Henry Pratt
Impact in
-
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA regulation and disease
- Epigenetics and DNA Methylation
-
- Cancer-related molecular mechanisms research
Papers in
-
- Genomics and Chromatin Dynamics 10
- RNA Research and Splicing 9
- RNA modifications and cancer 6
- RNA and protein synthesis mechanisms 5
- CRISPR and Genetic Engineering 3
- Genomics and Phylogenetic Studies 2
- RNA regulation and disease 2
-
- Cancer-related molecular mechanisms research 2
- Co-authors
- Zhiping Weng (15 shared papers)Jill E. Moore (9 shared papers)Michael Purcaro (5 shared papers)Kevin Struhl (2 shared papers)Mingshi Gao (2 shared papers)Lizhi He (2 shared papers)Xiao‐Ou Zhang (3 shared papers)Fengxiang Wei (1 shared paper)
- Journals
- Communications Biology (2 papers)Nucleic Acids Research (2 papers)Blood (1 paper)Mutation Research/Genetic Toxicology and Environmental Mutagenesis (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesChinaSouth Korea
In The Last Decade
Henry Pratt
24 papers receiving 524 citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 419
- Cancer Research 74
- Cell Biology 67
- Immunology 55
- Genetics 54
Countries citing papers authored by Henry Pratt
This map shows the geographic impact of Henry Pratt'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 Henry Pratt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Henry Pratt more than expected).
Fields of papers citing papers by Henry Pratt
This network shows the impact of papers produced by Henry Pratt. 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 Henry Pratt. The network helps show where Henry Pratt may publish in the future.
Co-authors
The 25 scholars most cited alongside Henry Pratt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 103 | |
| 2 | 2021 | 74 | |
| 3 | 2020 | 68 | |
| 4 | 2021 | 39 | |
| 5 | 2017 | 35 | |
| 6 | 2019 | 35 | |
| 7 | 2021 | 29 | |
| 8 | 2018 | 29 | |
| 9 | 2021 | 18 | |
| 10 | 2020 | 18 | |
| 11 | 2020 | 15 | |
| 12 | 2013 | 12 | |
| 13 | 2021 | 11 | |
| 14 | 2023 | 10 | |
| 15 | 2021 | 9 | |
| 16 | 2024 | 7 | |
| 17 | 2020 | 6 | |
| 18 | 2022 | 4 | |
| 19 | 2018 | 3 | |
| 20 | 2023 | 3 |
About Henry Pratt
Henry Pratt is a scholar working on Molecular Biology, Cancer Research, Genetics, Public Health, Environmental and Occupational Health and Hematology, having authored 24 papers that have together received 532 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (10 papers), RNA Research and Splicing (9 papers), RNA modifications and cancer (6 papers), RNA and protein synthesis mechanisms (5 papers), CRISPR and Genetic Engineering (3 papers), Genomics and Phylogenetic Studies (2 papers), Cancer-related molecular mechanisms research (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Molecular Biology (419 citations), Cancer Research (74 citations), Cell Biology (67 citations), Immunology (55 citations) and Genetics (54 citations). Henry Pratt has collaborated with scholars based in United States, China and South Korea. Frequent co-authors include Zhiping Weng, Jill E. Moore, Michael Purcaro, Kevin Struhl, Mingshi Gao, Lizhi He, Xiao‐Ou Zhang, Fengxiang Wei, Xinshu Xiao and Ei-Wen Yang. Their work appears in journals such as Communications Biology, Nucleic Acids Research, Blood, Mutation Research/Genetic Toxicology and Environmental Mutagenesis and Human Molecular 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.