Papers

2

Total Citations

53

H-Index

2

About

Robin Coope is a molecular diagnostics researcher whose work bridges clinical genomics and pandemic response. Their key contributions lie in hereditary cancer testing and high-throughput infectious disease detection. Coope’s most impactful work, a 2013 study on a clinically validated second-generation sequencing assay for hereditary *BRCA1* and *BRCA2* mutations (42 citations), established a robust diagnostic framework for identifying cancer-predisposing genetic variants. This assay has been instrumental in enabling accurate, scalable screening for patients at risk of breast and ovarian cancers. During the COVID-19 pandemic, Coope pivoted to address critical testing shortages. Their 2023 study on extraction-free SARS-CoV-2 detection from saline gargle samples using the Hamilton STARlet liquid handler (11 citations) demonstrated a rapid, cost-effective method that bypassed reagent bottlenecks. By optimizing self-collected samples and multiplex PCR workflows, this work directly supported high-throughput clinical testing, alleviating strain on overwhelmed laboratories. Coope’s research exemplifies translational impact—from advancing precision oncology to enabling agile pandemic diagnostics—showcasing a career dedicated to making molecular testing more accessible, efficient, and clinically actionable.

Research Focus

Key Achievements

2
H-Index
2
Papers
53
Total Citations
27
Avg Citations/Paper
🏆 Most Cited Paper
A Clinically Validated Diagnostic Second-Generation Sequencing Assay for Detection of Hereditary BRCA1 and BRCA2 Mutations
42 citations · 2013
📈 Most Prolific Year: 2013 (1 Papers)
🤝 Key Collaborators: 27
🏛 Institutions: BC Cancer Agency, Canada's Michael Smith Genome Sciences Centre

Top Papers

  1. 1
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Key Collaborators

Contact & Links

Available for collaboration
Content generated · 12 days ago