Howard E. Boudreau

765 total citations
17 papers, 652 citations indexed

About

Howard E. Boudreau is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Howard E. Boudreau has authored 17 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 6 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Howard E. Boudreau's work include Neutrophil, Myeloperoxidase and Oxidative Mechanisms (10 papers), Immune cells in cancer (4 papers) and Immune Response and Inflammation (3 papers). Howard E. Boudreau is often cited by papers focused on Neutrophil, Myeloperoxidase and Oxidative Mechanisms (10 papers), Immune cells in cancer (4 papers) and Immune Response and Inflammation (3 papers). Howard E. Boudreau collaborates with scholars based in United States, South Korea and Hungary. Howard E. Boudreau's co-authors include Thomas L. Leto, Agnieszka Korzeniowska, Benjamin W. Casterline, Balázs Rada, Suzanne U. Emerson, Usha N. Kasid, Deepak Kumar, Chuanbo Zhang, Jonathan J. Park and Debyani Chakravarty and has published in prestigious journals such as The Journal of Immunology, Journal of Virology and The FASEB Journal.

In The Last Decade

Howard E. Boudreau

16 papers receiving 651 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Howard E. Boudreau United States	11	333	232	121	110	101	17	652
Long Cui China	12	281 0.8×	223 1.0×	176 1.5×	65 0.6×	76 0.8×	27	762
Xuan Luo China	15	324 1.0×	171 0.7×	87 0.7×	170 1.5×	62 0.6×	24	608
Agnieszka Korzeniowska United States	7	222 0.7×	215 0.9×	47 0.4×	55 0.5×	128 1.3×	10	507
Peter Breslin United States	16	424 1.3×	176 0.8×	84 0.7×	184 1.7×	32 0.3×	34	737
Takamasa Kanbe Japan	11	484 1.5×	118 0.5×	114 0.9×	121 1.1×	146 1.4×	17	845
Monica Curto Italy	16	323 1.0×	131 0.6×	199 1.6×	115 1.0×	51 0.5×	22	829
Li Geng China	17	487 1.5×	220 0.9×	141 1.2×	347 3.2×	56 0.6×	54	932
Jianping Wang China	17	311 0.9×	67 0.3×	164 1.4×	145 1.3×	45 0.4×	39	661
Xiao‐Feng Lei Japan	13	258 0.8×	159 0.7×	59 0.5×	54 0.5×	57 0.6×	26	572

Countries citing papers authored by Howard E. Boudreau

Since Specialization

Citations

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

Fields of papers citing papers by Howard E. Boudreau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard E. Boudreau. 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 Howard E. Boudreau. The network helps show where Howard E. Boudreau may publish in the future.

Co-authorship network of co-authors of Howard E. Boudreau

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

All Works

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17 of 17 papers shown

Boudreau, Howard E., Jennifer Robinson, & Usha N. Kasid. (2023). Illuminating DEPDC1B in Multi-pronged Regulation of Tumor Progression. Methods in molecular biology. 2660. 295–310.

Boudreau, Howard E., Agnieszka Korzeniowska, & Thomas L. Leto. (2023). Mutant p53 and NOX4 are modulators of a CCL5-driven pro-migratory secretome. Free Radical Biology and Medicine. 199. 17–25. 5 indexed citations

Feng, Wei, Howard E. Boudreau, & Thomas L. Leto. (2021). Pan-Cancer Analysis Shows TP53 Mutations Modulate the Association of NOX4 with Genetic Programs of Cancer Progression and Clinical Outcome. Antioxidants. 10(2). 235–235. 7 indexed citations

Boudreau, Howard E. & Thomas L. Leto. (2019). Model Systems to Investigate NOX-Dependent Cell Migration and Invasiveness. Methods in molecular biology. 1982. 473–485. 2 indexed citations

Moody, Terry W., Lingaku Lee, Irene Ramos-Álvarez, et al.. (2018). PAC1 regulates receptor tyrosine kinase transactivation in a reactive oxygen species-dependent manner. Peptides. 120. 170017–170017. 13 indexed citations

Sugamata, Ryuichi, Ágnes Donkó, Yousuke Murakami, et al.. (2018). Duox1 Regulates Primary B Cell Function under the Influence of IL-4 through BCR-Mediated Generation of Hydrogen Peroxide. The Journal of Immunology. 202(2). 428–440. 7 indexed citations

Boudreau, Howard E., Wei Feng, Agnieszka Korzeniowska, et al.. (2017). Histone modifications affect differential regulation of TGFβ- induced NADPH oxidase 4 (NOX4) by wild-type and mutant p53. Oncotarget. 8(27). 44379–44397. 13 indexed citations

Kwon, Jaeyul, Aibing Wang, Howard E. Boudreau, et al.. (2016). Peroxiredoxin 6 (Prdx6) supports NADPH oxidase1 (Nox1)-based superoxide generation and cell migration. Free Radical Biology and Medicine. 96. 99–115. 44 indexed citations

Boudreau, Howard E., et al.. (2014). Wild-type and mutant p53 differentially regulate NADPH oxidase 4 in TGF-β-mediated migration of human lung and breast epithelial cells. British Journal of Cancer. 110(10). 2569–2582. 82 indexed citations

10.

Donkó, Ágnes, Stanislas Morand, Agnieszka Korzeniowska, et al.. (2014). Hypothyroidism-associated missense mutation impairs NADPH oxidase activity and intracellular trafficking of Duox2. Free Radical Biology and Medicine. 73. 190–200. 18 indexed citations

11.

Rada, Balázs, Howard E. Boudreau, Jonathan J. Park, & Thomas L. Leto. (2013). Histamine Stimulates Hydrogen Peroxide Production by Bronchial Epithelial Cells via Histamine H1 Receptor and Dual Oxidase. American Journal of Respiratory Cell and Molecular Biology. 50(1). 125–134. 34 indexed citations

12.

Boudreau, Howard E., Benjamin W. Casterline, Balázs Rada, Agnieszka Korzeniowska, & Thomas L. Leto. (2012). Nox4 involvement in TGF-beta and SMAD3-driven induction of the epithelial-to-mesenchymal transition and migration of breast epithelial cells. Free Radical Biology and Medicine. 53(7). 1489–1499. 172 indexed citations

13.

Boudreau, Howard E., Agnieszka Korzeniowska, & Thomas L. Leto. (2011). TGF‐beta Signaling Regulates NADPH Oxidase 4 (Nox4) – Dependent Oxidative Stress and Migration of Human Breast Epithelial Cells. The FASEB Journal. 25(S1). 2 indexed citations

14.

Boudreau, Howard E., et al.. (2009). Hepatitis C Virus (HCV) Proteins Induce NADPH Oxidase 4 Expression in a Transforming Growth Factor β-Dependent Manner: a New Contributor to HCV-Induced Oxidative Stress. Journal of Virology. 83(24). 12934–12946. 110 indexed citations

15.

Boudreau, Howard E., Constantinos G. Broustas, Prafulla C. Gokhale, et al.. (2007). Expression of BRCC3, a novel cell cycle regulated molecule, is associated with increased phospho-ERK and cell proliferation. International Journal of Molecular Medicine. 19(1). 29–39. 40 indexed citations

16.

Zhang, Chuanbo, Jin Pei, Deepak Kumar, et al.. (2006). Antisense Oligonucleotides: Target Validation and Development of Systemically Delivered Therapeutic Nanoparticles. Humana Press eBooks. 361. 163–186. 20 indexed citations

17.

Zhang, Chuanbo, Debyani Chakravarty, Howard E. Boudreau, et al.. (2006). Role of SCC-S2 in Experimental Metastasis and Modulation of VEGFR-2, MMP-1, and MMP-9 Expression. Molecular Therapy. 13(5). 947–955. 83 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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