Henry Pratt

18.7k total citations
24 papers, 532 citations indexed

About

Henry Pratt is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Henry Pratt has authored 24 papers receiving a total of 532 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 5 papers in Cancer Research and 2 papers in Genetics. Recurrent topics in Henry Pratt's work include Genomics and Chromatin Dynamics (10 papers), RNA Research and Splicing (9 papers) and RNA modifications and cancer (6 papers). Henry Pratt is often cited by papers focused on Genomics and Chromatin Dynamics (10 papers), RNA Research and Splicing (9 papers) and RNA modifications and cancer (6 papers). Henry Pratt collaborates with scholars based in United States, China and Singapore. Henry Pratt's co-authors include Zhiping Weng, Jill E. Moore, Michael Purcaro, Kevin Struhl, Lizhi He, Mingshi Gao, Fengxiang Wei, Xiao‐Ou Zhang, Brenton R. Graveley and Eric L. Van Nostrand and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Blood.

In The Last Decade

Henry Pratt

24 papers receiving 524 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Henry Pratt United States 12 419 74 67 55 54 24 532
Sónia Silva Portugal 14 489 1.2× 59 0.8× 80 1.2× 26 0.5× 54 1.0× 21 623
Austin J. Hepperla United States 12 419 1.0× 69 0.9× 75 1.1× 32 0.6× 32 0.6× 22 485
Semyon Kolmykov Russia 9 384 0.9× 92 1.2× 22 0.3× 54 1.0× 78 1.4× 19 528
Malini Mansharamani United States 9 417 1.0× 65 0.9× 71 1.1× 31 0.6× 47 0.9× 11 507
Chuanbing Zhu China 17 460 1.1× 93 1.3× 36 0.5× 71 1.3× 76 1.4× 32 602
Anne-Gaëlle Rio France 8 386 0.9× 79 1.1× 31 0.5× 33 0.6× 53 1.0× 11 486
Takeya Nakagawa Japan 12 710 1.7× 52 0.7× 46 0.7× 59 1.1× 97 1.8× 22 790
Parirokh Awasthi United States 11 307 0.7× 36 0.5× 68 1.0× 129 2.3× 77 1.4× 18 483
Janina Görnemann Belgium 10 593 1.4× 31 0.4× 93 1.4× 25 0.5× 30 0.6× 10 666
Sergio Lois Spain 12 421 1.0× 54 0.7× 18 0.3× 32 0.6× 83 1.5× 23 543

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-authorship network of co-authors of Henry Pratt

This figure shows the co-authorship network connecting the top 25 collaborators of Henry Pratt. A scholar is included among the top collaborators of Henry Pratt 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 Henry Pratt. Henry Pratt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pratt, Henry, Gregory Andrews, Nicole Shedd, et al.. (2024). Using a comprehensive atlas and predictive models to reveal the complexity and evolution of brain-active regulatory elements. Science Advances. 10(21). eadj4452–eadj4452. 7 indexed citations
2.
Pratt, Henry, et al.. (2023). Beyond genome-wide association studies: Investigating the role of noncoding regulatory elements in primary sclerosing cholangitis. Hepatology Communications. 7(10). 3 indexed citations
3.
Smith‐Roe, Stephanie L., Cheryl A. Hobbs, J. Todd Auman, et al.. (2023). Adopting duplex sequencing technology for genetic toxicity testing: A proof-of-concept mutagenesis experiment with N-ethyl-N-nitrosourea (ENU)-exposed rats. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 891. 503669–503669. 10 indexed citations
4.
He, Lizhi, Mingshi Gao, Henry Pratt, Zhiping Weng, & Kevin Struhl. (2022). MafB, WDR77, and ß-catenin interact with each other and have similar genome association profiles. PLoS ONE. 17(4). e0264799–e0264799. 1 indexed citations
5.
Pratt, Henry, Gregory Andrews, Jack Huey, et al.. (2021). Factorbook: an updated catalog of transcription factor motifs and candidate regulatory motif sites. Nucleic Acids Research. 50(D1). D141–D149. 18 indexed citations
6.
Velde, Arjan van der, Kaili Fan, Junko Tsuji, et al.. (2021). Annotation of Chromatin States in 66 Complete Mouse Epigenomes During Development (stateregexp). Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
7.
He, Lizhi, Henry Pratt, Mingshi Gao, et al.. (2021). YAP and TAZ are transcriptional co-activators of AP-1 proteins and STAT3 during breast cellular transformation. eLife. 10. 74 indexed citations
8.
Moore, Jill E., Xiao‐Ou Zhang, Shaimae I. Elhajjajy, et al.. (2021). Integration of high-resolution promoter profiling assays reveals novel, cell type–specific transcription start sites across 115 human cell and tissue types. Genome Research. 32(2). 389–402. 9 indexed citations
9.
Rodríguez, Tomás, et al.. (2021). Genome-wide detection and analysis of CRISPR-Cas off-targets. Progress in molecular biology and translational science. 181. 31–43. 11 indexed citations
10.
Velde, Arjan van der, Kaili Fan, Junko Tsuji, et al.. (2021). Annotation of chromatin states in 66 complete mouse epigenomes during development. Communications Biology. 4(1). 239–239. 39 indexed citations
11.
Zhang, Xiao‐Ou, Henry Pratt, & Zhiping Weng. (2021). Investigating the Potential Roles of SINEs in the Human Genome. Annual Review of Genomics and Human Genetics. 22(1). 199–218. 29 indexed citations
12.
Short, Nicholas J., Hagop M. Kantarjian, Rashmi Kanagal‐Shamanna, et al.. (2020). Ultra-accurate Duplex Sequencing for the assessment of pretreatment ABL1 kinase domain mutations in Ph+ ALL. Blood Cancer Journal. 10(5). 61–61. 18 indexed citations
13.
Moore, Jill E., Henry Pratt, Michael Purcaro, & Zhiping Weng. (2020). A curated benchmark of enhancer-gene interactions for evaluating enhancer-target gene prediction methods. Genome biology. 21(1). 17–17. 68 indexed citations
14.
Smith, Jordan L., Tomás Rodríguez, Haiwei Mou, et al.. (2020). YAP1 Withdrawal in Hepatoblastoma Drives Therapeutic Differentiation of Tumor Cells to Functional Hepatocyte‐Like Cells. Hepatology. 73(3). 1011–1027. 15 indexed citations
15.
Quinones-Valdez, Giovanni, Stephen Tran, Jae Hoon Bahn, et al.. (2019). Regulation of RNA editing by RNA-binding proteins in human cells. Communications Biology. 2(1). 19–19. 103 indexed citations
16.
Yang, Ei-Wen, Jae Hoon Bahn, Yiwei Sun, et al.. (2019). Allele-specific binding of RNA-binding proteins reveals functional genetic variants in the RNA. Nature Communications. 10(1). 1338–1338. 35 indexed citations
17.
Pratt, Henry, Charles C. Valentine, Lindsey N. Williams, et al.. (2019). Characterization of Clonal Dynamics after Hematopoietic Cell Transplantation Using Ultra-Sensitive Duplex Sequencing. Blood. 134(Supplement_1). 2483–2483. 1 indexed citations
18.
Pratt, Henry & Zhiping Weng. (2018). Decoding the non-coding genome: Opportunities and challenges of genomic and epigenomic consortium data. Current Opinion in Systems Biology. 11. 82–90. 3 indexed citations
19.
Fusco, Dahlene N., Henry Pratt, Wenyu Lin, et al.. (2017). HELZ2 Is an IFN Effector Mediating Suppression of Dengue Virus. Frontiers in Microbiology. 8. 240–240. 35 indexed citations
20.
Giallourakis, Cosmas, Yair Benita, Benoit Molinié, et al.. (2013). Genome-wide Analysis of Immune System Genes by Expressed Sequence Tag Profiling. The Journal of Immunology. 190(11). 5578–5587. 12 indexed citations

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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