T. Mohandas
- Molecular Biology
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Cellular and Molecular Neuroscience top 10%
- Surgery
- Co-authors
- Jonathan P. ParkMerry PassageVolker SchmiedenTeepu SiddiqueHeinrich BetzC.-M. BeckerGabriele GrenninglohPeter R. Schofield
- Topics
- Genomic variations and chromosomal abnormalities (15 papers)Prenatal Screening and Diagnostics (12 papers)Genetic Syndromes and Imprinting (6 papers)
- Journals
- Proceedings of the National Academy of SciencesJournal of Biological ChemistryThe EMBO Journal
- Partner nations
- United StatesJapanItaly
In The Last Decade
T. Mohandas
36 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 86
- Molecular Biology 627
- Genetics 463
- Pediatrics, Perinatology and Child Health 260
- Cellular and Molecular Neuroscience 202
- Surgery 111
Countries citing papers authored by T. Mohandas
This map shows the geographic impact of T. Mohandas'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 T. Mohandas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Mohandas more than expected).
Fields of papers citing papers by T. Mohandas
This network shows the impact of papers produced by T. Mohandas. 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 T. Mohandas. The network helps show where T. Mohandas may publish in the future.
Co-authorship network of co-authors of T. Mohandas
This figure shows the co-authorship network connecting the top 25 collaborators of T. Mohandas. A scholar is included among the top collaborators of T. Mohandas 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 T. Mohandas. T. Mohandas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 17 | |
| 3 | 24 | |
| 4 | 1 | |
| 5 | 18 | |
| 6 | 17 | |
| 7 | 9 | |
| 8 | 50 | |
| 9 | 30 | |
| 10 | 27 | |
| 11 | Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier. | 125 |
| 12 | 8 | |
| 13 | 11 | |
| 14 | 243 | |
| 15 | 4 | |
| 16 | 15 | |
| 17 | 8 | |
| 18 | Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion. | 26 |
| 19 | 5 | |
| 20 | 27 |
About T. Mohandas
T. Mohandas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 39 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (12 papers) and Genetic Syndromes and Imprinting (6 papers). The work is most often cited by research in Genetics (463 citations), Pediatrics, Perinatology and Child Health (260 citations) and Cellular and Molecular Neuroscience (202 citations). T. Mohandas has collaborated with scholars based in United States, Japan and Italy. Frequent co-authors include Jonathan P. Park, Merry Passage, Volker Schmieden, Teepu Siddique, Heinrich Betz, C.-M. Becker, Gabriele Grenningloh, Peter R. Schofield, Larry J. Shapiro and P. H. Seeburg. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The EMBO Journal.
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.