Taduru Sreenath

3.4k total citations
45 papers, 2.5k citations indexed

About

Taduru Sreenath is a scholar working on Molecular Biology, Rheumatology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Taduru Sreenath has authored 45 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 13 papers in Rheumatology and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Taduru Sreenath's work include Bone and Dental Protein Studies (13 papers), dental development and anomalies (12 papers) and Prostate Cancer Treatment and Research (10 papers). Taduru Sreenath is often cited by papers focused on Bone and Dental Protein Studies (13 papers), dental development and anomalies (12 papers) and Prostate Cancer Treatment and Research (10 papers). Taduru Sreenath collaborates with scholars based in United States, France and Belgium. Taduru Sreenath's co-authors include Ashok B. Kulkarni, Tamizchelvi Thyagarajan, Jeffrey T. Wright, Bradford Hall, Glenn Longenecker, Mary MacDougall, Carolyn W. Gibson, Andrew Cho, Naoto Haruyama and Rena N. D’Souza and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Taduru Sreenath

45 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taduru Sreenath United States 27 1.5k 1.1k 411 404 381 45 2.5k
Ken‐ichi Katsube Japan 28 1.4k 0.9× 467 0.4× 119 0.3× 221 0.5× 138 0.4× 68 2.4k
Kojiro Kurisu Japan 28 1.9k 1.3× 936 0.8× 58 0.1× 233 0.6× 290 0.8× 109 3.1k
B L Hogan United States 14 3.9k 2.6× 1.1k 0.9× 235 0.6× 264 0.7× 154 0.4× 19 5.2k
Marie A. Harris United States 28 2.0k 1.3× 707 0.6× 95 0.2× 246 0.6× 206 0.5× 46 2.9k
Eiki Koyama United States 34 2.0k 1.3× 1000 0.9× 130 0.3× 183 0.5× 317 0.8× 91 3.4k
Keigo Yoshizaki Japan 22 883 0.6× 397 0.4× 104 0.3× 90 0.2× 179 0.5× 65 1.3k
Marianna Bei United States 19 2.9k 1.9× 765 0.7× 43 0.1× 249 0.6× 938 2.5× 30 3.4k
Ron W. Pelton United States 13 2.1k 1.4× 393 0.3× 405 1.0× 199 0.5× 113 0.3× 13 2.8k
Tripti Gaur United States 18 2.4k 1.6× 381 0.3× 108 0.3× 97 0.2× 59 0.2× 22 3.1k

Countries citing papers authored by Taduru Sreenath

Since Specialization
Citations

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

Fields of papers citing papers by Taduru Sreenath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taduru Sreenath

This figure shows the co-authorship network connecting the top 25 collaborators of Taduru Sreenath. A scholar is included among the top collaborators of Taduru Sreenath 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 Taduru Sreenath. Taduru Sreenath 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.
Mohamed, Ahmed A., Charles P. Xavier, Gauthaman Sukumar, et al.. (2018). Identification of a Small Molecule That Selectively Inhibits ERG-Positive Cancer Cell Growth. Cancer Research. 78(13). 3659–3671. 44 indexed citations
2.
Mohamed, Ahmed A., Shyh‐Han Tan, Charles P. Xavier, et al.. (2017). Synergistic Activity with NOTCH Inhibition and Androgen Ablation in ERG-Positive Prostate Cancer Cells. Molecular Cancer Research. 15(10). 1308–1317. 33 indexed citations
3.
Griner, Nicholas B., Denise Young, Pankaj Chaudhary, et al.. (2014). ERG Oncoprotein Inhibits ANXA2 Expression and Function in Prostate Cancer. Molecular Cancer Research. 13(2). 368–379. 11 indexed citations
4.
Zhang, Chuanbo, Bhaskar Kallakury, Jeffrey S. Ross, et al.. (2012). The significance of TNFAIP8 in prostate cancer response to radiation and docetaxel and disease recurrence. International Journal of Cancer. 133(1). 31–42. 52 indexed citations
5.
Mohamed, Ahmed A., Shyh‐Han Tan, Chen Sun, et al.. (2011). ERGoncogene modulates prostaglandin signaling in prostate cancer cells. Cancer Biology & Therapy. 11(4). 410–417. 27 indexed citations
6.
Furusato, Bungo, Shyh‐Han Tan, Denise Young, et al.. (2010). ERG oncoprotein expression in prostate cancer: clonal progression of ERG-positive tumor cells and potential for ERG-based stratification. Prostate Cancer and Prostatic Diseases. 13(3). 228–237. 178 indexed citations
7.
Haruyama, Naoto, Taduru Sreenath, Shigeki Suzuki, et al.. (2009). Genetic evidence for key roles of decorin and biglycan in dentin mineralization. Matrix Biology. 28(3). 129–136. 44 indexed citations
8.
Hu, Ying, Albert Dobi, Taduru Sreenath, et al.. (2008). Delineation of TMPRSS2-ERG Splice Variants in Prostate Cancer. Clinical Cancer Research. 14(15). 4719–4725. 75 indexed citations
9.
Verdelis, Kostas, Taduru Sreenath, Naoto Haruyama, et al.. (2008). DSPP effects on in vivo bone mineralization. Bone. 43(6). 983–990. 69 indexed citations
10.
Septier, D., et al.. (2004). Is the lingual forming part of the incisor a structural entity?. Archives of Oral Biology. 50(2). 279–286. 14 indexed citations
11.
Shashidharan, P., Ruth H. Walker, David Weisz, et al.. (2004). Transgenic mouse model of early-onset DYT1 dystonia. Human Molecular Genetics. 14(1). 125–133. 115 indexed citations
12.
Hoe, Kwang‐Lae, Inés Armando, Gustavo Baiardi, et al.. (2003). Molecular cloning, characterization, and distribution of the gerbil angiotensin II AT2receptor. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 285(6). R1373–R1383. 3 indexed citations
13.
14.
Sreenath, Taduru, Yuji Hatakeyama, Tamizchelvi Thyagarajan, et al.. (2003). The Receptor Activator of Nuclear Factor-κB Ligand-mediated Osteoclastogenic Pathway Is Elevated in Amelogenin-null Mice. Journal of Biological Chemistry. 278(37). 35743–35748. 78 indexed citations
15.
Chen, Shuo, Ting Gu, Taduru Sreenath, et al.. (2002). Spatial Expression of Cbfa1/Runx2 Isoforms in Teeth and Characterization of Binding Sites in the DSPP Gene. Connective Tissue Research. 43(2-3). 338–344. 48 indexed citations
16.
Hirasawa, Motoyuki, Andrew Cho, Taduru Sreenath, et al.. (2001). Neuron-specific expression of Cre recombinase during the late phase of brain development. Neuroscience Research. 40(2). 125–132. 24 indexed citations
17.
Gibson, Carolyn W., Zhi-An Yuan, Bradford Hall, et al.. (2001). Amelogenin-deficient Mice Display an Amelogenesis Imperfecta Phenotype. Journal of Biological Chemistry. 276(34). 31871–31875. 397 indexed citations
18.
Sreenath, Taduru, Andrew Cho, Mary MacDougall, & Ashok B. Kulkarni. (1999). Spatial and temporal activity of the dentin sialophosphoprotein gene promoter: differential regulation in odontoblasts and ameloblasts. The International Journal of Developmental Biology. 43(6). 509–516. 29 indexed citations
19.
Lisziewicz, Julianna, J. Lesley Brown, Diego Breviario, et al.. (1990). Transcriptional regulatory elements of the RAS2 gene of Saccharomyces cerevisiae. Nucleic Acids Research. 18(14). 4167–4174. 1 indexed citations
20.
Sreenath, Taduru, et al.. (1988). Two different protein kinase activities phosphorylate RAS2 protein in saccharomycescerevisiae. Biochemical and Biophysical Research Communications. 157(3). 1182–1189. 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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