Y. S. Prakash

15.8k total citations · 1 hit paper
298 papers, 10.4k citations indexed

About

Y. S. Prakash is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Physiology. According to data from OpenAlex, Y. S. Prakash has authored 298 papers receiving a total of 10.4k indexed citations (citations by other indexed papers that have themselves been cited), including 99 papers in Molecular Biology, 97 papers in Pulmonary and Respiratory Medicine and 92 papers in Physiology. Recurrent topics in Y. S. Prakash's work include Asthma and respiratory diseases (55 papers), Neonatal Respiratory Health Research (52 papers) and Ion channel regulation and function (52 papers). Y. S. Prakash is often cited by papers focused on Asthma and respiratory diseases (55 papers), Neonatal Respiratory Health Research (52 papers) and Ion channel regulation and function (52 papers). Y. S. Prakash collaborates with scholars based in United States, Netherlands and India. Y. S. Prakash's co-authors include Gary C. Sieck, Christina M. Pabelick, Michael A. Thompson, Venkatachalem Sathish, Mathur Kannan, Elizabeth Townsend, Wen-Zhi Zhan, Virginia M. Miller, Bharathi Aravamudan and Vincent M. Rotello and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Y. S. Prakash

287 papers receiving 10.2k citations

Hit Papers

Effect of Nanoparticle Su... 2010 2026 2015 2020 2010 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Y. S. Prakash United States 59 3.6k 3.2k 2.9k 1.2k 1.1k 298 10.4k
Eduardo R. Lazarowski United States 56 5.1k 1.4× 2.2k 0.7× 1.9k 0.6× 1.7k 1.4× 1.2k 1.1× 124 11.7k
Armin Braun Germany 55 2.5k 0.7× 2.0k 0.6× 2.6k 0.9× 411 0.3× 1.7k 1.5× 274 10.0k
Karl Kunzelmann Germany 66 7.8k 2.2× 4.2k 1.3× 1.2k 0.4× 456 0.4× 1.6k 1.5× 219 12.8k
Søren Nielsen Denmark 66 7.6k 2.1× 3.0k 0.9× 3.0k 1.0× 640 0.5× 638 0.6× 279 13.8k
Stephen M. Black United States 62 4.5k 1.3× 3.8k 1.2× 3.6k 1.2× 672 0.6× 417 0.4× 317 11.7k
Wolfgang Liedtke United States 65 5.1k 1.4× 1.5k 0.5× 4.2k 1.5× 1.1k 0.9× 2.2k 2.0× 160 15.8k
Karl‐Erik Andersson Sweden 79 4.2k 1.2× 2.0k 0.6× 4.0k 1.4× 2.4k 2.0× 3.0k 2.8× 704 26.1k
Yushi Ito Japan 41 3.4k 1.0× 1.0k 0.3× 1.6k 0.6× 685 0.6× 1.9k 1.8× 335 7.8k
John W. Hanrahan Canada 56 4.4k 1.2× 5.6k 1.8× 1.2k 0.4× 437 0.4× 731 0.7× 170 10.0k
Stephanie A. Shore United States 53 1.4k 0.4× 3.5k 1.1× 5.5k 1.9× 944 0.8× 634 0.6× 169 9.5k

Countries citing papers authored by Y. S. Prakash

Since Specialization
Citations

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

Fields of papers citing papers by Y. S. Prakash

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Y. S. Prakash. 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 Y. S. Prakash. The network helps show where Y. S. Prakash may publish in the future.

Co-authorship network of co-authors of Y. S. Prakash

This figure shows the co-authorship network connecting the top 25 collaborators of Y. S. Prakash. A scholar is included among the top collaborators of Y. S. Prakash 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 Y. S. Prakash. Y. S. Prakash 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.
Drake, Li Y., et al.. (2025). Mechanical stretch promotes sustained proliferation and inflammation in developing human airway smooth muscle. American Journal of Physiology-Lung Cellular and Molecular Physiology. 329(2). L296–L306.
2.
Reza, Mohammad Irshad, Premanand Balraj, Michael A. Thompson, et al.. (2025). Asthma and inflammation transcriptionally up‐regulate the aryl hydrocarbon receptor in airway smooth muscle via p38/JNK‐AP1 signalling. British Journal of Pharmacology. 182(21). 5269–5285.
3.
Reza, Mohammad Irshad, Ashish Kumar, Christina M. Pabelick, et al.. (2024). Downregulation of protein phosphatase 2Aα in asthmatic airway smooth muscle. American Journal of Physiology-Lung Cellular and Molecular Physiology. 326(5). L651–L659. 4 indexed citations
4.
Balraj, Premanand, Nilesh Sudhakar Ambhore, Priyanka Banerjee, et al.. (2024). Kisspeptin/KISS1R Signaling Modulates Human Airway Smooth Muscle Cell Migration. American Journal of Respiratory Cell and Molecular Biology. 70(6). 507–518. 5 indexed citations
5.
Drake, Li Y., Sarah A. Wicher, Latifa Khalfaoui, et al.. (2024). Aging, brain-derived neurotrophic factor, and allergen-induced pulmonary responses in mice. American Journal of Physiology-Lung Cellular and Molecular Physiology. 328(2). L290–L300.
6.
Khalfaoui, Latifa, et al.. (2024). BMAL1 sex‐specific effects in the neonatal mouse airway exposed to moderate hyperoxia. Physiological Reports. 12(13). e16122–e16122. 4 indexed citations
7.
Kelley, Brian M., Emily Zhang, Latifa Khalfaoui, et al.. (2023). Piezo channels in stretch effects on developing human airway smooth muscle. American Journal of Physiology-Lung Cellular and Molecular Physiology. 325(5). L542–L551. 10 indexed citations
8.
Prakash, Y. S., et al.. (2021). Nicotinic α7 acetylcholine receptor (α7nAChR) in human airway smooth muscle. Archives of Biochemistry and Biophysics. 706. 108897–108897. 16 indexed citations
9.
Wicher, Sarah A., et al.. (2021). Aging increases senescence, calcium signaling, and extracellular matrix deposition in human airway smooth muscle. PLoS ONE. 16(7). e0254710–e0254710. 20 indexed citations
10.
Teske, Jacob J., Sarah A. Wicher, Andrea L. McConico, et al.. (2021). Glial‐derived neurotrophic factor in human airway smooth muscle. Journal of Cellular Physiology. 236(12). 8184–8196. 12 indexed citations
11.
Lazrak, Ahmed, Zhihong Yu, Stephen Doran, et al.. (2020). Upregulation of airway smooth muscle calcium-sensing receptor by low-molecular-weight hyaluronan. American Journal of Physiology-Lung Cellular and Molecular Physiology. 318(3). L459–L471. 13 indexed citations
12.
Wicher, Sarah A., Rodney D. Britt, L. Manlove, et al.. (2019). Calcium sensing receptor in developing human airway smooth muscle. Journal of Cellular Physiology. 234(8). 14187–14197. 14 indexed citations
13.
Kistemaker, Loes & Y. S. Prakash. (2019). Airway Innervation and Plasticity in Asthma. Physiology. 34(4). 283–298. 59 indexed citations
14.
Vogel, Elizabeth R., L. Manlove, Ine Kuipers, et al.. (2019). Caveolin-1 scaffolding domain peptide prevents hyperoxia-induced airway remodeling in a neonatal mouse model. American Journal of Physiology-Lung Cellular and Molecular Physiology. 317(1). L99–L108. 14 indexed citations
15.
Delmotte, Philippe, et al.. (2017). TNFα decreases mitochondrial movement in human airway smooth muscle. American Journal of Physiology-Lung Cellular and Molecular Physiology. 313(1). L166–L176. 30 indexed citations
16.
Singh, Suchita, Manish Bodas, Naveen Kumar Bhatraju, et al.. (2016). Hyperinsulinemia adversely affects lung structure and function. American Journal of Physiology-Lung Cellular and Molecular Physiology. 310(9). L837–L845. 79 indexed citations
17.
Sathish, Venkatachalem, Sarah Kay VanOosten, Bharathi Aravamudan, et al.. (2012). Brain-Derived Neurotrophic Factor in Cigarette Smoke–Induced Airway Hyperreactivity. American Journal of Respiratory Cell and Molecular Biology. 48(4). 431–438. 32 indexed citations
18.
Aravamudan, Bharathi, Sarah Kay VanOosten, Lucas W. Meuchel, et al.. (2012). Caveolin-1 knockout mice exhibit airway hyperreactivity. American Journal of Physiology-Lung Cellular and Molecular Physiology. 303(8). L669–L681. 30 indexed citations
19.
Prakash, Y. S., Erik H.F.M. van der Heijden, Esther M. Gallant, & Gary C. Sieck. (1999). Effects of salbutamol on intracellular Ca2+ regulation in skeletal myotubes. American Journal of Physiology-Legacy Content. 276. 1 indexed citations
20.
Zhan, Wen-Zhi, et al.. (1997). Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. Journal of Applied Physiology. 83(4). 1062–1067. 40 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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