Kumar Kastury
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- Chromatin Remodeling and Cancer
- Ubiquitin and proteasome pathways
- Cancer-related gene regulation
- RNA modifications and cancer
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 3
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- Chromatin Remodeling and Cancer 3
- Congenital heart defects research 3
- Renal and related cancers 3
- Signaling Pathways in Disease 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- Teresa Druck (16 shared papers)Masataka Ohta (7 shared papers)Kay Huebner (11 shared papers)Maria Grazia Cotticelli (3 shared papers)Raffaele Baffa (3 shared papers)Zurab Siprashvili (2 shared papers)Juan Palazzo (2 shared papers)Hiroshi Inoue (2 shared papers)
- Journals
- Genomics (5 papers)Genes Chromosomes and Cancer (3 papers)Proceedings of the National Academy of Sciences (2 papers)Cell (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)
- Partner nations
- United StatesItalyGermany
In The Last Decade
Kumar Kastury
21 papers receiving 2.2k citations
Kumar Kastury's Hit Papers
Peers
Comparison fields: 5 of 95
- Genetics 1.0k
- Molecular Biology 1.6k
- Cancer Research 236
- Cell Biology 253
- Oncology 350
Countries citing papers authored by Kumar Kastury
This map shows the geographic impact of Kumar Kastury'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 Kumar Kastury with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kumar Kastury more than expected).
Fields of papers citing papers by Kumar Kastury
This network shows the impact of papers produced by Kumar Kastury. 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 Kumar Kastury. The network helps show where Kumar Kastury may publish in the future.
Co-authors
The 25 scholars most cited alongside Kumar Kastury, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers Hit paper breakdown → | 1996 | 900 |
| 2 | 1995 | 300 | |
| 3 | 1994 | 241 | |
| 4 | Structure and expression of the human FHIT gene in normal and tumor cells. | 1997 | 177 |
| 5 | Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines. | 1996 | 100 |
| 6 | Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene. | 1997 | 88 |
| 7 | Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas. | 1995 | 60 |
| 8 | 1994 | 55 | |
| 9 | 2005 | 54 | |
| 10 | 1995 | 52 | |
| 11 | 1996 | 51 | |
| 12 | 2007 | 42 | |
| 13 | Gene structure, promoter activity, and chromosomal location of the DR-nm23 gene, a related member of the nm23 gene family. | 1997 | 35 |
| 14 | 1996 | 34 | |
| 15 | Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1). | 1993 | 29 |
| 16 | 1994 | 25 | |
| 17 | 1997 | 21 | |
| 18 | 1993 | 13 | |
| 19 | 1997 | 8 | |
| 20 | 1993 | 7 |
About Kumar Kastury
Kumar Kastury is a scholar working on Genetics, Molecular Biology, Cancer Research, Genetics and Hematology, having authored 21 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromatin Remodeling and Cancer (3 papers), Congenital heart defects research (3 papers), Renal and related cancers (3 papers), Signaling Pathways in Disease (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (1.6k citations), Cancer Research (236 citations), Cell Biology (253 citations) and Oncology (350 citations). Kumar Kastury has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Teresa Druck, Masataka Ohta, Kay Huebner, Maria Grazia Cotticelli, Raffaele Baffa, Zurab Siprashvili, Juan Palazzo, Hiroshi Inoue, Kay Huebner and Peter A. McCue. Their work appears in journals such as Genomics, Genes Chromosomes and Cancer, Proceedings of the National Academy of Sciences, Cell and The Journal of Clinical Endocrinology & Metabolism.
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.