Pelagia Deriziotis

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

Brian J. O’Roak, Pelagia Deriziotis, Choli Lee et al. · Nature Genetics · 2011 · 1.2K citations · Full text

Neurodevelopmental Disorders, Genetic Disorder, Exome Sequencing +7

Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome

Mark Kristiansen, Pelagia Deriziotis, Derek E. Dimcheff et al. · Molecular Cell · 2007 · 254 citations · Full text

Natural Sciences, Proteasome, Molecular Biology +3

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

Simon Mead, Mark Poulter, James Uphill et al. · The Lancet Neurology · 2008 · 153 citations · Full text

De novo TBR1 mutations in sporadic autism disrupt protein functions

Pelagia Deriziotis, Brian J. O’Roak, Sarah A. Graham et al. · Nature Communications · 2014 · 120 citations · Full text

Syndromic Autism, Genetic Disorder, Genetics +6

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

Pelagia Deriziotis, Ralph André, David M. Smith et al. · The EMBO Journal · 2011 · 116 citations · Full text

Protein Secretion, Substrate Entry, Signal Transduction +12