Citation:
Danielle Braun, Malka Gorfine, Hormuzd A Katki, Argyrios Ziogas, Hoda Anton-Culver, and Giovanni Parmigiani. 2014. “Extending mendelian risk prediction models to handle misreported family history”.
BayesMendel Lab
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Recent Publications
- Clinical implications of conflicting variant interpretations in the cancer genetics clinic
- Bayesian Meta-Analysis of Penetrance for Cancer Risk
- Variant-specific Mendelian Risk Prediction Model
- MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome
- SNIP: An adaptation of sorted neighborhood methods for deduplicating pedigree data
- Meta-Analysis of Breast Cancer Risk for Individuals with PALB2 Pathogenic Variants
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