Vikram Prasad

5.4k total citations · 2 hit papers
66 papers, 4.0k citations indexed

About

Vikram Prasad is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Vikram Prasad has authored 66 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 17 papers in Cardiology and Cardiovascular Medicine and 11 papers in Cell Biology. Recurrent topics in Vikram Prasad's work include Ion channel regulation and function (15 papers), Muscle Physiology and Disorders (8 papers) and Ion Transport and Channel Regulation (7 papers). Vikram Prasad is often cited by papers focused on Ion channel regulation and function (15 papers), Muscle Physiology and Disorders (8 papers) and Ion Transport and Channel Regulation (7 papers). Vikram Prasad collaborates with scholars based in United States, India and Poland. Vikram Prasad's co-authors include Gary E. Shull, Jeffery D. Molkentin, Marian L. Miller, Onur Kanisicak, Hadi Khalil, Xing Fu, Ronald J. Vagnozzi, Gbolahan W. Okunade, Robert N. Correll and Tobias G. Schips and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Vikram Prasad

66 papers receiving 3.9k citations

Hit Papers

Fibroblast-specific TGF-β–Smad2/3 signaling underlies car... 2017 2026 2020 2023 2017 2018 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vikram Prasad United States 29 2.6k 1.0k 580 430 365 66 4.0k
Mathias Mericskay France 32 2.6k 1.0× 694 0.7× 390 0.7× 774 1.8× 319 0.9× 65 4.3k
Bernhard Kühn United States 28 2.5k 1.0× 1.1k 1.1× 1.0k 1.8× 222 0.5× 255 0.7× 43 3.5k
Xiuqin Zhang China 32 2.8k 1.1× 381 0.4× 506 0.9× 479 1.1× 431 1.2× 109 4.6k
Thomas P. Zwaka United States 24 3.3k 1.2× 477 0.5× 859 1.5× 242 0.6× 502 1.4× 47 4.9k
Shohei Yamashina Japan 35 1.6k 0.6× 619 0.6× 543 0.9× 678 1.6× 532 1.5× 161 4.1k
Takayuki Morisaki Japan 34 2.1k 0.8× 645 0.6× 767 1.3× 223 0.5× 747 2.0× 154 3.7k
Keith R. Anderson United States 27 1.6k 0.6× 369 0.4× 657 1.1× 361 0.8× 272 0.7× 37 3.2k
David M. Bader United States 38 3.9k 1.5× 1.0k 1.0× 1.3k 2.2× 621 1.4× 734 2.0× 94 5.3k
Przemysław Błyszczuk Switzerland 29 1.6k 0.6× 877 0.8× 974 1.7× 120 0.3× 343 0.9× 71 3.3k
Lynn A. Megeney Canada 33 3.6k 1.4× 430 0.4× 594 1.0× 677 1.6× 308 0.8× 66 4.4k

Countries citing papers authored by Vikram Prasad

Since Specialization
Citations

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

Fields of papers citing papers by Vikram Prasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vikram Prasad

This figure shows the co-authorship network connecting the top 25 collaborators of Vikram Prasad. A scholar is included among the top collaborators of Vikram Prasad 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 Vikram Prasad. Vikram Prasad 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.
Bowers, Stephanie, Qinghang Meng, Yasuhide Kuwabara, et al.. (2023). Col1a2-Deleted Mice Have Defective Type I Collagen and Secondary Reactive Cardiac Fibrosis with Altered Hypertrophic Dynamics. Cells. 12(17). 2174–2174. 14 indexed citations
2.
Huo, Jiuzhou, Vikram Prasad, Kelly M. Grimes, et al.. (2023). MCUb is an inducible regulator of calcium-dependent mitochondrial metabolism and substrate utilization in muscle. Cell Reports. 42(11). 113465–113465. 13 indexed citations
3.
Boyer, Justin G., Jiuzhou Huo, Vikram Prasad, et al.. (2022). Depletion of skeletal muscle satellite cells attenuates pathology in muscular dystrophy. Nature Communications. 13(1). 2940–2940. 27 indexed citations
4.
Catalano, Michael A., Vikram Prasad, Alexander M. Spring, et al.. (2020). Heparin-induced thrombocytopenia in patients readmitted after open cardiac surgical procedures: A case series. JTCVS Open. 4. 36–42. 2 indexed citations
5.
Leikina, Evgenia, Dilani G. Gamage, Vikram Prasad, Leonid Chernomordik, & Douglas P. Millay. (2019). Myomaker and Myomerger Work Independently to Control Distinct Steps of Membrane Remodeling during Myoblast Fusion. Biophysical Journal. 116(3). 367a–367a. 1 indexed citations
6.
Boyer, Justin G., Vikram Prasad, Taejeong Song, et al.. (2019). ERK1/2 signaling induces skeletal muscle slow fiber-type switching and reduces muscular dystrophy disease severity. JCI Insight. 4(10). 61 indexed citations
7.
Nayak, Gowri, Yoshinobu Odaka, Vikram Prasad, et al.. (2018). Developmental vascular regression is regulated by a Wnt/β-catenin, MYC, P21 (CDKN1A) pathway that controls cell proliferation and cell death. Development. 145(12). 26 indexed citations
8.
Schips, Tobias G., Michelle A. Sargent, Davy Vanhoutte, et al.. (2016). Cathepsin S Contributes to the Pathogenesis of Muscular Dystrophy in Mice. Journal of Biological Chemistry. 291(19). 9920–9928. 18 indexed citations
9.
D’Astolfo, Diego S., Romina J. Pagliero, Wouter R. Karthaus, et al.. (2015). Efficient Intracellular Delivery of Native Proteins. Cell. 161(3). 674–690. 284 indexed citations
10.
Prasad, Vikram, John N. Lorenz, Valerie M. Lasko, et al.. (2014). Ablation of plasma membrane Ca2+-ATPase isoform 4 prevents development of hypertrophy in a model of hypertrophic cardiomyopathy. Journal of Molecular and Cellular Cardiology. 77. 53–63. 9 indexed citations
11.
Young, Richard M., Vikram Prasad, Joshua J. Wind, Wayne J. Olan, & Anthony J. Caputy. (2014). Novel technique for preoperative pedicle localization in spinal surgery with challenging anatomy. Journal of Neurosurgery Spine. 20(4). 400–403. 4 indexed citations
12.
Radhakrishnan, Rangasudhagar, et al.. (2014). A review on heat shock protein gene expressions and its association with Thermo tolerance in the silkworm of Bombyx mori (L). Journal of Entomology and Zoology Studies. 2(3). 170–176. 1 indexed citations
13.
Prasad, Vikram, Dheeraj Gandhi, & Gaurav Jindal. (2013). Pipeline endovascular reconstruction of traumatic dissecting aneurysms of the intracranial internal carotid artery. BMJ Case Reports. 2013. bcr2013010899–bcr2013010899. 6 indexed citations
14.
Shull, Gary E., Marian L. Miller, & Vikram Prasad. (2011). Secretory pathway stress responses as possible mechanisms of disease involving Golgi Ca2+ pump dysfunction. BioFactors. 37(3). 150–158. 30 indexed citations
15.
Prasad, Vikram, Ilona Bódi, Jamie W. Meyer, et al.. (2008). Impaired Cardiac Contractility in Mice Lacking Both the AE3 Cl/HCO3 Exchanger and the NKCC1 Na+-K+-2Cl– Cotransporter. Journal of Biological Chemistry. 283(46). 31303–31314. 28 indexed citations
16.
Okunade, Gbolahan W., Marian L. Miller, Mohamad Azhar, et al.. (2007). Loss of the Atp2c1 Secretory Pathway Ca2+-ATPase (SPCA1) in Mice Causes Golgi Stress, Apoptosis, and Midgestational Death in Homozygous Embryos and Squamous Cell Tumors in Adult Heterozygotes. Journal of Biological Chemistry. 282(36). 26517–26527. 93 indexed citations
17.
Noonan, William T., Alison L. Woo, Michelle L. Nieman, et al.. (2004). Blood pressure maintenance in NHE3-deficient mice with transgenic expression of NHE3 in small intestine. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 288(3). R685–R691. 53 indexed citations
18.
Okunade, Gbolahan W., Marian L. Miller, Gail J. Pyne, et al.. (2004). Targeted Ablation of Plasma Membrane Ca2+-ATPase (PMCA) 1 and 4 Indicates a Major Housekeeping Function for PMCA1 and a Critical Role in Hyperactivated Sperm Motility and Male Fertility for PMCA4. Journal of Biological Chemistry. 279(32). 33742–33750. 260 indexed citations
19.
Liu, Lynne H., Gregory P. Boivin, Vikram Prasad, Muthu Periasamy, & Gary E. Shull. (2001). Squamous Cell Tumors in Mice Heterozygous for a Null Allele of Atp2a2, Encoding the Sarco(endo)plasmic Reticulum Ca2+-ATPase Isoform 2 Ca2+Pump. Journal of Biological Chemistry. 276(29). 26737–26740. 86 indexed citations
20.
Prasad, Vikram, Sudeep Kumar, & Chinmoy Sankar Dey. (2000). Resistance to arsenite modulates levels of α-tubulin and sensitivity to paclitaxel in Leishmania donovani. Parasitology Research. 86(10). 838–842. 23 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026