Harminder Sehra
Impact in
- Cell Biology top 0.5%
- Zebrafish Biomedical Research Applications
- Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
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- Genomics and Chromatin Dynamics 7
- RNA and protein synthesis mechanisms 3
- RNA Interference and Gene Delivery 2
- Genomics and Phylogenetic Studies 2
- Co-authors
- Stephan Beck (4 shared papers)Sarah K. Sims (3 shared papers)Hidetoshi Inoko (2 shared papers)Takashi Shiina (2 shared papers)Jane Rogers (2 shared papers)Jennifer Harrow (2 shared papers)Helen L. Beasley (1 shared paper)Asako Ando (1 shared paper)
- Journals
- Nature (9 papers)Immunogenetics (1 paper)Nucleic Acids Research (1 paper)Genomics (1 paper)PLoS Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Harminder Sehra
16 papers receiving 7.5k citations
Harminder Sehra's Hit Papers
Peers
Comparison fields: 5 of 163
- Cell Biology 1.9k
- Genetics 1.8k
- Molecular Biology 3.8k
- Immunology 972
- Developmental Neuroscience 134
Countries citing papers authored by Harminder Sehra
This map shows the geographic impact of Harminder Sehra'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 Harminder Sehra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harminder Sehra more than expected).
Fields of papers citing papers by Harminder Sehra
This network shows the impact of papers produced by Harminder Sehra. 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 Harminder Sehra. The network helps show where Harminder Sehra may publish in the future.
Co-authors
The 25 scholars most cited alongside Harminder Sehra, 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 | The zebrafish reference genome sequence and its relationship to the human genome Hit paper breakdown → | 2013 | 3980 |
| 2 | The DNA sequence of the human X chromosome Hit paper breakdown → | 2005 | 857 |
| 3 | The DNA sequence of human chromosome 22 Hit paper breakdown → | 1999 | 846 |
| 4 | 2004 | 531 | |
| 5 | 2011 | 347 | |
| 6 | 2001 | 285 | |
| 7 | 2003 | 239 | |
| 8 | 2006 | 193 | |
| 9 | 2007 | 122 | |
| 10 | 2006 | 103 | |
| 11 | 2004 | 71 | |
| 12 | 2004 | 64 | |
| 13 | 2009 | 59 | |
| 14 | 2006 | 28 | |
| 15 | 2006 | 7 | |
| 16 | A high utility integrated map of the pig genome. | 2007 | 7 |
About Harminder Sehra
Harminder Sehra is a scholar working on Genetics, Molecular Biology, Immunology, Plant Science and Agronomy and Crop Science, having authored 16 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (7 papers), Chromosomal and Genetic Variations (6 papers), Immune Cell Function and Interaction (4 papers), T-cell and B-cell Immunology (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA and protein synthesis mechanisms (3 papers), RNA Interference and Gene Delivery (2 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Cell Biology (1.9k citations), Genetics (1.8k citations), Molecular Biology (3.8k citations), Immunology (972 citations) and Developmental Neuroscience (134 citations). Harminder Sehra has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Stephan Beck, Sarah K. Sims, Hidetoshi Inoko, Takashi Shiina, Jane Rogers, Jennifer Harrow, Helen L. Beasley, Asako Ando, Kevin Howe and P. Chardon. Their work appears in journals such as Nature, Immunogenetics, Nucleic Acids Research, Genomics and PLoS 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.