NIMH

Shining a light on night blindness

Vanderbilt researchers are studying how mutations in the receptor for light, rhodopsin, cause light blindness.

Visualizing data on network ‘maps’

The new web application NetGestalt will allow investigators to simultaneously visualize different types of data for the same gene – such as mutation, expression and modification.

time lapse traffic

Autism speeds motion perception

Children with autism spectrum disorder are better at perceiving the motion of certain objects than are typically developing children their age.

Biomarkers may offer autism clues

A combination of biomarkers may reveal new clues about causes of and potential interventions for autism.

Insights for neuroscience drug discovery

When discovering drugs for brain disorders, it’s important to test the candidates in multiple ways to avoid advancing those with restricted physiological effects.

New clue to ADHD

A rare genetic change adds support to the idea that altered dopamine signaling is a key risk factor for ADHD.

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