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Pandey GEMIN5 main 
Mutations Cause Rare Genetic Disease in Children

Mutations in a protein called GEMIN5 cause developmental delay and loss of coordination in young children.


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Kamboh NIA feature

Pitt Public Health geneticist to lead $10.7M study into the genetic underpinnings of Alzheimer's disease.


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ENIGMA Psychosis feature

"Sobering" results found in the largest study of brain scans in adolescents at risk for psychosis.

Pulm HTN blog feature
Pitt researchers describe new mechanism for pulmonary hypertension--study untangles the molecular process important for maintaining a healthy lining of the vessels supplying blood to the lungs.