Sangeetha Ramu

550 total citations
19 papers, 383 citations indexed

About

Sangeetha Ramu is a scholar working on Physiology, Immunology and Immunology and Allergy. According to data from OpenAlex, Sangeetha Ramu has authored 19 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Physiology, 11 papers in Immunology and 7 papers in Immunology and Allergy. Recurrent topics in Sangeetha Ramu's work include Asthma and respiratory diseases (15 papers), IL-33, ST2, and ILC Pathways (6 papers) and Pediatric health and respiratory diseases (5 papers). Sangeetha Ramu is often cited by papers focused on Asthma and respiratory diseases (15 papers), IL-33, ST2, and ILC Pathways (6 papers) and Pediatric health and respiratory diseases (5 papers). Sangeetha Ramu collaborates with scholars based in Sweden, Denmark and United States. Sangeetha Ramu's co-authors include Lena Uller, Mandy Menzel, Hamid Akbarshahi, Samuel Cerps, Irma Mahmutovic Persson, Celeste Porsbjerg, Asger Sverrild, Leif Bjermer, Juan José Nieto‐Fontarigo and Cecilia Andersson and has published in prestigious journals such as The Journal of Physical Chemistry B, American Journal of Respiratory and Critical Care Medicine and Frontiers in Immunology.

In The Last Decade

Sangeetha Ramu

18 papers receiving 380 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sangeetha Ramu Sweden 11 193 120 91 83 59 19 383
Maggie Lam Australia 12 214 1.1× 157 1.3× 51 0.6× 215 2.6× 109 1.8× 29 578
Chi‐Chang Shieh Taiwan 13 115 0.6× 111 0.9× 83 0.9× 29 0.3× 66 1.1× 36 378
Andrew J. Tan United Kingdom 8 196 1.0× 56 0.5× 90 1.0× 109 1.3× 41 0.7× 11 354
Patrycja Nejman‐Gryz Poland 14 256 1.3× 128 1.1× 41 0.5× 249 3.0× 84 1.4× 52 582
A. G. Alexander United States 7 254 1.3× 99 0.8× 67 0.7× 148 1.8× 48 0.8× 7 362
Jin‐Xin Liu China 11 111 0.6× 60 0.5× 110 1.2× 25 0.3× 44 0.7× 16 338
Matthias Nassimi Germany 7 57 0.3× 33 0.3× 22 0.2× 189 2.3× 70 1.2× 8 369
M. Zheng China 6 206 1.1× 28 0.2× 225 2.5× 37 0.4× 29 0.5× 9 394
Ka Lun Cheung Hong Kong 7 97 0.5× 156 1.3× 13 0.1× 27 0.3× 118 2.0× 9 374
Javier Millán Soria Spain 12 77 0.4× 22 0.2× 61 0.7× 17 0.2× 87 1.5× 32 544

Countries citing papers authored by Sangeetha Ramu

Since Specialization
Citations

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

Fields of papers citing papers by Sangeetha Ramu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sangeetha Ramu

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

All Works

19 of 19 papers shown
1.
Sverrild, Asger, Juan José Nieto‐Fontarigo, Sangeetha Ramu, et al.. (2023). Tezepelumab decreases airway epithelial IL‐33 and T2‐inflammation in response to viral stimulation in patients with asthma. Allergy. 79(3). 656–666. 19 indexed citations
2.
Ramu, Sangeetha, Asger Sverrild, Juan José Nieto‐Fontarigo, et al.. (2023). Allergen Immunotherapy Enhances Airway Epithelial Antiviral Immunity in Patients with Allergic Asthma (VITAL Study): A Double-Blind Randomized Controlled Trial. American Journal of Respiratory and Critical Care Medicine. 207(9). 1161–1170. 35 indexed citations
3.
Nieto‐Fontarigo, Juan José, Samuel Cerps, Sangeetha Ramu, et al.. (2023). C57Bl/6N mice have an attenuated lung inflammatory response to dsRNA compared to C57Bl/6J and BALB/c mice. Journal of Inflammation. 20(1). 6–6. 5 indexed citations
4.
5.
Cerps, Samuel, Asger Sverrild, Sangeetha Ramu, et al.. (2022). House dust mite sensitization and exposure affects bronchial epithelial anti‐microbial response to viral stimuli in patients with asthma. Allergy. 77(8). 2498–2508. 14 indexed citations
6.
Lidington, Darcy, Franziska E. Uhl, João M. N. Duarte, et al.. (2022). Restoring myocardial infarction-induced long-term memory impairment by targeting the cystic fibrosis transmembrane regulator. EBioMedicine. 86. 104384–104384. 9 indexed citations
7.
Porsbjerg, Celeste, Juan José Nieto‐Fontarigo, Samuel Cerps, et al.. (2022). Phenotype and severity of asthma determines bronchial epithelial immune responses to a viral mimic. 27–27. 2 indexed citations
8.
Porsbjerg, Celeste, Juan José Nieto‐Fontarigo, Samuel Cerps, et al.. (2021). Phenotype and severity of asthma determines bronchial epithelial immune responses to a viral mimic. European Respiratory Journal. 60(1). 2102333–2102333. 20 indexed citations
9.
Nieto‐Fontarigo, Juan José, Samuel Cerps, Asger Sverrild, et al.. (2021). Imiquimod Boosts Interferon Response, and Decreases ACE2 and Pro-Inflammatory Response of Human Bronchial Epithelium in Asthma. Frontiers in Immunology. 12. 743890–743890. 9 indexed citations
10.
Ramu, Sangeetha, Hamid Akbarshahi, Samuel Cerps, et al.. (2021). Direct effects of mast cell proteases, tryptase and chymase, on bronchial epithelial integrity proteins and anti-viral responses. BMC Immunology. 22(1). 35–35. 16 indexed citations
11.
Ramu, Sangeetha, et al.. (2021). Mast cell tryptase enhances wound healing by promoting migration in human bronchial epithelial cells. Cell Adhesion & Migration. 15(1). 202–214. 17 indexed citations
12.
Sverrild, Asger, Samuel Cerps, Juan José Nieto‐Fontarigo, et al.. (2021). Late Breaking Abstract - Effects of tezepelumab on host epithelial tolerance to virus in patients with uncontrolled asthma. OA1492–OA1492. 3 indexed citations
13.
Ramu, Sangeetha, Jenny Calvén, Charalambos Michaeloudes, et al.. (2020). TLR3/TAK1 signalling regulates rhinovirus-induced interleukin-33 in bronchial smooth muscle cells. ERJ Open Research. 6(4). 147–2020. 7 indexed citations
14.
Menzel, Mandy, Sangeetha Ramu, Jenny Calvén, et al.. (2019). Oxidative Stress Attenuates TLR3 Responsiveness and Impairs Anti-viral Mechanisms in Bronchial Epithelial Cells From COPD and Asthma Patients. Frontiers in Immunology. 10. 2765–2765. 31 indexed citations
15.
16.
Akbarshahi, Hamid, Mandy Menzel, Sangeetha Ramu, et al.. (2018). House dust mite impairs antiviral response in asthma exacerbation models through its effects on TLR3. Allergy. 73(5). 1053–1063. 32 indexed citations
17.
Persson, Irma Mahmutovic, Mandy Menzel, Sangeetha Ramu, et al.. (2018). IL-1β mediates lung neutrophilia and IL-33 expression in a mouse model of viral-induced asthma exacerbation. Respiratory Research. 19(1). 16–16. 87 indexed citations
18.
Ramu, Sangeetha, Mandy Menzel, Leif Bjermer, et al.. (2017). Allergens produce serine proteases‐dependent distinct release of metabolite DAMPs in human bronchial epithelial cells. Clinical & Experimental Allergy. 48(2). 156–166. 21 indexed citations
19.
Bao, Duoduo, Sangeetha Ramu, A. Contreras, et al.. (2010). Electrochemical Reduction of Quinones: Interfacing Experiment and Theory for Defining Effective Radii of Redox Moieties. The Journal of Physical Chemistry B. 114(45). 14467–14479. 53 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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