Arun Kumar
Impact in
- Ophthalmology top 2%
- Glaucoma and retinal disorders
- Cancer Research top 10%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Papers in
-
- Epigenetics and DNA Methylation 8
- RNA modifications and cancer 6
- Circular RNAs in diseases 5
- Genetics 17
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Satish Chandra Girimaji (6 shared papers)Susan H. Blanton (3 shared papers)Sanjukta Chakraborty (4 shared papers)K. S. Gopinath (6 shared papers)Venkatesh C. Prabhakaran (3 shared papers)KS Gopinath (3 shared papers)Farogh Ahsan (2 shared papers)Paramdeep Bagga (2 shared papers)
- Journals
- PLoS ONE (6 papers)Journal of Biosciences (5 papers)Gene (3 papers)Scientific Reports (3 papers)Human Molecular Genetics (3 papers)
- Partner nations
- IndiaUnited StatesIreland
In The Last Decade
Arun Kumar
87 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 128
- Ophthalmology 189
- Cancer Research 236
- Cell Biology 239
- Molecular Biology 942
- Genetics 374
Countries citing papers authored by Arun Kumar
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
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-authors
The 25 scholars most cited alongside Arun Kumar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 91 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 184 | |
| 2 | 1990 | 119 | |
| 3 | 2018 | 104 | |
| 4 | 2012 | 99 | |
| 5 | 2007 | 94 | |
| 6 | 2008 | 87 | |
| 7 | Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. | 2007 | 72 |
| 8 | 2008 | 71 | |
| 9 | Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11. | 2007 | 62 |
| 10 | 2010 | 58 | |
| 11 | 2011 | 48 | |
| 12 | 1998 | 46 | |
| 13 | 2003 | 44 | |
| 14 | 2013 | 40 | |
| 15 | 2020 | 38 | |
| 16 | 2004 | 35 | |
| 17 | Lipase from Bacillus pumilus RK31: Production, Purification and Some Properties | 2012 | 33 |
| 18 | 2017 | 31 | |
| 19 | 2020 | 31 | |
| 20 | Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature. | 2013 | 31 |
About Arun Kumar
Arun Kumar is a scholar working on Molecular Biology, Genetics, Physiology, Cancer Research and Plant Science, having authored 91 papers that have together received 2.1k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (10 papers), Epigenetics and DNA Methylation (8 papers), MicroRNA in disease regulation (8 papers), Cancer-related molecular mechanisms research (6 papers), Genetic Syndromes and Imprinting (6 papers), RNA modifications and cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Circular RNAs in diseases (5 papers). The work is most often cited by research in Ophthalmology (189 citations), Cancer Research (236 citations), Cell Biology (239 citations), Molecular Biology (942 citations) and Genetics (374 citations). Arun Kumar has collaborated with scholars based in India, United States and Ireland. Frequent co-authors include Satish Chandra Girimaji, Susan H. Blanton, Sanjukta Chakraborty, K. S. Gopinath, Venkatesh C. Prabhakaran, KS Gopinath, Farogh Ahsan, Paramdeep Bagga, Vishwanath Kumble Bhat and Pooja Singhmar. Their work appears in journals such as PLoS ONE, Journal of Biosciences, Gene, Scientific Reports and Human Molecular Genetics.
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.