Sabita K. Murthy
- Molecular Biology
- Genetics top 10%
- Cancer Research
- Pediatrics, Perinatology and Child Health
- Oncology
- Co-authors
- Douglas J. DemetrickLisa DifrancescoMeredith WernickJonathan M. LeeColin C. CollinsJoachim DieboldGudrun AmannLisa A. Porter
- Topics
- Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (7 papers)Chromosomal and Genetic Variations (6 papers)
- Journals
- Nature GeneticsMethods in enzymology on CD-ROM/Methods in enzymologyJournal of Medical Genetics
- Partner nations
- CanadaIndiaUnited Arab Emirates
In The Last Decade
Sabita K. Murthy
25 papers receiving 566 citations
Peers
Comparison fields: 5 of 80
- Molecular Biology 371
- Genetics 196
- Cancer Research 83
- Pediatrics, Perinatology and Child Health 61
- Oncology 61
Countries citing papers authored by Sabita K. Murthy
This map shows the geographic impact of Sabita K. Murthy'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 Sabita K. Murthy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sabita K. Murthy more than expected).
Fields of papers citing papers by Sabita K. Murthy
This network shows the impact of papers produced by Sabita K. Murthy. 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 Sabita K. Murthy. The network helps show where Sabita K. Murthy may publish in the future.
Co-authorship network of co-authors of Sabita K. Murthy
This figure shows the co-authorship network connecting the top 25 collaborators of Sabita K. Murthy. A scholar is included among the top collaborators of Sabita K. Murthy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sabita K. Murthy. Sabita K. Murthy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 8 | |
| 2 | 55 | |
| 3 | 18 | |
| 4 | 48 | |
| 5 | 8 | |
| 6 | 23 | |
| 7 | 49 | |
| 8 | 2 | |
| 9 | 217 | |
| 10 | 37 | |
| 11 | 22 | |
| 12 | 12 | |
| 13 | 12 | |
| 14 | Sporadic occurrence of nondeletion Prader-Willi syndrome in two cases: a female with maternal uniparental disomy and a male with complex chromosomal rearrangement. | 1 |
| 15 | 6 | |
| 16 | 1 | |
| 17 | 17 | |
| 18 | Mitotic disturbances associated with inversion 9qh. A case report. | 7 |
| 19 | Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report. | 6 |
| 20 | Nucleolar organizer region heteromorphism associated with trisomy-21: a risk factor for non-disjunction? | 2 |
About Sabita K. Murthy
Sabita K. Murthy is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 25 papers that have together received 585 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). The work is most often cited by research in Genetics (196 citations), Cancer Research (83 citations) and Molecular Biology (371 citations). Sabita K. Murthy has collaborated with scholars based in Canada, India and United Arab Emirates. Frequent co-authors include Douglas J. Demetrick, Lisa Difrancesco, Meredith Wernick, Jonathan M. Lee, Colin C. Collins, Joachim Diebold, Gudrun Amann, Lisa A. Porter, Joe W. Gray and Doug Demetrick. Their work appears in journals such as Nature Genetics, Methods in enzymology on CD-ROM/Methods in enzymology 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.