William F. Jester

1.7k total citations
34 papers, 1.3k citations indexed

About

William F. Jester is a scholar working on Physiology, Molecular Biology and Immunology. According to data from OpenAlex, William F. Jester has authored 34 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Physiology, 14 papers in Molecular Biology and 9 papers in Immunology. Recurrent topics in William F. Jester's work include Asthma and respiratory diseases (16 papers), Sperm and Testicular Function (8 papers) and IL-33, ST2, and ILC Pathways (5 papers). William F. Jester is often cited by papers focused on Asthma and respiratory diseases (16 papers), Sperm and Testicular Function (8 papers) and IL-33, ST2, and ILC Pathways (5 papers). William F. Jester collaborates with scholars based in United States, Sweden and Canada. William F. Jester's co-authors include Joanne M. Orth, Leping Li, Reynold A. Panettieri, Andrew L. Laslett, Jianping Qiu, Cynthia Koziol‐White, Stephen H. Pilder, Gautam Damera, Hengjiang Zhao and Kelan G. Tantisira and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and The FASEB Journal.

In The Last Decade

William F. Jester

34 papers receiving 1.2k citations

Peers

William F. Jester
Harri Hakovirta Finland
Theodore E. Whitmore United States
Talal El‐Hefnawy United States
Isoji Sasagawa Japan
Cecilia Varone Argentina
Pearl P.Y. Lie United States
Laura Milne United Kingdom
A. Ederveen Netherlands
Anita Kumar India
Heimo Syvälä Finland
Harri Hakovirta Finland
William F. Jester
Citations per year, relative to William F. Jester William F. Jester (= 1×) peers Harri Hakovirta

Countries citing papers authored by William F. Jester

Since Specialization
Citations

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

Fields of papers citing papers by William F. Jester

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William F. Jester

This figure shows the co-authorship network connecting the top 25 collaborators of William F. Jester. A scholar is included among the top collaborators of William F. Jester 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 William F. Jester. William F. Jester 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.
Kan, Mengyuan, Maoyun Sun, Xiaofeng Jiang, et al.. (2022). CEBPD modulates the airway smooth muscle transcriptomic response to glucocorticoids. Respiratory Research. 23(1). 193–193. 4 indexed citations
2.
Ghosh, Arnab, Cynthia Koziol‐White, William F. Jester, et al.. (2020). An inherent dysfunction in soluble guanylyl cyclase is present in the airway of severe asthmatics and is associated with aberrant redox enzyme expression and compromised NO-cGMP signaling. Redox Biology. 39. 101832–101832. 15 indexed citations
3.
Redes, Jamie, Nariman Balenga, Nathalie Fuentes, et al.. (2020). RGS4 promotes allergen- and aspirin-associated airway hyperresponsiveness by inhibiting PGE2 biosynthesis. Journal of Allergy and Clinical Immunology. 146(5). 1152–1164.e13. 13 indexed citations
4.
Kan, Mengyuan, Cynthia Koziol‐White, Maya Shumyatcher, et al.. (2019). Airway Smooth Muscle–Specific Transcriptomic Signatures of Glucocorticoid Exposure. American Journal of Respiratory Cell and Molecular Biology. 61(1). 110–120. 25 indexed citations
5.
Jude, Joseph A., et al.. (2019). Salicylic acid amplifies Carbachol-induced bronchoconstriction in human precision-cut lung slices. Respiratory Research. 20(1). 72–72. 14 indexed citations
6.
Pushkarsky, Ivan, Peter Tseng, Bryan France, et al.. (2018). Elastomeric sensor surfaces for high-throughput single-cell force cytometry. Nature Biomedical Engineering. 2(2). 124–137. 42 indexed citations
7.
Jude, Joseph A., Cynthia Koziol‐White, Edwin Yoo, et al.. (2016). Formaldehyde Induces Rho-Associated Kinase Activity to Evoke Airway Hyperresponsiveness. American Journal of Respiratory Cell and Molecular Biology. 55(4). 542–553. 14 indexed citations
8.
Himes, Blanca E., Xiaofeng Jiang, Peter J. Wagner, et al.. (2014). RNA-Seq Transcriptome Profiling Identifies CRISPLD2 as a Glucocorticoid Responsive Gene that Modulates Cytokine Function in Airway Smooth Muscle Cells. PLoS ONE. 9(6). e99625–e99625. 96 indexed citations
9.
Balenga, Nariman, et al.. (2014). Loss of regulator of G protein signaling 5 promotes airway hyperresponsiveness in the absence of allergic inflammation. Journal of Allergy and Clinical Immunology. 134(2). 451–459.e11. 26 indexed citations
10.
Banerjee, Audreesh, Chinmay M. Trivedi, Gautam Damera, et al.. (2011). Trichostatin A Abrogates Airway Constriction, but Not Inflammation, in Murine and Human Asthma Models. American Journal of Respiratory Cell and Molecular Biology. 46(2). 132–138. 64 indexed citations
11.
Damera, Gautam, William F. Jester, Hengjiang Zhao, et al.. (2010). Inhibition of myristoylated alanine-rich C kinase substrate (MARCKS) protein inhibits ozone-induced airway neutrophilia and inflammation. Experimental Lung Research. 36(2). 75–84. 26 indexed citations
12.
Wu, Ji, William F. Jester, & Joanne M. Orth. (2005). Short-type PB-cadherin promotes survival of gonocytes and activates JAK-STAT signalling. Developmental Biology. 284(2). 437–450. 30 indexed citations
13.
Jain, Deepika, Omar Tliba, William F. Jester, et al.. (2005). TGF-β potentiates airway smooth muscle responsiveness to bradykinin. American Journal of Physiology-Lung Cellular and Molecular Physiology. 289(4). L511–L520. 32 indexed citations
14.
Orth, Joanne M., et al.. (2000). Gonocyte-Sertoli cell interactions during development of the neonatal rodent testis. Current topics in developmental biology. 50. 103–124. 65 indexed citations
15.
Li, Leping, William F. Jester, & Joanne M. Orth. (1998). Effects of Relatively Low Levels of Mono-(2-Ethylhexyl) Phthalate on Cocultured Sertoli Cells and Gonocytes from Neonatal Rats. Toxicology and Applied Pharmacology. 153(2). 258–265. 128 indexed citations
16.
Li, Leping, William F. Jester, & Joanne M. Orth. (1998). Expression of 140‐kDa Neural Cell Adhesion Molecule in Developing TestesIn Vivoand in Long‐Term Sertoli Cell—Gonocyte Cocultures. Journal of Andrology. 19(3). 365–373. 20 indexed citations
17.
Orth, Joanne M., et al.. (1998). Use of in vitro systems to study male germ cell development in neonatal rats. Theriogenology. 49(2). 431–439. 21 indexed citations
18.
Pilder, Stephen H., et al.. (1997). Hst7: A Male Sterility Mutation Perturbing Sperm Motility, Flagellar Assembly, and Mitochondrial Sheath Differentiation. Journal of Andrology. 18(6). 663–671. 26 indexed citations
19.
Orth, Joanne M., Jianping Qiu, William F. Jester, & Stephen H. Pilder. (1997). Expression of the c-kit Gene is Critical for Migration of Neonatal Rat Gonocytes in Vitro1. Biology of Reproduction. 57(3). 676–683. 62 indexed citations
20.
Orth, Joanne M., William F. Jester, & Jianping Qiu. (1996). Gonocytes in testes of neonatal rats express thec-kit gene. Molecular Reproduction and Development. 45(2). 123–131. 43 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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