S. Patil
Impact in
- Hematology top 2%
- Acute Myeloid Leukemia Research
- Hematopoietic Stem Cell Transplantation
- Chronic Myeloid Leukemia Treatments
- Multiple Myeloma Research and Treatments
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Myeloproliferative Neoplasms: Diagnosis and Treatment
Papers in
-
- Epigenetics and DNA Methylation 2
- Cancer-related gene regulation 2
- Genetics 6
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- David Lawrence (1 shared paper)Mark J. Pettenati (1 shared paper)Andrew J. Carroll (1 shared paper)Robert J. Mayer (1 shared paper)Clara D. Bloomfield (1 shared paper)Charles A. Schiffer (1 shared paper)D Arthur (1 shared paper)Deborah Berg (1 shared paper)
- Journals
- Human Genetics (2 papers)Current Topics in Medicinal Chemistry (1 paper)Cytogenetic and Genome Research (1 paper)Journal of Medical Genetics (1 paper)Genomics (1 paper)
- Partner nations
- United StatesIndiaCanada
In The Last Decade
S. Patil
15 papers receiving 690 citations
S. Patil's Hit Papers
Peers
Comparison fields: 5 of 52
- Hematology 493
- Genetics 137
- Public Health, Environmental and Occupational Health 193
- Genetics 137
- Molecular Biology 321
Countries citing papers authored by S. Patil
This map shows the geographic impact of S. Patil'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 S. Patil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Patil more than expected).
Fields of papers citing papers by S. Patil
This network shows the impact of papers produced by S. Patil. 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 S. Patil. The network helps show where S. Patil may publish in the future.
Co-authors
The 25 scholars most cited alongside S. Patil, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid leukemia varies by cytogenetic subtype. Hit paper breakdown → | 1998 | 508 |
| 2 | Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. | 1995 | 42 |
| 3 | 1973 | 40 | |
| 4 | 1984 | 39 | |
| 5 | 1981 | 26 | |
| 6 | 1977 | 16 | |
| 7 | 1990 | 12 | |
| 8 | 1970 | 12 | |
| 9 | HLA alleles in pre-menopausal breast cancer patients from western India. | 2006 | 8 |
| 10 | 2024 | 7 | |
| 11 | 2009 | 5 | |
| 12 | 2004 | 5 | |
| 13 | 2019 | 2 | |
| 14 | 2024 | 1 | |
| 15 | 1980 | 1 |
About S. Patil
S. Patil is a scholar working on Molecular Biology, Genetics, Hematology, Oncology and Immunology, having authored 15 papers that have together received 724 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Epigenetics and DNA Methylation (2 papers), T-cell and B-cell Immunology (2 papers), Chromosomal and Genetic Variations (2 papers), Immune Cell Function and Interaction (2 papers), Cancer-related gene regulation (2 papers), Hemophilia Treatment and Research (1 paper) and Peptidase Inhibition and Analysis (1 paper). The work is most often cited by research in Hematology (493 citations), Genetics (137 citations), Public Health, Environmental and Occupational Health (193 citations), Genetics (137 citations) and Molecular Biology (321 citations). S. Patil has collaborated with scholars based in United States, India and Canada. Frequent co-authors include David Lawrence, Mark J. Pettenati, Andrew J. Carroll, Robert J. Mayer, Clara D. Bloomfield, Charles A. Schiffer, D Arthur, Deborah Berg, Frederick R. Davey and John C. Byrd. Their work appears in journals such as Human Genetics, Current Topics in Medicinal Chemistry, Cytogenetic and Genome Research, Journal of Medical Genetics and Genomics.
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.