People from isolated parts of the U.K. could have variations in their genetic code that increase their chance of developing certain diseases, a study suggests. The most genetically distinct ...

Model predicts effect of mutations on sequences up to 1 million base pairs in length and is adept at tackling complex ...

New research published in Scientific Reports provides evidence that the path from genetic predisposition to general ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized cutting-edge findings on Prader-Willi syndrome (PWS), revealing how this complex ...

Emma Broadbent had just turned one when her parents were told that, despite months of tests, physicians still had no explanation for her condition. Emma’s brain was not developing myelin, the fatty ...

Genome assemblies from 65 individuals, representing a variety of the world’s populations, are advancing the scientific exploration of complex genetic structural variation. Structural variations are ...

St. Jude Children's Research Hospital investigators have discovered inherited genetic variations that are associated with rapid hearing loss in young cancer patients treated with the drug cisplatin.

India's largest-ever genomic study has identified genetic variants unique to the country, marking a crucial step in closing a longstanding gap in global genomics research. The preliminary findings, ...