C. Backhouse

University of Alberta

Papers

2

Total Citations

42

H-Index

2

About

C. Backhouse is a pioneer in the development of microfluidic technologies for genetic analysis, with a primary focus on integrating complex biochemical assays onto miniaturized chip-based platforms. Their major contributions lie in advancing lab-on-a-chip systems for high-sensitivity mutation detection and DNA analysis. Notably, Backhouse’s 2004 work on integrating heteroduplex analysis with restriction fragment length polymorphism on an electrophoresis microchip for detecting hereditary haemochromatosis—cited 31 times—demonstrated a groundbreaking method for identifying subtle genetic variations like single nucleotide polymorphisms. This approach combined enzymatic digestion, heteroduplex analysis, and electrophoretic sizing in a single microfluidic device, significantly enhancing diagnostic efficiency. Additionally, their 2005 study on analyzing mitochondrial DNA within microfluidic systems, with 11 citations, expanded the application of these technologies to mitochondrial genetics, offering new avenues for studying inherited disorders and aging. Backhouse’s work has been instrumental in making genetic testing more rapid, portable, and accessible, laying foundational techniques for modern point-of-care diagnostics. Their innovative integration of multiple analytical steps onto a chip continues to influence researchers in microfluidics and molecular biology.

Research Focus

Key Achievements

2
H-Index
2
Papers
42
Total Citations
21
Avg Citations/Paper
🏆 Most Cited Paper
Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis
31 citations · 2004
📈 Most Prolific Year: 2004 (1 Papers)
🤝 Key Collaborators: 9
🏛 Institutions: University of Alberta

Top Papers

  1. 1
  2. 2

Key Collaborators

Contact & Links

Available for collaboration
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