Yogesh Srivastava

925 total citations
23 papers, 630 citations indexed

About

Yogesh Srivastava is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Yogesh Srivastava has authored 23 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Cancer Research and 4 papers in Oncology. Recurrent topics in Yogesh Srivastava's work include CRISPR and Genetic Engineering (8 papers), Pluripotent Stem Cells Research (5 papers) and Renal and related cancers (3 papers). Yogesh Srivastava is often cited by papers focused on CRISPR and Genetic Engineering (8 papers), Pluripotent Stem Cells Research (5 papers) and Renal and related cancers (3 papers). Yogesh Srivastava collaborates with scholars based in China, United States and India. Yogesh Srivastava's co-authors include Ralf Jauch, Bhudev C. Das, Linlin Hou, Alok C. Bharti, G. S. Verma, Gauri Shishodia, Shashank Masaldan, Ravi Mehrotra, Abhishek Tyagi and Kanchan Vishnoi and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Yogesh Srivastava

22 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yogesh Srivastava China 13 469 205 132 71 67 23 630
Tony M. Mertz United States 14 630 1.3× 217 1.1× 118 0.9× 51 0.7× 115 1.7× 19 726
Adam Langenbucher United States 8 333 0.7× 160 0.8× 118 0.9× 40 0.6× 72 1.1× 12 463
Sebastian M. Dieter Germany 8 285 0.6× 143 0.7× 268 2.0× 48 0.7× 62 0.9× 14 490
Artem G. Lada United States 14 518 1.1× 177 0.9× 82 0.6× 49 0.7× 94 1.4× 19 600
Masahiko Ajiro Japan 15 641 1.4× 178 0.9× 129 1.0× 153 2.2× 43 0.6× 28 809
Hua Cao China 16 366 0.8× 137 0.7× 115 0.9× 23 0.3× 120 1.8× 39 524
Yabin Guo China 14 439 0.9× 86 0.4× 99 0.8× 41 0.6× 64 1.0× 33 555
Chiara Vardabasso United States 9 740 1.6× 120 0.6× 159 1.2× 32 0.5× 51 0.8× 12 873
Veronika I. Zabarovska Sweden 13 508 1.1× 146 0.7× 98 0.7× 30 0.4× 88 1.3× 19 635
Sumanprava Giri United States 10 927 2.0× 572 2.8× 83 0.6× 44 0.6× 63 0.9× 11 1.0k

Countries citing papers authored by Yogesh Srivastava

Since Specialization
Citations

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

Fields of papers citing papers by Yogesh Srivastava

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yogesh Srivastava

This figure shows the co-authorship network connecting the top 25 collaborators of Yogesh Srivastava. A scholar is included among the top collaborators of Yogesh Srivastava 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 Yogesh Srivastava. Yogesh Srivastava 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.
Srivastava, Yogesh, et al.. (2024). Role of a Pdlim5:PalmD complex in directing dendrite morphology. Frontiers in Cellular Neuroscience. 18. 1315941–1315941. 3 indexed citations
2.
Srivastava, Yogesh, et al.. (2023). p120-catenin subfamily members have distinct as well as shared effects on dendrite morphology during neuron development in vitro. Frontiers in Cellular Neuroscience. 17. 1151249–1151249. 6 indexed citations
3.
Kumar, Reetesh, Yogesh Srivastava, Pandiyan Muthuramalingam, et al.. (2023). Understanding Mutations in Human SARS-CoV-2 Spike Glycoprotein: A Systematic Review & Meta-Analysis. Viruses. 15(4). 856–856. 24 indexed citations
4.
Kumar, Reetesh, Yogesh Srivastava, Rajeev K. Tyagi, et al.. (2023). In silico evaluation of natural compounds to confirm their anti-DNA gyrase activity. The Nucleus. 66(2). 167–182. 2 indexed citations
5.
Zhang, Baoyun, et al.. (2022). In-silico probing of AML related RUNX1 cancer-associated missense mutations: Predicted relationships to DNA binding and drug interactions. Frontiers in Molecular Biosciences. 9. 981020–981020. 1 indexed citations
6.
Srivastava, Yogesh, et al.. (2022). Delta-Catenin as a Modulator of Rho GTPases in Neurons. Frontiers in Cellular Neuroscience. 16. 939143–939143. 8 indexed citations
7.
Tan, Daisylyn Senna, Yanpu Chen, Ya Gao, et al.. (2021). Directed Evolution of an Enhanced POU Reprogramming Factor for Cell Fate Engineering. Molecular Biology and Evolution. 38(7). 2854–2868. 14 indexed citations
8.
Malik, Vikas, Sergiy Velychko, Yanpu Chen, et al.. (2019). Pluripotency reprogramming by competent and incompetent POU factors uncovers temporal dependency for Oct4 and Sox2. Nature Communications. 10(1). 3477–3477. 58 indexed citations
9.
Tan, Daisylyn Senna, et al.. (2019). SOX17 in cellular reprogramming and cancer. Seminars in Cancer Biology. 67(Pt 1). 65–73. 47 indexed citations
10.
Srivastava, Yogesh, et al.. (2018). Directed Evolution of Reprogramming Factors by Cell Selection and Sequencing. Stem Cell Reports. 11(2). 593–606. 20 indexed citations
11.
Wang, Xuecong, Yogesh Srivastava, Aleksander Jankowski, et al.. (2018). DNA-mediated dimerization on a compact sequence signature controls enhancer engagement and regulation by FOXA1. Nucleic Acids Research. 46(11). 5470–5486. 15 indexed citations
12.
Malik, Vikas, Yiming Chang, Yogesh Srivastava, et al.. (2017). Coop-Seq Analysis Demonstrates that Sox2 Evokes Latent Specificities in the DNA Recognition by Pax6. Journal of Molecular Biology. 429(23). 3626–3634. 4 indexed citations
13.
Tyagi, Abhishek, et al.. (2017). Cervical cancer stem cells manifest radioresistance: Association with upregulated AP-1 activity. Scientific Reports. 7(1). 4781–4781. 36 indexed citations
14.
Cornell, Thomas, Yogesh Srivastava, Ralf Jauch, Rongli Fan, & Brendan P. Orner. (2017). The Crystal Structure of a Maxi/Mini-Ferritin Chimera Reveals Guiding Principles for the Assembly of Protein Cages. Biochemistry. 56(30). 3894–3899. 7 indexed citations
15.
Tyagi, Abhishek, Kanchan Vishnoi, Sutapa Mahata, et al.. (2016). Cervical Cancer Stem Cells Selectively Overexpress HPV Oncoprotein E6 that Controls Stemness and Self-Renewal through Upregulation of HES1. Clinical Cancer Research. 22(16). 4170–4184. 81 indexed citations
16.
Hou, Linlin, Yogesh Srivastava, & Ralf Jauch. (2016). Molecular basis for the genome engagement by Sox proteins. Seminars in Cell and Developmental Biology. 63. 2–12. 83 indexed citations
17.
Prokoph, Nina, Mathias Girbig, Xuecong Wang, et al.. (2016). Structure and decoy-mediated inhibition of the SOX18/Prox1-DNA interaction. Nucleic Acids Research. 44(8). 3922–3935. 44 indexed citations
18.
Chang, Yiming, Yogesh Srivastava, Zheng Zuo, et al.. (2016). Quantitative profiling of selective Sox/POU pairing on hundreds of sequences in parallel by Coop-seq. Nucleic Acids Research. 45(2). 832–845. 30 indexed citations
19.
Shishodia, Gauri, Shirish Shukla, Yogesh Srivastava, et al.. (2015). Alterations in microRNAs miR-21 and let-7a correlate with aberrant STAT3 signaling and downstream effects during cervical carcinogenesis. Molecular Cancer. 14(1). 116–116. 78 indexed citations
20.
Shishodia, Gauri, G. S. Verma, Yogesh Srivastava, et al.. (2014). Deregulation of microRNAs Let-7a and miR-21 mediate aberrant STAT3 signaling during human papillomavirus-induced cervical carcinogenesis: role of E6 oncoprotein. BMC Cancer. 14(1). 996–996. 58 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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