Rajashree A. Deshpande

2.1k total citations
24 papers, 1.5k citations indexed

About

Rajashree A. Deshpande is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Rajashree A. Deshpande has authored 24 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 5 papers in Oncology and 4 papers in Genetics. Recurrent topics in Rajashree A. Deshpande's work include DNA Repair Mechanisms (20 papers), CRISPR and Genetic Engineering (8 papers) and DNA and Nucleic Acid Chemistry (4 papers). Rajashree A. Deshpande is often cited by papers focused on DNA Repair Mechanisms (20 papers), CRISPR and Genetic Engineering (8 papers) and DNA and Nucleic Acid Chemistry (4 papers). Rajashree A. Deshpande collaborates with scholars based in United States, India and Japan. Rajashree A. Deshpande's co-authors include Tanya T. Paull, Ji‐Hoon Lee, Vepatu Shankar, Zhi Guo, Thomas E. Wilson, Ilya J. Finkelstein, Michael M. Soniat, Logan R. Myler, Nodar Makharashvili and Yoori Kim and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Rajashree A. Deshpande

24 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rajashree A. Deshpande United States 17 1.4k 436 207 129 113 24 1.5k
Leyma P. De Haro United States 7 1.3k 0.9× 379 0.9× 235 1.1× 159 1.2× 72 0.6× 10 1.5k
Dongyi Xu China 20 1.7k 1.1× 569 1.3× 226 1.1× 136 1.1× 206 1.8× 31 1.8k
Hiroyuki Sasanuma Japan 23 1.6k 1.1× 492 1.1× 259 1.3× 129 1.0× 173 1.5× 67 1.7k
Hai Dang Nguyen United States 18 1.6k 1.1× 571 1.3× 159 0.8× 167 1.3× 197 1.7× 38 1.8k
Bianca M. Sirbu United States 9 1.2k 0.8× 332 0.8× 158 0.8× 149 1.2× 154 1.4× 9 1.3k
Yan Coulombe Canada 24 1.4k 1.0× 409 0.9× 220 1.1× 249 1.9× 87 0.8× 39 1.6k
Elda Cannavò Switzerland 18 1.9k 1.3× 458 1.1× 387 1.9× 183 1.4× 202 1.8× 30 2.1k
Dimitri G. Pestov United States 24 1.6k 1.1× 317 0.7× 133 0.6× 107 0.8× 79 0.7× 46 1.9k
Irina I. Dianova United Kingdom 23 1.7k 1.2× 653 1.5× 375 1.8× 172 1.3× 133 1.2× 25 1.9k
Olga M. Mazina United States 22 1.4k 0.9× 356 0.8× 225 1.1× 130 1.0× 91 0.8× 38 1.5k

Countries citing papers authored by Rajashree A. Deshpande

Since Specialization
Citations

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

Fields of papers citing papers by Rajashree A. Deshpande

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rajashree A. Deshpande. 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 Rajashree A. Deshpande. The network helps show where Rajashree A. Deshpande may publish in the future.

Co-authorship network of co-authors of Rajashree A. Deshpande

This figure shows the co-authorship network connecting the top 25 collaborators of Rajashree A. Deshpande. A scholar is included among the top collaborators of Rajashree A. Deshpande 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 Rajashree A. Deshpande. Rajashree A. Deshpande 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.
Deshpande, Rajashree A., et al.. (2023). Genome-wide analysis of DNA-PK-bound MRN cleavage products supports a sequential model of DSB repair pathway choice. Nature Communications. 14(1). 5759–5759. 14 indexed citations
2.
Deshpande, Rajashree A. & Tanya T. Paull. (2022). Characterization of DNA-PK-Bound End Fragments Using GLASS-ChIP. Methods in molecular biology. 2444. 171–182. 1 indexed citations
3.
Deshpande, Rajashree A., Logan R. Myler, Michael M. Soniat, et al.. (2020). DNA-dependent protein kinase promotes DNA end processing by MRN and CtIP. Science Advances. 6(2). eaay0922–eaay0922. 100 indexed citations
4.
Paiano, Jacob, Wei Wu, Shintaro Yamada, et al.. (2020). ATM and PRDM9 regulate SPO11-bound recombination intermediates during meiosis. Nature Communications. 11(1). 857–857. 80 indexed citations
5.
Myler, Logan R., Iluminada Gallardo, Michael M. Soniat, et al.. (2017). Single-Molecule Imaging Reveals How Mre11-Rad50-Nbs1 Initiates DNA Break Repair. Molecular Cell. 67(5). 891–898.e4. 151 indexed citations
6.
Deshpande, Rajashree A., Ji‐Hoon Lee, & Tanya T. Paull. (2017). Rad50 ATPase activity is regulated by DNA ends and requires coordination of both active sites. Nucleic Acids Research. 45(9). 5255–5268. 28 indexed citations
7.
Nguyen, Hoa N., Zhong‐Wei Zhou, Zhao‐Qi Wang, et al.. (2016). Mre11 Is Essential for the Removal of Lethal Topoisomerase 2 Covalent Cleavage Complexes. Molecular Cell. 64(3). 580–592. 152 indexed citations
8.
Broderick, Ronan, Jadwiga Nieminuszczy, Hannah T. Baddock, et al.. (2016). EXD2 promotes homologous recombination by facilitating DNA end resection. Nature Cell Biology. 18(3). 271–280. 60 indexed citations
9.
Deshpande, Rajashree A., et al.. (2016). Nbs1 Converts the Human Mre11/Rad50 Nuclease Complex into an Endo/Exonuclease Machine Specific for Protein-DNA Adducts. Molecular Cell. 64(3). 593–606. 136 indexed citations
10.
Makharashvili, Nodar, Anthony Tubbs, Hailong Wang, et al.. (2014). Catalytic and Noncatalytic Roles of the CtIP Endonuclease in Double-Strand Break End Resection. Molecular Cell. 54(6). 1022–1033. 148 indexed citations
11.
Deshpande, Rajashree A., Gareth J. Williams, Oliver Limbo, et al.. (2014). ATP-driven Rad50 conformations regulate DNA tethering, end resection, and ATM checkpoint signaling. The EMBO Journal. 33(5). 482–500. 126 indexed citations
12.
Paull, Tanya T. & Rajashree A. Deshpande. (2014). The Mre11/Rad50/Nbs1 complex: Recent insights into catalytic activities and ATP-driven conformational changes. Experimental Cell Research. 329(1). 139–147. 41 indexed citations
13.
Lee, Ji‐Hoon, et al.. (2013). Ataxia Telangiectasia-Mutated (ATM) Kinase Activity Is Regulated by ATP-driven Conformational Changes in the Mre11/Rad50/Nbs1 (MRN) Complex. Journal of Biological Chemistry. 288(18). 12840–12851. 88 indexed citations
14.
Guo, Zhi, Rajashree A. Deshpande, & Tanya T. Paull. (2010). ATM activation in the presence of oxidative stress . Cell Cycle. 9(24). 4805–4811. 146 indexed citations
15.
Deshpande, Rajashree A. & Thomas E. Wilson. (2007). Modes of interaction among yeast Nej1, Lif1 and Dnl4 proteins and comparison to human XLF, XRCC4 and Lig4. DNA repair. 6(10). 1507–1516. 46 indexed citations
16.
Deshpande, Rajashree A., M. Islam Khan, & Vepatu Shankar. (2003). Equilibrium unfolding of RNase Rs from Rhizopus stolonifer: pH dependence of chemical and thermal denaturation. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1648(1-2). 184–194. 18 indexed citations
17.
Deshpande, Rajashree A., et al.. (2003). The Role of Yeast DNA 3′-Phosphatase Tpp1 and Rad1/Rad10 Endonuclease in Processing Spontaneous and Induced Base Lesions. Journal of Biological Chemistry. 278(33). 31434–31443. 35 indexed citations
18.
Deshpande, Rajashree A. & Vepatu Shankar. (2002). Ribonucleases from T2 Family. Critical Reviews in Microbiology. 28(2). 79–122. 116 indexed citations
19.
Deshpande, Rajashree A., et al.. (2001). Ribonuclease Rs from Rhizopus stolonifer : lowering of optimum temperature in the presence of urea. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1545(1-2). 13–19. 8 indexed citations
20.
Deshpande, Rajashree A. & V. Shankar. (1998). Immobilization of RNase Rs via its carbohydrate moiety to aminoethyl-Bio-Gel P-2 and its application for the hydrolysis of RNA to 2′,3′ cyclic nucleotides. Process Biochemistry. 33(8). 819–824. 2 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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