Sanjeev S. Ranade

9.6k total citations · 9 hit papers
19 papers, 6.6k citations indexed

About

Sanjeev S. Ranade is a scholar working on Molecular Biology, Physiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Sanjeev S. Ranade has authored 19 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Physiology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Sanjeev S. Ranade's work include Erythrocyte Function and Pathophysiology (9 papers), Ion channel regulation and function (7 papers) and Congenital heart defects research (5 papers). Sanjeev S. Ranade is often cited by papers focused on Erythrocyte Function and Pathophysiology (9 papers), Ion channel regulation and function (7 papers) and Congenital heart defects research (5 papers). Sanjeev S. Ranade collaborates with scholars based in United States, Germany and France. Sanjeev S. Ranade's co-authors include Ardem Patapoutian, Bertrand Coste, Jayanti Mathur, Matt Petrus, Adrienne E. Dubin, Taryn J. Earley, Manuela Schmidt, Zhaozhu Qiu, Ruhma Syeda and Michael Bandell and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Sanjeev S. Ranade

18 papers receiving 6.6k citations

Hit Papers

Piezo1 and Piezo2 Are Essential Components of Distinct Me... 2010 2026 2015 2020 2010 2014 2014 2014 2015 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sanjeev S. Ranade United States 15 4.3k 3.6k 1.5k 1.3k 903 19 6.6k
Bertrand Coste France 30 5.3k 1.2× 4.4k 1.2× 1.7k 1.1× 1.5k 1.2× 1.3k 1.5× 47 8.0k
Jayanti Mathur United States 17 4.8k 1.1× 4.0k 1.1× 1.7k 1.1× 1.3k 1.0× 1.9k 2.1× 22 7.8k
Manuela Schmidt Germany 27 2.9k 0.7× 3.4k 1.0× 804 0.5× 1.5k 1.2× 981 1.1× 51 6.6k
Zhaozhu Qiu United States 21 1.7k 0.4× 2.3k 0.6× 564 0.4× 563 0.4× 529 0.6× 36 4.0k
Swetha E. Murthy United States 18 2.2k 0.5× 1.9k 0.5× 833 0.5× 636 0.5× 342 0.4× 28 3.3k
Ruhma Syeda United States 13 1.7k 0.4× 1.6k 0.5× 646 0.4× 542 0.4× 318 0.4× 22 2.7k
Takaya Abe Japan 45 697 0.2× 3.9k 1.1× 307 0.2× 907 0.7× 300 0.3× 170 7.3k
Andreas F. Mack Germany 44 467 0.1× 2.6k 0.7× 747 0.5× 530 0.4× 406 0.4× 160 5.7k
Linda Madisen United States 27 646 0.2× 4.1k 1.2× 391 0.3× 593 0.5× 564 0.6× 40 8.7k
Simon W. M. John United States 64 1.2k 0.3× 7.6k 2.1× 328 0.2× 1.3k 1.0× 130 0.1× 155 15.3k

Countries citing papers authored by Sanjeev S. Ranade

Since Specialization
Citations

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

Fields of papers citing papers by Sanjeev S. Ranade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanjeev S. Ranade

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

All Works

19 of 19 papers shown
1.
2.
Nishino, Tomohiro, Sanjeev S. Ranade, Angelo Pelonero, et al.. (2023). Single-cell multimodal analyses reveal epigenomic and transcriptomic basis for birth defects in maternal diabetes. Nature Cardiovascular Research. 2(12). 1190–1203. 5 indexed citations
3.
Krup, Alexis Leigh, Sanjeev S. Ranade, Ayushi Agrawal, et al.. (2023). A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors. Development. 150(9). 6 indexed citations
4.
Theodoris, Christina V., Ping Zhou, Lei Liu, et al.. (2020). Network-based screen in iPSC-derived cells reveals therapeutic candidate for heart valve disease. Science. 371(6530). 66 indexed citations
5.
Gifford, Casey A., Sanjeev S. Ranade, Hazel T. Salunga, et al.. (2019). Oligogenic inheritance of a human heart disease involving a genetic modifier. Science. 364(6443). 865–870. 127 indexed citations
6.
Soysa, T. Yvanka de, Sanjeev S. Ranade, Satoshi Okawa, et al.. (2019). Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects. Nature. 572(7767). 120–124. 169 indexed citations
7.
Nonomura, Keiko, Viktor Lukacs, Daniel T. Sweet, et al.. (2018). Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation. Proceedings of the National Academy of Sciences. 115(50). 12817–12822. 197 indexed citations breakdown →
8.
Theodoris, Christina V., Foteini Mourkioti, Yu Huang, et al.. (2017). Long telomeres protect against age-dependent cardiac disease caused by NOTCH1 haploinsufficiency. Journal of Clinical Investigation. 127(5). 1683–1688. 36 indexed citations
9.
Nonomura, Keiko, Rui B. Chang, Astrid Gillich, et al.. (2016). Piezo2 senses airway stretch and mediates lung inflation-induced apnoea. Nature. 541(7636). 176–181. 300 indexed citations breakdown →
10.
Wu, Zizhen, Nicolas Grillet, Bo Zhao, et al.. (2016). Mechanosensory hair cells express two molecularly distinct mechanotransduction channels. Nature Neuroscience. 20(1). 24–33. 98 indexed citations
11.
Ranade, Sanjeev S., Ruhma Syeda, & Ardem Patapoutian. (2015). Mechanically Activated Ion Channels. Neuron. 88(2). 433–433. 7 indexed citations
12.
Ranade, Sanjeev S., Ruhma Syeda, & Ardem Patapoutian. (2015). Mechanically Activated Ion Channels. Neuron. 87(6). 1162–1179. 459 indexed citations breakdown →
13.
Retailleau, Kevin, Fabrice Duprat, Malika Arhatte, et al.. (2015). Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling. Cell Reports. 13(6). 1161–1171. 269 indexed citations
14.
Cahalan, Stuart M., Viktor Lukacs, Sanjeev S. Ranade, et al.. (2015). Piezo1 links mechanical forces to red blood cell volume. eLife. 4. 439 indexed citations breakdown →
15.
Maksimovic, Srdjan, Masashi Nakatani, Yoshichika Baba, et al.. (2014). Epidermal Merkel cells are mechanosensory cells that tune mammalian touch receptors. Nature. 509(7502). 617–621. 405 indexed citations breakdown →
16.
Ranade, Sanjeev S., Adrienne E. Dubin, Rabih Moshourab, et al.. (2014). Piezo2 is the major transducer of mechanical forces for touch sensation in mice. Nature. 516(7529). 121–125. 639 indexed citations breakdown →
17.
Ranade, Sanjeev S., Zhaozhu Qiu, Sung Sik Hur, et al.. (2014). Piezo1, a mechanically activated ion channel, is required for vascular development in mice. Proceedings of the National Academy of Sciences. 111(28). 10347–10352. 643 indexed citations breakdown →
18.
Ranade, Sanjeev S., Andy Weyer, Adrienne E. Dubin, et al.. (2014). Piezo2 is required for Merkel-cell mechanotransduction. Nature. 509(7502). 622–626. 551 indexed citations breakdown →
19.
Coste, Bertrand, Jayanti Mathur, Manuela Schmidt, et al.. (2010). Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels. Science. 330(6000). 55–60. 2230 indexed citations breakdown →

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