Parag Tamhankar
- Co-authors
- Sarita AgarwalShubha R. PhadkeUrvashi GuptaRavindra KumarJayesh ShethMehul MistriDhanjit Kumar DasFrenny Sheth
- Topics
- Hemoglobinopathies and Related Disorders (4 papers)Genomics and Rare Diseases (3 papers)Lysosomal Storage Disorders Research (3 papers)
- Cited by
- GeneticsHematology
- Partner nations
- IndiaJapanUnited States
In The Last Decade
Parag Tamhankar
28 papers receiving 263 citations
Peers
Comparison fields: 5 of 66
- Molecular Biology 95
- Genetics 67
- Physiology 57
- Genetics 52
- Hematology 51
Countries citing papers authored by Parag Tamhankar
This map shows the geographic impact of Parag Tamhankar'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 Parag Tamhankar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Parag Tamhankar more than expected).
Fields of papers citing papers by Parag Tamhankar
This network shows the impact of papers produced by Parag Tamhankar. 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 Parag Tamhankar. The network helps show where Parag Tamhankar may publish in the future.
Co-authorship network of co-authors of Parag Tamhankar
This figure shows the co-authorship network connecting the top 25 collaborators of Parag Tamhankar. A scholar is included among the top collaborators of Parag Tamhankar 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 Parag Tamhankar. Parag Tamhankar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 3 | |
| 4 | 1 | |
| 5 | 5 | |
| 6 | 9 | |
| 7 | 5 | |
| 8 | 22 | |
| 9 | Phenotypic variability in congenital lipoid adrenal hyperplasia. | 3 |
| 10 | 7 | |
| 11 | 6 | |
| 12 | 20 | |
| 13 | 31 | |
| 14 | 11 | |
| 15 | 8 | |
| 16 | 2 | |
| 17 | 16 | |
| 18 | 5 | |
| 19 | 2 | |
| 20 | 4 |
About Parag Tamhankar
Parag Tamhankar is a scholar working on Genetics, Hematology and Genetics, having authored 32 papers that have together received 272 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Genetics (52 citations), Hematology (51 citations) and Genetics (67 citations). Parag Tamhankar has collaborated with scholars based in India, Japan and United States. Frequent co-authors include Sarita Agarwal, Shubha R. Phadke, Urvashi Gupta, Ravindra Kumar, Jayesh Sheth, Mehul Mistri, Dhanjit Kumar Das, Frenny Sheth, Shalu Jain and C. Alexander Valencia. Their work appears in journals such as PLoS ONE, Human Mutation and Prenatal Diagnosis.
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.