Last Updated: 09/26/2026
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Found 30 publications
Benchmarking Interpretability in Healthcare Using Pattern Discovery and Disentanglement.
Journal: Bioengineering (Basel, Switzerland)
Published: February 10, 2025
Myelodysplastic syndrome diagnosed by genetic testing for hereditary cancer: a case report.
Journal: NPJ genomic medicine
Published: August 16, 2024
Improving Access to Hereditary Testing in Pancreatic Ductal Carcinoma.
Journal: JCO precision oncology
Published: August 05, 2024
An Unsupervised Error Detection Methodology for Detecting Mislabels in Healthcare Analytics.
Journal: Bioengineering (Basel, Switzerland)
Published: June 30, 2024
Variant classification changes over time in the clinical molecular diagnostic laboratory setting.
Journal: Journal of medical genetics
Published: November 20, 2023
Validation of low-pass genome sequencing for prenatal diagnosis.
Journal: Prenatal diagnosis
Published: August 11, 2023
Improving RNA Fusion Call Confidence and Reliability in Molecular Diagnostic Testing.
Journal: The Journal of molecular diagnostics : JMD
Published: November 11, 2022
Theory and rationale of interpretable all-in-one pattern discovery and disentanglement system.
Journal: NPJ digital medicine
Published: August 08, 2022
Correction to: Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario.
Journal: Journal of cancer research and clinical oncology
Published: September 25, 2020
Tumor BRCA Testing in High Grade Serous Carcinoma: Mutation Rates and Optimal Tissue Requirements.
Journal: Cancers
Published: September 04, 2020
Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario.
Journal: Journal of cancer research and clinical oncology
Published: July 20, 2020
Explanation and prediction of clinical data with imbalanced class distribution based on pattern discovery and disentanglement.
Journal: BMC medical informatics and decision making
Published: May 08, 2020
Last Updated: 09/26/2026