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CASE STUDY · YRI FELLOW

Decoded genetic variants behind a hidden heart disease, accepted at an IEEE conference

Arrhythmogenic cardiomyopathy is an inherited heart disease that can cause sudden cardiac death in young, healthy people. Ajwa studied missense variants in the five desmosomal genes linked to it, interpreting each variant by where it sits on the protein interfaces that hold heart cells together, to help tell disease-causing mutations from harmless ones.

FIELDGenetics & Cardiology
RESULTFirst-author paper accepted at an IEEE conference
VENUEIEEE, 2026
BEFORE THE FELLOWSHIP

An 11th grader at Highland Park High School interested in genetics and medicine.

AFTER

First author of a structural study of genetic variants in arrhythmogenic cardiomyopathy, accepted at an IEEE conference.

THE LEDGER
01First-author paper accepted at an IEEE conference
02Analyzed variants across five desmosomal genes
03Interface-aware approach to classifying disease-causing mutations
NEXT CASE STUDYAriham Jain, First-author paper accepted at an IEEE conference

Every case study starts with one application.

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