Shale Dames

1.8k total citations · 1 hit paper
18 papers, 1.2k citations indexed

About

Shale Dames is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Shale Dames has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in Shale Dames's work include Advanced biosensing and bioanalysis techniques (5 papers), Molecular Biology Techniques and Applications (4 papers) and RNA modifications and cancer (3 papers). Shale Dames is often cited by papers focused on Advanced biosensing and bioanalysis techniques (5 papers), Molecular Biology Techniques and Applications (4 papers) and RNA modifications and cancer (3 papers). Shale Dames collaborates with scholars based in United States and Taiwan. Shale Dames's co-authors include Karl V. Voelkerding, Jacob Durtschi, Angelika Niemz, Eric Tan, Susan E. Mango, Matthew N. Alder, Bruce Irvine, Tanya M. Ferguson, Rebecca L. Margraf and Carl T. Wittwer and has published in prestigious journals such as Biochemistry, Genetics and Clinical Chemistry.

In The Last Decade

Shale Dames

18 papers receiving 1.1k citations

Hit Papers

Next-Generation Sequencing: From Basic Research to Diagno... 2009 2026 2014 2020 2009 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shale Dames United States 14 783 260 185 158 107 18 1.2k
Brian Libby United States 10 619 0.8× 235 0.9× 152 0.8× 88 0.6× 91 0.9× 11 959
Robert Palais United States 17 1.0k 1.3× 266 1.0× 157 0.8× 133 0.8× 221 2.1× 30 1.8k
Paul Ajuh United Kingdom 21 1.5k 1.9× 125 0.5× 56 0.3× 146 0.9× 114 1.1× 36 1.9k
Rhiannon K. Macrae United States 18 1.3k 1.7× 299 1.1× 64 0.3× 56 0.4× 179 1.7× 33 1.6k
Maarten H. Geurts Netherlands 12 1.5k 1.9× 353 1.4× 167 0.9× 92 0.6× 164 1.5× 18 1.9k
Roeland W. Dirks Netherlands 27 1.6k 2.0× 146 0.6× 56 0.3× 102 0.6× 108 1.0× 48 2.3k
Michael Liew United States 13 554 0.7× 190 0.7× 62 0.3× 60 0.4× 132 1.2× 21 1.1k
Palakodeti V.N. Dasaradhi India 9 813 1.0× 111 0.4× 42 0.2× 150 0.9× 203 1.9× 10 1.2k
Gregory J. Porreca United States 12 1.3k 1.7× 522 2.0× 171 0.9× 194 1.2× 223 2.1× 15 1.8k

Countries citing papers authored by Shale Dames

Since Specialization
Citations

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

Fields of papers citing papers by Shale Dames

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shale Dames

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

All Works

18 of 18 papers shown
1.
Brunelli, Luca, Steven B. Bleyl, Christine E. Miller, et al.. (2019). Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants. Molecular Genetics & Genomic Medicine. 7(7). e00796–e00796. 27 indexed citations
2.
Dames, Shale, Karen Eilbeck, & Rong Mao. (2015). A High-Throughput Next-Generation Sequencing Assay for the Mitochondrial Genome. Methods in molecular biology. 1264. 77–88. 14 indexed citations
3.
Hall, Deborah J., et al.. (2015). BCAP 31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing. Movement Disorders Clinical Practice. 3(2). 197–199. 7 indexed citations
4.
Dames, Shale, et al.. (2013). The Development of Next-Generation Sequencing Assays for the Mitochondrial Genome and 108 Nuclear Genes Associated with Mitochondrial Disorders. Journal of Molecular Diagnostics. 15(4). 526–534. 40 indexed citations
5.
Margraf, Rebecca L., et al.. (2011). Variant identification in multi-sample pools by illumina genome analyzer sequencing.. PubMed. 22(2). 74–84. 13 indexed citations
6.
Voelkerding, Karl V., Shale Dames, & Jacob Durtschi. (2010). Next Generation Sequencing for Clinical Diagnostics-Principles and Application to Targeted Resequencing for Hypertrophic Cardiomyopathy. Journal of Molecular Diagnostics. 12(5). 539–551. 87 indexed citations
7.
Dames, Shale, et al.. (2010). Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.. PubMed. 21(2). 73–80. 25 indexed citations
8.
Margraf, Rebecca L., et al.. (2010). Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database development.. PubMed. 21(3). 126–40. 9 indexed citations
9.
Voelkerding, Karl V., Shale Dames, & Jacob Durtschi. (2009). Next-Generation Sequencing: From Basic Research to Diagnostics. Clinical Chemistry. 55(4). 641–658. 500 indexed citations breakdown →
10.
Tan, Eric, Shale Dames, Tanya M. Ferguson, et al.. (2008). Specific versus Nonspecific Isothermal DNA Amplification through Thermophilic Polymerase and Nicking Enzyme Activities. Biochemistry. 47(38). 9987–9999. 159 indexed citations
11.
Dames, Shale, et al.. (2007). Characterization of Aberrant Melting Peaks in Unlabeled Probe Assays. Journal of Molecular Diagnostics. 9(3). 290–296. 38 indexed citations
12.
Liew, Michael, Michael Seipp, Jacob Durtschi, et al.. (2007). Closed-Tube SNP Genotyping Without Labeled Probes/A Comparison Between Unlabeled Probe and Amplicon Melting. American Journal of Clinical Pathology. 127(3). 341–348. 1 indexed citations
13.
Liew, Michael, Michael Seipp, Jacob Durtschi, et al.. (2007). Closed-Tube SNP Genotyping Without Labeled Probes. American Journal of Clinical Pathology. 127(3). 341–348. 45 indexed citations
14.
Tan, Eric, et al.. (2007). Isothermal DNA Amplification with Gold Nanosphere-Based Visual Colorimetric Readout for Herpes Simplex Virus Detection. Clinical Chemistry. 53(11). 2017–2020. 47 indexed citations
15.
Dames, Shale, et al.. (2007). Unlabeled Probes for the Detection and Typing of Herpes Simplex Virus. Clinical Chemistry. 53(10). 1847–1854. 19 indexed citations
16.
Dames, Shale, L Kathryn Bromley, Mark G. Herrmann, et al.. (2006). A Single-Tube Nucleic Acid Extraction, Amplification, and Detection Method Using Aluminum Oxide. Journal of Molecular Diagnostics. 8(1). 16–21. 13 indexed citations
17.
Alder, Matthew N., et al.. (2003). Gene silencing in Caenorhabditis elegans by transitive RNA interference. RNA. 9(1). 25–32. 89 indexed citations
18.
Link, Christopher D., et al.. (1992). Characterization of Caenorhabditis elegans lectin-binding mutants.. Genetics. 131(4). 867–881. 54 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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