Arun Kumar

2.7k total citations
89 papers, 2.0k citations indexed

About

Arun Kumar is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Arun Kumar has authored 89 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 22 papers in Genetics and 14 papers in Cancer Research. Recurrent topics in Arun Kumar's work include Epigenetics and DNA Methylation (11 papers), MicroRNA in disease regulation (10 papers) and Tuberous Sclerosis Complex Research (10 papers). Arun Kumar is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), MicroRNA in disease regulation (10 papers) and Tuberous Sclerosis Complex Research (10 papers). Arun Kumar collaborates with scholars based in India, United States and United Kingdom. Arun Kumar's co-authors include Satish Chandra Girimaji, Susan H. Blanton, Sanjukta Chakraborty, K. S. Gopinath, Venkatesh C. Prabhakaran, KS Gopinath, Pooja Singhmar, Vishwanath Kumble Bhat, Farogh Ahsan and Paramdeep Bagga and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Arun Kumar

86 papers receiving 1.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Arun Kumar 1.1k 404 292 254 223 89 2.0k
Wai Kit Chu 1.7k 1.6× 235 0.6× 308 1.1× 220 0.9× 117 0.5× 98 2.8k
S. Priya Narayanan 1.1k 1.0× 106 0.3× 226 0.8× 152 0.6× 368 1.7× 47 2.4k
Yang Wu 855 0.8× 181 0.4× 278 1.0× 72 0.3× 131 0.6× 91 1.7k
Nazar Mashtalir 1.9k 1.8× 378 0.9× 183 0.6× 176 0.7× 653 2.9× 33 3.0k
Yixin Li 895 0.8× 235 0.6× 135 0.5× 80 0.3× 115 0.5× 54 1.4k
U. Krause 1.6k 1.5× 192 0.5× 206 0.7× 522 2.1× 529 2.4× 72 3.1k
Jeong Ae Park 947 0.9× 152 0.4× 341 1.2× 282 1.1× 129 0.6× 34 1.7k
Dafna Lotan 2.1k 2.0× 379 0.9× 358 1.2× 275 1.1× 74 0.3× 68 3.1k
Lixia Lü 1.3k 1.2× 96 0.2× 249 0.9× 87 0.3× 167 0.7× 111 2.5k

Countries citing papers authored by Arun Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Arun Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arun Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Arun Kumar. A scholar is included among the top collaborators of Arun 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 Arun Kumar. Arun 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.
Kumar, Arun, et al.. (2025). Rewiring the Epigenetic Landscape of Cancer: The Role of 5-Azacytidine and 5-Aza-2′-Deoxycytidine. 6(1). 11–21. 1 indexed citations
2.
Kumar, Arun, et al.. (2024). An LC-MS/MS method for the determination of W18 in urine samples. European Psychiatry. 67(S1). S216–S217. 1 indexed citations
3.
Singh, Nivedita, et al.. (2024). Intronic miR-6741-3p targets the oncogene SRSF3: Implications for oral squamous cell carcinoma pathogenesis. PLoS ONE. 19(5). e0296565–e0296565. 4 indexed citations
4.
Kumar, Arun, et al.. (2023). Phenothiazines as anti-cancer agents: SAR overview and synthetic strategies. European Journal of Medicinal Chemistry. 254. 115337–115337. 22 indexed citations
5.
Netravathi, M, Renu Kumari, Pushkar Dakle, et al.. (2015). Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. BMC Medical Genetics. 16(1). 5–5. 12 indexed citations
6.
Gopinath, K. S., et al.. (2015). Genomic amplification upregulates estrogen-related receptor alpha and its depletion inhibits oral squamous cell carcinoma tumors in vivo. Scientific Reports. 5(1). 17621–17621. 17 indexed citations
7.
Bhat, Vishwanath Kumble, et al.. (2014). Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.. PubMed. 20. 790–6. 24 indexed citations
8.
Venkatesh, Thejaswini, et al.. (2013). Primary Microcephaly Gene MCPH1 Shows Signatures of Tumor Suppressors and Is Regulated by miR-27a in Oral Squamous Cell Carcinoma. PLoS ONE. 8(3). e54643–e54643. 40 indexed citations
9.
Kumar, Pavan, B. D. Sharma, Rajiv Kumar, & Arun Kumar. (2012). Optimization of the level of wheat gluten in analogue meat nuggets. 21(1). 54–59. 16 indexed citations
10.
Kumar, Arun, et al.. (2009). Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly. The American Journal of Human Genetics. 84(2). 286–290. 170 indexed citations
11.
Chakraborty, Sanjukta, et al.. (2008). Involvement of TSC genes and differential expression of other members of the mTOR signaling pathway in oral squamous cell carcinoma. BMC Cancer. 8(1). 163–163. 88 indexed citations
12.
Kumar, Arun, et al.. (2007). Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients.. PubMed. 13. 667–76. 72 indexed citations
13.
Kumar, Arun, et al.. (2007). Missense mutation G296S in <i>GATA4</i> is not responsible for cardiac septal defects. Indian journal of human genetics. 13(1). 30–30. 7 indexed citations
14.
Chakraborty, Sanjukta, et al.. (2007). Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis. Genomics. 90(3). 344–353. 92 indexed citations
15.
Kumar, Arun, et al.. (2004). Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).. PubMed. 10. 445–9. 16 indexed citations
16.
Kumar, Arun & Raman Seth. (2004). A rapid method for the determination of protein content in skim milk powder using Pyne method. Indian Journal of Dairy Science. 57(1). 67–68. 3 indexed citations
17.
Astbury, Caroline, Laurie A. Christ, David J. Aughton, et al.. (2004). Detection of deletions in de novo “balanced” chromosome rearrangements: Further evidence for their role in phenotypic abnormalities. Genetics in Medicine. 6(2). 81–89. 34 indexed citations
18.
Raghunath, Arathi, et al.. (2001). Linkage of congenital fibrosis of the extraocular muscles to chromosome 12 in an Indian family. NOT FOUND REPOSITORY (Indian Institute of Science Bangalore). 1 indexed citations
19.
Kumar, Arun, et al.. (1999). Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl. American Journal of Medical Genetics. 86(3). 227–231. 15 indexed citations
20.
Gilbert, John R., Arun Kumar, Chantelle M. Wolpert, et al.. (1998). Mutation and polymorphism analysis in the tuberous sclerosis 2 ( TSC2 ) gene. Neurogenetics. 1(4). 267–272. 13 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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