Sudhir Krishna

1.6k total citations
39 papers, 1.3k citations indexed

About

Sudhir Krishna is a scholar working on Molecular Biology, Oncology and Epidemiology. According to data from OpenAlex, Sudhir Krishna has authored 39 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 13 papers in Oncology and 9 papers in Epidemiology. Recurrent topics in Sudhir Krishna's work include Cervical Cancer and HPV Research (9 papers), Developmental Biology and Gene Regulation (7 papers) and Cancer-related Molecular Pathways (6 papers). Sudhir Krishna is often cited by papers focused on Cervical Cancer and HPV Research (9 papers), Developmental Biology and Gene Regulation (7 papers) and Cancer-related Molecular Pathways (6 papers). Sudhir Krishna collaborates with scholars based in India, United States and Italy. Sudhir Krishna's co-authors include Oishee Chakrabarti, Pradip Nair, Kumaravel Somasundaram, Lawrence Banks, Annapoorni Rangarajan, Geetashree Mukherjee, Karthikeyan Veeraraghavalu, Tessy Thomas Maliekal, Sweta Srivastava and Deepa Subramanyam and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Sudhir Krishna

39 papers receiving 1.3k citations

Peers

Sudhir Krishna
Ramiro E. Verdún United States
Sudhir Krishna
Citations per year, relative to Sudhir Krishna Sudhir Krishna (= 1×) peers Ramiro E. Verdún

Countries citing papers authored by Sudhir Krishna

Since Specialization
Citations

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

Fields of papers citing papers by Sudhir Krishna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sudhir Krishna

This figure shows the co-authorship network connecting the top 25 collaborators of Sudhir Krishna. A scholar is included among the top collaborators of Sudhir Krishna 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 Sudhir Krishna. Sudhir Krishna 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.
Krishna, Sudhir, et al.. (2024). Computational Analysis of the Accumulation of Mutations in Therapeutically Important RNA Viral Proteins During Pandemics with Special Emphasis on SARS-CoV-2. Journal of Molecular Biology. 436(19). 168716–168716. 1 indexed citations
2.
Arora, Reety, Bharat Rekhi, Pratik Chandrani, Sudhir Krishna, & Amit Dutt. (2019). Merkel cell polyomavirus is implicated in a subset of Merkel cell carcinomas, in the Indian subcontinent. Microbial Pathogenesis. 137. 103778–103778. 3 indexed citations
3.
Krishna, Sudhir, et al.. (2019). RhoC regulates radioresistance via crosstalk of ROCK2 with the DNA repair machinery in cervical cancer. Journal of Experimental & Clinical Cancer Research. 38(1). 392–392. 27 indexed citations
4.
Ross, Cecil, et al.. (2017). MiRNA182 regulates percentage of myeloid and erythroid cells in chronic myeloid leukemia. Cell Death and Disease. 8(1). e2547–e2547. 16 indexed citations
5.
Maliekal, Tessy Thomas, et al.. (2016). CD66 and CD49f expressing cells are associated with distinct neoplastic phenotypes and progression in human cervical cancer. European Journal of Cancer. 60. 166–178. 18 indexed citations
6.
Zhang, Yanzhou, Sudhir Krishna, Deepa Rajagopalan, et al.. (2016). TIP60 inhibits metastasis by ablating DNMT1−SNAIL2-driven epithelial-mesenchymal transition program. Journal of Molecular Cell Biology. 8(5). 1–16. 16 indexed citations
7.
Pattabiraman, Chitra, Shiyuan Hong, Vignesh Gunasekharan, et al.. (2014). CD66+ Cells in Cervical Precancers Are Partially Differentiated Progenitors with Neoplastic Traits. Cancer Research. 74(22). 6682–6692. 7 indexed citations
8.
Nagasaka, Kazunori, Aki Yamashita, Paola Massimi, et al.. (2013). A Novel Interaction between hScrib and PP1γ Downregulates ERK Signaling and Suppresses Oncogene-Induced Cell Transformation. PLoS ONE. 8(1). e53752–e53752. 24 indexed citations
9.
Krishna, Sudhir, Nisha Narayan, Paola Massimi, & Lawrence Banks. (2012). Regulation of the DLG tumor suppressor by β‐catenin. International Journal of Cancer. 131(10). 2223–2233. 16 indexed citations
10.
Kumar, Mahesh, Surya Ramachandran, Geetashree Mukherjee, et al.. (2012). Toll-Like Receptors 7, 8, and 9 Expression and Function in Primary Human Cervical Cancer Langerhans Cells. International Journal of Gynecological Cancer. 23(1). 184–192. 11 indexed citations
11.
Bajaj, Jeevisha, Tessy Thomas Maliekal, Chitra Pattabiraman, et al.. (2011). Notch Signaling in CD66+ Cells Drives the Progression of Human Cervical Cancers. Cancer Research. 71(14). 4888–4897. 32 indexed citations
12.
Nagasaka, Kazunori, Paola Massimi, David Pim, et al.. (2010). The mechanisms and implications of hScrib regulation of ERK. Small GTPases. 1(2). 108–112. 9 indexed citations
13.
Narayan, Nisha, Sudhir Krishna, & Lawrence Banks. (2009). The high-risk HPV E6 oncoprotein preferentially targets phosphorylated nuclear forms of hDlg. Virology. 387(1). 1–4. 21 indexed citations
14.
Srivastava, Sweta, et al.. (2009). Notch1 regulates the functional contribution of RhoC to cervical carcinoma progression. British Journal of Cancer. 102(1). 196–205. 53 indexed citations
15.
Maliekal, Tessy Thomas, et al.. (2008). The role of Notch signaling in human cervical cancer: implications for solid tumors. Oncogene. 27(38). 5110–5114. 73 indexed citations
16.
Maliekal, Tessy Thomas, S. Lakshmi, Michael Rehman, et al.. (2006). Coexpression of Notch1 and NF-κB signaling pathway components in human cervical cancer progression. Gynecologic Oncology. 104(2). 352–361. 82 indexed citations
17.
Subramanyam, Deepa & Sudhir Krishna. (2005). c-Myc substitutes for Notch1-CBF1 functions in cooperative transformation with papillomavirus oncogenes. Virology. 347(1). 191–198. 12 indexed citations
18.
Chakrabarti, Oishee & Sudhir Krishna. (2003). Molecular interactions of ‘high risk’ human papillomaviruses E6 and E7 oncoproteins: implications for tumour progression. Journal of Biosciences. 28(3). 337–348. 38 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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