Pelagia Deriziotis

Disease-associated prion protein oligomers inhibit the 26S proteasome.

Prions and the proteasome.

Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry.

Neurogenomics of speech and language disorders: the road ahead.