Alexandra Hicks

693 total citations
27 papers, 348 citations indexed

About

Alexandra Hicks is a scholar working on Genetics, Physiology and Immunology. According to data from OpenAlex, Alexandra Hicks has authored 27 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Physiology and 8 papers in Immunology. Recurrent topics in Alexandra Hicks's work include Hemoglobinopathies and Related Disorders (7 papers), Asthma and respiratory diseases (4 papers) and Iron Metabolism and Disorders (3 papers). Alexandra Hicks is often cited by papers focused on Hemoglobinopathies and Related Disorders (7 papers), Asthma and respiratory diseases (4 papers) and Iron Metabolism and Disorders (3 papers). Alexandra Hicks collaborates with scholars based in United States, United Kingdom and Japan. Alexandra Hicks's co-authors include S.A. Levison, Walter B. Dandliker, Robert A. Goodnow, Ann F. Hoffman, Adolf Portmann, R. James Brawn, Robert W. Coatney, Gerald P. McCafferty, Mark Pullen and David P. Brooks and has published in prestigious journals such as Blood, PLoS ONE and Biochemistry.

In The Last Decade

Alexandra Hicks

25 papers receiving 330 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexandra Hicks United States 9 116 74 72 46 41 27 348
Yuji Saita Japan 11 161 1.4× 66 0.9× 35 0.5× 122 2.7× 43 1.0× 16 449
Katsuya Nakano Japan 10 186 1.6× 34 0.5× 68 0.9× 13 0.3× 154 3.8× 30 422
Li You China 13 251 2.2× 22 0.3× 19 0.3× 51 1.1× 36 0.9× 33 454
Kimio Nasu Japan 10 149 1.3× 30 0.4× 252 3.5× 50 1.1× 89 2.2× 15 688
Masaki Kanazawa Japan 14 336 2.9× 71 1.0× 4 0.1× 51 1.1× 57 1.4× 29 599
Marta García Spain 13 252 2.2× 17 0.2× 10 0.1× 27 0.6× 174 4.2× 26 496
Giacomo Quilici Italy 12 448 3.9× 46 0.6× 6 0.1× 79 1.7× 50 1.2× 24 758
Yehong Yang China 9 228 2.0× 51 0.7× 6 0.1× 35 0.8× 28 0.7× 24 406
P D Ottosen Denmark 8 427 3.7× 62 0.8× 9 0.1× 23 0.5× 286 7.0× 9 589

Countries citing papers authored by Alexandra Hicks

Since Specialization
Citations

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

Fields of papers citing papers by Alexandra Hicks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandra Hicks. 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 Alexandra Hicks. The network helps show where Alexandra Hicks may publish in the future.

Co-authorship network of co-authors of Alexandra Hicks

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra Hicks. A scholar is included among the top collaborators of Alexandra Hicks 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 Alexandra Hicks. Alexandra Hicks 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.
Bachert, Claus, Alexandra Hicks, Simon Gane, et al.. (2024). The interleukin-4/interleukin-13 pathway in type 2 inflammation in chronic rhinosinusitis with nasal polyps. Frontiers in Immunology. 15. 1356298–1356298. 26 indexed citations
2.
Daak, Ahmed, David R. Light, Fuad Abdulla, et al.. (2024). Bruton Tyrosine Kinase Inhibitor Rilzabrutinib Reduces Vaso-Occlusion and Markers of Inflammation and Adhesion in Transgenic Mice with Sickle Cell Disease. Blood. 144(Supplement 1). 2482–2482. 1 indexed citations
3.
Wang, Yui‐Hsi, Hamid Mattoo, Joo‐Hye Song, et al.. (2024). TSLP AND IL-13 Dual Blockade By Lunsekimig Provides Broader Benefits On Type-2 Inflammation. PA4861–PA4861. 2 indexed citations
4.
Han, Hongwei, Jennifer Johnson, Joseph Gans, et al.. (2023). Cellular mechanisms and effects of IL-4 receptor blockade in experimental conjunctivitis evoked by skin inflammation. JCI Insight. 8(3). 5 indexed citations
5.
Lemgart, Viktor T., Nis Halland, Kiana Mahdaviani, et al.. (2023). SGK1 inhibition induces fetal hemoglobin expression and delays polymerization in sickle erythroid cells. Blood Advances. 7(11). 2317–2323. 2 indexed citations
6.
Jha, Mithilesh Kumar, Hamid Mattoo, Scott D. Nash, et al.. (2023). Interleukin 4 directly activates olfactory neurons and induces loss of smell in mice. Journal of Allergy and Clinical Immunology. 151(2). AB128–AB128. 8 indexed citations
7.
Alving, Kim, et al.. (2021). SGK1 Inhibition Induces Fetal Hemoglobin in Erythroid Cells. Blood. 138(Supplement 1). 963–963.
8.
Demers, Mélanie, Kevin R. Guertin, Dipti Gupta, et al.. (2021). MetAP2 inhibition modifies hemoglobin S to delay polymerization and improves blood flow in sickle cell disease. Blood Advances. 5(5). 1388–1402. 5 indexed citations
9.
10.
Guo, Jane, Laura Engstrom, Hyun‐Hee Lee, et al.. (2017). A human tissue-based functional assay platform to evaluate the immune function impact of small molecule inhibitors that target the immune system. PLoS ONE. 12(7). e0180870–e0180870. 2 indexed citations
11.
Nahid, Md A., et al.. (2016). TLR4, TLR7/8 agonist-induced miR-146a promotes macrophage tolerance to MyD88-dependent TLR agonists. Journal of Leukocyte Biology. 100(2). 339–349. 30 indexed citations
12.
Hicks, Alexandra, Huseyin Mehmet, Melody K. Morris, et al.. (2015). Pharmacological Inhibition of O-GlcNAcase Does Not Increase Sensitivity of Glucocorticoid Receptor-Mediated Transrepression. PLoS ONE. 10(12). e0145151–e0145151. 5 indexed citations
13.
Brandish, Philip E., et al.. (2014). Development and pharmacological validation of novel methods of B cell activation in rat whole blood. Journal of Pharmacological and Toxicological Methods. 71. 61–67. 2 indexed citations
14.
Tare, Nadine S., Donald Lavelle, H Michel, et al.. (2010). Dual bronchodilatory and pulmonary anti‐inflammatory activity of RO5024118, a novel agonist at vasoactive intestinal peptide VPAC2receptors. British Journal of Pharmacology. 161(6). 1329–1342. 14 indexed citations
15.
Hicks, Alexandra, Holly Hilton, Hongli Li, et al.. (2009). Cellular and Molecular Characterization of Ozone-Induced Pulmonary Inflammation in the Cynomolgus Monkey. Inflammation. 33(3). 144–156. 10 indexed citations
16.
Cornelissen, Laura, et al.. (2008). Influence of genetic background and gender on bladder function in the mouse. Autonomic Neuroscience. 140(1-2). 53–58. 24 indexed citations
17.
Hilton, Holly, Xin Wei, Thomas H. March, et al.. (2008). Lung and Blood Gene Expression Profiles from Cynomolgus Monkeys Exposed to Ozone. The FASEB Journal. 22(S2). 212–212. 1 indexed citations
18.
Hicks, Alexandra, Gerald P. McCafferty, Nambi Aiyar, et al.. (2007). GW427353 (Solabegron), a Novel, Selective β3-Adrenergic Receptor Agonist, Evokes Bladder Relaxation and Increases Micturition Reflex Threshold in the Dog. Journal of Pharmacology and Experimental Therapeutics. 323(1). 202–209. 70 indexed citations
19.
Hicks, Alexandra, et al.. (2007). Leukotriene B4receptor antagonists as therapeutics for inflammatory disease: preclinical and clinical developments. Expert Opinion on Investigational Drugs. 16(12). 1909–1920. 61 indexed citations
20.
Dandliker, Walter B., Alexandra Hicks, S.A. Levison, & R. James Brawn. (1977). A fluorescein-labeled derivative of estradiol with binding affinity towards cellular receptors. Biochemical and Biophysical Research Communications. 74(2). 538–544. 29 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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