Raj Kishore

10.3k total citations
143 papers, 7.1k citations indexed

About

Raj Kishore is a scholar working on Molecular Biology, Cancer Research and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Raj Kishore has authored 143 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 36 papers in Cancer Research and 35 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Raj Kishore's work include Extracellular vesicles in disease (24 papers), Angiogenesis and VEGF in Cancer (22 papers) and Cardiac Fibrosis and Remodeling (19 papers). Raj Kishore is often cited by papers focused on Extracellular vesicles in disease (24 papers), Angiogenesis and VEGF in Cancer (22 papers) and Cardiac Fibrosis and Remodeling (19 papers). Raj Kishore collaborates with scholars based in United States, China and Japan. Raj Kishore's co-authors include Douglas W. Losordo, Gangjian Qin, Prasanna Krishnamurthy, Tina Thorne, Mohsin Khan, Suresh K Verma, Erin Lambers, Venkata Naga Srikanth Garikipati, Megan R. McMullen and Laura E. Nagy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Raj Kishore

140 papers receiving 7.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Raj Kishore United States	49	4.3k	1.7k	1.5k	1.2k	1.1k	143	7.1k
Anton Jan van Zonneveld Netherlands	57	5.0k 1.2×	3.1k 1.9×	1.1k 0.7×	1.3k 1.1×	1.1k 1.0×	211	10.6k
Maria B. Grant United States	55	5.4k 1.3×	1.0k 0.6×	984 0.7×	940 0.8×	920 0.8×	235	11.2k
Tatiana V. Byzova United States	50	4.2k 1.0×	1.2k 0.7×	1000 0.7×	1.0k 0.9×	1.4k 1.3×	124	8.9k
Giuseppe Vassalli Switzerland	42	3.5k 0.8×	1.5k 0.9×	2.2k 1.5×	1.4k 1.2×	695 0.6×	137	6.6k
George E. Sandusky United States	46	5.3k 1.2×	1.3k 0.8×	983 0.7×	1.6k 1.3×	770 0.7×	201	9.6k
Anton J.G. Horrevoets Netherlands	43	4.2k 1.0×	1.8k 1.1×	1.1k 0.8×	1.0k 0.9×	1.3k 1.1×	106	7.1k
Guo‐Chang Fan United States	55	6.4k 1.5×	2.7k 1.6×	2.6k 1.8×	1.1k 0.9×	1.2k 1.0×	150	9.9k
Jean‐Marie Freyssinet France	44	4.6k 1.1×	1.2k 0.7×	1.3k 0.9×	939 0.8×	2.1k 1.9×	86	8.3k
Krzysztof Reiss United States	49	4.9k 1.1×	1.2k 0.7×	1.4k 0.9×	692 0.6×	701 0.6×	158	8.0k
Maria Felice Brizzi Italy	45	3.4k 0.8×	1.5k 0.9×	540 0.4×	665 0.6×	1.0k 0.9×	142	5.8k

Countries citing papers authored by Raj Kishore

Since Specialization

Citations

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

Fields of papers citing papers by Raj Kishore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raj Kishore

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

All Works

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20 of 20 papers shown

Thakur, Abhimanyu & Raj Kishore. (2025). Neurobiology of the circadian clock and its role in cardiovascular disease: Mechanisms, biomarkers, and chronotherapy. PubMed. 19. 100131–100131. 1 indexed citations

Kishore, Raj & Ajit Magadum. (2024). Cell-Specific mRNA Therapeutics for Cardiovascular Diseases and Regeneration. Journal of Cardiovascular Development and Disease. 11(2). 38–38. 9 indexed citations

Thej, Charan, Rajika Roy, Zhongjian Cheng, et al.. (2024). Epigenetic mechanisms regulate sex differences in cardiac reparative functions of bone marrow progenitor cells. npj Regenerative Medicine. 9(1). 17–17. 7 indexed citations

Kośmider, Beata, Thomas Brandt, Wissam Chatila, et al.. (2023). The Regulation of Fatty Acid Synthase by Exosomal miR-143-5p and miR-342-5p in Idiopathic Pulmonary Fibrosis. American Journal of Respiratory Cell and Molecular Biology. 70(4). 259–282. 13 indexed citations

Magadum, Ajit, Vandana Mallaredy, Rajika Roy, et al.. (2022). Abstract 12785: Psat1 Promotes Serine Synthesis Pathway and Cardiac Regeneration After Myocardial Infarction. Circulation. 146(Suppl_1). 1 indexed citations

Huang, Grace, Zhongjian Cheng, Chunlin Wang, et al.. (2022). Diabetes impairs cardioprotective function of endothelial progenitor cell-derived extracellular vesicles via H3K9Ac inhibition. Theranostics. 12(9). 4415–4430. 34 indexed citations

Cimini, Maria, Venkata Naga Srikanth Garikipati, Claudio de Lucia, et al.. (2019). Podoplanin neutralization improves cardiac remodeling and function after myocardial infarction. JCI Insight. 4(15). 25 indexed citations

Yue, Yujia, Venkata Naga Srikanth Garikipati, Suresh K Verma, David A. Goukassian, & Raj Kishore. (2017). Interleukin-10 Deficiency Impairs Reparative Properties of Bone Marrow-Derived Endothelial Progenitor Cell Exosomes. Tissue Engineering Part A. 23(21-22). 1241–1250. 41 indexed citations

Joladarashi, Darukeshwara, Venkata Naga Srikanth Garikipati, Rajarajan A. Thandavarayan, et al.. (2015). Enhanced Cardiac Regenerative Ability of Stem Cells After Ischemia-Reperfusion Injury. Journal of the American College of Cardiology. 66(20). 2214–2226. 60 indexed citations

10.

Verma, Suresh K, Prasanna Krishnamurthy, David Y. Barefield, et al.. (2012). Interleukin-10 Treatment Attenuates Pressure Overload–Induced Hypertrophic Remodeling and Improves Heart Function via Signal Transducers and Activators of Transcription 3–Dependent Inhibition of Nuclear Factor-κB. Circulation. 126(4). 418–429. 162 indexed citations

11.

Kishore, Raj & Suresh K Verma. (2012). Roles of STATs signaling in cardiovascular diseases. PubMed. 1(2). 118–124. 43 indexed citations

12.

Hoxha, Eneda & Raj Kishore. (2012). Induced Pluripotent Cells in Cardiovascular Biology. Progress in molecular biology and translational science. 111. 27–49.

13.

Xu, Yan, Heiko Enderling, Daniel Park, et al.. (2011). Breaking the ‘harmony’ of TNF-α signaling for cancer treatment. Oncogene. 31(37). 4117–4127. 55 indexed citations

14.

Zattra, Edoardo, Elizabeth Helms, Evelyn Bord, et al.. (2009). Polypodium leucotomos Extract Decreases UV-Induced Cox-2 Expression and Inflammation, Enhances DNA Repair, and Decreases Mutagenesis in Hairless Mice. American Journal Of Pathology. 175(5). 1952–1961. 72 indexed citations

15.

Suriano, Robert, et al.. (2008). 17β-Estradiol Mobilizes Bone Marrow–Derived Endothelial Progenitor Cells to Tumors. Cancer Research. 68(15). 6038–6042. 42 indexed citations

16.

Qin, Gangjian, Masaaki Ii, Marcy Silver, et al.. (2006). Functional disruption of α4 integrin mobilizes bone marrow–derived endothelial progenitors and augments ischemic neovascularization. The Journal of Experimental Medicine. 203(1). 153–163. 91 indexed citations

17.

Chen, Yahui, Elizabeth Helms, Hiroyasu Inoue, et al.. (2005). T-oligo Treatment Decreases Constitutive and UVB-induced COX-2 Levels through p53- and NFκB-dependent Repression of the COX-2 Promoter. Journal of Biological Chemistry. 280(37). 32379–32388. 33 indexed citations

18.

Kishore, Raj, et al.. (1998). Development and characterization of mouse anti‐human LMP2, LMP7, TAP1 and TAP2 monoclonal antibodies. Tissue Antigens. 51(2). 129–140. 12 indexed citations

19.

Chatterjee‐Kishore, Moitreyee, Raj Kishore, Daniel J. Hicklin, Francesco M. Marincola, & Soldano Ferrone. (1998). Different Requirements for Signal Transducer and Activator of Transcription 1α and Interferon Regulatory Factor 1 in the Regulation of Low Molecular Mass Polypeptide 2 and Transporter Associated with Antigen Processing 1 Gene Expression. Journal of Biological Chemistry. 273(26). 16177–16183. 90 indexed citations

20.

Kishore, Raj, et al.. (1996). HLA Sharing, Anti‐Paternal Cytotoxic Antibodies and MLR Blocking Factors in Women with Recurrent Spontaneous Abortion. Journal of obstetrics and gynaecology research. 22(2). 177–183. 27 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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