Muthu Periasamy

17.7k total citations · 1 hit paper
258 papers, 14.3k citations indexed

About

Muthu Periasamy is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Organic Chemistry. According to data from OpenAlex, Muthu Periasamy has authored 258 papers receiving a total of 14.3k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Molecular Biology, 115 papers in Cardiology and Cardiovascular Medicine and 52 papers in Organic Chemistry. Recurrent topics in Muthu Periasamy's work include Cardiac electrophysiology and arrhythmias (64 papers), Cardiomyopathy and Myosin Studies (60 papers) and Ion channel regulation and function (55 papers). Muthu Periasamy is often cited by papers focused on Cardiac electrophysiology and arrhythmias (64 papers), Cardiomyopathy and Myosin Studies (60 papers) and Ion channel regulation and function (55 papers). Muthu Periasamy collaborates with scholars based in United States, India and Canada. Muthu Periasamy's co-authors include Naresh C. Bal, Gopal J. Babu, Anuradha Kalyanasundaram, Marina Arai, Santosh K. Maurya, B Nadal-Ginard, Philip Babij, David H. MacLennan, Norman R. Alpert and Poornima Bhupathy and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Muthu Periasamy

253 papers receiving 14.0k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Sarcolipin is a newly identified regulator of muscle-based thermogenesis in mammals

2012 428 citations Naresh C. Bal, Santosh K. Maurya et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Muthu Periasamy United States	68	8.4k	5.7k	2.9k	1.3k	1.1k	258	14.3k
Wolfgang Dillmann United States	71	9.9k 1.2×	5.2k 0.9×	2.4k 0.8×	1.4k 1.1×	715 0.7×	212	16.2k
Takeshi Nakano Japan	57	10.2k 1.2×	3.6k 0.6×	2.8k 0.9×	3.5k 2.6×	968 0.9×	509	19.6k
Takashi Matsui Japan	57	6.9k 0.8×	2.9k 0.5×	1.6k 0.6×	530 0.4×	666 0.6×	271	13.0k
Kenneth D. Bloch United States	75	6.4k 0.8×	5.7k 1.0×	6.0k 2.0×	992 0.7×	643 0.6×	264	18.6k
Thomas Michel United States	66	8.1k 1.0×	4.2k 0.7×	8.6k 2.9×	3.0k 2.2×	1.3k 1.2×	179	18.3k
Akiyoshi Fukamizu Japan	75	10.8k 1.3×	4.5k 0.8×	2.3k 0.8×	1.2k 0.9×	1.4k 1.3×	365	20.9k
Michael P. Walsh Canada	65	8.3k 1.0×	3.2k 0.6×	1.9k 0.6×	2.0k 1.5×	1.4k 1.3×	261	12.5k
Joseph A. Beavo United States	72	16.6k 2.0×	3.1k 0.5×	3.8k 1.3×	1.0k 0.8×	2.9k 2.7×	169	22.2k
Giuseppe Cirino Italy	72	5.5k 0.7×	1.6k 0.3×	4.7k 1.6×	866 0.6×	774 0.7×	288	17.9k
Steven J. Sollott United States	39	8.1k 1.0×	2.3k 0.4×	2.4k 0.8×	734 0.5×	1.0k 1.0×	80	14.7k

Countries citing papers authored by Muthu Periasamy

Since Specialization

Citations

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

Fields of papers citing papers by Muthu Periasamy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muthu Periasamy

This figure shows the co-authorship network connecting the top 25 collaborators of Muthu Periasamy. A scholar is included among the top collaborators of Muthu Periasamy 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 Muthu Periasamy. Muthu Periasamy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Cilenti, Lucia, et al.. (2024). Inactivation of mitochondrial MUL1 E3 ubiquitin ligase deregulates mitophagy and prevents diet-induced obesity in mice. Frontiers in Molecular Biosciences. 11. 1397565–1397565. 3 indexed citations

Sarver, Dylan C., Cheng Xu, Susana Rodriguez, et al.. (2023). Hypermetabolism in mice carrying a near-complete human chromosome 21. eLife. 12. 9 indexed citations

Petrosino, Jennifer M., Srinivasagan Ramkumar, Xianyao Xu, et al.. (2021). Paracardial fat remodeling affects systemic metabolism through alcohol dehydrogenase 1. Journal of Clinical Investigation. 131(4). 14 indexed citations

Maurya, Santosh K., José Luís Herrera, Sanjaya Kumar Sahoo, et al.. (2018). Sarcolipin Signaling Promotes Mitochondrial Biogenesis and Oxidative Metabolism in Skeletal Muscle. Cell Reports. 24(11). 2919–2931. 93 indexed citations

Pant, Meghna, Naresh C. Bal, & Muthu Periasamy. (2016). Sarcolipin: A Key Thermogenic and Metabolic Regulator in Skeletal Muscle. Trends in Endocrinology and Metabolism. 27(12). 881–892. 106 indexed citations

Borniger, Jeremy C., Michelle M. Williams, Michael F. Tweedle, et al.. (2016). Photoperiod Affects Organ Specific Glucose Metabolism in Male Siberian Hamsters (Phodopus sungorus). 1(2). 2 indexed citations

Schill, Kevin E., Jeovanna Lowe, Muthu Periasamy, et al.. (2015). Muscle damage, metabolism, and oxidative stress in mdx mice: Impact of aerobic running. Muscle & Nerve. 54(1). 110–117. 28 indexed citations

Shaikh, Sana, Sanjaya Kumar Sahoo, & Muthu Periasamy. (2015). Phospholamban and sarcolipin: Are they functionally redundant or distinct regulators of the Sarco(Endo)Plasmic Reticulum Calcium ATPase?. Journal of Molecular and Cellular Cardiology. 91. 81–91. 70 indexed citations

Glukhov, Alexey V., Anuradha Kalyanasundaram, Qing Lou, et al.. (2013). Calsequestrin 2 deletion causes sinoatrial node dysfunction and atrial arrhythmias associated with altered sarcoplasmic reticulum calcium cycling and degenerative fibrosis within the mouse atrial pacemaker complex1. European Heart Journal. 36(11). 686–697. 94 indexed citations

10.

Kumar, Amit, Naresh C. Bal, Nivedita Jena, et al.. (2013). Identification of calcium binding sites on calsequestrin 1 and their implications for polymerization. Molecular BioSystems. 9(7). 1949–1957. 26 indexed citations

11.

Shanmugam, Mayilvahanan, Shumin Gao, Chull Hong, et al.. (2010). Ablation of phospholamban and sarcolipin results in cardiac hypertrophy and decreased cardiac contractility. Cardiovascular Research. 89(2). 353–361. 33 indexed citations

12.

Periasamy, Muthu, Poornima Bhupathy, & Gopal J. Babu. (2007). Regulation of sarcoplasmic reticulum Ca2+ ATPase pump expression and its relevance to cardiac muscle physiology and pathology. Cardiovascular Research. 77(2). 265–273. 191 indexed citations

13.

Babu, Gopal J. & Muthu Periasamy. (2005). Transgenic Mouse Models for Cardiac Dysfunction by a Specific Gene Manipulation. Humana Press eBooks. 112. 365–377. 9 indexed citations

14.

Babu, Gopal J., Gail J. Pyne, Yingbi Zhou, et al.. (2004). Isoform switching from SM-B to SM-A myosin results in decreased contractility and altered expression of thin filament regulatory proteins. American Journal of Physiology-Cell Physiology. 287(3). C723–C729. 33 indexed citations

15.

Katoh, Youichi & Muthu Periasamy. (1996). Growth and differentiation of smooth muscle cells during vascular development. Trends in Cardiovascular Medicine. 6(3). 100–106. 32 indexed citations

16.

Woodcock‐Mitchell, Janet, Sheryl L. White, William S. Stirewalt, et al.. (1993). Myosin Isoform Expression in Developing and Remodeling Rat Lung. American Journal of Respiratory Cell and Molecular Biology. 8(6). 617–625. 33 indexed citations

17.

Fujii, Junichi, et al.. (1993). Chromosome Mapping of Five Human Cardiac and Skeletal Muscle Sarcoplasmic Reticulum Protein Genes. Genomics. 17(2). 507–509. 55 indexed citations

18.

Saitoh, Osamu, Atsuko Fujisawa‐Sehara, Yo-ichi Nabeshima, & Muthu Periasamy. (1993). Expression of myogenic factors in denervated chicken breast muscle: isolation of the chicken Myf5 gene. Nucleic Acids Research. 21(10). 2503–2509. 46 indexed citations

19.

Alpert, Norman R., et al.. (1989). Genetic and non-genetic control of myocardial calcium. Basic Research in Cardiology. 84(1). 55–66. 7 indexed citations

20.

Periasamy, Muthu, et al.. (1989). Regulation of myosin heavy-chain gene expression during skeletal-muscle hypertrophy. Biochemical Journal. 257(3). 691–698. 39 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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