Rachel Brouwer (assistant professor CNCR - CTG) recently published her work in Nature Neuroscience. The study is a large-scale collaboration of research groups worldwide and identifies genetic variants that are associated with the speed of structural brain changes over time.
We bike together to raise money for research towards new treatments for the rare disorder STXBP1 Encephalopathy!
An international consortium analysed DNA from more than 300,000 people with and without the disorder. The SYNGO consortium, coordinated by CNCR, performed the analyses of synaptic genes. The study is published in Nature on April 11th