Srinivas M. Tipparaju

1.7k total citations
50 papers, 1.3k citations indexed

About

Srinivas M. Tipparaju is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Srinivas M. Tipparaju has authored 50 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 17 papers in Cardiology and Cardiovascular Medicine and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Srinivas M. Tipparaju's work include Cardiac electrophysiology and arrhythmias (13 papers), Ion channel regulation and function (13 papers) and Cardiac Ischemia and Reperfusion (9 papers). Srinivas M. Tipparaju is often cited by papers focused on Cardiac electrophysiology and arrhythmias (13 papers), Ion channel regulation and function (13 papers) and Cardiac Ischemia and Reperfusion (9 papers). Srinivas M. Tipparaju collaborates with scholars based in United States, Russia and India. Srinivas M. Tipparaju's co-authors include Aruni Bhatnagar, Oleg A. Barski, Kalyan C. Chapalamadugu, Peter J. Kilfoil, Narasaiah Kolliputi, Siva K. Panguluri, Ravikumar Manickam, Rajiv Kumar, Wanling Xuan and Sanjay Srivastava and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Circulation Research.

In The Last Decade

Srinivas M. Tipparaju

47 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Srinivas M. Tipparaju United States 18 629 307 235 208 127 50 1.3k
Sujoy Bhattacharya United States 24 1.1k 1.8× 150 0.5× 117 0.5× 289 1.4× 163 1.3× 55 1.9k
Ken Chen China 21 723 1.1× 119 0.4× 225 1.0× 371 1.8× 110 0.9× 63 1.5k
Reiko Matsui United States 23 822 1.3× 112 0.4× 151 0.6× 377 1.8× 88 0.7× 48 1.5k
Ute Gödtel‐Armbrust Germany 21 512 0.8× 91 0.3× 398 1.7× 366 1.8× 94 0.7× 29 1.5k
Xupei Huang United States 25 875 1.4× 99 0.3× 509 2.2× 90 0.4× 99 0.8× 83 1.5k
E. Schleicher Germany 26 791 1.3× 185 0.6× 205 0.9× 416 2.0× 155 1.2× 77 2.5k
Pu Fang United States 18 834 1.3× 96 0.3× 92 0.4× 204 1.0× 75 0.6× 28 1.9k
Edward G. Lynn Canada 21 459 0.7× 159 0.5× 78 0.3× 138 0.7× 69 0.5× 32 1.1k
Peter K.M. Kim United States 17 867 1.4× 121 0.4× 69 0.3× 341 1.6× 102 0.8× 21 1.5k
Yingfeng Deng United States 26 1.1k 1.8× 492 1.6× 268 1.1× 769 3.7× 76 0.6× 43 2.5k

Countries citing papers authored by Srinivas M. Tipparaju

Since Specialization
Citations

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

Fields of papers citing papers by Srinivas M. Tipparaju

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Srinivas M. Tipparaju. 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 Srinivas M. Tipparaju. The network helps show where Srinivas M. Tipparaju may publish in the future.

Co-authorship network of co-authors of Srinivas M. Tipparaju

This figure shows the co-authorship network connecting the top 25 collaborators of Srinivas M. Tipparaju. A scholar is included among the top collaborators of Srinivas M. Tipparaju 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 Srinivas M. Tipparaju. Srinivas M. Tipparaju 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.
Fahim, M., et al.. (2025). The heart-brain crosstalk in age related cardiovascular and neurodegenerative diseases. Fluids and Barriers of the CNS. 22(1). 89–89.
2.
Manickam, Ravikumar, et al.. (2025). Nampt: a new therapeutic target for modulating NAD+ levels in metabolic, cardiovascular, and neurodegenerative diseases. Canadian Journal of Physiology and Pharmacology. 103(7). 208–224. 1 indexed citations
3.
4.
Carris, Nicholas W., et al.. (2024). Association of Common Foods with Inflammation and Mortality: Analysis from a Large Prospective Cohort Study. Journal of Medicinal Food. 27(3). 267–274. 1 indexed citations
5.
Kim, Joung W., et al.. (2024). P7C3 ameliorates barium chloride‐induced skeletal muscle injury activating transcriptomic and epigenetic modulation of myogenic regulatory factors. Journal of Cellular Physiology. 239(9). e31346–e31346. 2 indexed citations
6.
Tipparaju, Srinivas M., et al.. (2024). Sarcopenia: recent advances for detection, progression, and metabolic alterations along with therapeutic targets. Canadian Journal of Physiology and Pharmacology. 102(12). 697–708. 10 indexed citations
7.
Manickam, Ravikumar, et al.. (2023). Genetic deletion of Kvβ2 (AKR6) causes loss of muscle function and increased inflammation in mice. SHILAP Revista de lepidopterología. 4. 1175510–1175510. 1 indexed citations
8.
Sutariya, Vijaykumar, Priyanka Bhatt, Sachin L. Badole, et al.. (2023). Development and testing of nanoparticles delivery for P7C3 small molecule using injury models. Molecular and Cellular Biochemistry. 479(9). 2429–2445. 4 indexed citations
9.
Carris, Nicholas W., et al.. (2022). Novel biomarkers of inflammation in heart failure with preserved ejection fraction: analysis from a large prospective cohort study. BMC Cardiovascular Disorders. 22(1). 221–221. 7 indexed citations
10.
Xuan, Wanling, Srinivas M. Tipparaju, & Muhammad Ashraf. (2022). Transformational Applications of Human Cardiac Organoids in Cardiovascular Diseases. Frontiers in Cell and Developmental Biology. 10. 936084–936084. 9 indexed citations
11.
Badole, Sachin L., et al.. (2017). Corticosteroids and aldose reductase inhibitor Epalrestat modulates cardiac action potential via Kvβ1.1 (AKR6A8) subunit of voltage-gated potassium channel. Molecular and Cellular Biochemistry. 436(1-2). 71–78. 3 indexed citations
12.
Chapalamadugu, Kalyan C., et al.. (2016). Deletion of Kvβ1.1 subunit leads to electrical and haemodynamic changes causing cardiac hypertrophy in female murine hearts. Experimental Physiology. 101(4). 494–508. 18 indexed citations
13.
Chapalamadugu, Kalyan C., Siva K. Panguluri, Eric S. Bennett, Narasaiah Kolliputi, & Srinivas M. Tipparaju. (2014). High level of oxygen treatment causes cardiotoxicity with arrhythmias and redox modulation. Toxicology and Applied Pharmacology. 282(1). 100–107. 30 indexed citations
14.
15.
Panguluri, Siva K., et al.. (2013). MicroRNA-301a Mediated Regulation of Kv4.2 in Diabetes: Identification of Key Modulators. PLoS ONE. 8(4). e60545–e60545. 46 indexed citations
16.
Xie, Zhengzhi, Oleg A. Barski, Jian Cai, Aruni Bhatnagar, & Srinivas M. Tipparaju. (2011). Catalytic reduction of carbonyl groups in oxidized PAPC by Kvβ2 (AKR6). Chemico-Biological Interactions. 191(1-3). 255–260. 14 indexed citations
17.
Tipparaju, Srinivas M., Oleg A. Barski, Sanjay Srivastava, & Aruni Bhatnagar. (2008). Catalytic Mechanism and Substrate Specificity of the β-Subunit of the Voltage-Gated Potassium Channel. Biochemistry. 47(34). 8840–8854. 47 indexed citations
18.
Wagner, Mary B., Yanggan Wang, Rajiv Kumar, Srinivas M. Tipparaju, & Ronald W. Joyner. (2004). Calcium Transients in Infant Human Atrial Myocytes. Pediatric Research. 57(1). 28–34. 9 indexed citations
19.
Tipparaju, Srinivas M., Rajiv Kumar, Yanggan Wang, Ronald W. Joyner, & Mary B. Wagner. (2004). Developmental differences in L-type calcium current of human atrial myocytes. American Journal of Physiology-Heart and Circulatory Physiology. 286(5). H1963–H1969. 15 indexed citations
20.
Bhatnagar, Aruni, et al.. (2003). Differential pyridine nucleotide coenzyme binding to the β-subunit of the voltage-sensitive K+ channel: a mechanism for redox regulation of excitability?. Chemico-Biological Interactions. 143-144. 613–620. 1 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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