R. William Henry

1.7k total citations
42 papers, 1.4k citations indexed

About

R. William Henry is a scholar working on Molecular Biology, Oncology and Ophthalmology. According to data from OpenAlex, R. William Henry has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 15 papers in Oncology and 6 papers in Ophthalmology. Recurrent topics in R. William Henry's work include RNA Research and Splicing (17 papers), Genomics and Chromatin Dynamics (17 papers) and Cancer-related Molecular Pathways (14 papers). R. William Henry is often cited by papers focused on RNA Research and Splicing (17 papers), Genomics and Chromatin Dynamics (17 papers) and Cancer-related Molecular Pathways (14 papers). R. William Henry collaborates with scholars based in United States, Russia and Poland. R. William Henry's co-authors include Nouria Hernandez, Ryûji Kobayashi, Craig S. Hinkley, Susan Lobo, Sui Huang, Beicong Ma, Danyang Chen, Satyaki Sengupta, David N. Arnosti and Liping Gu and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

R. William Henry

41 papers receiving 1.4k citations

Peers

R. William Henry

ONCOL

GENET

Craig R. Stumpf United States

Xiang-Jiao Yang Canada

Laura A. Lee United States

Jan P. Gerlach Netherlands

Takbum Ohn South Korea

Abhinav Dhall United States

Jeremy L. Balsbaugh United States

Marc Kenzelmann Germany

A. A. Karavanov United States

Ulrika Nyman Sweden

Craig R. Stumpf United States

R. William Henry

1.7k ×1.4

210 ×1.0

ONCOL

196 ×1.7

124 ×1.3

GENET

122 ×1.4

Citations per year, relative to R. William Henry R. William Henry (= 1×) peers Craig R. Stumpf

Countries citing papers authored by R. William Henry

Since Specialization

Citations

This map shows the geographic impact of R. William Henry'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 R. William Henry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. William Henry more than expected).

Fields of papers citing papers by R. William Henry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. William Henry. 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 R. William Henry. The network helps show where R. William Henry may publish in the future.

Co-authorship network of co-authors of R. William Henry

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

All Works

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20 of 20 papers shown

Sengupta, Satyaki & R. William Henry. (2015). Regulation of the retinoblastoma–E2F pathway by the ubiquitin–proteasome system. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1849(10). 1289–1297. 30 indexed citations

Henry, R. William, et al.. (2012). RNA polymerase III repression by the retinoblastoma tumor suppressor protein. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1829(3-4). 385–392. 27 indexed citations

Raj, Nitin, Liang Zhang, Yiliang Wei, David N. Arnosti, & R. William Henry. (2012). Ubiquitination of Retinoblastoma Family Protein 1 Potentiates Gene-specific Repression Function. Journal of Biological Chemistry. 287(50). 41835–41843. 10 indexed citations

Lansdell, Theresa A., Michelle A. Hurchla, Jingyu Xiang, et al.. (2012). Noncompetitive Modulation of the Proteasome by Imidazoline Scaffolds Overcomes Bortezomib Resistance and Delays MM Tumor Growth in Vivo. ACS Chemical Biology. 8(3). 578–587. 30 indexed citations

Lansdell, Theresa A., Sandra O’Reilly, Stacy Hovde, et al.. (2012). Attenuation of collagen-induced arthritis by orally available imidazoline-based NF-κB inhibitors. Bioorganic & Medicinal Chemistry Letters. 22(14). 4816–4819. 5 indexed citations

Henry, R. William, et al.. (2012). Regulation of Human RNA Polymerase III Transcription by DNMT1 and DNMT3a DNA Methyltransferases. Journal of Biological Chemistry. 287(10). 7039–7050. 24 indexed citations

Wang, Kai, Satyaki Sengupta, Luca Magnani, et al.. (2010). Brg1 Is Required for Cdx2-Mediated Repression of Oct4 Expression in Mouse Blastocysts. PLoS ONE. 5(5). e10622–e10622. 54 indexed citations

Acharya, Pankaj, Nitin Raj, Liang Zhang, et al.. (2010). Paradoxical Instability–Activity Relationship Defines a Novel Regulatory Pathway for Retinoblastoma Proteins. Molecular Biology of the Cell. 21(22). 3890–3901. 15 indexed citations

Norton, John T., et al.. (2008). The Perinucleolar Compartment Is Directly Associated with DNA. Journal of Biological Chemistry. 284(7). 4090–4101. 26 indexed citations

10.

Gu, Liping, et al.. (2007). The Protein Kinase CK2 Phosphorylates SNAP190 to Negatively Regulate SNAPC DNA Binding and Human U6 Transcription by RNA Polymerase III. Journal of Biological Chemistry. 282(38). 27887–27896. 13 indexed citations

11.

Ullah, Zakir, et al.. (2007). Retinoblastoma Protein Regulation by the COP9 Signalosome. Molecular Biology of the Cell. 18(4). 1179–1186. 36 indexed citations

12.

Feig, Michael, et al.. (2006). The Unorthodox SNAP50 Zinc Finger Domain Contributes to Cooperative Promoter Recognition by Human SNAPC. Journal of Biological Chemistry. 281(41). 31050–31060. 15 indexed citations

13.

Hinkley, Craig S., et al.. (2006). Co-expression of multiple subunits enables recombinant SNAPC assembly and function for transcription by human RNA polymerases II and III. Protein Expression and Purification. 48(2). 215–223. 6 indexed citations

14.

Gu, Liping, Walter J. Esselman, & R. William Henry. (2005). Cooperation between Small Nuclear RNA-activating Protein Complex (SNAPC) and TATA-box-binding Protein Antagonizes Protein Kinase CK2 Inhibition of DNA Binding by SNAPC. Journal of Biological Chemistry. 280(30). 27697–27704. 5 indexed citations

15.

Hovde, Stacy, Craig S. Hinkley, Katie L. Strong, et al.. (2002). Activator recruitment by the general transcription machinery: X-ray structural analysis of the Oct-1 POU domain/human U1 octamer/SNAP190 peptide ternary complex. Genes & Development. 16(21). 2772–2777. 16 indexed citations

16.

Chen, Danyang, Craig S. Hinkley, R. William Henry, & Sui Huang. (2002). TBP Dynamics in Living Human Cells: Constitutive Association of TBP with Mitotic Chromosomes. Molecular Biology of the Cell. 13(1). 276–284. 127 indexed citations

17.

Henry, R. William, Beicong Ma, Ryûji Kobayashi, et al.. (1998). The Large Subunit of Basal Transcription Factor SNAP _c Is a Myb Domain Protein That Interacts with Oct-1. Molecular and Cellular Biology. 18(1). 368–377. 79 indexed citations

18.

Henry, R. William, Ethan Ford, Renu Mital, Vivek Mittal, & Nouria Hernandez. (1998). Crossing the Line between RNA Polymerases: Transcription of Human snRNA Genes by RNA Polymerases II and III. Cold Spring Harbor Symposia on Quantitative Biology. 63(0). 111–120. 32 indexed citations

19.

Grueneberg, Dorre A., R. William Henry, Andrew W. Brauer, et al.. (1997). A multifunctional DNA-binding protein that promotes the formation of serum response factor/homeodomain complexes: identity to TFII-I. Genes & Development. 11(19). 2482–2493. 117 indexed citations

20.

Atkin, Audrey L., R. William Henry, Kenneth L. Roy, & John B. Bell. (1992). Characterization of the tRNATrp genes of Saccharomyces cerevisiae. Gene. 119(1). 57–63. 3 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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