Evin M. Padhi
Impact in
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- Acute Myeloid Leukemia Research
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- Cancer Genomics and Diagnostics
Papers in
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- Genomics and Phylogenetic Studies 1
- Single-cell and spatial transcriptomics 1
- Congenital heart defects research 1
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- Prenatal Screening and Diagnostics 1
- Co-authors
- Tychele N. Turner (2 shared papers)Tim Coorens (1 shared paper)Stephen B. Montgomery (1 shared paper)Andrew R. Marderstein (1 shared paper)Marco De Zuani (1 shared paper)Ana Cvejic (1 shared paper)Jon Bezney (1 shared paper)Timothy T. Harkins (1 shared paper)
- Partner nations
- United StatesUnited KingdomSouth Sudan
In The Last Decade
Evin M. Padhi
3 papers receiving 15 citations
Peers
Comparison fields: 5 of 11
- Hematology 4
- Cancer Research 3
- Genetics 5
- Genetics 1
- Immunology 2
Countries citing papers authored by Evin M. Padhi
This map shows the geographic impact of Evin M. Padhi'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 Evin M. Padhi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Evin M. Padhi more than expected).
Fields of papers citing papers by Evin M. Padhi
This network shows the impact of papers produced by Evin M. Padhi. 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 Evin M. Padhi. The network helps show where Evin M. Padhi may publish in the future.
Co-authors
The 13 scholars most cited alongside Evin M. Padhi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
About Evin M. Padhi
Evin M. Padhi is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Cancer Research and Infectious Diseases, having authored 3 papers that have together received 15 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (1 paper), Genomics and Rare Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Cancer Genomics and Diagnostics (1 paper), Single-cell and spatial transcriptomics (1 paper), Prenatal Screening and Diagnostics (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Hematology (4 citations), Cancer Research (3 citations), Genetics (5 citations), Genetics (1 citation) and Immunology (2 citations). Evin M. Padhi has collaborated with scholars based in United States, United Kingdom and South Sudan. Frequent co-authors include Tychele N. Turner, Tim Coorens, Stephen B. Montgomery, Andrew R. Marderstein, Marco De Zuani, Ana Cvejic, Jon Bezney, Timothy T. Harkins, Pankaj Vats and Shawn Leonard. Their work appears in journals such as Nature, Human Mutation and Bioinformatics.
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.