brain disease

Researchers identified somatic KRAS mutations in affected tissue from more than 60 percent of people with sporadic arteriovenous malformations of the brain.

A pair of papers has linked mutations in the DCC gene to agenesis of the corpus callosum as well as to a new syndrome.

A study of twins, unrelated individuals, and post-mortem brain samples suggests genetic factors contribute to cortical features and functions in humans.

Using a modified single-nuclei RNA sequencing pipeline adapted to deal with postmortem tissue, researchers have uncovered 16 neuronal subtypes.

NEW YORK (GenomeWeb News) – Agilent Technologies and South Korea's Daegu Gyeongbuk Institute of Science and Technology (DGIST) today announced a collaboration focused on neurometabolomics research.

A new analysis examines the gender gap among paper authors in the sciences and says it may take decades or more to close.

Researchers have uncovered signals of selection that may enable the Bajau people to free five hundreds of feet deep, Reuters reports.

In Science this week: paternally inherited cis-regulatory structural variants in autism, and more.

A new report outlines issues facing the implementation of personalized medicine in the UK, the Independent reports.