A single mutation in one gene can impair inhibitory signaling in the brain and cause multiple types of seizures and behavioral abnormalities.

Biochemistry investigators at Vanderbilt have discovered a new DNA repair mechanism that prevents gene mutations during DNA replication.

The identification of a genetic culprit for hypoplastic left heart syndrome could lead to new treatments for the condition.

A newly identified genetic risk factor for heart block after surgery may help guide the course of postoperative care.

Researchers at Vanderbilt have identified what may be a genetic “smoking gun” for autism spectrum disorder (ASD) — a mutation in the gene for the critical neuronal protein CaMKII.

Vanderbilt researchers developed a new algorithm to find clinically targetable gene rearrangements in cancers.

A new report released this week raises questions about “gene drives,” a biological process that can profoundly and rapidly alter the characteristics of entire species.