Mary J. Kennett

4.9k total citations · 2 hit papers
72 papers, 3.9k citations indexed

About

Mary J. Kennett is a scholar working on Molecular Biology, Epidemiology and Microbiology. According to data from OpenAlex, Mary J. Kennett has authored 72 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Epidemiology and 12 papers in Microbiology. Recurrent topics in Mary J. Kennett's work include Bacterial Infections and Vaccines (11 papers), Peroxisome Proliferator-Activated Receptors (9 papers) and Gut microbiota and health (7 papers). Mary J. Kennett is often cited by papers focused on Bacterial Infections and Vaccines (11 papers), Peroxisome Proliferator-Activated Receptors (9 papers) and Gut microbiota and health (7 papers). Mary J. Kennett collaborates with scholars based in United States, China and India. Mary J. Kennett's co-authors include Na Xiong, Yanming Wang, Ming Li, Pingxin Li, Michael Lindberg, Joshua D. Lambert, Jihyeung Ju, Kenneth R. Reuhl, Shengmin Sang and Chung S. Yang and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Mary J. Kennett

72 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps

2010 1.1k citations Mary J. Kennett, Na Xiong et al. profile →
Dysregulated Microbial Fermentation of Soluble Fiber Induces Cholestatic Liver Cancer

2018 397 citations Vishal Singh, Beng San Yeoh et al. Cell profile →

Peers

Mary J. Kennett

IMMUN

EPIDE

PHYSI

PFM

Harald Carlsen Norway

Asima Bhattacharyya India

Lei Wan Taiwan

Liping Luo China

Venkatakrishna R. Jala United States

Suhkneung Pyo South Korea

Zhengtao Yang China

Carole Elbim France

Hiroki Tanabe Japan

Mónica Comalada Spain

Harald Carlsen Norway

Mary J. Kennett

1.7k ×1.1

1.5k ×1.3

IMMUN

633 ×1.0

EPIDE

409 ×0.9

PHYSI

198 ×0.4

PFM

Citations per year, relative to Mary J. Kennett Mary J. Kennett (= 1×) peers Harald Carlsen

Countries citing papers authored by Mary J. Kennett

Since Specialization

Citations

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

Fields of papers citing papers by Mary J. Kennett

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary J. Kennett. 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 Mary J. Kennett. The network helps show where Mary J. Kennett may publish in the future.

Co-authorship network of co-authors of Mary J. Kennett

This figure shows the co-authorship network connecting the top 25 collaborators of Mary J. Kennett. A scholar is included among the top collaborators of Mary J. Kennett 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 Mary J. Kennett. Mary J. Kennett 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

Allen, Joselyn Natasha, Adwitia Dey, Jingwei Cai, et al.. (2020). Metabolic Profiling Reveals Aggravated Non-Alcoholic Steatohepatitis in High-Fat High-Cholesterol Diet-Fed Apolipoprotein E-Deficient Mice Lacking Ron Receptor Signaling. Metabolites. 10(8). 326–326. 5 indexed citations

Hu, Shaomin, Jie Yang, Yang‐Ding Lin, et al.. (2020). Coordinated co-migration of CCR10+ antibody-producing B cells with helper T cells for colonic homeostatic regulation. Mucosal Immunology. 14(2). 420–430. 13 indexed citations

Snyder, Lindsay M., Juhi Arora, Mary J. Kennett, Veronika Weaver, & Margherita T. Cantorna. (2020). Retinoid Signaling in Intestinal Epithelial Cells Is Essential for Early Survival From Gastrointestinal Infection. Frontiers in Immunology. 11. 559635–559635. 8 indexed citations

Singh, Vishal, Beng San Yeoh, Benoît Chassaing, et al.. (2018). Dysregulated Microbial Fermentation of Soluble Fiber Induces Cholestatic Liver Cancer. Cell. 175(3). 679–694.e22. 397 indexed citations breakdown →

Yeoh, Beng San, Rodrigo Aguilera Olvera, Vishal Singh, et al.. (2016). Epigallocatechin-3-Gallate Inhibition of Myeloperoxidase and Its Counter-Regulation by Dietary Iron and Lipocalin 2 in Murine Model of Gut Inflammation. American Journal Of Pathology. 186(4). 912–926. 41 indexed citations

Wijetunge, Dona Saumya S., et al.. (2016). Growth in Egg Yolk Enhances Salmonella Enteritidis Colonization and Virulence in a Mouse Model of Human Colitis. PLoS ONE. 11(3). e0150258–e0150258. 19 indexed citations

Kudva, Avinash K., et al.. (2015). Chemopreventive Effects of Dietary Eicosapentaenoic Acid Supplementation in Experimental Myeloid Leukemia. Cancer Prevention Research. 8(10). 989–999. 6 indexed citations

Gandhi, Ujjawal H., Naveen Kaushal, Shailaja Hegde, et al.. (2014). Selenium Suppresses Leukemia through the Action of Endogenous Eicosanoids. Cancer Research. 74(14). 3890–3901. 21 indexed citations

Kudva, Avinash K., Naveen Kaushal, Sonia Mohinta, et al.. (2013). Evaluation of the Stability, Bioavailability, and Hypersensitivity of the Omega-3 Derived Anti-Leukemic Prostaglandin: Δ12-Prostaglandin J3. PLoS ONE. 8(12). e80622–e80622. 13 indexed citations

10.

Kennett, Mary J., et al.. (2013). Immunization with Pneumococcal Polysaccharide Serotype 3 and Lipopolysaccharide Modulates Lung and Liver Inflammation during a Virulent Streptococcus pneumoniae Infection in Mice. Clinical and Vaccine Immunology. 20(5). 639–650. 3 indexed citations

11.

Weyrich, Laura S., Jihye Park, Nicholas A. Spidale, et al.. (2012). A Type VI Secretion System Encoding Locus Is Required for Bordetella bronchiseptica Immunomodulation and Persistence In Vivo. PLoS ONE. 7(10). e45892–e45892. 31 indexed citations

12.

Werner, Jacob, et al.. (2011). Human Electromuscular Incapacitation Devices Characterization: A Comparative Study on Stress and the Physiological Effects on Swine. The Journal of Strength and Conditioning Research. 26(3). 804–810. 5 indexed citations

13.

Kennett, Mary J., et al.. (2011). IACUC Issues Related to Animal Models of Aging. ILAR Journal. 52(1). 106–109. 2 indexed citations

14.

Pérez‐Lorenzo, Rolando, et al.. (2010). Use of a TGFβ type I receptor inhibitor in mouse skin carcinogenesis reveals a dual role for TGFβ signaling in tumor promotion and progression. Carcinogenesis. 31(12). 2127–2135. 27 indexed citations

15.

Wolfe, Daniel, et al.. (2009). IL-10 Induction by Bordetella parapertussis Limits a Protective IFN-γ Response. The Journal of Immunology. 184(3). 1392–1400. 16 indexed citations

16.

Bility, Moses T., Meghann K Devlin-Durante, Nicholas Blazanin, et al.. (2008). Ligand activation of peroxisome proliferator-activated receptor β/δ (PPARβ/δ) inhibits chemically induced skin tumorigenesis. Carcinogenesis. 29(12). 2406–2414. 33 indexed citations

17.

Shan, Weiwei, Christopher J.B. Nicol, Shinji Ito, et al.. (2007). Peroxisome proliferator-activated receptor-β/δ protects against chemically induced liver toxicity in mice. Hepatology. 47(1). 225–235. 79 indexed citations

18.

Pilione, Mylisa R., Luis M. Agosto, Mary J. Kennett, & Eric T. Harvill. (2005). CD11b is required for the resolution of inflammation induced by Bordetella bronchiseptica respiratory infection. Cellular Microbiology. 8(5). 758–768. 18 indexed citations

19.

Kim, Dae Joon, Taro E. Akiyama, F. S. Harman, et al.. (2004). Peroxisome Proliferator-activated Receptor β (δ)-dependent Regulation of Ubiquitin C Expression Contributes to Attenuation of Skin Carcinogenesis. Journal of Biological Chemistry. 279(22). 23719–23727. 82 indexed citations

20.

Kennett, Mary J., et al.. (2004). Toll‐Like Receptor 4 Is Critical to Innate Host Defense in a Murine Model of Bordetellosis. The Journal of Infectious Diseases. 189(5). 833–836. 47 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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