Raman Kumar
Impact in
- Cancer Research top 10%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
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- Ubiquitin and proteasome pathways
- RNA modifications and cancer
- Epigenetics and DNA Methylation
Papers in
-
- Epigenetics and DNA Methylation 5
- Ubiquitin and proteasome pathways 4
- RNA Research and Splicing 3
- RNA and protein synthesis mechanisms 3
- Genetics 13
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 4
- Co-authors
- David F. Callen (9 shared papers)Paul M. Neilsen (8 shared papers)Jozef Gécz (16 shared papers)Fares Al‐Ejeh (3 shared papers)Renèe B. Schulz (3 shared papers)Jacqueline E. Noll (2 shared papers)Jessie Jeffery (3 shared papers)Kum Kum Khanna (3 shared papers)
- Journals
- Oncogene (3 papers)Translational Psychiatry (2 papers)European Journal of Human Genetics (2 papers)Human Molecular Genetics (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- AustraliaUnited StatesFrance
In The Last Decade
Raman Kumar
36 papers receiving 956 citations
Peers
Comparison fields: 5 of 88
- Cancer Research 147
- Molecular Biology 601
- Genetics 224
- Oncology 201
- Applied Microbiology and Biotechnology 14
Countries citing papers authored by Raman Kumar
This map shows the geographic impact of Raman 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 Raman Kumar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Raman Kumar more than expected).
Fields of papers citing papers by Raman Kumar
This network shows the impact of papers produced by Raman 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 Raman Kumar. The network helps show where Raman Kumar may publish in the future.
Co-authors
The 25 scholars most cited alongside Raman 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 150 | |
| 2 | 2014 | 105 | |
| 3 | 2018 | 90 | |
| 4 | 2012 | 75 | |
| 5 | 2011 | 61 | |
| 6 | 2010 | 59 | |
| 7 | 2014 | 45 | |
| 8 | 2009 | 38 | |
| 9 | 2012 | 34 | |
| 10 | 2016 | 30 | |
| 11 | 2016 | 28 | |
| 12 | 2020 | 27 | |
| 13 | 2012 | 24 | |
| 14 | 2017 | 23 | |
| 15 | 2010 | 21 | |
| 16 | 2022 | 18 | |
| 17 | 2020 | 15 | |
| 18 | 2018 | 14 | |
| 19 | 1995 | 12 | |
| 20 | 1995 | 11 |
About Raman Kumar
Raman Kumar is a scholar working on Molecular Biology, Genetics, Oncology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 38 papers that have together received 967 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Epigenetics and DNA Methylation (5 papers), Ubiquitin and proteasome pathways (4 papers), Genomics and Rare Diseases (4 papers), Cancer-related Molecular Pathways (3 papers), RNA Research and Splicing (3 papers), RNA and protein synthesis mechanisms (3 papers) and Epilepsy research and treatment (3 papers). The work is most often cited by research in Cancer Research (147 citations), Molecular Biology (601 citations), Genetics (224 citations), Oncology (201 citations) and Applied Microbiology and Biotechnology (14 citations). Raman Kumar has collaborated with scholars based in Australia, United States and France. Frequent co-authors include David F. Callen, Paul M. Neilsen, Jozef Gécz, Fares Al‐Ejeh, Renèe B. Schulz, Jacqueline E. Noll, Jessie Jeffery, Kum Kum Khanna, Lachlan A. Jolly and Rachel J. Suetani. Their work appears in journals such as Oncogene, Translational Psychiatry, European Journal of Human Genetics, Human Molecular Genetics and The American Journal of Human 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.