Chris Cassa
Computational geneticist working on rare variant interpretation, population-scale genomic data, and translational genomics.
Assistant Professor of Medicine
Brigham & Women’s Hospital / Harvard Medical School
Associate Member
Broad Institute
Lecturer
MIT Center for Transportation & Logistics
Research
My research focuses on using population-scale genomic datasets to improve interpretation of rare variants and understand the genetic basis of disease.
Key areas include:
- Variant interpretation using population evidence
- Rare disease genetics
- Familial hypercholesterolemia and lipid genetics
- Large-scale biobank analysis
Publications
Selected publications and full publication list.
Projects
Research projects, tools, and datasets.
→ Projects
Resources
Tools, datasets, and research materials.
Teaching
Courses and educational materials.
→ Teaching
Contact
→ Contact