Samantha Cooper

1.3k total citations
20 papers, 940 citations indexed

About

Samantha Cooper is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Samantha Cooper has authored 20 papers receiving a total of 940 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Samantha Cooper's work include Cancer Genomics and Diagnostics (7 papers), CRISPR and Genetic Engineering (5 papers) and Estrogen and related hormone effects (4 papers). Samantha Cooper is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), CRISPR and Genetic Engineering (5 papers) and Estrogen and related hormone effects (4 papers). Samantha Cooper collaborates with scholars based in United States, Germany and Switzerland. Samantha Cooper's co-authors include Keith R. Yamamoto, George Karlin‐Neumann, Ashley Acevedo, Adam S. Lauring, Raul Andino, Amanda H. Chan, Steven J. Mayerl, Jennifer R. Berman, Bin Zhang and Bruce R. Conklin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Samantha Cooper

20 papers receiving 926 citations

Peers

Samantha Cooper
Xueqiu Lin United States
Brian Florence United States
W M Lee United States
Osman V. Patel United States
Samantha Cooper
Citations per year, relative to Samantha Cooper Samantha Cooper (= 1×) peers A. Gordon Robertson

Countries citing papers authored by Samantha Cooper

Since Specialization
Citations

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

Fields of papers citing papers by Samantha Cooper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samantha Cooper

This figure shows the co-authorship network connecting the top 25 collaborators of Samantha Cooper. A scholar is included among the top collaborators of Samantha Cooper 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 Samantha Cooper. Samantha Cooper 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.
Chang, Gregory, Samantha Cooper, Yongzhao Shao, et al.. (2018). Development of Novel Mutation-Specific Droplet Digital PCR Assays Detecting TERT Promoter Mutations in Tumor and Plasma Samples. Journal of Molecular Diagnostics. 21(2). 274–285. 41 indexed citations
2.
Mellert, Hestia, Trudi Foreman, Leisa Jackson, et al.. (2017). Development and Clinical Utility of a Blood-Based Test Service for the Rapid Identification of Actionable Mutations in Non–Small Cell Lung Carcinoma. Journal of Molecular Diagnostics. 19(3). 404–416. 29 indexed citations
3.
Mellert, Hestia, et al.. (2017). Abstract 1784: Early feasibility and development of multiplexed, single-reaction assays for ALK, ROS1 and RET novel ddPCR RNA fusions. Cancer Research. 77(13_Supplement). 1784–1784. 1 indexed citations
5.
Boot, Erik, Nancy J. Butcher, Samantha Cooper, et al.. (2016). Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine. 19(2). 204–208. 55 indexed citations
6.
Miyaoka, Yuichiro, Jennifer R. Berman, Samantha Cooper, et al.. (2016). Systematic quantification of HDR and NHEJ reveals effects of locus, nuclease, and cell type on genome-editing. Scientific Reports. 6(1). 23549–23549. 183 indexed citations
7.
Love, Michael I., Matthew R. Huska, Marcel Jurk, et al.. (2016). Role of the chromatin landscape and sequence in determining cell type-specific genomic glucocorticoid receptor binding and gene regulation. Nucleic Acids Research. 45(4). 1805–1819. 37 indexed citations
8.
Regan, John F., Nolan Kamitaki, Tina C. Legler, et al.. (2015). A Rapid Molecular Approach for Chromosomal Phasing. PLoS ONE. 10(3). e0118270–e0118270. 48 indexed citations
9.
Yang, Wei, Dawne N. Shelton, Jennifer R. Berman, et al.. (2015). Droplet Digital™ PCR: Multiplex Detection of KRAS Mutations in Formalin-Fixed, Paraffin-Embedded Colorectal Cancer Samples. BioTechniques. 58(5). 270–271. 1 indexed citations
10.
Yang, Wei, Dawne N. Shelton, Jennifer R. Berman, et al.. (2015). Droplet Digital™ PCR: Multiplex Detection of KRAS Mutations in Formalin-Fixed, Paraffin-Embedded Colorectal Cancer Samples. BioTechniques. 58(4). 205–206. 2 indexed citations
11.
Halkias, Joanna, Heather J. Melichar, Jenny O. Ross, et al.. (2013). Opposing chemokine gradients control human thymocyte migration in situ. Journal of Clinical Investigation. 123(5). 2131–2142. 51 indexed citations
12.
Chen, Sheng‐hong, et al.. (2013). Incoherent feed-forward regulatory logic underpinning glucocorticoid receptor action. Proceedings of the National Academy of Sciences. 110(5). 1964–1969. 25 indexed citations
13.
Thomas‐Chollier, Morgane, Lisa Watson, Samantha Cooper, et al.. (2013). A naturally occuring insertion of a single amino acid rewires transcriptional regulation by glucocorticoid receptor isoforms. Proceedings of the National Academy of Sciences. 110(44). 17826–17831. 51 indexed citations
14.
Cann, Gordon, Zulfiqar Gulzar, Samantha Cooper, et al.. (2012). mRNA-Seq of Single Prostate Cancer Circulating Tumor Cells Reveals Recapitulation of Gene Expression and Pathways Found in Prostate Cancer. PLoS ONE. 7(11). e49144–e49144. 107 indexed citations
15.
Lauring, Adam S., Ashley Acevedo, Samantha Cooper, & Raul Andino. (2012). Codon Usage Determines the Mutational Robustness, Evolutionary Capacity, and Virulence of an RNA Virus. Cell Host & Microbe. 12(5). 623–632. 105 indexed citations
16.
Holdorf, Meghan, Samantha Cooper, Keith R. Yamamoto, & JJ L. Miranda. (2011). Occupancy of chromatin organizers in the Epstein–Barr virus genome. Virology. 415(1). 1–5. 35 indexed citations
17.
Cooper, Samantha. (2010). Glucocorticoid receptor DNA occupancy and transcriptional regulation across cell types. eScholarship (California Digital Library). 2 indexed citations
18.
So, Alex Yick‐Lun, et al.. (2008). Conservation analysis predicts in vivo occupancy of glucocorticoid receptor-binding sequences at glucocorticoid-induced genes. Proceedings of the National Academy of Sciences. 105(15). 5745–5749. 74 indexed citations
19.
Taubert, Stefan, Malene Hansen, Marc R. Van Gilst, Samantha Cooper, & Keith R. Yamamoto. (2008). The Mediator Subunit MDT-15 Confers Metabolic Adaptation to Ingested Material. PLoS Genetics. 4(2). e1000021–e1000021. 90 indexed citations
20.
Taubert, Stefan, Malene Plejdrup Hansen, Marc R. Van Gilst, Samantha Cooper, & Keith R. Yamamoto. (2005). The Mediator Subunit MDT-15 Confers Metabolic Adaptation to Ingested Material. PLoS Genetics. preprint(2008). e40–e40. 2 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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