Ewart de Bruijn

Hartwig Medical Foundation

Papers

1

Total Citations

86

H-Index

1

About

Ewart de Bruijn is a leading figure in the field of cancer genomics, with a primary focus on the clinical translation of whole genome sequencing (WGS) for oncology diagnostics. His most impactful work centers on demonstrating the feasibility and superiority of using WGS as a comprehensive, single-test alternative to traditional multi-biomarker assays. In his landmark 2021 study, which has garnered 86 citations, de Bruijn provided critical clinical validation for applying WGS to fresh-frozen tumor tissue and matched blood samples. This work directly addresses the pressing need for a more complete genetic tumor test, especially given the increasing prevalence of small biopsies and the growing number of actionable biomarkers. By advocating for an all-inclusive genomic approach, de Bruijn’s contributions are helping to streamline cancer diagnostics, reduce turnaround times, and improve the detection of clinically relevant mutations. His research is pivotal for moving precision oncology toward more efficient, cost-effective, and comprehensive testing paradigms, solidifying his reputation as a key translator of genomic technology into routine clinical practice.

Research Focus

Key Achievements

1
H-Index
1
Papers
86
Total Citations
86
Avg Citations/Paper
🏆 Most Cited Paper
Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics
86 citations · 2021
📈 Most Prolific Year: 2021 (1 Papers)
🤝 Key Collaborators: 18
🏛 Institutions: Hartwig Medical Foundation

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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