Rakesh Kumar

6.6k total citations
121 papers, 3.5k citations indexed

About

Rakesh Kumar is a scholar working on Molecular Biology, Oncology and Organic Chemistry. According to data from OpenAlex, Rakesh Kumar has authored 121 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 41 papers in Oncology and 23 papers in Organic Chemistry. Recurrent topics in Rakesh Kumar's work include Histone Deacetylase Inhibitors Research (13 papers), Metal-Catalyzed Oxygenation Mechanisms (12 papers) and Hydrology and Drought Analysis (11 papers). Rakesh Kumar is often cited by papers focused on Histone Deacetylase Inhibitors Research (13 papers), Metal-Catalyzed Oxygenation Mechanisms (12 papers) and Hydrology and Drought Analysis (11 papers). Rakesh Kumar collaborates with scholars based in India, United States and United Kingdom. Rakesh Kumar's co-authors include Ratna K. Vadlamudi, Chandranath Chatterjee, Suresh K. Rayala, Dana S. Levy, Kazufumi Ohshiro, Christopher J. Barnes, Jason A. Kahana, Richard G. Pestell, Caroline Holm and Göran Landberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Rakesh Kumar

118 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rakesh Kumar India 35 2.1k 1.1k 504 388 359 121 3.5k
Jenny L. Persson Sweden 33 2.0k 1.0× 677 0.6× 655 1.3× 287 0.7× 180 0.5× 85 3.3k
Patricia Müller United Kingdom 29 4.9k 2.3× 2.7k 2.4× 1.5k 2.9× 615 1.6× 211 0.6× 48 8.0k
Luyuan Li China 29 1.3k 0.6× 355 0.3× 413 0.8× 134 0.3× 226 0.6× 122 3.1k
Mei Wang China 34 2.4k 1.2× 617 0.5× 718 1.4× 285 0.7× 295 0.8× 146 4.0k
Hiroshi Tauchi Japan 29 3.0k 1.4× 1.1k 0.9× 1.0k 2.0× 363 0.9× 311 0.9× 90 3.6k
Aaron A. Goodarzi Canada 35 4.8k 2.3× 2.0k 1.7× 1.2k 2.4× 447 1.2× 254 0.7× 60 5.7k
Alice C. Fan United States 25 1.3k 0.6× 676 0.6× 464 0.9× 102 0.3× 103 0.3× 74 2.7k
Shigeru Hashimoto Japan 36 2.3k 1.1× 702 0.6× 454 0.9× 1.1k 2.8× 151 0.4× 143 3.8k
Noriaki Nakamura Japan 27 2.8k 1.3× 1.1k 1.0× 556 1.1× 298 0.8× 126 0.4× 88 4.3k
Hiroshi Miwa Japan 28 1.5k 0.7× 575 0.5× 218 0.4× 122 0.3× 333 0.9× 132 3.4k

Countries citing papers authored by Rakesh Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Rakesh Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rakesh Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Rakesh Kumar. A scholar is included among the top collaborators of Rakesh Kumar 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 Rakesh Kumar. Rakesh Kumar 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.
Rana, Garima, Rakesh Kumar, Devendra Singh, et al.. (2025). Recent advances in phosphorus nano-fertilizers: Impacts on crop productivity and soil sustainability. Physiological and Molecular Plant Pathology. 140. 102885–102885.
2.
Singh, Baghendra, Rakesh Kumar, & Apparao Draksharapu. (2024). Multimetallic Prussian Blue Analogue Nanoparticles for Oxygen Evolution Reaction and Efficient Benzyl Alcohol Oxidation. ACS Applied Nano Materials. 7(13). 15763–15771. 15 indexed citations
3.
Singh, Baghendra, et al.. (2024). Nitrate-coordinated FeNi(OH)2 for hydrazine oxidation assisted seawater splitting at the industrial-level current density. Chemical Communications. 60(70). 9432–9435. 15 indexed citations
4.
George, Bijesh, et al.. (2023). Hyperactivation of p21-Activated Kinases in Human Cancer and Therapeutic Sensitivity. Biomedicines. 11(2). 462–462. 4 indexed citations
5.
Choudhury, Chinmayee, Vivek Kumar, & Rakesh Kumar. (2023). smProdrugs: A repository of small molecule prodrugs. European Journal of Medicinal Chemistry. 249. 115153–115153. 4 indexed citations
6.
Mallojjala, Sharath Chandra, et al.. (2023). Altering the Localization of an Unpaired Spin in a Formal Ni(V) Species. Chemistry - A European Journal. 30(4). e202302824–e202302824. 2 indexed citations
7.
Sharma, Raju, Sameer Bakhshi, Amit Mehndiratta, et al.. (2022). Chemotherapy response evaluation using diffusion weighted MRI in Ewing Sarcoma: A single center experience. Acta Radiologica. 64(4). 1508–1517. 2 indexed citations
8.
Kumar, Rakesh, et al.. (2022). Formation and Reactivity of a Fleeting NiIII Bisphenoxyl Diradical Species. Angewandte Chemie International Edition. 61(41). e202211345–e202211345. 15 indexed citations
9.
Kumar, Rakesh, et al.. (2022). Formation and Reactivity of a Fleeting NiIII Bisphenoxyl Diradical Species. Angewandte Chemie. 134(41). 4 indexed citations
10.
Pakala, Suresh B., Suresh K. Rayala, Rui‐An Wang, et al.. (2013). MTA1 Promotes STAT3 Transcription and Pulmonary Metastasis in Breast Cancer. Cancer Research. 73(12). 3761–3770. 55 indexed citations
11.
Eswaran, Jeyanthy, et al.. (2012). Molecular Pathways: Targeting P21-Activated Kinase 1 Signaling in Cancer—Opportunities, Challenges, and Limitations. Clinical Cancer Research. 18(14). 3743–3749. 65 indexed citations
12.
Ohshiro, Kazufumi, Arnold M. Schwartz, Paul H. Levine, & Rakesh Kumar. (2012). Alternate Estrogen Receptors Promote Invasion of Inflammatory Breast Cancer Cells via Non-Genomic Signaling. PLoS ONE. 7(1). e30725–e30725. 41 indexed citations
13.
Kumar, Rakesh, Sanjay Thulkar, Raju Sharma, et al.. (2012). Magnetic resonance imaging and positron emission tomography-computed tomography evaluation of soft tissue sarcoma with surgical and histopathological correlation. Indian Journal of Nuclear Medicine. 27(4). 213–213. 6 indexed citations
14.
Xu, Yingjie, Tarek A. Bismar, Jie Su, et al.. (2010). Filamin A regulates focal adhesion disassembly and suppresses breast cancer cell migration and invasion. The Journal of Experimental Medicine. 207(11). 2421–2437. 143 indexed citations
15.
Kumar, Rakesh, Seetharaman Balasenthil, Suresh B. Pakala, et al.. (2010). Metastasis-Associated Protein 1 Short Form Stimulates Wnt1 Pathway in Mammary Epithelial and Cancer Cells. Cancer Research. 70(16). 6598–6608. 21 indexed citations
16.
Altomare, Deborah A., Lili Zhang, Jing Deng, et al.. (2010). GSK690693 Delays Tumor Onset and Progression in Genetically Defined Mouse Models Expressing Activated Akt. Clinical Cancer Research. 16(2). 486–496. 43 indexed citations
17.
Nair, Binoj C., Sujit S. Nair, Dimple Chakravarty, et al.. (2010). Cyclin-Dependent Kinase–Mediated Phosphorylation Plays a Critical Role in the Oncogenic Functions of PELP1. Cancer Research. 70(18). 7166–7175. 35 indexed citations
18.
Rabindran, Sridhar K., Peter Sabbatini, Susan Korenchuk, et al.. (2009). Abstract #1740: Characterization of GSK1838705A, a small molecule inhibitor of the insulin-like growth factor-1 receptor and anaplastic lymphoma kinase that delays growth of IGF-1R-dependent tumors and causes regression of ALK-dependent tumors in vivo. Cancer Research. 69. 1740–1740. 2 indexed citations
19.
Naresh, Anjali, Ann D. Thor, Susan M. Edgerton, et al.. (2008). The HER4/4ICD Estrogen Receptor Coactivator and BH3-Only Protein Is an Effector of Tamoxifen-Induced Apoptosis. Cancer Research. 68(15). 6387–6395. 54 indexed citations
20.
Bagheri‐Yarmand, Rozita, Seetharaman Balasenthil, Anupama E. Gururaj, et al.. (2007). Metastasis-Associated Protein 1 Transgenic Mice: A New Model of Spontaneous B-Cell Lymphomas. Cancer Research. 67(15). 7062–7067. 12 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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