Samuel Darko

5.9k total citations · 1 hit paper
35 papers, 2.0k citations indexed

About

Samuel Darko is a scholar working on Immunology, Virology and Infectious Diseases. According to data from OpenAlex, Samuel Darko has authored 35 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Immunology, 11 papers in Virology and 6 papers in Infectious Diseases. Recurrent topics in Samuel Darko's work include Immune Cell Function and Interaction (17 papers), T-cell and B-cell Immunology (16 papers) and HIV Research and Treatment (11 papers). Samuel Darko is often cited by papers focused on Immune Cell Function and Interaction (17 papers), T-cell and B-cell Immunology (16 papers) and HIV Research and Treatment (11 papers). Samuel Darko collaborates with scholars based in United States, United Kingdom and Canada. Samuel Darko's co-authors include Daniel C. Douek, Jorge R. Almeida, James Chih‐Hsin Yang, Mark E. Dudley, Eric Tran, Simon Turcotte, Alena Gros, Paul F. Robbins, John R. Wunderlich and Ken‐ichi Hanada and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Samuel Darko

34 papers receiving 2.0k citations

Hit Papers

PD-1 identifies the patient-specific CD8+ tumor-reactive ... 2014 2026 2018 2022 2014 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samuel Darko United States 18 1.4k 882 399 226 135 35 2.0k
Laura M. McLane United States 12 1.7k 1.2× 1.1k 1.3× 649 1.6× 100 0.4× 258 1.9× 13 2.6k
Grzegorz K. Przybylski Poland 25 1.6k 1.2× 625 0.7× 528 1.3× 97 0.4× 251 1.9× 75 2.7k
Dagmar Breitfeld Germany 5 2.7k 2.0× 1.0k 1.2× 405 1.0× 163 0.7× 191 1.4× 7 3.3k
Tao Zou United States 13 1.8k 1.3× 907 1.0× 436 1.1× 121 0.5× 294 2.2× 18 2.3k
Md. Zahidunnabi Dewan Japan 21 1.5k 1.0× 1.5k 1.7× 579 1.5× 156 0.7× 252 1.9× 34 2.8k
Tatyana Chtanova Australia 21 2.0k 1.4× 518 0.6× 471 1.2× 65 0.3× 252 1.9× 36 2.8k
Mohamed S. Abdel-Hakeem Egypt 14 1.8k 1.3× 1.3k 1.5× 509 1.3× 102 0.5× 368 2.7× 26 2.6k
Monika Srivastava Australia 7 2.4k 1.7× 354 0.4× 362 0.9× 114 0.5× 138 1.0× 9 2.8k
Isharat Yusuf United States 13 2.3k 1.7× 454 0.5× 493 1.2× 117 0.5× 165 1.2× 13 2.8k
Armanda Casrouge France 22 2.0k 1.5× 646 0.7× 410 1.0× 95 0.4× 394 2.9× 36 2.7k

Countries citing papers authored by Samuel Darko

Since Specialization
Citations

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

Fields of papers citing papers by Samuel Darko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuel Darko

This figure shows the co-authorship network connecting the top 25 collaborators of Samuel Darko. A scholar is included among the top collaborators of Samuel Darko 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 Samuel Darko. Samuel Darko 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.
Chaimongkol, Natthawan, Bianca M. Nagata, Samuel Darko, et al.. (2024). A non-human primate model for human norovirus infection. Nature Microbiology. 9(3). 776–786. 7 indexed citations
2.
Simpson, Jennifer, Carly E. Starke, Alexandra M. Ortiz, et al.. (2024). Immunotoxin-mediated depletion of Gag-specific CD8+ T cells undermines natural control of SIV. JCI Insight. 9(14). 1 indexed citations
3.
Schramm, Chaim A., Noemia S. Lima, Kristin L. Boswell, et al.. (2023). Interaction dynamics between innate and adaptive immune cells responding to SARS-CoV-2 vaccination in non-human primates. Nature Communications. 14(1). 7961–7961. 5 indexed citations
4.
Singh, Satya P., Hongwei H. Zhang, Jinguo Chen, et al.. (2023). Human CCR6+ Th Cells Show Both an Extended Stable Gradient of Th17 Activity and Imprinted Plasticity. The Journal of Immunology. 210(11). 1700–1716. 5 indexed citations
5.
Naing, Aung, Hirva Mamdani, Minal Barve, et al.. (2023). 652 NT-I7 (efineptakin alfa), a long-acting IL-7, in combination with pembrolizumab improves T cell fitness in heavily pretreated subjects with gastrointestinal tumors. SHILAP Revista de lepidopterología. A743–A743. 1 indexed citations
6.
Simpson, Jennifer, Carly E. Starke, Alexandra M. Ortiz, et al.. (2022). Multiple modes of antigen exposure induce clonotypically diverse epitope-specific CD8+ T cells across multiple tissues in nonhuman primates. PLoS Pathogens. 18(7). e1010611–e1010611. 5 indexed citations
7.
Guo, Shuang, Brian T. Luke, Amy R. Henry, et al.. (2022). HIV infected CD4+ T cell clones are more stable than uninfected clones during long-term antiretroviral therapy. PLoS Pathogens. 18(8). e1010726–e1010726. 5 indexed citations
8.
Wegrecki, Marcin, T. Praveena, Lijing Bu, et al.. (2021). The molecular assembly of the marsupial γμ T cell receptor defines a third T cell lineage. Science. 371(6536). 1383–1388. 16 indexed citations
9.
Padhan, Kartika, Eirini Moysi, Alessandra Noto, et al.. (2021). Acquisition of optimal TFH cell function is defined by specific molecular, positional, and TCR dynamic signatures. Proceedings of the National Academy of Sciences. 118(18). 14 indexed citations
10.
Quiniou, Valentin, Mikhail Shugay, Evgeniy S. Egorov, et al.. (2020). Benchmarking of T cell receptor repertoire profiling methods reveals large systematic biases. Nature Biotechnology. 39(2). 236–245. 77 indexed citations
11.
Wen, Ting, Bruce J. Aronow, Yrina Rochman, et al.. (2019). Single-cell RNA sequencing identifies inflammatory tissue T cells in eosinophilic esophagitis. Journal of Clinical Investigation. 129(5). 2014–2028. 140 indexed citations
12.
Hataye, Jason, Joseph P. Casazza, Katharine Best, et al.. (2019). Principles Governing Establishment versus Collapse of HIV-1 Cellular Spread. Cell Host & Microbe. 26(6). 748–763.e20. 28 indexed citations
13.
Wieland, Andreas, Alice O. Kamphorst, Volkan Adsay, et al.. (2018). T cell receptor sequencing of activated CD8 T cells in the blood identifies tumor-infiltrating clones that expand after PD-1 therapy and radiation in a melanoma patient. Cancer Immunology Immunotherapy. 67(11). 1767–1776. 49 indexed citations
14.
Ramesh, Akshaya, Samuel Darko, Axin Hua, et al.. (2017). Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies. Frontiers in Immunology. 8. 1407–1407. 43 indexed citations
15.
Covacu, Ruxandra, Merja Jaronen, Jorge R. Almeida, et al.. (2016). System-wide Analysis of the T Cell Response. Cell Reports. 14(11). 2733–2744. 31 indexed citations
16.
Yu, Xiaomin, Jorge R. Almeida, Samuel Darko, et al.. (2014). Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development. Journal of Allergy and Clinical Immunology. 133(4). 1109–1115.e14. 43 indexed citations
17.
Boswell, Kristin L., Robert Paris, Eli Boritz, et al.. (2014). Loss of Circulating CD4 T Cells with B Cell Helper Function during Chronic HIV Infection. PLoS Pathogens. 10(1). e1003853–e1003853. 140 indexed citations
18.
Hill, Brenna J., Patricia A. Darrah, Zachary Ende, et al.. (2014). Epitope Specificity Delimits the Functional Capabilities of Vaccine-Induced CD8 T Cell Populations. The Journal of Immunology. 193(11). 5626–5636. 7 indexed citations
19.
Ryberg, Henrik, Jiyan An, Samuel Darko, et al.. (2010). Discovery and verification of amyotrophic lateral sclerosis biomarkers by proteomics. Muscle & Nerve. 42(1). 104–111. 90 indexed citations
20.
Bonneh‐Barkay, Dafna, Stephanie J. Bissel, Kenneth N. Fish, et al.. (2008). YKL-40, a Marker of Simian Immunodeficiency Virus Encephalitis, Modulates the Biological Activity of Basic Fibroblast Growth Factor. American Journal Of Pathology. 173(1). 130–143. 102 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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