Amanda P. Henry

2.6k total citations
15 papers, 439 citations indexed

About

Amanda P. Henry is a scholar working on Molecular Biology, Physiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Amanda P. Henry has authored 15 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Physiology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Amanda P. Henry's work include Epigenetics and DNA Methylation (5 papers), Asthma and respiratory diseases (4 papers) and Neonatal Respiratory Health Research (3 papers). Amanda P. Henry is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Asthma and respiratory diseases (4 papers) and Neonatal Respiratory Health Research (3 papers). Amanda P. Henry collaborates with scholars based in United Kingdom, United States and Singapore. Amanda P. Henry's co-authors include Ian P. Hall, Ching Lam, Gulzar Singh, Peter J. Whorwell, Robert E. Spiller, Klara Garsed, Margaret Hastings, Luca Marciani, Julia Chernova and Ian Sayers and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Amanda P. Henry

15 papers receiving 433 citations

Peers

Amanda P. Henry

GASTR

PHYSI

PRM

SURGE

David O. Prichard United States

Fumihiko Hatao Japan

Dario Ummarino Italy

Minghui Bao China

Takuya Okugawa Japan

Yasuo Tokita Japan

W. F. Caspary Germany

Eiji Takeshita Japan

Brad Snyder United States

David O. Prichard United States

Amanda P. Henry

274 ×1.7

GASTR

105 ×0.7

PHYSI

77 ×0.6

PRM

57 ×0.5

342 ×3.1

SURGE

Citations per year, relative to Amanda P. Henry Amanda P. Henry (= 1×) peers David O. Prichard

Countries citing papers authored by Amanda P. Henry

Since Specialization

Citations

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

Fields of papers citing papers by Amanda P. Henry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda P. Henry

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda P. Henry. A scholar is included among the top collaborators of Amanda P. 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 Amanda P. Henry. Amanda P. 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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15 of 15 papers shown

Henry, Amanda P., et al.. (2021). Association study between asthma and single nucleotide polymorphisms of ORMDL3, GSDMB, and IL1RL1 genes in an Algerian population. SHILAP Revista de lepidopterología. 22(1). 1 indexed citations

Hall, Robert J., Michael A. Portelli, Amanda P. Henry, et al.. (2021). Extended lifespan of bronchial epithelial cells maintains normal cellular phenotype and transcriptome integrity. ERJ Open Research. 7(1). 254–2020. 1 indexed citations

Mahapatra, Parth Sarathi, Amanda P. Henry, Charlotte K. Billington, et al.. (2020). Proinflammatory Effects in Ex Vivo Human Lung Tissue of Respirable Smoke Extracts from Indoor Cooking in Nepal. Annals of the American Thoracic Society. 17(6). 688–698. 9 indexed citations

Liu, Bo, Amanda P. Henry, Sheyda Azimi, et al.. (2019). Exposure to lipopolysaccharide (LPS) reduces contractile response of small airways from GSTCD-/- mice. PLoS ONE. 14(9). e0221899–e0221899. 2 indexed citations

Henry, Amanda P., et al.. (2019). Defining a role for lung function associated gene GSTCD in cell homeostasis. Respiratory Research. 20(1). 172–172. 7 indexed citations

Gunn, David, Klara Garsed, Ching Lam, et al.. (2019). Abnormalities of mucosal serotonin metabolism and 5‐HT₃ receptor subunit 3C polymorphism in irritable bowel syndrome with diarrhoea predict responsiveness to ondansetron. Alimentary Pharmacology & Therapeutics. 50(5). 538–546. 28 indexed citations

Henry, Amanda P., et al.. (2019). Modelling Virus-Host Interactions: TLR-Induced Release of Inflammatory Mediators in Human Lung Explants. A5213–A5213. 1 indexed citations

Лю, Бо, et al.. (2018). Chloride intracellular channel 1 (CLIC1) contributes to modulation of cyclic AMP-activated whole-cell chloride currents in human bronchial epithelial cells. Physiological Reports. 6(2). e13508–e13508. 11 indexed citations

Ware, James S., Louise V. Wain, Victoria E. Jackson, et al.. (2017). Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia. Journal of Clinical Investigation. 127(9). 3367–3374. 58 indexed citations

10.

Garsed, Klara, Julia Chernova, Margaret Hastings, et al.. (2013). A randomised trial of ondansetron for the treatment of irritable bowel syndrome with diarrhoea. Gut. 63(10). 1617–1625. 166 indexed citations

11.

Obeidat, Ma’en, S. Miller, Charlotte K. Billington, et al.. (2013). GSTCD and INTS12 Regulation and Expression in the Human Lung. PLoS ONE. 8(9). e74630–e74630. 21 indexed citations

12.

Nelson, Carl P., S. Miller, Charlotte K. Billington, et al.. (2013). HTR4 gene structure and altered expression in the developing lung. Respiratory Research. 14(1). 77–77. 17 indexed citations

13.

Glover, Mark, James S. Ware, Amanda P. Henry, et al.. (2013). Detection of mutations inKLHL3andCUL3in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). Clinical Science. 126(10). 721–726. 40 indexed citations

14.

Sayers, Ian, et al.. (2009). Pharmacogenetic characterization of indacaterol, a novel β₂‐adrenoceptor agonist. British Journal of Pharmacology. 158(1). 277–286. 11 indexed citations

15.

Barton, Sheila J., Gerard H. Koppelman, Judith M. Vonk, et al.. (2009). PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline. Journal of Allergy and Clinical Immunology. 123(6). 1391–1400.e17. 66 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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