× 69 0.4× 36 0.4× 60 0.8× 37 0.5× 29 787
Ming‐Chih Lai Taiwan 11 780 1.9× 61 0.4× 45 0.5× 68 0.8× 47 0.6× 11 877

Countries citing papers authored by Baskar Bakthavachalu

Since Specialization
Citations

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

Fields of papers citing papers by Baskar Bakthavachalu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baskar Bakthavachalu

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

All Works

16 of 16 papers shown
1.
Singh, Amanjot, Jens Hillebrand, Chunghun Lim, et al.. (2024). Structured and disordered regions of Ataxin-2 contribute differently to the specificity and efficiency of mRNP granule formation. PLoS Genetics. 20(5). e1011251–e1011251. 4 indexed citations
2.
Bakthavachalu, Baskar, et al.. (2024). Distinct developmental patterns in Anopheles stephensi organ systems. Developmental Biology. 508. 107–122. 2 indexed citations
3.
Bakthavachalu, Baskar, et al.. (2023). Eggs of the mosquito Aedes aegypti survive desiccation by rewiring their polyamine and lipid metabolism. PLoS Biology. 21(10). e3002342–e3002342. 10 indexed citations
4.
Chen, Nannan, Yunpeng Zhang, Elena A. Kuklin, et al.. (2022). Local translation provides the asymmetric distribution of CaMKII required for associative memory formation. Current Biology. 32(12). 2730–2738.e5. 7 indexed citations
5.
Singh, Amanjot, et al.. (2021). Antagonistic roles for Ataxin-2 structured and disordered domains in RNP condensation. eLife. 10. 19 indexed citations
7.
Bakthavachalu, Baskar, Indulekha P. Sudhakaran, Jens Hillebrand, et al.. (2018). RNP-Granule Assembly via Ataxin-2 Disordered Domains Is Required for Long-Term Memory and Neurodegeneration. Neuron. 98(4). 754–766.e4. 80 indexed citations
8.
Kuklin, Elena A., Baskar Bakthavachalu, Indulekha P. Sudhakaran, et al.. (2017). The Long 3′UTR mRNA ofCaMKIIIs Essential for Translation-Dependent Plasticity of Spontaneous Release inDrosophila melanogaster. Journal of Neuroscience. 37(44). 10554–10566. 19 indexed citations
9.
Mukherjee, Chandrama, Baskar Bakthavachalu, & Daniel R. Schoenberg. (2014). The Cytoplasmic Capping Complex Assembles on Adapter Protein Nck1 Bound to the Proline-Rich C-Terminus of Mammalian Capping Enzyme. PLoS Biology. 12(8). e1001933–e1001933. 32 indexed citations
10.
Bakthavachalu, Baskar, Joonhee Han, Deepak P. Patil, et al.. (2012). Identification of the human PMR1 mRNA endonuclease as an alternatively processed product of the gene for peroxidasin-like protein. RNA. 18(6). 1186–1196. 8 indexed citations
11.
Mukherjee, Chandrama, et al.. (2012). Identification of Cytoplasmic Capping Targets Reveals a Role for Cap Homeostasis in Translation and mRNA Stability. Cell Reports. 2(3). 674–684. 66 indexed citations
12.
Rajaram, Murugesan V. S., Bin Ni, Tracy Carlson, et al.. (2011). Mycobacterium tuberculosis lipomannan blocks TNF biosynthesis by regulating macrophage MAPK-activated protein kinase 2 (MK2) and microRNA miR-125b. Proceedings of the National Academy of Sciences. 108(42). 17408–17413. 228 indexed citations
13.
Muralidharan, Bhavana, et al.. (2011). Glucose-stimulated Translation Regulation of Insulin by the 5′ UTR-binding Proteins. Journal of Biological Chemistry. 286(16). 14146–14156. 32 indexed citations
14.
Bakthavachalu, Baskar, et al.. (2010). Dense cataract and microphthalmia (dcm) in BALB/c mice is caused by mutations in the GJA8 locus. Journal of Genetics. 89(2). 147–154. 7 indexed citations
15.
Panda, Amaresh C., et al.. (2010). Novel splice variant of mouse insulin2 mRNA: Implications for insulin expression. FEBS Letters. 584(6). 1169–1173. 10 indexed citations
16.
Muralidharan, Bhavana, Baskar Bakthavachalu, Anuj Pathak, & Vasudevan Seshadri. (2007). A minimal element in 5′UTR of insulin mRNA mediates its translational regulation by glucose. FEBS Letters. 581(21). 4103–4108. 16 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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