Henry Pratt

19.5k citations
25 papers · 569 · h-index 13

Impact in

    • RNA Research and Splicing
    • Genomics and Chromatin Dynamics
    • RNA modifications and cancer
    • RNA regulation and disease
    • RNA and protein synthesis mechanisms
    • Epigenetics and DNA Methylation
    • Cancer-related molecular mechanisms research

Papers in

    • Genomics and Chromatin Dynamics 10
    • RNA Research and Splicing 8
    • RNA modifications and cancer 5
    • RNA and protein synthesis mechanisms 4
    • CRISPR and Genetic Engineering 3
    • Gene expression and cancer classification 2

Henry Pratt

24 papers receiving 564 citations

Peers

Henry Pratt
Comparison fields: 5 of 63
  • Molecular Biology 416
  • Cancer Research 67
  • Cell Biology 70
  • Immunology 53
  • Genetics 55
Replace Evangelia Koutelou with:
Evangelia Koutelou United States
Alicia Lindeman Switzerland
Zhongcheng Zhou China
Takeya Nakagawa Japan
Veronika I. Zabarovska Sweden
Marta Seczyńska United Kingdom
Calley Hirsch United States
Matthew Wollerton United Kingdom
Robin Mjelle Norway
Melanie Oakes United States
Henry Pratt relative to Evangelia Koutelou United States Evangelia Koutelou's profile →
Citations per field
00.5×2.8×
Evangelia Koutelou · 1×
Citations per year

Countries citing papers authored by Henry Pratt

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Henry Pratt Line = papers co-authored together Henry Pratt links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2019104
2 202179
3 202073
4 202147
5 201738
6 201936
7 202130
8 201829
9 202120
10 202019
11 202018
12 201312
13 202112
14 202310
15 202410
16 20219
17 20207
18 20225
19 20234
20 20183

About Henry Pratt

Henry Pratt is a scholar working on Molecular Biology, Cancer Research, Public Health, Environmental and Occupational Health, Hematology and Genetics, having authored 25 papers that have together received 569 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (10 papers), RNA Research and Splicing (8 papers), RNA modifications and cancer (5 papers), RNA and protein synthesis mechanisms (4 papers), CRISPR and Genetic Engineering (3 papers), Gene expression and cancer classification (2 papers), Chronic Myeloid Leukemia Treatments (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). The work is most often cited by research in Molecular Biology (416 citations), Cancer Research (67 citations), Cell Biology (70 citations), Immunology (53 citations) and Genetics (55 citations). Henry Pratt has collaborated with scholars based in United States, China and Singapore. Frequent co-authors include Zhiping Weng, Jill E. Moore, Michael Purcaro, Mingshi Gao, Lizhi He, Fengxiang Wei, Kevin Struhl, Xiao‐Ou Zhang, Brenton R. Graveley and Giovanni Quinones-Valdez. Their work appears in journals such as Blood, Nucleic Acids Research, Communications Biology, Bioinformatics 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.

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