Joy Sarkar

1.4k total citations
28 papers, 1.2k citations indexed

About

Joy Sarkar is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Joy Sarkar has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Radiology, Nuclear Medicine and Imaging and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Joy Sarkar's work include Corneal Surgery and Treatments (12 papers), Ocular Surface and Contact Lens (11 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). Joy Sarkar is often cited by papers focused on Corneal Surgery and Treatments (12 papers), Ocular Surface and Contact Lens (11 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). Joy Sarkar collaborates with scholars based in United States, Japan and Netherlands. Joy Sarkar's co-authors include J. Usha Raj, Deming Gou, Ramaswamy Ramchandran, Sandeep Jain, Shweta Chaudhary, Abed Namavari, Snehal Sonawane, Vishakha Khanolkar, Lisette Yco and Janardan K. Reddy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Joy Sarkar

28 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joy Sarkar United States 19 496 328 286 260 185 28 1.2k
Nihal Kaplan United States 18 465 0.9× 148 0.5× 139 0.5× 216 0.8× 80 0.4× 39 1.0k
Gaël Cagnone Canada 17 508 1.0× 299 0.9× 80 0.3× 83 0.3× 38 0.2× 37 916
Xuejiao Yang China 14 483 1.0× 49 0.1× 150 0.5× 113 0.4× 160 0.9× 47 969
Katayoon B. Ebrahimi United States 18 679 1.4× 86 0.3× 68 0.2× 349 1.3× 64 0.3× 29 1.4k
Pachiappan Arjunan United States 16 510 1.0× 51 0.2× 141 0.5× 68 0.3× 62 0.3× 28 1.0k
Hiroshi Mochimaru Japan 15 209 0.4× 41 0.1× 56 0.2× 175 0.7× 169 0.9× 25 748
Shai Erlich United States 13 840 1.7× 41 0.1× 140 0.5× 74 0.3× 31 0.2× 16 1.2k
Akihiko Kudo Japan 25 715 1.4× 111 0.3× 61 0.2× 28 0.1× 97 0.5× 69 1.5k

Countries citing papers authored by Joy Sarkar

Since Specialization
Citations

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

Fields of papers citing papers by Joy Sarkar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joy Sarkar

This figure shows the co-authorship network connecting the top 25 collaborators of Joy Sarkar. A scholar is included among the top collaborators of Joy Sarkar 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 Joy Sarkar. Joy Sarkar 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.
Sarkar, Joy, Yuncin Luo, Qiang Zhou, et al.. (2022). VEGF receptor heterodimers and homodimers are differentially expressed in neuronal and endothelial cell types. PLoS ONE. 17(7). e0269818–e0269818. 6 indexed citations
2.
Sarkar, Joy, et al.. (2022). Benzalkonium chloride, a common ophthalmic preservative, compromises rat corneal cold sensitive nerve activity. The Ocular Surface. 26. 88–96. 13 indexed citations
3.
Zhou, Qiang, Victor H. Guaiquil, Ghasem Yazdanpanah, et al.. (2021). Hydrogels derived from acellular porcine corneal stroma enhance corneal wound healing. Acta Biomaterialia. 134. 177–189. 26 indexed citations
4.
Sarkar, Joy, Behrad Y. Milani, Eun Jae Kim, et al.. (2019). Corneal nerve healing after in situ laser nerve transection. PLoS ONE. 14(6). e0218879–e0218879. 7 indexed citations
5.
Byun, Yong‐Soo, Sapna Tibrewal, Eun Jae Kim, et al.. (2014). Keratocytes Derived from Spheroid Culture of Corneal Stromal Cells Resemble Tissue Resident Keratocytes. PLoS ONE. 9(11). e112781–e112781. 10 indexed citations
6.
Sonawane, Snehal, Vishakha Khanolkar, Abed Namavari, et al.. (2012). Ocular Surface Extracellular DNA and Nuclease Activity Imbalance: A New Paradigm for Inflammation in Dry Eye Disease. Investigative Ophthalmology & Visual Science. 53(13). 8253–8253. 91 indexed citations
7.
Jia, Yuzhi, Navin Viswakarma, Susan E. Crawford, et al.. (2012). Early embryonic lethality of mice with disrupted transcription cofactor PIMT/NCOA6IP/Tgs1 gene. Mechanisms of Development. 129(9-12). 193–207. 22 indexed citations
8.
Chaudhary, Shweta, Abed Namavari, Lisette Yco, et al.. (2012). Neurotrophins and Nerve Regeneration-Associated Genes are Expressed in the Cornea After Lamellar Flap Surgery. Cornea. 31(12). 1460–1467. 50 indexed citations
9.
Sarkar, Joy, Shweta Chaudhary, Abed Namavari, et al.. (2012). Corneal Neurotoxicity Due to Topical Benzalkonium Chloride. Investigative Ophthalmology & Visual Science. 53(4). 1792–1792. 112 indexed citations
10.
Namavari, Abed, Shweta Chaudhary, Jin‐Hong Chang, et al.. (2012). Semaphorin 7a Links Nerve Regeneration and Inflammation in the Cornea. Investigative Ophthalmology & Visual Science. 53(8). 4575–4575. 47 indexed citations
11.
12.
Namavari, Abed, Shweta Chaudhary, Jin‐Hong Chang, et al.. (2011). Cyclosporine Immunomodulation Retards Regeneration of Surgically Transected Corneal Nerves. Investigative Ophthalmology & Visual Science. 53(2). 732–732. 28 indexed citations
13.
Namavari, Abed, Shweta Chaudhary, Joy Sarkar, et al.. (2011). In Vivo Serial Imaging of Regenerating Corneal Nerves after Surgical Transection in Transgenic Thy1-YFP mice. Investigative Ophthalmology & Visual Science. 52(11). 8025–8025. 35 indexed citations
14.
Vluggens, Aurore, Pierre Andreoletti, Navin Viswakarma, et al.. (2010). Functional significance of the two ACOX1 isoforms and their crosstalks with PPARα and RXRα. Laboratory Investigation. 90(5). 696–708. 77 indexed citations
15.
Xia, Jun, Lan Liao, Joy Sarkar, et al.. (2007). Redundant enhancement of mouse constitutive androstane receptor transactivation by p160 coactivator family members. Archives of Biochemistry and Biophysics. 468(1). 49–57. 10 indexed citations
16.
Matsumoto, Kojiro, Songtao Yu, Yuzhi Jia, et al.. (2007). Critical Role for Transcription Coactivator Peroxisome Proliferator-activated Receptor (PPAR)-binding Protein/TRAP220 in Liver Regeneration and PPARα Ligand-induced Liver Tumor Development. Journal of Biological Chemistry. 282(23). 17053–17060. 47 indexed citations
17.
Guo, Dongsheng, Joy Sarkar, Kelly Suino-Powell, et al.. (2007). Induction of Nuclear Translocation of Constitutive Androstane Receptor by Peroxisome Proliferator-activated Receptor α Synthetic Ligands in Mouse Liver. Journal of Biological Chemistry. 282(50). 36766–36776. 31 indexed citations
18.
Viswakarma, Navin, Songtao Yu, Swati Naik, et al.. (2007). Transcriptional Regulation of Cidea, Mitochondrial Cell Death-inducing DNA Fragmentation Factor α-Like Effector A, in Mouse Liver by Peroxisome Proliferator-activated Receptor α and γ. Journal of Biological Chemistry. 282(25). 18613–18624. 80 indexed citations
19.
Guo, Dongsheng, Joy Sarkar, Navin Viswakarma, et al.. (2006). Peroxisome proliferator-activated receptor (PPAR)-binding protein (PBP) but not PPAR-interacting protein (PRIP) is required for nuclear translocation of constitutive androstane receptor in mouse liver. Biochemical and Biophysical Research Communications. 347(2). 485–495. 20 indexed citations
20.

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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