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CFH gene triggers the eye disease in white patients but not Black patients
Systems genetics approach sets stage for lab testing of simvastatin and other candidate drugs
Consortium is uncovering risk factors that spur disease development in an understudied group
New Cleveland Clinic fellowship fosters expertise in the genetics of epilepsy
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Genome-wide association study identifies potential risk loci in a little-studied population
Association of the COMT gene Val/Met polymorphism and suicidality in children and adolescents
Goal is to pinpoint therapeutic targets, improve risk prediction in an understudied population
Some of the first epidemiologic insights into brain disorders caused by de novo variants
Largest study of epilepsy genetics identifies polygenic risk score
New podcast episode ranges from genetics insights to patient selection for tafamidis
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