Shannon Callen

3.0k total citations
52 papers, 2.4k citations indexed

About

Shannon Callen is a scholar working on Virology, Neurology and Molecular Biology. According to data from OpenAlex, Shannon Callen has authored 52 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Virology, 23 papers in Neurology and 16 papers in Molecular Biology. Recurrent topics in Shannon Callen's work include HIV Research and Treatment (27 papers), Neuroinflammation and Neurodegeneration Mechanisms (23 papers) and Tryptophan and brain disorders (9 papers). Shannon Callen is often cited by papers focused on HIV Research and Treatment (27 papers), Neuroinflammation and Neurodegeneration Mechanisms (23 papers) and Tryptophan and brain disorders (9 papers). Shannon Callen collaborates with scholars based in United States, China and India. Shannon Callen's co-authors include Shilpa Buch, Ke Liao, Palsamy Periyasamy, Ming‐Lei Guo, Fang Niu, Lu Yang, Y.-S. Lau, G.E. Meredith, Susan Totterdell and Honghong Yao and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Shannon Callen

52 papers receiving 2.4k citations

Peers

Shannon Callen
Ke Liao United States
Huangui Xiong United States
Pamela E. Knapp United States
Jerel Adam Fields United States
Alessia Bachis United States
Avi Nath United States
Raghava Potula United States
Étienne Jacotot France
Evan B. Dreyer United States
Sunhee C. Lee United States
Ke Liao United States
Shannon Callen
Citations per year, relative to Shannon Callen Shannon Callen (= 1×) peers Ke Liao

Countries citing papers authored by Shannon Callen

Since Specialization
Citations

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

Fields of papers citing papers by Shannon Callen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shannon Callen

This figure shows the co-authorship network connecting the top 25 collaborators of Shannon Callen. A scholar is included among the top collaborators of Shannon Callen 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 Shannon Callen. Shannon Callen 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.
Callen, Shannon, et al.. (2025). Single-Cell RNA-Seq Uncovers Robust Glial Cell Transcriptional Changes in Methamphetamine-Administered Mice. International Journal of Molecular Sciences. 26(2). 649–649. 2 indexed citations
2.
Ray, Sudipta, Dinesh Y. Gawande, Shashank M. Dravid, et al.. (2024). Neuropathogenic role of astrocyte‐derived extracellular vesicles in HIV‐associated neurocognitive disorders. Journal of Extracellular Vesicles. 13(4). e12439–e12439. 8 indexed citations
3.
Sil, Susmita, Shannon Callen, Hitendra S. Chand, et al.. (2023). Inflammation-Associated Lung Tissue Remodeling and Fibrosis in Morphine-Dependent SIV-Infected Macaques. American Journal Of Pathology. 193(4). 380–391. 4 indexed citations
4.
Kutchy, Naseer A., Amelia Palermo, Rong Ma, et al.. (2023). Changes in Plasma Metabolic Signature upon Acute and Chronic Morphine Administration in Morphine-Tolerant Mice. Metabolites. 13(3). 434–434. 5 indexed citations
5.
Fox, Howard S., Meng Niu, Brenda Morsey, et al.. (2022). Morphine suppresses peripheral responses and transforms brain myeloid gene expression to favor neuropathogenesis in SIV infection. Frontiers in Immunology. 13. 1012884–1012884. 10 indexed citations
6.
Chivero, Ernest T., Susmita Sil, Seema Singh, et al.. (2021). Protective Role of Lactobacillus rhamnosus Probiotic in Reversing Cocaine-Induced Oxidative Stress, Glial Activation and Locomotion in Mice. Journal of Neuroimmune Pharmacology. 17(1-2). 62–75. 13 indexed citations
7.
Sil, Susmita, Guoku Hu, Ke Liao, et al.. (2020). HIV-1 Tat-mediated astrocytic amyloidosis involves the HIF-1α/lncRNA BACE1-AS axis. PLoS Biology. 18(5). e3000660–e3000660. 29 indexed citations
8.
Chand, Hitendra S., Rodrigo Vazquez Guillamet, Christopher M. Royer, et al.. (2018). Cigarette smoke and HIV synergistically affect lung pathology in cynomolgus macaques. Journal of Clinical Investigation. 128(12). 5428–5433. 21 indexed citations
9.
Periyasamy, Palsamy, Annadurai Thangaraj, Ming‐Lei Guo, et al.. (2018). Epigenetic Promoter DNA Methylation of miR-124 Promotes HIV-1 Tat-Mediated Microglial Activation via MECP2-STAT3 Axis. Journal of Neuroscience. 38(23). 5367–5383. 52 indexed citations
10.
Hu, Guoku, Ke Liao, Fang Niu, et al.. (2018). Astrocyte EV-Induced lincRNA-Cox2 Regulates Microglial Phagocytosis: Implications for Morphine-Mediated Neurodegeneration. Molecular Therapy — Nucleic Acids. 13. 450–463. 90 indexed citations
11.
Chivero, Ernest T., Ming‐Lei Guo, Palsamy Periyasamy, et al.. (2017). HIV-1 Tat Primes and Activates Microglial NLRP3 Inflammasome-Mediated Neuroinflammation. Journal of Neuroscience. 37(13). 3599–3609. 162 indexed citations
12.
Kevadiya, Bhavesh D., Prasanta K. Dash, Balasrinivasa R. Sajja, et al.. (2017). Multimodal Theranostic Nanoformulations Permit Magnetic Resonance Bioimaging of Antiretroviral Drug Particle Tissue-Cell Biodistribution. Theranostics. 8(1). 256–276. 40 indexed citations
13.
Liao, Ke, Ming‐Lei Guo, Fang Niu, et al.. (2016). Cocaine-mediated induction of microglial activation involves the ER stress-TLR2 axis. Journal of Neuroinflammation. 13(1). 33–33. 98 indexed citations
14.
Cai, Yu, Lu Yang, Shannon Callen, & Shilpa Buch. (2016). Multiple Faceted Roles of Cocaine in Potentiation of HAND. Current HIV Research. 14(5). 412–416. 23 indexed citations
15.
Marcario, Joanne K., Gurudutt Pendyala, Kandace Fleming, et al.. (2016). Effects of Morphine on Behavioral Task Performance in SIV-Infected Rhesus Macaques. Journal of Neuroimmune Pharmacology. 11(2). 348–357. 8 indexed citations
16.
Villeneuve, Lance M., Phillip R. Purnell, Kelly L. Stauch, et al.. (2016). HIV-1 transgenic rats display mitochondrial abnormalities consistent with abnormal energy generation and distribution. Journal of NeuroVirology. 22(5). 564–574. 31 indexed citations
17.
Sharma, Madhulika, Shannon Callen, Da Zhang, et al.. (2010). Activation of Notch signaling pathway in HIV-associated nephropathy. AIDS. 24(14). 2161–2170. 60 indexed citations
18.
Yao, Honghong, Fuwang Peng, Navneet K. Dhillon, et al.. (2009). Involvement of TRPC Channels in CCL2-Mediated Neuroprotection against Tat Toxicity. Journal of Neuroscience. 29(6). 1657–1669. 63 indexed citations
19.
Dhillon, Navneet K., Xuhui Zhu, Fuwang Peng, et al.. (2008). Molecular mechanism(s) involved in the synergistic induction of CXCL10 by human immunodeficiency virus type 1 Tat and interferon-γ in macrophages. Journal of NeuroVirology. 14(3). 196–204. 16 indexed citations
20.
Dhillon, Navneet K., Fuwang Peng, Sirosh Bokhari, et al.. (2007). Cocaine-mediated Alteration in Tight Junction Protein Expression and Modulation of CCL2/CCR2 Axis Across the Blood-Brain Barrier: Implications for HIV-Dementia. Journal of Neuroimmune Pharmacology. 3(1). 52–56. 65 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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