Dhavendra Kumar
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 26
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 7
- BRCA gene mutations in cancer 7
- Connective tissue disorders research 2
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- Genetic Neurodegenerative Diseases 3
- Co-authors
- Viswanathan Mohan (1 shared paper)Venkatesan Radha (1 shared paper)Carani B. Sanjeevi (1 shared paper)Madhukar Mittal (1 shared paper)RUTH F. CHADWICK (1 shared paper)Catherine Lynn T. Silao (1 shared paper)Bin Alwi Zilfalil (1 shared paper)Ajith Kumar (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Neurology (1 paper)Genetics in Medicine (1 paper)Science (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomIndiaAustralia
In The Last Decade
Dhavendra Kumar
31 papers receiving 959 citations
Peers
Comparison fields: 5 of 99
- Genetics 516
- Psychiatry and Mental health 100
- Nephrology 49
- Molecular Biology 421
- Genetics 46
Countries citing papers authored by Dhavendra Kumar
This map shows the geographic impact of Dhavendra 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 Dhavendra Kumar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dhavendra Kumar more than expected).
Fields of papers citing papers by Dhavendra Kumar
This network shows the impact of papers produced by Dhavendra 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 Dhavendra Kumar. The network helps show where Dhavendra Kumar may publish in the future.
Co-authors
The 11 scholars most cited alongside Dhavendra 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 207 | |
| 2 | 2018 | 146 | |
| 3 | 2017 | 111 | |
| 4 | 2018 | 91 | |
| 5 | 2015 | 69 | |
| 6 | 1998 | 64 | |
| 7 | 2019 | 62 | |
| 8 | 2019 | 50 | |
| 9 | 2021 | 39 | |
| 10 | 2017 | 34 | |
| 11 | 2008 | 27 | |
| 12 | 2011 | 23 | |
| 13 | 2007 | 21 | |
| 14 | 2007 | 14 | |
| 15 | 2004 | 9 | |
| 16 | 2008 | 5 | |
| 17 | 2020 | 3 | |
| 18 | 2015 | 3 | |
| 19 | 2007 | 2 | |
| 20 | 2019 | 2 |
About Dhavendra Kumar
Dhavendra Kumar is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Cancer Research and Modeling and Simulation, having authored 36 papers that have together received 993 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), BRCA gene mutations in cancer (7 papers), Genetic Neurodegenerative Diseases (3 papers), CRISPR and Genetic Engineering (2 papers), Cancer Genomics and Diagnostics (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Genetics (516 citations), Psychiatry and Mental health (100 citations), Nephrology (49 citations), Molecular Biology (421 citations) and Genetics (46 citations). Dhavendra Kumar has collaborated with scholars based in United Kingdom, India and Australia. Frequent co-authors include Viswanathan Mohan, Venkatesan Radha, Carani B. Sanjeevi, Madhukar Mittal, RUTH F. CHADWICK, Catherine Lynn T. Silao, Bin Alwi Zilfalil, Ajith Kumar, Ishwar C. Verma and Shahida Moosa. Their work appears in journals such as The American Journal of Human Genetics, Neurology, Genetics in Medicine, Science and Journal of Medical 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.