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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Genetic discoveries are leading to new treatments for alopecia areata.