Margaret Solon

2.3k total citations
20 papers, 1.3k citations indexed

About

Margaret Solon is a scholar working on Molecular Biology, Immunology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Margaret Solon has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Immunology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Margaret Solon's work include interferon and immune responses (3 papers), Cell death mechanisms and regulation (3 papers) and Asthma and respiratory diseases (3 papers). Margaret Solon is often cited by papers focused on interferon and immune responses (3 papers), Cell death mechanisms and regulation (3 papers) and Asthma and respiratory diseases (3 papers). Margaret Solon collaborates with scholars based in United States, France and Japan. Margaret Solon's co-authors include Prescott G. Woodruff, John V. Fahy, Owen D. Solberg, Joshua D. Webster, Sukhvinder Sidhu, Kim Newton, Ryan H. Dougherty, George H. Caughey, Allie Maltzman and Katherine E. Wickliffe and has published in prestigious journals such as Nature, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

Margaret Solon

20 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Margaret Solon United States	15	670	550	349	227	220	20	1.3k
Sudipta Das United States	17	409 0.6×	451 0.8×	362 1.0×	276 1.2×	118 0.5×	30	1.1k
Carla Mazzeo Spain	15	607 0.9×	281 0.5×	146 0.4×	94 0.4×	235 1.1×	19	983
Anna Maria Merendino Italy	13	437 0.7×	365 0.7×	549 1.6×	470 2.1×	103 0.5×	15	1.2k
Corinne Hiéblot France	18	496 0.7×	341 0.6×	117 0.3×	323 1.4×	149 0.7×	25	1.1k
Wei-ping Zheng United States	5	472 0.7×	1.5k 2.7×	322 0.9×	80 0.4×	149 0.7×	7	2.0k
Joseph A. Kitzmiller United States	18	523 0.8×	255 0.5×	309 0.9×	677 3.0×	99 0.5×	28	1.3k
Y Katsura Japan	19	565 0.8×	890 1.6×	189 0.5×	105 0.5×	53 0.2×	70	1.7k
Carla Eponina Carvalho-Pinto Brazil	19	225 0.3×	873 1.6×	113 0.3×	126 0.6×	112 0.5×	33	1.4k
Alla Pritsker United States	13	460 0.7×	334 0.6×	147 0.4×	86 0.4×	237 1.1×	18	1.3k
Lap-Ping Chung United Kingdom	21	423 0.6×	585 1.1×	93 0.3×	218 1.0×	85 0.4×	27	1.4k

Countries citing papers authored by Margaret Solon

Since Specialization

Citations

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

Fields of papers citing papers by Margaret Solon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margaret Solon

This figure shows the co-authorship network connecting the top 25 collaborators of Margaret Solon. A scholar is included among the top collaborators of Margaret Solon 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 Margaret Solon. Margaret Solon 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

Solon, Margaret, Nianfeng Ge, Susan Haller, et al.. (2024). ZBP1 and TRIF trigger lethal necroptosis in mice lacking caspase-8 and TNFR1. Cell Death and Differentiation. 31(5). 672–682. 21 indexed citations

Himmels, Patricia, Alfonso Arrazate, Robyn Clark, et al.. (2023). T cell‐dependent bispecific antibodies alter organ‐specific endothelial cell–T cell interaction. EMBO Reports. 24(3). e55532–e55532. 6 indexed citations

Herzner, Anna‐Maria, Zia Khan, Eric L. Van Nostrand, et al.. (2021). ADAR and hnRNPC deficiency synergize in activating endogenous dsRNA-induced type I IFN responses. The Journal of Experimental Medicine. 218(9). 15 indexed citations

Thomas, Adrien Le, Elena Ferri, Scot A. Marsters, et al.. (2021). Decoding non-canonical mRNA decay by the endoplasmic-reticulum stress sensor IRE1α. Nature Communications. 12(1). 7310–7310. 41 indexed citations

Webster, Joshua D., Margaret Solon, & Katherine N. Gibson‐Corley. (2020). Validating Immunohistochemistry Assay Specificity in Investigative Studies: Considerations for a Weight of Evidence Approach. Veterinary Pathology. 58(5). 829–840. 13 indexed citations

Webster, Joshua D., Margaret Solon, Susan Haller, & Kim Newton. (2018). Detection of Necroptosis by Phospho-RIPK3 Immunohistochemical Labeling. Methods in molecular biology. 1857. 153–160. 19 indexed citations

Choy, Lisa, Thijs J. Hagenbeek, Margaret Solon, et al.. (2017). Constitutive NOTCH3 Signaling Promotes the Growth of Basal Breast Cancers. Cancer Research. 77(6). 1439–1452. 73 indexed citations

Januario, Thomas, Xiaofen Ye, Russell Bainer, et al.. (2017). Abstract 2790: PRC2 mediated repression of SMARCA2 predicts for EZH2 inhibitor activity in tumors with SWI/SNF mutations. Cancer Research. 77(13_Supplement). 2790–2790. 1 indexed citations

Newton, Kim, Katherine E. Wickliffe, Allie Maltzman, et al.. (2016). RIPK1 inhibits ZBP1-driven necroptosis during development. Nature. 540(7631). 129–133. 307 indexed citations

10.

Rogers, Roy S., Jeff Eastham-Anderson, Jason DeVoss, et al.. (2015). Image Analysis-Based Approaches for Scoring Mouse Models of Colitis. Veterinary Pathology. 53(1). 200–210. 14 indexed citations

11.

Merchant, Mark, Jocelyn Chan, Jin Cheng, et al.. (2014). 387 Combination of the ERK inhibitor GDC-0994 with the MEK inhibitor cobimetinib significantly enhances anti-tumor activity in KRAS and BRAF mutant tumor models. European Journal of Cancer. 50. 124–124. 7 indexed citations

12.

McCleland, Mark L., Adam S. Adler, Ely Cosino, et al.. (2012). Lactate Dehydrogenase B Is Required for the Growth of KRAS-Dependent Lung Adenocarcinomas. Clinical Cancer Research. 19(4). 773–784. 93 indexed citations

13.

Solberg, Owen D., Edwin J. Ostrin, Michael I. Love, et al.. (2012). Airway Epithelial miRNA Expression Is Altered in Asthma. American Journal of Respiratory and Critical Care Medicine. 186(10). 965–974. 199 indexed citations

14.

Gordon, Erin, Sukhvinder Sidhu, Prescott G. Woodruff, et al.. (2011). A protective role for periostin and TGF‐β in IgE‐mediated allergy and airway hyperresponsiveness. Clinical & Experimental Allergy. 42(1). 144–155. 75 indexed citations

15.

Koth, Laura L., Margaret Solon, Lydia Hou, et al.. (2010). DAP12 Is Required for Macrophage Recruitment to the Lung in Response to Cigarette Smoke and Chemotaxis toward CCL2. The Journal of Immunology. 184(11). 6522–6528. 29 indexed citations

16.

Innes, Anh L., Kevin McGrath, Ryan H. Dougherty, et al.. (2010). The H Antigen at Epithelial Surfaces Is Associated with Susceptibility to Asthma Exacerbation. American Journal of Respiratory and Critical Care Medicine. 183(2). 189–194. 25 indexed citations

17.

Dougherty, Ryan H., Sukhvinder Sidhu, Margaret Solon, et al.. (2010). Accumulation of intraepithelial mast cells with a unique protease phenotype in TH2-high asthma. Journal of Allergy and Clinical Immunology. 125(5). 1046–1053.e8. 210 indexed citations

18.

Kerr, Sheena C., Stephen D. Carrington, Shaopeng Yuan, Margaret Solon, & John V. Fahy. (2010). Galactose Binding Lectins Cross-link Airway Mucins And Are A Novel Mediator Of Mucus Plug Formation In Acute Asthma. A5510–A5510. 2 indexed citations

19.

Woodruff, Prescott G., et al.. (2009). Alveolar Macrophage Recruitment and Activation by Chronic Second Hand Smoke Exposure in Mice. COPD Journal of Chronic Obstructive Pulmonary Disease. 6(2). 86–94. 28 indexed citations

20.

Seibold, Max A., Samantha Donnelly, Margaret Solon, et al.. (2008). Chitotriosidase is the primary active chitinase in the human lung and is modulated by genotype and smoking habit. Journal of Allergy and Clinical Immunology. 122(5). 944–950.e3. 78 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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