Researchers have uncovered a surprising mechanism by which a single genetic mutation in the BCL11B gene causes both immune dysfunction and brain development issues.

A seminal study has uncovered a new genetic cause of neurodevelopmental disorders (NDDs). The discovery offers both closure and hope to potentially thousands of families worldwide who have long been ...

A new multicenter study by researchers at the Icahn School of Medicine at Mount Sinai, in collaboration with the National Cancer Institute-funded Clinical Proteomic Tumor Analysis Consortium (CPTAC) ...

A seminal study by researchers at the Icahn School of Medicine at Mount Sinai and their collaborators in the United Kingdom, ...

Researchers from the Department of Pathology, School of Clinical Medicine at the LKS Faculty of Medicine of the University of ...

A new multicenter study by researchers at the Icahn School of Medicine at Mount Sinai, in collaboration with the Clinical Proteomic Tumor Analysis Consortium (CPTAC) and colleagues around the world, ...

GenomeIndia project publishes preliminary findings from sequencing 10,000 Indian genomes, highlighting unique genetic ...

A major new study has revealed that the genes we inherit at birth play a much larger role in cancer than previously ...

By analyzing the flowerpot snake's unique genome, scientists are uncovering how the tiny reptile repairs its DNA and prevents harmful mutations. The findings provides valuable insights into genetic ...

The disease has an early onset form, which affects patients before they reach age 50, and is due to genetic mutations; mutations that alter a protein called PINK1 were identified many years ago as a ...

Horizontal gene transfer (HGT) is the movement of genetic material from one organism to another. In this article, we will discuss what HGT is, how it is used in research, how to detect it and the ...

A new study analyzes the evolutionary history of 11 deep-sea species from environments stretching from the central Indian ...